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Copanlisib in the Treatment of Relapsed Follicular Lymphoma: Utility and Experience from the Clinic

Authors Chauhan AF, Cheson BD 

Received 3 October 2020

Accepted for publication 30 December 2020

Published 25 January 2021 Volume 2021:13 Pages 677—692


Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 2

Editor who approved publication: Dr Antonella D'Anneo

Video abstract presented by Ayushi F Chauhan.

Views: 106

Ayushi F Chauhan,1 Bruce D Cheson2

1Department of Hematology and Oncology, Lombardi Comprehensive Cancer Center, MedStar Georgetown University Hospital, Washington DC, USA; 2Scientific Advisory Board, Lymphoma Research Foundation, Washington, DC, USA

Correspondence: Ayushi F Chauhan Email [email protected]

Abstract: The phosphatidylinositol-3-kinase (PI3K) pathway is ubiquitous to multiple cellular processes and is intricately implicated in lymphomagenesis. The development of PI3K inhibitors has broadened treatment options for relapsed and/or refractory follicular lymphoma (FL) and currently three PI3K inhibitors have been approved in the third-line setting for FL, including idelalisib (oral), duvelisib (oral), and copanlisib (intravenous), with other agents under investigation. In this review, we discuss the clinical advance of copanlisib through preclinical to Phase III trials, its unique cellular targets and side effect profile that have poised it as a safer and equally efficacious option when compared to the older-generation oral PI3Kis, and its utility to the clinician as part of the therapeutic armamentarium for relapsed and/or refractory FL.

Keywords: copanlisib, follicular lymphoma, PI3K inhibitors


Follicular lymphoma (FL) is an indolent non-Hodgkin lymphoma (NHL) derived from germinal center B-cells. Significant improvements in outcomes have been attained in the rituximab era such that most patients will experience a prolonged remission after frontline therapy. However, FL is still considered an incurable disease in most patients and exhibits a relapsing, remitting course. Thus, the majority of patients will be exposed to multiple lines of therapy during their lifetime. Therapies used to treat progressive disease have mostly utilized anti-CD20 monoclonal antibodies (class I and II), with or without cytotoxic chemotherapy, or with lenalidomide.1 Also, survival outcomes progressively decline with subsequent lines of therapy.2 The unmet need for additional tolerable and effective treatment options in subsequent relapses has led to the development of targeted agents, amongst them phosphatidylinositol-3-kinase (PI3K) pathway inhibitors.

Background and Rationale

FL can be considered to possess three pathobiological targets: the cell surface, the intracellular compartment, and the tumor microenvironment. The PI3K pathway mediates signaling in each of these domains and has prognostic implications. PI3Ks belong to a conserved family of lipid kinases, activated by growth factor receptor tyrosine kinases which, in turn, lead to the recruitment and stimulation of a wide range of downstream, including the serine-threonine protein kinase Akt and mechanistic target of rapamycin (mTOR). Phosphatase and tensin homolog (PTEN) is a notable negative regulator of this pathway. PI3K pathway is at the epicenter of an extraordinarily broad range of cellular regulatory processes, including cell growth and proliferation, metabolism, migration, and secretion and upregulation of PI3K signaling has been considered a hallmark of cancer.3–5

Human cells express 3 classes of PI3K enzymes, of which class I are implicated in lymphoid malignancies and pertinent to the current review. Class I is subdivided in class IA and IB based on modes of regulation. Class IA are heterodimers, containing one catalytic subunit p110α, p110β, or p110δ, that associates with any of the regulatory subunits p85α, p55α, p50α, p85β, or p55γ forming PI3Kα, PI3Kβ, and PI3Kδ, respectively. Class IB is also a heterodimer, consisting of the catalytic subunit p110γ and the regulatory subunit p101 or p84 forming PI3Kγ. p110α and p110β are ubiquitously expressed in various tissues while p110γ and p110δ are mainly expressed in leukocytes. Sixty percent of PI3K activity in B-cells is accounted for by the p110δ isoform and this, hence, has been the focus of drug development in lymphomas.6

At the B-cell surface, the B-cell receptor (BCR) is a ubiquitously expressed protein with BCR signaling regulating multiple B-cell biological functions, such as growth, proliferation, differentiation, and survival. BCR also plays a role in follicular lymphomagenesis, both through auto-reactivity7 and antigen-independent signaling via interaction of mannosyl residues on surface-expressed BCR with lectins expressed on stromal cells in the tumor microenvironment.8–10 Intracellular signal transduction of BCRs is almost invariably dependent on PI3K signaling and in mature B cells, PI3K activity interweaves with B-cell receptor (BCR) signaling, regulated in both a B-cell receptor (BCR) dependent and BCR-independent manner.6 This interdependence underscores the critical role of PI3K pathway in FL lymphomagenesis.

Intracellularly, PI3K activation, at least in part, enhances the apoptosis-resistance provided by Bcl-2 overexpression, which is central to FL pathogenesis.11 FL cells demonstrate elevated basal levels of spleen tyrosine kinase (Syk), a downstream molecule in the PI3K pathway, and studies have shown a key role of the Syk/mTOR axis in FL survival.12 Ablation of p110δ in mice blocks pro-B cell differentiation with decreased numbers of circulating, mature B cells, suggesting an indispensable role in B-cell follicular maturation and survival. Class I PI3K aberrancy has been frequently implicated in many forms of B-cell malignancies, such as chronic lymphocytic leukemia (CLL), mantle cell lymphoma (MCL), and diffuse large B-cell lymphoma (DLBCL). A subset of FL patients shows activation of PI3K, demonstrated by Akt phosphorylation, a downstream kinase of PI3Ks.

The tumor microenvironment is key to lymphomagenesis. There is extensive, bi-directional cross-talk between FL and stromal cells. Stromal cells promote FL cell survival through recruitment of cell adhesion molecules, cytokines, and chemokines.13 PI3Kδ blockade in mice models has been shown to abrogate production of cytokines such as IL-6 and IL-1014 and NK-cell chemokine production.15 Idelalisib (formerly CAL-101), a PI3δ inhibitor, disrupted T and NK-cell cytokine production in CLL preclinical models supporting the pathogenetic role of this pathway.16 PI3Kδ inhibition also interrupts CXCR12 mediated chemotaxis.17 Overall, PI3K inhibition disrupts supportive lymphoma-tumor microenvironment interactions contributing to anti-tumor activity.

p110δ expression also appears to have a prognostic role in FL. Dong et al examined expression of p110δ and CD9 (a tetraspanin protein involved in diverse cellular processes such as motility, adhesion, and differentiation) on 76 FL tumor tissues and 15 normal tissues with immunohistochemistry (IHC). FL patients expressed high levels of p110δ and low levels of CD9. The upregulation of PIK3CD and downregulation of CD9 was associated with higher Ann Arbor stages and a shorter progression-free survival (PFS). These results suggested that gain of p110δ increases the recurrence risk of FL and could be a predictor of tumor progression and FL aggressiveness.18 Taken together, there is a sound biological rationale for targeting PI3K pathway in FL (Figure 1).

Figure 1 The PI3K pathway in the context of BCR signaling along with various targets. The BCR pathway is activated through antigen binding followed by recruitment and stimulation of LYN/SYK, resulting in phosphorylation of tyrosine residues on adapter proteins on the BCR as well as CD19. This enables the docking of PI3K regulator subunit to the BCR and CD19 and activation of the PI3K pathway. Activated PI3K phosphorylates PIP2 into PIP3 which stimulates PH domain signaling molecules including Akt. LYN/SYK also activate the BTK pathway which instigates PLCγ2 activation. The result of these processes is intranuclear transcriptional activation promoting cell survival. PTEN is a prominent negative regulator of this pathway. Also shown is the role of follicular T-helper cells and the PD-1/PDL-1 pathway. Created with

Abbreviations: Akt, a serine/threonine-specific protein kinase; BCR, B-cell receptor; BTK, Bruton tyrosine kinase; CAR, chimeric-antigen receptor; CR, chemokine receptor; ERK, extracellular-signal-regulated kinase (major signaling cassette of mitogen-activated kinase pathway); IKK-α/β, inhibitor of NF-κB; IRAK 1/4, interleukin-1 receptor-associated kinase 4; JAK, Janus tyrosine kinase; LYN, Lck/yes novel tyrosine kinase; mTOR, mechanistic target of rapamycin; MYD88, myeloid differentiation primary response 88; NEMO, NF-κB essential modulator; NFATc1, nuclear factor of activated T-cells cytoplasmic 1; NF-κB, nuclear factor kappa-B; PD-1, programmed death-1; PDL-1, programmed death-1 ligand; PH, pleckstrin homology; PIP2, phosphatidylinositol 4,5-bisphosphate; PI3K, phosphatidylinositol-3 kinase; PIP3, phosphatidylinositol 3,4,5-triphosphate; PLCγ2, phospholipase C-gamma PTEN, phosphatase and tensin homolog; STAT, signal transducer and activator of transcription; SYK, spleen tyrosine kinase; TLR, toll-like receptor; TRAF6, tumor necrosis factor receptor-associated factor 6.

Pi3k Inhibitor Development in Lymphoma

The biggest challenge in PI3K inhibitor (PI3Ki) development has been achieving the balance between sufficient depth of target inhibition in tumor tissue and dose-limiting toxicities. Initially, pan-specific PI3K/mTOR and pan-PI3K inhibitors were developed in an attempt to augment therapeutic efficacy. However, trials in solid tumors demonstrated unacceptable toxicities.5 Isoform-selective and isoform-sparing PI3K inhibitors, by circumventing intrinsic toxicity of pan-PI3K inhibition and allowing exploration of combination therapies, thus, became the new focus for research.

Given the prominent role played by p110δ in lymphoid malignancies, isoform-specific PI3Kδ inhibitors were investigated. Idelalisib (selective PI3K-δ inhibitor) and duvelisib (PI3K δ/γ dual isoform-specific inhibitor) have been approved for FL, relapsed/refractory (R/R) after 2 prior lines of therapy.1,19 Unfortunately, the initial enthusiasm concerning these agents was dampened by a high incidence of gastrointestinal and immune-mediated toxicities.20,21

Copanlisib (BAY 80–6946; Bayer Pharma AG, Berlin, Germany) is an intravenous, potent, highly selective, pan-class I PI3K inhibitor with preferential activity against the p110α and p110δ isoforms, compared with the p110β and p110γ isoforms.22 Copanlisib is indicated in the US for the treatment of patients with relapsed follicular lymphoma (FL) who have received at least two prior systemic therapies.23

Preclinical Studies

The in vivo antitumor efficacy (determined as a function of tumor growth inhibition) of copanlisib was studied in athymic nude rats or nude mice using xenograft models of human tumors.22 Following a single intravenous dose of 6.0L/kg, copanlisib potently inhibited the catalytic activity of all class I PI3K isoforms with highest inhibition of α and γ isoforms (IC50 values for α, β, γ, and δ isoforms were 0.5, 3.7, 6.4, and 0.7 nmol/L, respectively).

This study showed potent antiproliferative activity of copanlisib against a diverse panel of human tumor cell lines, many of which exhibited constitutively activated PI3K signaling.22 Several breast cancer, endometrial cancer, and hematologic tumor cell lines were particularly sensitive at IC50 values less than 10 nmol/L. Cell proliferation inhibition was thought to correlate with the strong activity of copanlisib against the α and δ isoforms.


Copanlisib exhibited a very large volume of distribution (Vss = 32 L/kg) resulting in high tumor penetrance as well as a high plasma clearance (3.95 L/kg/hour (h)) and long half-life (6.0 h).22 At 48 h, copanlisib levels in tumors were 100-fold higher than in plasma. There was a strong pharmacokinetic (PK)-pharmacodynamic relationship with tumor Copanlisib levels correlating well with inhibition of tumor AKT phosphorylation. Levels of pAKT-Ser473 in tumors showed more than 90% inhibition at 24 h after intravenous dosing and remained suppressed for 48 to 72 h. pAKT reduction was observed as early as 1 h after intravenous dosing. Elimination of copanlisib and its metabolites is predominantly through hepatic metabolism and biliary excretion with more than 90% of in vitro metabolism mediated by cytochrome P450 (CYP) 3A4 and less than 1% by CYP1A1.24

Aforementioned exposure and other PK parameters remained similar following multiple administrations (every second day × 5), signifying lack of compound accumulation of compound or metabolic process alterations. An alternative dosing schedule of intravenous copanlisib twice a day once weekly for also showed equivalent antitumor activity.

Subsequently, Paul et al performed PI3K isoform and PTEN expression analysis with primary tumors from 45 FL and 45 DLBCL patients.25 High PI3Kδ expression was noted in 87% of FL patients. Only 18% of FL patients demonstrated both PI3Kδ and PI3Kα overexpression however PI3Kα overexpression correlated with a late disease stage (p=0.06) and a high Follicular Lymphoma International Prognostic Index (FLIPI) risk score (p= 0.01) indicating PI3Kα contribution to disease progression and a prognostic role. Hence, dual inhibition of the α and δ isoforms could be especially pertinent in FL with poor prognostic features, which, in turn, is more likely to exhibit refractoriness to front-line therapies, paving the way for study of copanlisib in the Phase I setting.

Phase I Trials

Patnaik et al conducted the first-in-human study of copanlisib in patients with advanced solid tumors and NHL.26 Fifty-seven patients were treated with copanlisib on days 1, 8, and 15 of a 28-day cycle. Preclinical studies showed a lack of drug accumulation despite multiple doses potentially translating to lower rates of cumulative toxicities. This, in conjunction with the observation that pAKT phosphorylation remained suppressed 48–72 h post copanlisib administration and equivalent efficacy of the twice a day weekly schedule with every other day schedule, established the clinical rationale for weekly, intermittent dosing. The dose escalation cohort included 17 solid-tumor patients and 9 NHL patients out of which 6 had FL. The maximal tolerated dose (MTD) was 0.8 mg/kg due to multiple grade 3–4 dose-limiting toxicities (DLTs) experienced by one patient with metastatic colon carcinoma. These DLTs included grade 3–4 transaminitis, grade 4 hyperglycemia with lactic acidosis, elevated anion gap and increased serum ketones, and grade 3 left ventricular systolic dysfunction, starting on the day of the first copanlisib infusion, resolving after drug discontinuation.

Patients with NHL received a median of 10 treatment cycles (range, 1–49 which was higher than that in the solid-tumor expansion cohort (median of 2 treatment cycles (range, 1–14)). Of note, the longest duration of study treatment was received by 2 FL patients, one of whom was treated for >4 years before disease progression and another who remained on treatment for >3 years (at time of data cut off). The NHL patients were heavily pretreated, suggesting a better tolerability profile of copanlisib in NHL, especially FL.

The aforementioned study also had a distinct cohort for patients with Type 2 diabetes mellitus (T2DM) who were treated at a lower dose level of 0.4 mg/kg. Most common (≥20%) drug-related adverse events (AEs) of any grade were hyperglycemia (63%), nausea (37%), and hypertension (21%). However, both blood glucose and blood pressure elevations were relatively transient returning to baseline within 24–48 h.26,27

Copanlisib exhibited a distinct gastrointestinal (GI) toxicity profile compared to what was previously seen with the orally administered PI3K inhibitors. For the orally administered PI3K inhibitors idelalisib and duvelisib, the reported incidence of all-grade and grade ≥3 diarrhea ranged from 32% to 92% and 9% to 20%, respectively, while the reported incidence of grade ≥3 elevations in aminotransferases was up to 25%, and serious GI toxicity, such as colitis, was reported in 4% of patients. In contrast, with copanlisib administration, nausea was the most common drug-related GI toxicity (37%; all events grade ≤2) and diarrhea was less common (all-grades: 16%; grade ≥3: 2%). Elevated aminotransferases were primarily an incidental laboratory toxicity finding and mostly grade 1. GI toxicities were noted to be class effects of PI3K inhibitors, however, their reduced incidence and severity associated with copanlisib was thought to suggest a beneficial role for intravenous administration which would bypass high gut concentrations and first-pass metabolism due to oral agents. Gedatolisib (PKI-587), another intravenous dual PI3K/mTOR inhibitor with pan-PI3K inhibitory activity, similarly demonstrated a low incidence of diarrhea and transaminitis supporting the advantage of bypassing the gut.28

Another smaller Phase 1 study evaluated 10 Japanese patients with advanced or refractory solid tumors.27 Copanlisib was administered at 0.8 mg/kg. The toxicity profile was similar to Patnaik et al albeit with a slightly higher incidence of all-grade hypertension (70% vs 21%) and hyperglycemia (80% vs 63%), respectively.

Overall, Copanlisib was noted to be safe with a significantly lower GI toxicity rate as compared to the commercially available oral PI3K inhibitors.

Phase II Trials

CHRONOS-1 was a pivotal phase II trial of copanlisib in relapsed/refractory aggressive and indolent lymphomas. In Part A, 33 patients with indolent lymphoma and 51 with aggressive lymphoma received copanlisib at a dose of 0.8 mg/kg intravenously over a 1-h infusion on days 1, 8, and 15 of a 28-day cycle.29 FL comprised 48.5% of patients. Most patients (78.6%) had received prior rituximab and 54.8% were rituximab-refractory. Median duration of treatment was 23 and 8 weeks in the indolent and aggressive cohorts, respectively. Of 80 patients evaluable for efficacy, the objective response rate (ORR) was 43.7% in the indolent cohort and 27.1% in the aggressive cohort with a median progression-free survival (PFS) of 9.7 and 2.3 months and median duration of response (DOR) of 12.8 and 5.5 months, respectively. The ORR of 40% in FL patients was slightly lower than reported with idelalisib (48–57%) in a similar indolent lymphoma population.30,31 The AE profile was consistent with that noted in phase I studies, with the most common being hyperglycemia (57.1%; grade ≥3, 23.8%) and hypertension (54.8%; grade ≥3, 40.5%). Diarrhea was more frequent than noted in phase 1 trials with an incidence of 40.5% (grade ≥3, 4.8%). However, as in phase 1 studies, both hyperglycemia and hypertension were transient, with blood pressure peaking 1 to 2 h after the start of infusion, and plasma glucose levels peaking 5 to 8 h after the start of infusion, followed by a decline to baseline levels. Neither of these required treatment discontinuations. Neutropenia also occurred in 28.6% of patients (grade 4, 11.9%). Copanlisib dosage and administration schedule was as established in phase 1 studies (0.8 mg/kg on days 1, 8, and 15 of a 28-day cycle).

The authors also conducted tumor gene expression and mutation analyses that confirmed low prevalence of PIK3CA mutations and frequent upregulation of PI3K pathway gene expression in lymphomas. Copanlisib exhibited increased antitumor activity in cases with activated PI3K/BCR signaling and this, taken together with low expression of unfavorable tumor microenvironment genes, was a proof-of-principle for its mechanism of action. Based on these results, the efficacy of copanlisib was studied in an extension cohort of patients with indolent lymphoma (Part B).

CHRONOS-1 part B included relapsed/refractory indolent lymphoma patients and the and safety of copanlisib (60 mg IV dose), based on promising results noted in part A.32 The study accrued 142 patients relapsed/refractory after at least 2 prior lines of therapy; 104 patients had FL (73%) and 23 (16.2%) had MZL. The ORR was 58.7% vs 70% with complete remissions (CR) in 14.4% vs 9%, respectively, in FL versus marginal zone lymphoma (MZL). Median DOR was 22.6 months, and the median PFS was 11.2 months. High expression of PI3K/BCR pathway genes was found in 75% of evaluated patients with an ORR, including 6 of 8 with a CR, and in 25 of 33 (76%) evaluable patients with FL with an objective response and in 5 of 6 with a CR. 9 of 17 FL (53%) patients with low PI3K/BCR gene expression did not respond to copanlisib (stable (SD) or progressive disease (PD) or tumors that were not evaluable for gene expression profiling) while only 12 of 37 FL (32.4%) patients with high PI3K/BCR expression were non-responders. Upregulation of PI3K pathway genes, hence, appears to portend an improved response to copanlisib. Most common AEs were transient hyperglycemia (41%) and transient hypertension (24%).

Of the FL subset, 62% were refractory to their last regimen.30 Patients had received a median of 3 prior lines of treatment. In addition to an ORR of 58.7%, 44.2% patients had a partial response (PR). The median DOR was 12.2 months in patients with CR or PR. Most patients were able to remain on treatment with median duration of treatment being 22 weeks and 32% patients remaining on treatment at the initial data cut off of June 2016. Most common AEs were (all grade/grade 3+): diarrhea (34%/5%), neutropenia (30%/24%), fatigue (30%/2%), and fever (25%/4%). Hyperglycemia (50%/41%) and hypertension (30%/24%) were transient. All toxicities were manageable, with a low incidence of severe AEs associated with other PI3K inhibitors, especially hepatic enzymopathy, opportunistic infections, and colitis.

A 2-year updated analysis of CHRONOS-1 supported continued efficacy and safety benefit for copanlisib in relapsed/refractory indolent lymphomas.33 The efficacy analysis showed an improved ORR of 60.6% with 24 CRs and 62 PRs as compared to 21 CRs and 40 PRs at the time of primary analysis. There were 3 new CRs since primary analysis and 4 partial responses that became CR endpoints of median DOR, PFS, and overall survival (OS) were 14.1 months (median follow‐up, 16.1 months), 12.5 months (median follow‐up, 14.0 months), and 42.6 months (median follow‐up, 31.5 months), respectively. Median safety follow‐up was 6.7 months and 26% of patients received treatment for more than 1 year. Common treatment‐emergent adverse events (TEAEs) (all grade/grade 3/grade 4) were transient hyperglycemia (50.0%/33.1%/7.0%), diarrhea (35.2%/8.5%/0%), transient hypertension (29.6%/23.9%/0%), and neutropenia (28.9%/9.2%/14.8%). These serious AEs were largely unchanged, with no new cases of pneumonitis (4.2%), diarrhea (2.8%), or grade 5 events. Unlike orally administered PI3K inhibitors, there were no black box warnings or chronic adverse events. These long-term data are highly encouraging with improving responses without new safety concerns.

Phase III Trials

Ongoing phase III trials using copanlisib in indolent lymphomas include CHRONOS-2 (NCT02369016), CHRONOS-3 (NCT02367040) and CHRONOS-4 (NCT02626455) (Table 1), all of which are currently active. CHRONOS-2 is a randomized, double-blind phase III Study of copanlisib versus placebo in patients with rituximab-refractory indolent NHL.34 CHRONOS-3 and 4 aim to evaluate efficacy of copanlisib in combination with other therapies for relapsed iNHLs (with rituximab and standard chemo-immunotherapy RCHOP or BR, respectively).

Table 1 Ongoing Phase III Trials Studying Copanlisib in NHL


CHRONOS-1 study established that copanlisib can be administered in the outpatient setting at 60 mg intravenously infused over 1 h on days 1, 8, and 15 of a 28-day cycle with treatment continuation until unacceptable toxicity or disease progression. There is no requirement for pre-medications.

Given the predominant hepatic elimination of copanlisib,24 concomitant use of copanlisib with a strong CYP3A inducer should be avoided and the package insert recommends a dose decrement to 45 mg in this setting. Manufacturers also recommend a dose decrease to 45 mg in case with moderate hepatic impairment (Child Pugh Class B). The pharmacokinetics of copanlisib in severe hepatic (Child Pugh Class C) and renal impairment (creatinine clearance < 30 mL/min, with or without dialysis) are unknown and no dosage adjustments provided in the package insert.23

Safety Profile

Zinzani et al published a pooled safety analyses from eight phase I and phase II studies of copanlisib in 364 patients with hematologic malignancies, out of which 42% (n= 153) had FL.35 These updated data reported all-grade TEAEs in 97.8% of patients with grade 3 or 4 TEAEs in 51.4% and 24.7% of patients, respectively. Of these, copanlisib-related TEAEs of all grades were reported for 88.7% patients with grade 3 and 4 events occurring in 54.1% and 18.4% of patients, respectively. The most common (≥20%) TEAEs (all grade/g3/g4) were hyperglycemia (50.5%/28.3%/4.4%), hypertension (38.7%/29.1%/0%), and diarrhea (37.1%/4.9%/0%). Hyperglycemia and hypertension were infusion-related, transient, and manageable. Of note, AEs were commonly reported early with a greater incidence occurring at ≤180 days with no increased incidence of grade 3 or higher events with prolonged exposure, apart from diarrhea. Patients treated for more than 1 year exhibited a similar adverse event trend as 22 patients who were treated for more than 2 years, despite prolonged exposure in the latter group, indicating low rates of cumulative toxicity and a favorable long-term safety profile. Diarrhea was an exception, as mentioned above, and the incidence of grade 3 diarrheal events increased with prolonged exposure, occurring at 8.9% at ≤180 days, 7.1% between 181 and 360 days, and increasing to 12.5% at ≥361 days. Pneumonitis was infrequent (all grade and grade 3 or higher 5.2% and 2.7%, respectively, without a significant increase in incidence in patients treated for more than 1 year (10.7%/3.6%). Serious adverse events (SAEs) trends paralleled TEAEs. As high as 10.7% patients (n=39) died either during copanlisib treatment or within 35 days post discontinuation of treatment; however, that was most commonly due to disease progression (4.7%) and not deemed a drug-effect. In distinction to inflammatory AEs noted with oral PI3K inhibitors, there were no grade 4 late-onset colitis, hepatotoxicity, or other intestinal toxicity that occurred after 6 months of copanlisib treatment. Overall, these data provide evidence for the manageable safety profile of long-term copanlisib treatment, with no late-onset toxicities or worsening of severity of TEAEs, few severe gastrointestinal TEAEs, and no new unexpected safety signals.


Transient hyperglycemia is a predictable, on-target effect of PI3Kα inhibition due to abrogation of downstream insulin receptor signaling.17 The p110α isozyme and AKT2 mediate insulin-driven glucose uptake in muscle, liver, and fat cells, mainly attributable to the translocation of glucose transporters (GLUT) to the plasma membrane. As a result, acute, systemic inhibition of PI3Kα/AKT blocks insulin action, preventing glucose uptake in adipose tissue and skeletal muscle, and promoting hepatic gluconeogenesis through glycogenolysis. The resultant hyperglycemia is transient due to insulin feedback and compensatory insulin release from the pancreas resulting in normalization of glucose levels.5,35,36

Grade 3 or 4 hyperglycemia (blood glucose 250 mg/dL or greater) occurred in 32.7% of 364 patients with hematologic malignancies treated with copanlisib, with serious hyperglycemic events occurring in 4.1% of patients.37 Infusion-related hyperglycemia, peaking about 5 to 8 h post copanlisib infusion, was noted in both diabetic and non-diabetic patients in the phase I first-in-human trial of copanlisib by Patnaik et al as well as the phase 1 pharmacodynamic study by Morschhauser et al.26,38 Plasma glucose levels returned to baseline within 24 h. Similar results regarding onset, peak, and nadir of glucose elevation were demonstrated in the phase IIB CHRONOS-I study.32 Only 17.7% of patients exhibited elevated blood glucose levels 1 day after infusion.23 The prevalence of hyperglycemia decreases after the 1st cycle (48.48%) and remains relatively constant (6.9 to 16.1%) during subsequent cycles which is possibly due to down-regulation of alpha receptors and development of glycemic tolerance. Hemoglobin A1c (HgbA1c) values do show an overall increase during copanlisib treatment indicating a cumulative effect. The mean HgbA1c values increment was 0.64 in diabetics and 0.50 in non-diabetics.39 However, HgbA1c values 3 months after drug discontinuation were not reported in this study (the time when post-treatment changes in glycated hemoglobin would be expected to emerge).35 In pooled analyses, of 155 patients with baseline HbA1c <5.7%, 10% had HbA1c >6.5% after about 15 cycles; however, the time to normalization of HgbA1c is unclear.23 Reassuringly, hyperglycemia, both as a TEAE and SAE, emerges early during the treatment course (higher incidence ≤180 days) and there is no increased incidence of grade 3 or higher events with prolonged exposure.37 In patients with pre-existing diabetes (n=20 in CHRONOS-I) however, incidence of all-grade hyperglycemia was nearly twice that seen in the non-diabetic cohort (85% vs 44.3%) likely due to blunting of the insulin feedback loop from insulin resistance, with 35% (n=7) patients developing grade 4 hyperglycemia and two discontinuing treatment due to it.39 Interestingly, the ORR, PFS, and median DOR were lower in the diabetic subset as compared to the non-diabetic subset (40% vs >60%; 7.2 months vs 13.8 months; 7.1 months vs 14.9 months, respectively); however, the study was not powered to detect such an efficacy difference.

In clinical trials, stringent glucose monitoring was done pre- and post-copanlisib infusion, and monitoring was continued on days 2 and 3. In the phase I study, patients also fasted for 8 h prior to copanlisib infusion and up to 3 h post-infusion.26 Cheson et al35 recommended against immediate post-infusion glucose monitoring in non-diabetic patients, although blood glucose levels could be re-checked 24 h post infusion at the clinician’s discretion. The use of insulin for management of infusion-related hyperglycemia is not recommended in insulin-naïve, non-diabetic patients given transient nature of hyperglycemia which could normalize before onset of action of insulin and risk of hypoglycemia. In CHRONOS-I, insulin was administered to 17 out of 84 patients to manage infusion-related hyperglycemia; however, owing to hypoglycemic events following short-acting insulin use, further recommendations were to use only intravenous hydration in insulin-naive patients.35

In patients at risk for diabetes, including those with obesity and/or a family history of diabetes, HbA1c screening is recommended to be performed prior to treatment to identify prediabetic or uncontrolled diabetic patients. In newly or previously diagnosed diabetic patients, it is imperative to ensure adequate glycemic control prior to initiation of copanlisib which requires close consultation with the patient’s primary care provider or endocrinologist. Consideration should be given to use oral diabetic agents, in particular, sodium-glucose co-transporter-2 (SGLT-2) inhibitors and adherence to American diabetic association (ADA) recommended diabetic diet should be encouraged pre-and post-infusion. Post-infusion glucose monitoring for several hours is recommended in diabetic patients; however, the optimal duration of monitoring has not yet been determined.35

Role of Ketogenic Diet, Metformin, and SGLT-2 Inhibitors

It has been hypothesized that the insulin feedback induced by PI3K inhibitors may reactivate the PI3K-mTOR signaling axis in tumors, thereby compromising treatment effectiveness. Hopkins et al, in mouse tumor models, reported on dietary and pharmaceutical strategies aimed at preventing insulin feedback and in turn, enhancing the efficacy and reduce the toxicity of PI3K inhibitors.36,40 These included the antidiabetic drug metformin, which increases insulin sensitivity and reduces insulin levels; sodium glucose cotransporter 2 (SGLT2) inhibitors, which reduce glucose reabsorption in kidney tubules; and a ketogenic diet, which depletes glycogen stores and thus limits the acute hepatic glucose efflux upon PI3K inhibition. In preclinical animal models, SGLT2 inhibitors and a ketogenic diet prevented insulin feedback and enhanced the antitumor effect of PI3K pathway inhibitors in both PIK3CA-mutant and PIK3CA wild-type tumors. Although, yet to be tested clinically, should a diabetic patient need pharmacotherapy for adequate pre-treatment glucose control, strong consideration should be given to initiation of SGLT-2 inhibitors.

Based on the aforementioned data, the FDA-approved package insert recommends to withhold copanlisib in patients with a pre-infusion fasting plasma glucose of ≥160 mg/dL or a random glucose of ≥200 mg/dL until the fasting glucose is ≤160 mg/dL or the random glucose is ≤200 mg/dL. For those patients with a post-dose blood glucose ≥500 mg/dL, on first occurrence, copanlisib should be withheld until the fasting glucose is ≤160 mg/dL or the random blood glucose is ≤200 mg/dL. Dose reductions (60 mg to 45 mg and then to 30 mg) or discontinuation should only be considered in situations of severe or recurrent events or if progressive metabolic derangement persists after therapeutic interventions have been attempted for a sufficient duration per a National Cancer Institute task force.41


In updated pooled analyses of patients with hematologic malignancies treated with copanlisib, transient, infusion-related hypertension of all grades occurred in 38.7% (n-364) of patients. Grade 3 hypertension was seen in 29.1% of patients with no grade 4 events.37

Hypertension was not a previously reported AE for other pan-PI3K inhibitors. In the phase I trials, multiple factors were posited by the authors to account for this AE including frequent monitoring, dysregulation of endothelial-derived vasoconstriction, and dilators based on peripheral vasoconstriction noted in laboratory animals following copanlisib administration, and acute insulin elevation and resultant vasoconstriction due to PI3K blockade.26,27

All-grade hypertension was noted in 43.9% of hypertensive patients in CHRONOS-1-part B and was principally grade 3 (39.0%), compared to 23.8% and 17.8%, respectively, in non-hypertensives. No grade 4 hypertension events were noted and 1 patient discontinued treatment due to grade 2 hypertension. There were 2 grade 3 cardiac-related events (atrial fibrillation and left ventricular dysfunction) and one grade 4 event (arrhythmia) in the hypertensive group.39 The authors also noted a longer PFS and DOR in the hypertensive cohort as compared to the non-hypertensive patients (19 and 22.6 mos vs 11.3 and 10.9 mos, respectively).

Similar to hyperglycemia, hypertension associated with copanlisib appears to be infusion-related and consistent with an on-target effect. Blood pressures (BP) peak 2 h post-infusion and normalize within 24 h.23,35 The mean change of systolic and diastolic BP from baseline to 2 h post-infusion on Cycle 1 Day 1 was 16.8 mmHg and 7.8 mmHg, respectively. The mean BP usually starts to decrease approximately 2 h post-infusion and BP may remain elevated for 6 to 8 h after the start of the infusion.

Optimal BP control should be achieved before initiating copanlisib with dietary or pharmacologic measures. In CHRONOS-I, antihypertensive use was permitted based on investigator clinical judgment.32 It is recommended to monitor BP pre- and post-infusion. For patients with a pre-dose BP of ≥150/90 mm Hg, the recommendation is to hold copanlisib until 2 consecutive readings of <150/90 mm Hg have been achieved, measured at least 15 min apart. The decision of whether to treat copanlisib-induced hypertension with antihypertensive therapy should be individualized based on baseline blood pressure, the severity of blood pressure elevation during treatment, and preexisting cardiovascular risk factors (eg, diabetes or chronic kidney disease) or cardiovascular disease (eg, ischemic heart disease, stroke or transient ischemic attack, peripheral vascular disease, or heart failure). Given the short, anticipated duration of elevated blood pressure secondary to copanlisib treatment, short-acting antihypertensives are preferred. For patients with a post-dose blood pressure of <150/90 mm Hg, if antihypertensive therapy was not required, copanlisib should be continued at the previous dose. However, if blood pressure remains uncontrolled (≥150/90 mm Hg) despite initiation or optimization of antihypertensive therapy, copanlisib can be reduced from 60 to 45 mg, or from 45 to 30 mg.23,35

Whereas the hypertensive cohort exhibited similar ORR of 61% vs 60.4%; the PFS and DOR appeared to be longer at 19 months vs 11.3 months, and 22.6 months vs 10.9 months, respectively.

In summary, treatment-related hyperglycemia and hypertension are common infusion-related side effects of copanlisib with a greater incidence in those patients with these pre-existing conditions; however, these were mostly lower grade and manageable. Hyperglycemic events in diabetic patients were not severe, not associated with ketoacidosis states and did not impact overall glycemic control with only minor increases in A1c values from baseline. Treatment discontinuations due to these AEs were uncommon. Overall, data support the low likelihood of these adverse events translating into long-term consequences and support use of copanlisib in indolent lymphoma patients with well-controlled diabetes or hypertension.


PI3K activation in leukocytes is predominantly mediated by p110γ and p110δ isoforms which produce phosphatidylinositol (3,4,5)-trisphosphate (PIP3) following receptor engagement. This signal transduction can act as an activation or dampening switch for immune response depending on the receptor, the cell type, and the degree of PI3K activation. p110α and p110β are also expressed in immune cells; however, their roles are restricted.5 Overall, PI3K inhibition causes immune reprogramming and a pro-inflammatory effect however these effects are predominantly mediated by the p110δ isoform.

Inactivation of p110δ impairs differentiation of effector CD4+ and CD8+ T cells, yet also impairs regulatory T-cell (Treg) function. This Treg defect has been thought to be responsible for the autoimmune colitis that develops in p110δ-deficient mice and likewise, to mediate diarrhea and colitis which are frequent side effects of idelalisib (a PI3Kδ inhibitor).5 The principal action of copanlisib on the α and γ isoforms as well the intravenous route of administration could contribute to the lower incidence of GI toxicity seen with this drug.

In pooled analyses, all-grade diarrhea occurred in 37.1% of 364 patients treated with copanlisib; however, grade 3 events were significantly lower at 4.9% in comparison to 13–14% seen with idelalisib and duvelisib.21,31 There were no grade 4 diarrhea events.37 This finding is in contrast to the oral agents idelalisib and duvelisib where grade 3 diarrheal events were seen in 14% and 18% of patients, respectively.35 Also, both of these oral agents carry FDA Black Box warnings for severe diarrhea or colitis. Interestingly, the incidence of diarrhea as a grade 3 event did increase with prolonged exposure to copanlisib with a rate of 3% at ≤180days, 4.2% at 181–360 days, and 12.5% at >360 days. This trend is unlike what has been noted for hyperglycemia and hypertension. The difference could be due to the fact that hypertension and hyperglycemia are on-target effects while diarrhea is likely due to durable immune perturbances caused by copanlisib.

In patients with grade 3 diarrhea, copanlisib should be withheld until diarrhea resolves to grade 1 or better and the drug should be restarted at 45 mg. If diarrhea of grade 3 or worse recurs, copanlisib should be discontinued.


Due to the high incidence of infections seen with idelalisib, close monitoring for infectious complications was done in CHRONOS-I. Copanlisib was found to be associated with relatively low rates of myelosuppression and pulmonary infections in the trial. All grade, grade 3, and grade 4 neutropenia in pooled analysis was noted to be 23.1%, 9.3%, and 9.6%, respectively. Of 142 patients in the CHRONOS-1 Part B trial, there were 2 (1.4%) patients with a grade 3 upper respiratory infection; 9.9% of patients had grade 3 or 4 (1.4% grade 4) pneumonia, and there was a single (0.7% of patients) death from lung infection that was considered to be treatment-related. Prophylaxis was not routinely given to subjects receiving copanlisib as a monotherapy in CHRONOS-1, although 18 patients did receive it at the investigator’s discretion. In pooled analyses, pneumonia was the most frequent SAE with a frequency of pneumonia 6.0% (all grade) and 5.5% (grade 3 or higher). Given infrequency of pneumonia during therapy, routine prophylaxis is not recommended (unlike idelalisib); however, absolute neutrophil counts are recommended to be monitored weekly, and treatment should be withheld if the absolute neutrophil count (ANC) is less than 0.5 × 103 cells/mm3.35 When ANC is greater than 0.5 x 103 cells/mm3, it is recommended to resume copanlisib at the previous dose. However, if the grade 4 neutropenia recurs, a dose-reduction to 45 mg is recommended. Granulocyte colony-stimulating factor (G-CSF) has not been routinely used in clinical trials and use is not standardized. If a patient has shown a good response to copanlisib, G-CSF could be used to maximize treatment duration especially given the R/R setting and decisions should be individualized for the patients.

Early Progressing FL

Recent data have highlighted that the strongest predictor of long‐term FL outcomes is the length of first remission after front‐line therapy. Patients with disease progression within 24 months of completing induction chemoimmunotherapy with R-CHOP, R-CHOP like regimens, or rituximab-based immunotherapy doublets (POD24) have inferior OS compared with those with longer remission durations.42,43 Idelalisib has previously been shown to have clinical activity in POD24 FL patients (n=46; POD24=37) with an ORR of 56.7%, including 5 (13.5%) CRs and mPFS of 11.1 mos,44 which was equivalent to that noted in non-POD24 patients (ORR 54%). Similarly, exploratory analysis from the CHRONOS-1 data showed robust activity of copanlisib in POD24 patients (n=104; POD24=37) and comparable to that noted in the non-POD24 cohort (n=68; ORR 60.3%).45 ORR and CR rates were slightly higher than that seen with idelalisib at 58.9% and 17.7% (n=6) however given small numbers in both studies, meaningful comparisons cannot be drawn. mPFS and mOS were similar in both groups: 11.3 vs 10.8 mos and 38.3 vs 31.0 mos, in non-POD24 and POD24, respectively. Results were similar in patients previously treated with R‐CHOP. These data emphasize that the efficacy of copanlisib is not impacted by POD24 status and can offset the inferior survival noted in this high-risk group in previous trials and this finding should be further characterized in larger patient samples to ensure generalizability.


PI3K inhibitors are approved for treatment of R/R FL in the third-line setting. Copanlisib is unique in this class in that it is a pan–class I PI3K inhibitor, with preferential inhibitory activity against the PI3Kα and PI3Kδ isoforms. It is an intravenous drug that is administered weekly, whereas the other FDA-approved PI3K inhibitors (idelalisib and duvelisib) are oral formulations with twice-daily dosing.

Despite the intravenous route of administration, copanlisib provides an advantage over the oral agents given an extremely favorable toxicity profile and lack of cumulative, progressive, long-term toxicities, while maintaining efficacy. The intermittent dosing schedule has been designed to achieve optimal target inhibition within the tumor while sparing normal tissue, a strategy which was shown to be more effective than continuous dosing in mice bearing breast cancer xenografts. Weekly dosing along with isoform inhibition preference results in the distinctive AE profile of copanlisib and confers an advantage over the approved oral PI3K inhibitors – idelalisib and duvelisib. PI3Kδ inhibition is linked to myelosuppression, transaminitis, and autoimmune toxicities and both idelalisib and duvelisib are associated with a prohibitive, treatment-limiting toxicity and carry boxed warnings. Immunosuppression-related toxic effects, including infections, have been noted to be higher in real-world outcomes study of idelalisib, as compared to those observed in trials, likely due to frequent dose reductions and exclusion of patients with ongoing infections in the trial setting.20 This toxicity profile counterweighs the feasibility of oral agents.

Dual PI3K α and δ inhibition is also an astute strategy for overcoming PI3K resistance. Iyengar et al studied PI3K class IA isoforms in primary patient mantle cell lymphoma samples and demonstrated that although p110δ was widely overexpressed, p110α expression was variable, and significant increases occurred with disease progression.46,47 Further, combined inhibition of p110-α and p110-δ isoforms was noted to be a more effective strategy for inhibiting constitutive PI3K activation in cell lines. Whole-exome sequencing identified PI3KCA gain-of-function mutations (N345K, P539R, E970K) in 3 independently generated idelalisib-resistant WSU-FSCCL FL cell line clones and compensatory activation in SFK and WNT pathways indicating a mechanistic role of p110α in resistance.48 Hence, simultaneous targeting of both PI3K-α and PI3K-δ could bypass this resistance mechanism.

Regarding concerns of financial toxicity incurred on patients due to intravenous dosing, a budget impact model noted that over a 1-year period, addition of copanlisib to a formulary resulted in a small increase in total budget of $242,641, corresponding to $0.02 per patient per month. This assessment accounted for a concurrent increase in the use of obinutuzumab plus bendamustine and lenalidomide plus rituximab. The analysis concluded that the addition of copanlisib was an affordable option for payers thus alleviating, to some extent, concerns of financial toxicity incurred on the patients.49 The more favorable safety profile of copanlisib compared to other agents in its class without late-onset or treatment-limiting toxicities makes it an agent with immense clinical utility and significance in the third-line setting.

Optimal sequencing of therapies in R/R FL remains unknown. Existing and evolving prognostic models utilize clinical,50,51 gene mutation status52 or gene expression profiling53 of the tumor microenvironment to predict FL outcomes. The prognostic value of the clinicogenetic risk models is dependent on the therapeutic regimen. These perform inadequately in predicting early progression42 and are not prognostic in patients who receive chemo-free regimens upfront.54 A 23-gene predictive score developed in the post-rituximab era was able to identify a high-risk FL population which was at an increased risk of progression after frontline rituximab-chemotherapy, independent of rituximab maintenance and FLIPI score.53 However, given that novel agents can interfere with gene expression signatures in both tumor B-cells and their microenvironment, its validity in this scenario needs further investigation.

In the absence of a universal prediction model, positioning of copanlisib in the R/R setting is dependent on individualized risk-benefit assessment which should account for patient’s disease status whether relapsed or refractory, tumor burden, presence or absence of transformation, performance status, and co-existing medical conditions especially diabetes or hypertension. Low-risk patients (non-chemo-refractory, non-POD24, low tumor burden, etc.) could benefit from shorter duration and less toxic therapy whereas high-risk patients should ideally be referred for clinical trials including those evaluating chimeric-antigen receptor modified T (CAR-T) cell therapy.55 Anti-CD19 CAR-T cell therapy has shown high ORR and CR rates in both progressive and transformed FL and could be considered for high-risk R/R FL patients especially those who are young and with high tumor burden, given increased durable complete remission rates.56 Copanlisib could be considered in older patients desiring to avoid the side-effects associated with lymphodepleting chemotherapy or cytokine release syndrome seen with CAR-T cells.

Future Directions

Acquired and inherent drug resistance is always a potential concern with monotherapy leading to further investigations of copanlisib as combination therapy. Based on preclinical studies, potential drug combinations include chemotherapy, immune-checkpoint inhibitors (ICIs), bcl-2 inhibitors, and other kinase inhibitors. In vitro studies of idelalisib showed augmented DNA damage when it was used with bendamustine providing a therapeutic rationale for administration of PI3Kis concomitantly with chemotherapy.57 CHRONOS-4 is investigating use of copanlisib with standard chemoimmunotherapy (B-R or R-CHOP) and a phase 1 study (NCT04156828) is assessing R-CGD (carboplatin, gemcitabine, and dexamethasone) with copanlisib for R/R grade 3b FL and DLBCL. The role of ICIs is also being examined in lymphoid malignancies and the anti-PD1 antibody nivolumab has shown an ORR of 40% as a single-agent in R/R FL.58 PI3Kδ inhibition is thought to abrogate T-cell immune tolerance to cancer, leading to potential for combination with ICIs.59 A study of duvelisib with immune checkpoint (anti-PD-1, RMP1-14) or co-stimulatory (anti-OX40, clone OX86) antibodies in a murine B-cell lymphoma model showed that the combination of duvelisib with anti-PD1 antibodies caused synergistic tumor regression as well as development of immune memory that prohibited new tumor growth upon oncogenic rechallenge in mice treated with the combination.60 The lack of autoimmune AEs with copanlisib as compared to idelalisib or duvelisib makes it a more favorable PI3K inhibitor for use with ICIs and a phase 1B trial is assessing the safety and efficacy of nivolumab in combination with copanlisib in advanced solid tumors and lymphomas.61

Clinical trials utilizing combinations of idelalisib with immunomodulatory agents, anti-CD20 monoclonal antibodies and, kinase inhibitors have shown undue toxicities. The phase 1 Alliance trial- A051202, evaluating the combination of idelalisib, lenalidomide, and rituximab in R/R/FL had to be terminated due to dose-limiting rash, transaminitis, and infections.62 A trial of idelalisib with bendamustine and rituximab was conducted in R/R chronic lymphocytic leukemia exhibited increased rates of serious adverse events of febrile neutropenia, pneumonia, and pyrexia in the idelalisib cohort versus placebo, including 6 deaths attributed to infections with idelalisib.63 Similarly, combination of idelalisib with a SYK inhibitor, entospletinib, resulted in high rates of treatment-emergent, life-threatening, and fatal pneumonitis.64 With the improved safety profile of copanlisib, these combinations could be revisited.

Another promising research direction is combining copanlisib with the bcl-2 inhibitor venetoclax, supported by preclinical data showing synergy between PI3K α/δ inhibition with BCL-2 blockade in some DLBCL subtypes. Concurrent bcl-2 and PI3K inhibition has also been able to overcome acquired venetoclax resistance in vitro.65 A recent cell-viability screen identified venetoclax as the strongest partner for copanlisib in B-cell lymphomas66 and this preclinical foundation has led to the SAKK 66/18 phase 1 study (NCT03886649) exploring the combination of copanlisib and venetoclax in relapsed/refractory lymphomas.

The potential for translation of in vitro synergy to efficacious therapeutic combinations is promising and could lead to wider applications of copanlisib in FL.

Newer PI3k Inhibitors

The established efficacy of PI3K inhibitors in lymphoid malignancies has been often overshadowed by their adverse event profile (Table 2). There is a need for safe and tolerable PI3K inhibitors with equivalent efficacy and improved feasibility. This has led to the development of umbralisib (TGR-1202) and ME-40, both of which are oral PI3Kis with once daily administration schedules. Umbralisib is a dual inhibitor of PI3Kδ and casein kinase-1-ε which has shown a 53% ORR in R/R FL in a phase 1 dose escalation trial (FL n=22).67 Updated safety data from the UNITY trial show that, similar to the idelalisib and duvelisib studies, the most frequent AEs were diarrhea (44%), nausea (39%), and fatigue (35%);68 however, the incidence of grade 3 or higher adverse events was lower (2–9% grade ≥3 diarrhea on the umbralisib monotherapy study. Of note, late onset diarrhea or colitis commonly seen with first-generation PI3Kδ inhibitors was uncommon. In patients who had been on umbralisib for at least 6 months (n=167, median umbralisib exposure 15.6 mos; range 6.4–60.6 mos), the incidence of diarrhea remained low with a 25% incidence of all grade diarrhea of which only 7% were grade 3 or higher. Umbralisib is currently being studied in UNITY-CLL Phase 3 randomized trial (NCT02612311) and UNITY-NHL Phase 2b randomized trial (NCT02793583).

Table 2 Efficacy and Safety Profile of PI3K Inhibitors in FL

ME-401 is a PI3Ki selective for p110δ and is currently being investigated in the phase 1b (NCT02914938) and II (TIDAL study, NCT03768505) setting. The phase 1b study is evaluating ME-401 as both monotherapy and in combination with rituximab or the BTK inhibitor zanubrutinib with a continuous (CS) and intermittent (IS) dosage schedule. Preliminary data have shown an ORR of 83% with ME-401 monotherapy in R/R FL.69 In keeping with the lower toxicity of intermittent PI3K inhibition, the IS dosing of ME-401 had a lower rate of immune-mediated AEs as compared to CS (11% vs 30%, respectively) and there was a potential to salvage disease progressions on IS by switching to CS.70

Intermittent PI3K inhibition seems to be a key factor in reducing adverse events while maintaining efficacy. The investigation of the newer oral PI3Kis could not only prove superior to copanlisib in terms of their safety profile and ease of administration but also pave the way for exploration of similar, intermittent schedules for the existing oral PI3K inhibitors.


Copanlisib provides a significant advantage over the oral PI3K inhibitors due to its tolerability; however, newer oral agents including those with an intermittent dosing schedule could prove more advantageous. Combinations with chemo-immunotherapy, immune-checkpoint inhibitors, or bcl-2 inhibitors could lead to expanded indications for copanlisib and are under study. A significant impediment to developing novel therapies in FL and developing rational therapeutic combinations is lack of accurate biomarkers which implies that most novel combinations being studied are relatively empiric. Studies are investigating the role of PI3K and macrophage activation gene expression profiles to predict responses to copanlisib which, if possible, at outset, would enable a risk-adapted decision-making approach. The intravenous dosing schedule of copanlisib and requirement for blood glucose and blood pressure monitoring does impact feasibility of administration in the outpatient setting and studies should explore a more pragmatic maintenance schedule after an initial loading period. In summary, copanlisib is a safe and efficacious addition to our therapeutic armamentarium against FL and should allow us to improve current and future outcomes of these patients.


Bruce D Cheson reports research funding to prior institution from AstraZeneca, Bristol-Myers-Squibb, Seattle Genetics, Trillium, TG Therapeutics, Abbvie, Pharmacyclics, and Epizyme.  He also reports consulting and advisory boards for Symbio, Morphosys, Beigene, Karyopharm, TG Therapeutics, and Merck, outside the submitted work. The authors report no other potential conflicts of interest for this work.


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