Radiation-induced esophagitis in lung cancer
Authors Baker S, Fairchild A
Received 31 May 2016
Accepted for publication 22 July 2016
Published 13 October 2016 Volume 2016:7 Pages 119—127
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Editor who approved publication: Prof. Dr. Pan-Chyr Yang
Sarah Baker, Alysa Fairchild
Department of Radiation Oncology, Cross Cancer Institute, University of Alberta, Edmonton, AB, Canada
Abstract: Radiation-induced esophagitis is the most common local acute toxicity of radiotherapy (RT) delivered for the curative or palliative intent treatment of lung cancer. Although concurrent chemotherapy and higher RT dose are associated with increased esophagitis risk, advancements in RT techniques as well as adherence to esophageal dosimetric constraints may reduce the incidence and severity. Mild acute esophagitis symptoms are generally self-limited, and supportive management options include analgesics, acid suppression, diet modification, treatment for candidiasis, and maintenance of adequate nutrition. Esophageal stricture is the most common late sequela from esophageal irradiation and can be addressed with endoscopic dilatation. Approaches to prevent or mitigate these toxicities are also discussed.
Keywords: non–small cell lung cancer, acute, late, toxicity, stricture
Radiation-induced esophagitis is a frequent and dose-limiting toxicity of thoracic radiotherapy (RT), especially when delivered concurrently with cytotoxic chemotherapy. The specific incidence is sensitive to the timing and methods used to measure it.1 For example, acute dysphagia resulting from irradiation of the esophagus was reported in one study on 13% of patients’ quality of life questionnaires, 18% of weekly physician ratings, and in 28% of patients’ verbal descriptions.2 In a meta-analysis of 13 palliative thoracic RT studies, physician-assessed dysphagia was more common after higher versus lower RT schedules (20.5% vs 14.9%; P=0.01); however, pooling of patients’ self-report data could not be performed due to heterogeneity.3
RT esophagitis can be classified as acute or late. The time frame of acute side effects is generally taken to mean ≤3 months after completion of treatment, although RT esophagitis most commonly onsets 2–3 weeks after the initiation of RT, lasting up to 4 weeks after RT completion.3,4 Symptoms tend to be cumulative, may peak after RT is finished, are generally self-limited, and can be addressed by conservative supportive care measures.1 As it is a predictable side effect of RT, esophagitis should probably not be described as a “complication” unless it is significant enough to interfere with the planned treatment.1
By definition, “late” refers to >3 months after the completion of RT; median time of onset of late esophageal injury is 6 months,5 with some instances diagnosed at 1 year or later.1 Late side effects more often require invasive management such as surgical intervention, and even then may not be reversible.1 Although RT dose schedules are generally chosen to limit the risk of long-term side effects to ≤5%, prevalence depends on the proportion of patients alive and at risk after treatment, and whether they are investigated for toxicity routinely, only if presenting with symptoms, or not at all.1
There is no evidence that incidence or severity of side effects correlates with eventual tumor response and that degree of toxicity does not generally correlate with pre-RT symptom burden.1 Although one group described that the severity of acute esophagitis predicted late esophageal toxicity,6 this finding has not been widely confirmed.
There are no specific criteria that can reliably distinguish between post-RT symptoms caused by tumor progression versus the same ones due to treatment.1,7,8 This uncertainty in causation can result in under- or overreporting of toxicity depending on the interpretation by individual clinicians.2 Some authors attribute complications to tumor if present at the symptomatic site, whereas others score all adverse outcomes following RT as treatment-induced, regardless of whether tumor is actually controlled.1 It is essential that tumor progression be ruled out before ascribing worsening symptoms after treatment to RT toxicity.
This article focuses on toxicity related to external beam RT only; brachytherapy is not discussed. Most of the available data are the results of RT for non-small cell lung cancer (NSCLC), but much of the data would theoretically be generalizable to small cell lung cancer. There is a paucity of data on esophagitis related to stereotactic body RT at present.
Radiation-induced injury involves DNA damage that activates stress-induced signaling pathways and proinflammatory cytokines leading to cell death by various mechanisms.5 The esophagus is vulnerable particularly to RT injury due to its continuous mucosal cell turnover. Mucosal inflammation and basal epithelial thinning can progress to denudation and ulceration.9 Different mechanisms may predominate in the pathogenesis of acute versus chronic radiation GI injury and have been recently reviewed.5
Acute esophagitis symptoms include dysphagia, nausea, anorexia, odynophagia, and substernal discomfort.10 If severe, these symptoms may lead to dehydration, malnutrition, aspiration, and weight loss.6,11 The most frequently employed grading scheme for acute esophagitis is the grade 0–4 Common Terminology Criteria for Adverse Events Version 4.03 (Table 1).12 Severely altered eating or swallowing that requires tube feeding, total parenteral nutrition (TPN), or hospitalization constitutes grade 3 esophagitis. Rarely, perforation or bleeding occurs,9 and these and other potentially life-threatening complications are classified as grade 4. Symptom scores have been noted in a large prospective study to correlate closely with acute esophageal mucosal injury grade after RT alone or concurrent chemoradiotherapy (CRT).13
Table 1 Common Terminology Criteria for Adverse Events Version 4.03 grading for acute esophagitis
Notes: Adapted from National Cancer Institute; National Institutes of Health; US Department of Health and Human Services. Common Terminology Criteria for Adverse Events (CTCAE); Version 4.0. Available from: http://evs.nci.nih.gov/ftp1/CTCAE/CTCAE_4.03_2010-06-14_QuickReference_5x7.pdf. Source: the website of the National Cancer Institute (https://www.cancer.gov). Accessed August 31, 2016.12
Symptoms from late radiation strictures typically include mechanical dysphagia from stenosis or impaired motility secondary to nerve damage4,10 and odynophagia from chronic ulceration.14,15 The rate of stricture requiring dilatation after radical RT is ~3%.16 The Radiation Therapy Oncology Group/European Organization for Research and Treatment of Cancer Late Esophagitis Morbidity Grading Criteria are commonly used to assess severity (Table 2). RT may also result in late perforation, submucosal fibrosis, mucosal atrophy, or ulceration.8,17 Recurrent pulmonary infections can result from chronic aspiration or bronchoesophageal fistula.5
Table 2 RTOG/EORTC late esophagitis morbidity grading criteria
Notes: Adapted from RTOG Foundation Inc. RTOG/EORTC Late Radiation Morbidity Scoring Schema. Available from: https://www.rtog.org/ResearchAssociates/AdverseEventReporting/RTOGEORTCLateRadiationMorbidityScoringSchema.aspx. Accessed August 31, 2016. Copyright 2016 RTOG.66
Abbreviations: RTOG, Radiation Therapy Oncology Group; EORTC, European Organisation for Research and Treatment of Cancer.
Patient and disease factors
Patient characteristics associated with higher rates of severe acute esophagitis include Caucasian race,10 age ≥70 years,6,18 female sex,19 poor initial performance status,19 low body mass index,20 gastroesophageal reflux disease,16 and potentially pretreatment dysphagia.19 De Ruysscher et al reported that worse neutropenia during CRT correlated with higher maximal dysphagia.21 Higher tumor and nodal stage19 and the presence of N2 disease are associated with higher rates of esophagitis, likely as surrogates for the volume of esophagus irradiated. Esophageal erosion secondary to tumor is also associated with higher rates,16 and tumors infiltrating the esophagus or proximal bronchial tree especially may put patients at risk of late fistula or perforation. Germline polymorphisms may render some patients more susceptible to injury than others.5
Factors that contribute to RT toxicity include volume of tissue irradiated, total dose, dose per day (fraction size), overall treatment time, concurrent systemic therapy, and RT technique (Table 3).1,8,22
A meta-analysis of 19 randomized trials of radical CRT versus RT alone, including concurrent and sequential systemic therapy, reported that the addition of chemotherapy increases acute esophagitis by approximately five times.23 In a study by Byhardt et al in patients with locally advanced NSCLC, the incidence of severe acute esophagitis with standard RT alone (60–69 Gy/30) was 1.3%; concurrent chemotherapy increased this to 14%–49%.24 In esophageal cancer, as an example, when systemic therapy is given in conjunction with RT, symptomatic toxicity occurs on average 1 week earlier, higher proportions of patients cannot complete planned treatment, and there is a higher risk of treatment-related death.17,25
Radical RT alone results in significantly lower rates of grade 3 or higher esophagitis (1%–2%).24 Hyperfractionated and hyperfractionated accelerated RT techniques have high rates of esophagitis10,26 even without the addition of chemotherapy and have not conclusively improved survival outcomes, so are not in common use.
RT from different eras is not directly comparable in terms of likelihood of toxicity: older techniques using two-dimensional (2D) planning and lower energy machines such as Cobalt-60 are more likely to cause side effects than modern technologies.1 2D RT techniques with concurrent chemotherapy result in grade 2 esophagitis in 75%, grade 3 in 22%, and grade 4 in 2% of patients.10
The emergence of advanced three-dimensional conformal RT and especially intensity-modulated RT results in more precise dose delivery to the target and therefore more sparing of normal structures such as the esophagus. In comparison with the aforementioned 2D incidences, using 3D conformal RT or intensity-modulated RT to deliver CRT results in grade 2 esophagitis in 32%, grade 3 in 17%, and grade 4 in 0.9%.27 Approximately 10%–20% of patients undergoing modern CRT will experience grade 3 esophagitis, which by definition indicates severely altered swallowing requiring hospitalization and/or TPN or tube feeding (Table 1).27,28 The potential gains in toxicity rates of these techniques must be weighed against the increased cost, time, and resources required for planning and treatment,1 and a steep institutional learning curve in achieving lower rates of toxicity seems to exist.7
Palliative regimens are the most frequently prescribed RT schedules for patients with NSCLC, as 75%–85% of patients present with incurable disease.29 While a lower total dose is usually delivered, often 30 Gy in 10 daily fractions, the relatively high daily dose still carries a risk of esophagitis: mild in 34% and moderate to severe esophagitis in 10% (Table 3).30
Prevention: dose constraints for acute esophagitis
Parameters from the Quantitative Analyses of Normal Tissue Effects in the Clinic report provide estimates of acute esophagitis risk in relation to mean organ dose (eg, mean dose to the entire esophagus <34 Gy results in 5%–20% incidence of grade >3 esophagitis).31 Other parameters reported as predictive include maximal esophageal point dose (69 Gy for RT alone and 58 Gy with concurrent chemotherapy), and percentage of esophageal surface area receiving >50 Gy.16,32,33 An individual patient data meta-analysis including 1,082 patients undergoing curative-intent CRT for locally advanced NSCLC found that esophageal volume receiving ≥60 Gy (V60) was the best predictor, with a V60 <0.07% associated with <5% risk of grade 3 or higher esophagitis, but V60 ≥17% conferring a 59% risk of grade ≥2 and 22% of grade ≥3 esophagitis.27 A previous analysis of 12 studies described no single best parameter but noted that higher esophageal volumes receiving >40–50 Gy correlated with higher rates of acute esophagitis.34 Other authors have reported maximum point dose exceeding 55 Gy and esophageal surface area receiving a dose exceeding 58 Gy as predictive.32,33 Figure 1 demonstrates the RT plan and esophageal dosimetric indices of a patient who developed grade 3 esophagitis requiring hospital admission and a treatment break.
Prevention: dose constraints for late esophageal toxicity
Emami et al estimated the dose at which 5% of patients develop stricture or perforation at 5 years to be 60 Gy when one-third of the esophagus length was irradiated, 58 Gy when two-thirds was irradiated, and 55 Gy after irradiation of the entire esophagus.35 With one-third of the esophagus irradiated to 72 Gy, 50% of patients developed late complications at 5 years.35 However, it must be acknowledged that these results are inferred largely on the basis of historic techniques.
Prevention: systemic agents
Amifostine, an organic thiophosphate, has been studied as a potential radioprotective agent. The active metabolite WR-1065 acts as a scavenger of the free-oxygen radicals produced by ionizing radiation,36 and early reports suggested the potential to reduce RT esophagitis without compromising tumor control.36–39 A subsequent phase III study in locally advanced NSCLC patients undergoing CRT, however, found no significant reduction in grade 3 or higher esophagitis.40 It did improve swallowing dysfunction and pain based on patients’ self-report but was associated with higher rates of nausea, vomiting, cardiotoxicity, and febrile neutropenia.41 Currently, the American Society of Clinical Oncology recommends against the use of amifostine.42
Another potential radioprotective agent, glutamine, has been associated with lower rates of mucositis, weight loss, and TPN use based on a retrospective cohort study in patients with head and neck and thoracic malignancies.43 A small prospective trial included NSCLC patients treated prophylactically with glutamine powder and reported no esophagitis in 49% of those undergoing radical CRT and 73% receiving sequential CRT.44 A phase III trial is currently underway.45
Nonsteroidal compounds have been studied to prevent RT esophagitis but have not yet been proved effective.46,47 Nonrandomized trials have suggested the potential efficacy of granulocyte macrophage colony stimulating factor.48 The use of honey to prevent mucositis in head and neck patients has been demonstrated in several small randomized trials;49,50 however, in a phase II trial reported in abstract form, there was no added benefit of Manuka honey compared to standard care for reducing odynophagia in patients with lung cancer undergoing CRT.51
In the absence of systemic agents with a proven ability to prevent RT esophagitis, pretreatment supportive care consultation to optimize baseline status and quality of life, such as clinical nutrition referral, should be undertaken.1
Acute radiation esophagitis can be generally diagnosed clinically and seldom is specific workup needed. Endoscopy is helpful not only in diagnosing and treating late esophageal strictures but also in differentiating radiation injury from infectious esophagitis (Table 4).52 Histologic findings typical of late RT esophagitis include chronic-appearing inflammation, fibrosis, and atypia in biopsies taken from the radiated field,53 with tissue sampling essential to rule out recurrent malignancy.5
Optimal management (Table 5) of esophagitis is important to not only reduce morbidity and maintain patient quality of life but also prevent further nutritional deterioration. Although short treatment breaks can be considered for severe symptoms,14 interruptions should be avoided if at all possible as they can decrease overall and disease-free survival.54
Table 5 Management strategies for acute radiation esophagitis
Notes: aProphylaxis may be considered. bRecommended at first symptoms of esophagitis.
Diet and nutritional support
Certain foods including tobacco, alcohol, coffee, spicy foods, and very hot or very cold items may irritate the esophageal mucosa.55 A soft or pureed bland diet is preferred. A dietician assessment can provide estimates of daily nutritional requirements and advice for optimizing protein and calorie intake, such as use of liquid meal replacements. Patients with dysphagia to fluids will require intravenous fluid hydration. In patients with weight loss, tube feeding or TPN may be required.56 Although placement of a nasogastric tube may irritate esophageal mucosa, enteral feeding is generally preferred over parental nutrition due to lower rates of infection and faster return to normal intake.57 Interventional radiology placement of a gastrostomy tube can be alternatively considered.
Mild to moderate odynophagia responds to topical analgesics such as oral viscous lidocaine.55 Treatment with nonsteroidal anti-inflammatory agents has been proposed56 since murine models demonstrate elevated prostaglandins following RT;9 however, opioid analgesics such as morphine are often necessary. Significant dysphagia typically requires a liquid formulation or intravenous, subcutaneous, or transdermal route of analgesic administration.
Patients with esophagitis have reduced lower esophageal sphincter pressure and are prone to reflux and should be prescribed a proton-pump inhibitor (PPI) or H2 receptor blocker.9 Proton-pump inhibitors, but not H2 receptor blockers, may reduce the healing time for erosive esophagitis.58 Antacids can provide symptomatic relief and help prevent candida infection based on their alkalotic properties.56
Prophylactic antifungal agents are recommended due to a high incidence of thrush and candidal esophagitis, particularly in patients receiving chemotherapy or steroids. Mixtures containing nystatin and equal parts of viscous xylocaine 2%, aluminum hydroxide-magnesium carbonate, and diphenhydramine can concurrently manage odynophagia and treat thrush.53 Nitrates or calcium-channel blockers may be effective for esophageal spasm,14 and prokinetic agents such as metoclopramide help address dysfunctional peristalsis.14,55
An early trial randomizing esophageal cancer patients to sucralfate or a control antacid containing sodium alginate reported significant symptom relief in 80% of patients treated with sucralfate compared to 10% of patients receiving the control and faster ulcer healing with sucralfate.59 However, a subsequent study found minor relief of symptoms in only 40% of patients and showed with TC99m-labeled sucralfate that the suspension adhered to the esophageal mucosa for a short period of time.60 McGinnis et al reported that sucralfate did not improve esophagitis in patients undergoing thoracic RT compared to placebo and actually found high rates of gastrointestinal toxicity (58% of sucralfate patients versus 14% of placebo, P<0.0001).61
Dilatation for esophageal stenosis
Dysphagia, especially when resulting in weight loss, is an indication for dilation of late esophageal stricture.5 Multiple dilatation procedures may be required for achievement of a minimum luminal diameter of 13 mm, which is needed for sustained symptomatic improvement.62 Major complications with dilatation include bleeding and aspiration, with a perforation risk of <0.4%.5 Gastrostomy tube feeding is recommended in the setting of strictures resistant to endoscopic dilatation to maintain adequate nutritional status, as is continued acid suppression with proton-pump inhibitor therapy.5
Despite improvements in RT delivery techniques, treatment-induced esophagitis continues to be a common and at times severe side effect for patients undergoing treatment for lung cancer. With aggressive symptomatic intervention and nutritional support, few patients require treatment breaks. Ongoing research in radioprotective agents and continued refinements of RT, such as adaptive image-guided therapy, may continued reduce the detrimental impact of acute and late esophageal toxicity in the future.
The authors report no conflicts of interest in this work.
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