A Novel MYH9-RET Fusion Occurrence and EGFR T790M Loss as an Acquired Resistance Mechanism to Osimertinib in a Patient with Lung Adenocarcinoma: A Case Report
Authors Sun Y, Pei L, Luo N, Chen D, Meng L
Received 18 June 2020
Accepted for publication 29 September 2020
Published 2 November 2020 Volume 2020:13 Pages 11177—11181
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 4
Editor who approved publication: Dr Sanjay Singh
Yanwei Sun,1 Lina Pei,2 Ningning Luo,3 Dongsheng Chen,3 Lingxin Meng1
1Department of Oncology, People’s Hospital of Rizhao, Rizhao, People’s Republic of China; 2Department of Pharmacy, People’s Hospital of Rizhao, Rizhao, People’s Republic of China; 3The State Key Laboratory of Translational Medicine and Innovative Drug Development, Jiangsu Simcere Diagnostics Co., Ltd, Nanjing, People’s Republic of China
Correspondence: Lingxin Meng
Department of Oncology, People’s Hospital of Rizhao, Rizhao, People’s Republic of China
Email [email protected]
Background: Osimertinib is a novel and irreversible epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitor (TKI) targeting EGFR sensitive mutations and EGFR exon20 p.T790M mutation, which demonstrated superior progression-free survival (PFS) and overall survival (OS).
Case Presentation: We report a patient with lung adenocarcinoma harboring EGFR exon 19 deletion mutant treatment with icotinib. After 6 months, she developed EGFR exon20 p.T790M and then the patient received osimertinib treatment. A novel MYH9 (exon41)-RET (exon12) fusion and EGFR exon20 p.T790M loss were identified using plasma circulation tumor DNA (ctDNA) after osimertinib treatment, which led to rapid progression after osimertinib five months and suggested a potential resistance mechanism.
Conclusion: Our findings expanded the spectrum of RET arrangement types and provided the basis for this hypothesis: acquired RET rearrangement and EGFR exon20 p.T790M loss potentially serve an additional resistance mechanism to osimertinib in EGFR-mutated non-small-cell lung cancer (NSCLC).
Keywords: MYH9-RET fusion, EGFR exon20 p.T790M loss, lung adenocarcinoma, acquired resistance, osimertinib
Approximately half of Asia-patients with NSCLC harbor EGFR mutation, and oral EGFR-TKIs have been used as one routine clinical therapeutic approach.1 Osimertinib is approved for both EGFR-TKI sensitive and EGFR exon20 p.T790M mutations in NSCLC patients.2,3 Previous studies described different resistance mechanisms to osimertinib, including EGFR tertiary mutations, like C797S,4 KRAS mutations, and targetable gene fusions.5 In all NSCLC patients, RET fusion accounts for 1–2%, involving various common fusion partners such as KIF5B and CCDC6.6 RET fusions have been proved that can mediate acquired resistance to EGFR-TKIs.7,8 Here, we reported a lung adenocarcinoma patient harboring a novel myosin heavy chain-9 (MYH9)-RET fusion, EGFR exon19 deletion (exon19del) and EGFR exon20 p.T790M loss and exerted resistance to osimertinib.
A non-smoking 48-year-old female was admitted to the hospital with intermittent cough and sputum for more than 4 months. Space occupying lesions were detected in the basal segment of the lower lobe of the left lung and intracranial site on admission examination. The immunohistochemistry staining results of pulmonary biopsy were CK5/6-positive, CK7-positive, thyroid transcription factor-1–positive, Naspin A–negative, P63-negative, P40-negative and Ki-67 positive index 30% (Figure 1). The disease was diagnosed as advanced lung adenocarcinoma (poorly differentiated). To seek for precision therapy, next-generation sequencing (NGS) (14-gene panel) was performed in primary lung cancer lesion. EGFR exon19 p. E746_A750del and EGFR amplification were detected (Table 1). The patient was immediately treated with icotinib. However, after 6 months, the patient’s condition deteriorated and the left lung tumor expanded. Then the detection of EGFR exon20 p.T790M was performed by ddPCR in plasma ctDNA and T790M positive was found. After that, the patient received osimertinib treatment and achieved a partial response with progression-free survival (PFS) of 5 months. Subsequently, the disease progressed with the left lung tumor enlarged.
Table 1 Findings of Gene Sequencing During Treatment
Figure 1 Histopathologic stains from the pulmonary biopsy. (A) hematoxylin and eosin. (B) CK5/6 (C) CK7. (D) thyroid transcription factor-1. (E) Naspin A. (F) P63. (G) P40. (H) Ki67. (×400). cytokeratin (CK).
Plasma ctDNA of patients after osimertinib treatment was tested by hybrid capture NGS method using 9-gene panel (Simceredx, CAP certified Laboratory), and EGFR exon19 p. E746_A750del, EGFR amplification as well as a novel MYH9 (exon41)-RET (exon12) fusion (Figure 2) were identified, without EGFR exon20 p.T790M. The findings of gene sequencing during treatment were given in Table 1 and time line of the treatments and the effects of different types of therapy were presented in Figure 3.
Figure 2 Next-generation sequencing findings of MYH9-RET fusion. (A) The Integrative Genomics Viewer snapshot of MYH9-RET. (B) Schematic representation of the MYH9-RET fusion protein domain structure.
In summary, this is the first case report that a novel MYH9-RET fusion and EGFR exon20 p.T790M loss occurred in lung adenocarcinoma patient who acquired resistance to osimertinib treatment. MYH9-RET fusion retains the complete kinase domain of RET. Besides, the partner gene MYH9 contains a coiled-coil domain. MYH9-ALK fusion has been reported in 2003, which makes MYH9 a plausible partner for RET as well.9 This novel fusion is considered to promote ligand-independent dimerization and constitutive activation of RET. Previously reported that acquired RET fusions can overcome the osimertinib inhibitory effect by the activation of MAPK and PI3K signal pathway, which was sufficient to cause EGFR TKI resistance.10,11 The NSCLC patients harboring RET fusion may benefit from new highly selective RET inhibitors, such as BLU-667 and LOXO-292. Previously reported that RET fusion coexisted with EGFR sensitive mutation in EGFR-mutated NSCLC patients who had progressed after first- or second-generation EGFR TKI treatment.8
EGFR exon 20 p.T790M loss has been reported in some osimertinib resistant cases.12–14 Genomic heterogeneity and clonal evolution including T790M-positive clones loss and selection of pre-existing resistance clones may contribute to the emergence of drug resistance. EGFR exon20 p.T790M was detected by NGS assay using ctDNA rather than tissue sample after osimertinib resistance. However, it might be due to the low sensitivity of the ctDNA assay. This is one limitation of this case. But RET fusions as mechanisms of resistance to osimertinib have so far always been accompanied by T790M loss in EGFR-mutant Lung Cancers.7,10
Because of the patient achieving the partial response and the progression-free survival (PFS) of osimertinib treatment was merely 5 months, and no other resistance mechanisms identified, we considered that this novel MYH9-RET fusion acquired and T790M loss was an acquired resistance mechanism. One study has demonstrated that osimertinib and BLU-667 (one of RET inhibitors) might be a well tolerated and effective approach for EGFR-mutated NSCLC acquired RET fusion.7 However, the patient did not have a chance to receive this combination therapy and died 3 months later. Moreover, the patient did not undergo a biopsy at disease progression after osimertinib, so we did not confirm whether there was a potential histological transformation or not.
As a routine genetic testing approach, NGS is essential in identifying mutations that mediate primary or acquired resistance during treatment. Our case report expanded the spectrum of RET arrangement types and provided the basis for this hypothesis: acquired RET rearrangement and T790M loss can potentially serve an additional resistance mechanism to osimertinib in EGFR-mutated NSCLC.
Ethics Approval and Consent for Publication
A written informed consent was obtained from the patient’s family for publication of the case details and any accompanying images and the research was approved by the Institutional Ethics Review Board of People’s hospital of Rizhao.
The authors thank Mr. Chuang Qi, Mr. Hao Guo, Mr. Chao Song, Ms. Si Li and Ms. Xueyu Yang from Simceredx for the kindly assistance.
First author: Yanwei Sun; Department of oncology, People’s hospital of Rizhao, Rizhao, China.
The authors have declared no conflicts of interest.
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