EGFR-mutant adenocarcinomas that transform to small-cell lung cancer and other neuroendocrine carcinomas: Clinical outcomes Journal Article


Authors: Marcoux, N.; Gettinger, S. N.; O'Kane, G.; Arbour, K. C.; Neal, J. W.; Husain, H.; Evans, T. L.; Brahmer, J. R.; Muzikansky, A.; Bonomi, P. D.; del Prete, S.; Wurtz, A.; Farago, A. F.; Dias-Santagata, D.; Mino-Kenudson, M.; Reckamp, K. L.; Yu, H. A.; Wakelee, H. A.; Shepherd, F. A.; Piotrowska, Z.; Sequist, L. V.
Article Title: EGFR-mutant adenocarcinomas that transform to small-cell lung cancer and other neuroendocrine carcinomas: Clinical outcomes
Abstract: PURPOSE Approximately 3% to 10% of EGFR (epidermal growth factor receptor) -mutant non-small cell lung cancers (NSCLCs) undergo transformation to small-cell lung cancer (SCLC), but their clinical course is poorly characterized. METHODS We retrospectively identified patients with EGFR-mutant SCLC and other high-grade neuroendocrine carcinomas seen at our eight institutions. Demographics, disease features, and outcomes were analyzed. RESULTS We included 67 patients-38 women and 29 men; EGFR mutations included exon 19 deletion (69%), L858R (25%), and other (6%). At the initial lung cancer diagnosis, 58 patients had NSCLC and nine had de novo SCLC or mixed histology. All but these nine patients received one or more EGFR tyrosine kinase inhibitor before SCLC transformation. Median time to transformation was 17.8 months (95% CI, 14.3 to 26.2 months). After transformation, both platinum-etoposide and taxanes yielded high response rates, but none of 17 patients who received immunotherapy experienced a response. Median overall survival since diagnosis was 31.5 months (95% CI, 24.8 to 41.3 months), whereas median survival since the time of SCLC transformation was 10.9 months (95% CI, 8.0 to 13.7 months). Fifty-nine patients had tissue genotyping at first evidence of SCLC. All maintained their founder EGFR mutation, and 15 of 19 with prior EGFR T790M positivity were T790 wild-type at transformation. Other recurrent mutations included TP53, Rb1, and PIK3CA. Re-emergence of NSCLC clones was identified in some cases. CNS metastases were frequent after transformation. CONCLUSION There is a growing appreciation that EGFR-mutant NSCLCs can undergo SCLC transformation. We demonstrate that this occurs at an average of 17.8 months after diagnosis and cases are often characterized by Rb1, TP53, and PIK3CA mutations. Responses to platinum-etoposide and taxanes are frequent, but checkpoint inhibitors yielded no responses. Additional investigation is needed to better elucidate optimal strategies for this group.
Keywords: erlotinib; paclitaxel; phase-ii; acquired-resistance
Journal Title: Journal of Clinical Oncology
Volume: 37
Issue: 4
ISSN: 0732-183X
Publisher: American Society of Clinical Oncology  
Date Published: 2019-02-01
Start Page: 278
End Page: 285
Language: English
ACCESSION: WOS:000457744000004
DOI: 10.1200/jco.18.01585
PROVIDER: wos
PUBMED: 30550363
Notes: Article -- Source: Wos
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MSK Authors
  1. Helena Alexandra Yu
    89 Yu
  2. Kathryn Cecilia Arbour
    15 Arbour