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J Clin Oncol. 2019 Feb 1;37(4):278-285. doi: 10.1200/JCO.18.01585. Epub 2018 Dec 14.

EGFR-Mutant Adenocarcinomas That Transform to Small-Cell Lung Cancer and Other Neuroendocrine Carcinomas: Clinical Outcomes.

Author information

1
1 Massachusetts General Hospital, Boston, MA.
2
12 CHU de Qu├ębec, Quebec City, Quebec, Canada.
3
2 Yale Cancer Center, New Haven, CT.
4
3 Princess Margaret Cancer Centre, Toronto, Ontario, Canada.
5
4 Memorial Sloan Kettering Cancer Center, New York, NY.
6
5 Stanford Cancer Institute, Palo Alto, CA.
7
6 University of California San Diego, La Jolla, CA.
8
7 Abramson Cancer Center, Philadelphia, PA.
9
13 Lankenau Medical Center, Wynnewood, PA.
10
8 Johns Hopkins Sidney Kimmel Comprehensive Cancer Center, Baltimore, MD.
11
9 Rush University Medical Center, Chicago, IL.
12
10 Bennett Cancer Center, Stamford CT.
13
11 City of Hope National Medical Center, Duarte, CA.

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.

PMID:
30550363
DOI:
10.1200/JCO.18.01585

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