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EGFR-Mutant Adenocarcinomas That Transform to Small-Cell Lung Cancer and Other Neuroendocrine Carcinomas: Clinical Outcomes.
- Source :
-
Journal of clinical oncology : official journal of the American Society of Clinical Oncology [J Clin Oncol] 2019 Feb 01; Vol. 37 (4), pp. 278-285. Date of Electronic Publication: 2018 Dec 14. - Publication Year :
- 2019
-
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.<br />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.<br />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.<br />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.
- Subjects :
- Adenocarcinoma of Lung drug therapy
Adenocarcinoma of Lung mortality
Adenocarcinoma of Lung secondary
Adult
Aged
Aged, 80 and over
Antineoplastic Combined Chemotherapy Protocols therapeutic use
Carcinoma, Non-Small-Cell Lung drug therapy
Carcinoma, Non-Small-Cell Lung mortality
Carcinoma, Non-Small-Cell Lung secondary
Class I Phosphatidylinositol 3-Kinases genetics
ErbB Receptors genetics
Female
Genetic Predisposition to Disease
Humans
Lung Neoplasms drug therapy
Lung Neoplasms mortality
Lung Neoplasms pathology
Male
Middle Aged
Neoplasm Grading
North America
Phenotype
Retinoblastoma Binding Proteins genetics
Retrospective Studies
Small Cell Lung Carcinoma drug therapy
Small Cell Lung Carcinoma mortality
Small Cell Lung Carcinoma secondary
Time Factors
Treatment Outcome
Tumor Suppressor Protein p53 genetics
Ubiquitin-Protein Ligases genetics
Adenocarcinoma of Lung genetics
Biomarkers, Tumor genetics
Carcinoma, Non-Small-Cell Lung genetics
Lung Neoplasms genetics
Mutation
Small Cell Lung Carcinoma genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1527-7755
- Volume :
- 37
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Journal of clinical oncology : official journal of the American Society of Clinical Oncology
- Publication Type :
- Academic Journal
- Accession number :
- 30550363
- Full Text :
- https://doi.org/10.1200/JCO.18.01585