Intratumoral heterogeneity of ALK-rearranged and ALK/EGFR coaltered lung adenocarcinoma

Weijing Cai, Dongmei Lin, Chunyan Wu, Xuefei Li, Chao Zhao, Limou Zheng, Shannon Chuai, Ke Fei, Caicun Zhou, Fred R. Hirsch

Research output: Contribution to journalArticlepeer-review

119 Scopus citations


Purpose: Genetic intratumoral heterogeneity has a profound influence on the selection of clinical treatment strategies and on addressing resistance to targeted therapy. The purpose of this study was to explore the potential effect of intratumoral heterogeneity on both genetic and pathologic characteristics of ALK-rearranged lung adenocarcinoma (LADC) Methods: We tested ALK fusions and EGFR mutations in 629 patients with LADC by using laser-capture microdissection to capture spatially separated tumor cell subpopulations in various adenocarcinoma subtypes and to test for ALK fusions and EGFR mutations in ALK-rearranged, EGFR-mutated, and ALK/EGFR coaltered LADCs to compare the oncogenic driver status between different tumor cell subpopulations in the same primary tumor. Results: Among the 629 patients, 30 (4.8%) had ALK fusions, 364 (57.9%) had EGFR mutations, and two had ALKfusions that coexisted with EGFR mutations. Intratumoral heterogeneity of ALK fusions were identified in nine patients by reverse-transcriptase polymerase chain reaction. In the two patients with an ALK/EGFR coaltered status, genetic intratumoral heterogeneity was observed both between different growth patterns and within the same growth pattern. The relative abundance of ALK and EGFR alterations was different in the same captured area. ALK fusions were positively associated with a micropapillary pattern (P =.002) and were negatively associated with a lepidic pattern (P =.008) in an expanded statistical analysis of 900 individual adenocarcinoma components, although they appeared to be more common in acinar-predominant LADCs in the analysis of 629 patients. Conclusion: Intratumoral genetic heterogeneity was demonstrated to coexist with histologic heterogeneity in both single-driver and ALK/EGFR coaltered LADCs.

Original languageEnglish
Pages (from-to)3701-3709
Number of pages9
JournalJournal of Clinical Oncology
Issue number32
StatePublished - 10 Nov 2015
Externally publishedYes


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