3rd-line anaplastic lymphoma kinase (ALK) inhibitors (ALKi) in advanced non-small cell lung cancer (aNSCLC): Real-world comparison to non-ALKi therapy.

Natalie Maimon(Tel Aviv University), Elizabeth Dudnik(Rabin Medical Center), Yakir Rottenberg(Hadassah Medical Center), Noa Popovits‐Hadari(Carmel Medical Center), Noam Asna(Barzilai Medical Center), Mira Wollner(Rambam Health Care Campus), Alona Zer(Rabin Medical Center), Maya Gottfried(Meir Medical Center), Moshe Mishaeli(Meir Medical Center), Yulia Rovitsky-Gelis(Carmel Medical Center), Anastasiya Lobachov(Sheba Medical Center), Amir Onn(Sheba Medical Center), Damien Urban(Sheba Medical Center), Mor Moskovitz(Rambam Health Care Campus), Jair Bar(Sheba Medical Center), Israel Lung Cancer Group
Journal of Clinical Oncology
May 20, 2020
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Abstract

e21685 Background: ALKi represent the standard 1 st - and 2 nd -line treatment (Tx) for ALK+ aNSCLC patients (pts). The value of ALKi in the 3 rd -line setting is unclear. We retrospectively assessed the real-world impact of a 3 rd -line ALKi vs. non-ALKi Tx in ALK+ aNSCLC pts. Methods: Consecutive ALK+ aNSCLC pts were identified in the working databases of 7 Israeli oncology centers; pts receiving any systemic Tx beyond 2 different ALKi were selected for the comparative analysis. Pts whose immediate next Tx line (post-2 nd -ALKi) was a 3 rd ALKi (Group (Gr) A) were compared to pts whose immediate next Tx line (post-2 nd -ALKi) was non-ALKi Tx (Gr B), in terms of overall survival (OS) and time to next Tx line (TNT). Results: 158 consecutive ALK+ aNSCLC pts diagnosed in January 2011 - March 2019 were included, median follow up from diagnosis of aNSCLC was 41 months (mo) (IQR 8-45). Median OS from aNSCLC diagnosis was 56 mo (95% CI 36-66). Post-2 nd -ALKi line was a 3 rd ALKi for 23 pts (Gr A) and a non-ALKi Tx for 10 pts (Gr B). 7 of Gr B (70%) received ALKi as a later line Tx. Median OS after initiation of post-2 nd -ALKi Tx was 27 mo (95% CI, 7-NA) for Gr A vs. 16 mo (95% CI, 7-NA) for Gr B; p-non-significant (NS) with or without adjustment for sex, age, brain metastases. TNT on post-2 nd -ALKi Tx was 6 mo (95% CI, 2-27) for Gr A vs. 2.5 mo (95% CI, 0-NA) for Gr B; p-NS. Conclusions: Following progression on a 2 nd ALKi, OS and TNT were numerically higher for pts receiving a 3 rd ALKi, but statistically NS. Extensive exposure of pts in the non-ALKi Tx Gr to an ALKi at a later stage might have impacted these results. Further studies are required to identify patients likely to benefit from ALKi after progressing on 2 or more ALKi Tx lines. [Table: see text]


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