1. Clinical outcome, long‐term survival and tolerability of sequential therapy of first‐line crizotinib followed by alectinib in advanced <scp>ALK</scp> + <scp>NSCLC</scp> : A multicenter retrospective analysis in China
- Author
-
Yumei Peng, Yangchun Gu, Li Liang, Yan Zhang, Puyuan Xing, Haojing Li, Junling Li, Li Shan, Kewei Ma, Z. Zou, Guilan Dong, Xuezhi Hao, Cuiying Zhang, and Ye Guo
- Subjects
Male ,Pulmonary and Respiratory Medicine ,Oncology ,Alectinib ,China ,medicine.medical_specialty ,Lung Neoplasms ,medicine.medical_treatment ,Population ,Carbazoles ,ALK+ NSCLC ,Systemic therapy ,Targeted therapy ,Piperidines ,Crizotinib ,Carcinoma, Non-Small-Cell Lung ,Internal medicine ,Humans ,Medicine ,Anaplastic Lymphoma Kinase ,Adverse effect ,education ,Protein Kinase Inhibitors ,RC254-282 ,Aged ,Retrospective Studies ,education.field_of_study ,business.industry ,Neoplasms. Tumors. Oncology. Including cancer and carcinogens ,Original Articles ,General Medicine ,Middle Aged ,Progression-Free Survival ,Discontinuation ,Tolerability ,Original Article ,Female ,business ,medicine.drug - Abstract
Background There is limited data on the clinical outcome, long‐term survival and tolerability of sequential therapy of first‐line crizotinib followed by alectinib in a real‐world setting for Chinese patients with advanced ALK+ NSCLC. Methods The medical records of patients who received sequential therapy with first‐line crizotinib followed by alectinib (no intermittent systemic therapy was allowed between the two ALK‐TKIs) were collected from six centers in China. Combined time treatment to failure (C‐TTF) was defined as the period from the start of crizotinib to the complete discontinuation of alectinib due to any cause. Results A total of 61 patients were included in our study. Fifty‐two patients were switched to alectinib due to disease progression, seven as a result of toxicity, and two due to patient preference. At the time of data cutoff, alectinib treatment was discontinued in 31 patients on account of disease progression while severe adverse events resulted in cessation of alectinib in another two patients. Rebiopsy was conducted in 21 patients following disease progression on alectinib in whom ALK secondary mutation was found in 13 patients. Patients with ALK secondary mutation demonstrated better PFS during treatment with subsequent ALK‐TKIs compared with those without (10.4 vs. 3.1 m, p = 0.0018, HR = 0.08). With a median follow‐up of 34.3 months, C‐TTF was 39.2 months and estimated 5‐year OS was 68.6% in the overall population. Conclusion Sequential therapy with first‐line crizotinib followed by alectinib demonstrated long‐term benefits. Different efficacy in subsequent ALK‐TKI between patients with or without ALK secondary mutation further emphasized the importance of rebiopsy to guide targeted therapy more precisely., Sequential therapy with first‐line crizotinib followed by alectinib demonstrated long‐term benefits in a Chinese population. Different efficacy in subsequent ALK‐TKI between patients with or without ALK secondary mutation further emphasized the importance of rebiopsy to guide targeted therapy more precisely.
- Published
- 2021