Early dose reduction of osimertinib in advanced EGFR-mutated non-small cell lung cancer

被引:1
作者
Ferreira, Marion [1 ,2 ]
Ebia, Matthew I. [3 ]
Reckamp, Karen L. [3 ]
机构
[1] Univ Hosp Tours, Dept Pneumol & Resp Funct Explorat, Tours, France
[2] Ctr Etud Pathol Resp, INSERM, Tours, France
[3] Cedars Sinai Med Ctr, Dept Med, Los Angeles, CA USA
关键词
dose reduction; EGFR mutation; lung cancer; osimertinib;
D O I
10.1097/CAD.0000000000001609
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Osimertinib has become the standard of care for epidermal growth factor receptor (EGFR)-mutated non-small cell lung cancer (NSCLC). In order to prevent or treat toxicity, the osimertinib dose may be reduced. However, data regarding the impact of dose reduction during treatment are limited. We aimed to compare the efficacy of osimertinib early dose reduction during the first 3 months of treatment with late dose reduction in EGFR-mutated advanced NSCLC. This retrospective study included patients with EGFR-mutated advanced NSCLC who received osimertinib. We constituted two groups: 'early dose reduction' (early) with patients receiving a reduced dose of osimertinib from 80 to 40 mg within the 3 months of osimertinib initiation and 'late dose reduction' (late) with patients receiving a reduced dose after 3 months of full-dose treatment. Thirty-five patients were included, with 17 and 18 patients in the early and late groups, respectively, and a higher median age in the early group (76 vs. 67 years). The real-world progression-free survival (rwPFS) at 1 year was 70.5% in the early group and 88.9% in the late group (P = 0.31). Median rwPFS was 32.7 and 24.6 months (P = 0.98), and the median overall survival was 46.9 versus not reached in early and late groups, respectively (P = 0.17). Central nervous system rwPFS was not different between the early and late groups: 29.8 and 35.8 months, respectively (P = 0.39). We showed that a reduced dose of osimertinib within the first 3 months of treatment, compared to a later reduced dose, could influence treatment response or patient survival. Anti-Cancer Drugs 35: 672-679 Copyright (c) 2024 Wolters Kluwer Health, Inc. All rights reserved.
引用
收藏
页码:672 / 679
页数:8
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