Clinical experience and management of adverse events in patients with advanced ALK-positive non-small-cell lung cancer receiving alectinib

被引:20
作者
Dziadziuszko, R. [1 ]
Peters, S. [2 ]
Ruf, T. [3 ]
Cardona, A. [3 ]
Guerini, E. [3 ]
Kurtsikidze, N. [3 ]
Smoljanovic, V. [3 ]
Planchard, D. [4 ,5 ]
机构
[1] Med Univ Gdansk, Dept Oncol & Radiotherapy, Gdansk, Poland
[2] Ctr Hosp Univ Vaudois CHUV, Lausanne Univ Hosp, Lausanne, Switzerland
[3] F Hoffmann La Roche Ltd, Basel, Switzerland
[4] Gustave Roussy Canc Campus, Dept Med Oncol, Thorac Oncol Unit, Villejuif, France
[5] Gustave Roussy Canc Campus, Dept Canc Med, Thorac Oncol Unit, 114 Edouard Vaillant St, F-94805 Villejuif, France
关键词
alectinib; ALK-positive NSCLC; clinical experience; safety; tolerability; INHIBITOR ALECTINIB; ANTITUMOR-ACTIVITY; J-ALEX; CRIZOTINIB; SURVIVAL; MODELS;
D O I
10.1016/j.esmoop.2022.100612
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Alectinib is a preferred first-line therapy for patients with advanced anaplastic lymphoma kinase (ALK)-positive non -small-cell lung cancer (NSCLC) in several national clinical practice guidelines. The randomized, global, phase III ALEX study has demonstrated significant improvement in progression-free survival for alectinib over crizotinib in treatment-naive ALK-positive NSCLC. It was also the first study to show clinically meaningful improvement in overall survival for a next-generation ALK tyrosine kinase inhibitor relative to crizotinib. The J-ALEX and ALESIA phase III studies confirmed the clinical benefit of alectinib relative to crizotinib in the first-line ALK-positive NSCLC treatment setting in Japanese and Asian patients, respectively. Across these pivotal phase III trials, alectinib had a manageable, well-characterized safety profile. Here, we review the safety and tolerability of long-term alectinib treatment in patients with advanced ALK-positive NSCLC and provide guidance for physicians, based on clinical experience, on the management of the most frequently reported adverse events (AEs). Most AEs associated with alectinib can be managed by dose reduction. Some alectinib-related AEs are not yet fully characterized, including myalgia and peripheral oedema and deciphering their underlying mechanism of action could enhance their management. With longer-term follow-up, the safety profile of alectinib continues to remain consistent in the ALEX study, with no new safety signals observed. Safety and tolerability data from the first-line phase III alectinib trials are also consistent with those observed in clinical trials of alectinib in later-line settings. These results add to the weight of evidence recommending alectinib as a preferred therapy for treatment-naive advanced ALK-positive NSCLC.Key words: alectinib, ALK-positive NSCLC, clinical experience, safety, tolerability
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页数:10
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