Long-Term Efficacy and Safety of Entrectinib in ROS1 Fusion-Positive NSCLC

被引:82
作者
Drilon, Alexander [1 ,2 ]
Chiu, Chao-Hua [3 ]
Fan, Yun [4 ]
Cho, Byoung Chul [5 ]
Lu, Shun [6 ]
Ahn, Myung-Ju [7 ]
Krebs, Matthew G. [8 ,9 ]
Liu, Stephen, V [10 ]
John, Thomas [11 ,12 ]
Otterson, Gregory A. [13 ,14 ]
Tan, Daniel S. W. [15 ]
Patil, Tejas [16 ]
Dziadziuszko, Rafal [17 ,18 ]
Massarelli, Erminia [19 ]
Seto, Takashi [20 ]
Doebele, Robert C. [16 ]
Pitcher, Bethany [21 ]
Kurtsikidze, Nino [22 ]
Heinzmann, Sebastian [23 ]
Siena, Salvatore [23 ,24 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Med, New York, NY USA
[2] Weill Cornell Med Coll, New York, NY USA
[3] Taipei Vet Gen Hosp, Dept Chest Med, Taipei, Taiwan
[4] Zhejiang Canc Hosp, Hangzhou, Peoples R China
[5] Yonsei Canc Ctr, Div Med Oncol, Seoul, South Korea
[6] Shanghai Jiao Tong Univ, Shanghai Chest Hosp, Sch Med, Dept Med Oncol,Shanghai Lung Canc Ctr, Shanghai, Peoples R China
[7] Sungkyunkwan Univ, Div Hematol Oncol, Dept Med, Samsung Med Ctr,Sch Med, Seoul, South Korea
[8] Univ Manchester, Div Canc Sci, Fac Biol Med & Hlth, Manchester, England
[9] Christie Natl Hlth Serv NHS Fdn Trust, Manchester Acad Hlth Sci Ctr, Manchester, England
[10] Georgetown Univ, Washington, DC USA
[11] Peter MacCallum Canc Ctr, Dept Med Oncol, Melbourne, Australia
[12] Austin Hlth, Olivia Newton John Canc Ctr, Melbourne, Australia
[13] Ohio State Univ, Arthur G James Canc Hosp, Comprehens Canc Ctr, Columbus, OH USA
[14] Ohio State Univ, Richard J Solove Res Inst, Comprehens Canc Ctr, Columbus, OH USA
[15] Duke Nat Univ Singapore NUS, Div Med Oncol, Natl Canc Ctr Singapore, Med Sch, Singapore, Singapore
[16] Univ Colorado, Div Med Oncol, Dept Med, Aurora, CO USA
[17] Med Univ Gdansk, Dept Oncol & Radiotherapy, Gdansk, Poland
[18] Med Univ Gdansk, Early Clin Trials Ctr, Gdansk, Poland
[19] City Hope Comprehens Canc Ctr, Dept Med Oncol & Therapeut Res, Duarte, CA USA
[20] Natl Hosp Org Kyushu Canc Ctr, Dept Thorac Oncol, Fukuoka, Japan
[21] F Hoffmann La Roche Ltd, Mississauga, ON, Canada
[22] F Hoffmann La Roche Ltd, Basel, Switzerland
[23] Grande Osped Metropolitano Niguarda, Niguarda Canc Ctr, Milan, Italy
[24] Univ Milan, Dept Oncol & Hematooncol, Milan, Italy
关键词
Entrectinib; Intracranial efficacy; NSCLC; ROS1; fusions; Treatment post-crizotinib; CELL LUNG-CANCER; INTEGRATED ANALYSIS; ROS1; CRIZOTINIB; INHIBITOR; SURVIVAL; ALK;
D O I
10.1016/j.jtocrr.2022.100332
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: Entrectinib is an approved tyrosine kinase inhibitor (TKI) for ROS1 fusion-positive NSCLC. An updated integrated analysis of entrectinib from the ALKA-372-001, STARTRK-1, and STARTRK-2 trials is presented, with sub-stantially longer follow-up, more patients, and the first description of the median overall survival (OS). An explor-atory analysis of entrectinib in ROS1 fusion-positive NSCLC with the central nervous system (CNS)-only progression post-crizotinib is reported. Methods: Adults with ROS1 fusion-positive, locally advanced or metastatic NSCLC who received at least one dose of entrectinib and had 12 months or longer of follow-up were included in the analysis. Co-primary end points were confirmed objective response rate (ORR) and duration of response (DoR) by blinded independent central review. The data cutoff was on August 31, 2020. Results: The efficacy-assessable population comprised 168 ROS1 TKI-naive patients. The median survival follow-up was 29.1 months (interquartile range, 21.8-35.9). The ORR was 68% (95% confidence interval [CI]: 60.2-74.8); the median DoR was 20.5 months. The median progression-free survival (PFS) was 15.7 months and the median OS was 47.8 months. In the 25 patients with measurable baseline CNS metastases, the intracranial ORR was 80% (95% CI: 59.3-93.2), median intracranial DoR was 12.9 months, and median intracranial PFS was 8.8 months. Among 18 patients with CNS-only pro-gression on previous crizotinib treatment, two achieved a partial response (11%) and four had stable disease (22%). In seven patients with measurable CNS disease from this cohort, the intracranial ORR was 14% (1 partial response). Conclusions: Entrectinib is active and achieves prolonged survival in ROS1 TKI-naive patients with ROS1 fusion- positive NSCLC. Modest activity is seen in patients with CNS-only progression post-crizotinib. (c) 2022 The Authors. Published by Elsevier Inc. on behalf of the International Association for the Study of Lung Cancer. This is an open access article under the CC BY-NC-ND li-cense (http://creativecommons.org/licenses/by-nc-nd/ 4.0/).
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页数:13
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