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Updated efficacy and safety of entrectinib in NTRK fusion-positive non-small cell lung cancer.
Cho, Byoung Chul; Chiu, Chao-Hua; Massarelli, Erminia; Buchschacher, Gary L; Goto, Koichi; Overbeck, Tobias R; Loong, Herbert H F; Chee, Cheng E; Garrido, Pilar; Dong, Xiaorong; Fan, Yun; Lu, Shun; Schwemmers, Sven; Bordogna, Walter; Zeuner, Harald; Osborne, Stuart; John, Thomas.
Afiliação
  • Cho BC; Division of Medical Oncology, Yonsei Cancer Center, Yonsei University College of Medicine, 50-1 Yonsei-ro, Sinchon-dong, Seodaemun-gu, Seoul, Republic of Korea. Electronic address: CBC1971@yuhs.ac.
  • Chiu CH; Taipei Cancer Center and Taipei Medical University Hospital, Taipei Medical University, No. 252, Wuxing St, Xinyi District, Taipei City, Taipei 110, Taiwan. Electronic address: chaohuachiu@tmu.edu.tw.
  • Massarelli E; Department of Medical Oncology, City of Hope Comprehensive Cancer Center, 1500 E Duarte Rd, Duarte, CA 91702, USA. Electronic address: emassarelli@coh.org.
  • Buchschacher GL; Department of Hematology/Oncology, Kaiser Permanente Southern California, Los Angeles Medical Center, 4950 W Sunset Blvd, Los Angeles, CA 90027 USA. Electronic address: Gary.L.Buchschacher@kp.org.
  • Goto K; National Cancer Center Hospital East, 6-5-1 Kashiwanoha, Kashiwa, Chiba 277-8577, Japan. Electronic address: kgoto@east.ncc.go.jp.
  • Overbeck TR; Department of Hematology and Medical Oncology, University Medical Center Göttingen, Robert-Koch-Straße 40, 37075 Göttingen, Germany. Electronic address: tobias.overbeck@med.uni-goettingen.de.
  • Loong HHF; Department of Clinical Oncology, The Chinese University of Hong Kong, Central Ave, Hong Kong, Hong Kong Special Administrative Region. Electronic address: h_loong@clo.cuhk.edu.hk.
  • Chee CE; Department of Haematology-Oncology, National University Cancer Institute, Singapore 119074, Singapore. Electronic address: cheng_ean_chee@nuhs.edu.sg.
  • Garrido P; Medical Oncology Department, Ramón y Cajal University Hospital, M-607, 9, 100, 28034 Madrid, Spain. Electronic address: pilargarridol@gmail.com.
  • Dong X; Cancer Center, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China. Electronic address: xhzzdxr@126.com.
  • Fan Y; Department of Medical Thoracic Oncology, Zhejiang Cancer Hospital, Hangzhou, China. Electronic address: fanyun@zjcc.org.cn.
  • Lu S; Department of Medical Oncology, Shanghai Chest Hospital, Shanghai Jiao Tong University, Shanghai, China. Electronic address: shunlu@sjtu.edu.cn.
  • Schwemmers S; F. Hoffmann-La Roche Ltd, Grenzacherstrasse 124, 4070 Basel, Switzerland. Electronic address: sven.schwemmers@roche.com.
  • Bordogna W; F. Hoffmann-La Roche Ltd, Grenzacherstrasse 124, 4070 Basel, Switzerland. Electronic address: walter.bordogna@roche.com.
  • Zeuner H; F. Hoffmann-La Roche Ltd, Grenzacherstrasse 124, 4070 Basel, Switzerland. Electronic address: harald.zeuner@roche.com.
  • Osborne S; F. Hoffmann-La Roche Ltd, Grenzacherstrasse 124, 4070 Basel, Switzerland. Electronic address: stuart.osborne@roche.com.
  • John T; Department of Medical Oncology, Peter McCallum Cancer Center, 305 Grattan St, Melbourne, VIC 3000, Australia. Electronic address: tom.john@petermac.org.
Lung Cancer ; 188: 107442, 2024 02.
Article em En | MEDLINE | ID: mdl-38171156
ABSTRACT

OBJECTIVES:

NTRK fusions result in constitutively active oncogenic TRK proteins responsible for âˆ¼ 0.2 % of non-small cell lung cancer (NSCLC) cases. Approximately 40 % of patients with advanced NSCLC develop CNS metastases; therefore, treatments with intracranial (IC) efficacy are needed. In an integrated analysis of three phase I/II studies (ALKA-372-001 EudraCT 2012-000148-88; STARTRK-1 NCT02097810; STARTRK-2 NCT02568267), entrectinib, a potent, CNS-active, TRK inhibitor, demonstrated efficacy in patients with NTRK fusion-positive (fp) NSCLC (objective response rate [ORR] 64.5 %; 2 August 2021 data cut-off). We present updated data for this cohort. MATERIALS AND

METHODS:

Eligible patients were ≥ 18 years with locally advanced/metastatic, NTRK-fp NSCLC with ≥ 12 months of follow-up. Tumor responses were assessed by blinded independent central review (BICR) per RECIST v1.1 at Week 4 and every eight weeks thereafter. Co-primary endpoints ORR; duration of response (DoR). Secondary endpoints included progression-free survival (PFS); overall survival (OS); IC efficacy; safety. Enrolment cut-off 2 July 2021; data cut-off 2 August 2022.

RESULTS:

The efficacy-evaluable population included 51 patients with NTRK-fp NSCLC. Median age was 60.0 years (range 22-88); 20 patients (39.2 %) had investigator-assessed baseline CNS metastases. Median survival follow-up was 26.3 months (95 % CI 21.0-34.1). ORR was 62.7 % (95 % CI 48.1-75.9), with six complete and 26 partial responses. Median DoR and PFS were 27.3 months (95 % CI 19.9-30.9) and 28.0 months (95 % CI 15.7-30.4), respectively. Median OS was 41.5 months. In patients with BICR-assessed baseline CNS metastases, IC-ORR was 64.3 % (n = 9/14; 95 % CI 35.1-87.2), including seven complete responders, and IC-DoR was 55.7 months. In the safety-evaluable population (n = 55), most treatment-related adverse events were grade 1/2; no treatment-related deaths were reported.

CONCLUSION:

Entrectinib has continued to demonstrate deep and durable systemic and IC responses in patients with NTRK-fp NSCLC.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Benzamidas / Neoplasias do Sistema Nervoso Central / Carcinoma Pulmonar de Células não Pequenas / Neoplasias Pulmonares / Antineoplásicos Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Benzamidas / Neoplasias do Sistema Nervoso Central / Carcinoma Pulmonar de Células não Pequenas / Neoplasias Pulmonares / Antineoplásicos Idioma: En Ano de publicação: 2024 Tipo de documento: Article