Targeted and Cytotoxic Therapy in Coordinated Sequence (TACTICS): Erlotinib, Bevacizumab, and Standard Chemotherapy for Non-Small-Cell Lung Cancer, A Phase II Trial

被引:9
|
作者
Cohen, Ezra E. W. [2 ,3 ]
Subramanian, Janakiraman [1 ,4 ]
Gao, Feng [5 ]
Szeto, Livia [2 ,3 ]
Kozloff, Mark [2 ,3 ]
Faoro, Leonardo [2 ,3 ]
Karrison, Theodore [6 ]
Salgia, Ravi [2 ,3 ]
Govindan, Ramaswamy [1 ,4 ]
Vokes, Everett E. [2 ,3 ]
机构
[1] Washington Univ, Sch Med, Div Oncol, Dept Med, St Louis, MO 63110 USA
[2] Univ Chicago, Dept Med, Sect Hematol & Oncol, Chicago, IL 60637 USA
[3] Univ Chicago, Ctr Comprehens Canc, Chicago, IL 60637 USA
[4] Washington Univ, Sch Med, Alvin J Siteman Canc Ctr, St Louis, MO 63110 USA
[5] Washington Univ, Sch Med, Div Biostat, St Louis, MO 63110 USA
[6] Univ Chicago, Dept Hlth Studies, Chicago, IL 60637 USA
关键词
Bevacizumab; EGFR TK mutation; Erlotinib; NSCLC advanced stage; VINORELBINE PLUS CISPLATIN; RECEPTOR TYROSINE KINASE; MONOCLONAL-ANTIBODY; CARBOPLATIN; PACLITAXEL; COMBINATION; GEFITINIB; GEMCITABINE; STATISTICS; RECURRENT;
D O I
10.1016/j.cllc.2011.10.001
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The aim of this phase II study (ClinicalTrials.gov ID: NCT00607165) was to effectively combine existing targeted and cytotoxic chemotherapy in unselected patients with non small-cell lung cancer (NSCLC). The study achieved it primary endpoint, with a nonprogression rate of 46%, and the combination of erlotinib and bevacizumab was well tolerated. Given the modest benefit and the fact that frontline treatment with erlotinib is primarily indicated in patients with activating epidermal growth factor receptor (EGFR) tyrosine kinase (TK) mutations, we do not feel that this regimen requires further evaluation in unselected patients with NSCLC. Background: This trial focused on optimally combining existing targeted therapies and cytotoxic chemotherapy in the treatment of unselected patients with advanced non-small-cell lung cancer (NSCLC). Methods: Patients with previously untreated advanced-stage nonsquamous NSCLC were eligible for this trial. In module A, patients received up to 4 cycles of erlotinib 150 mg daily and bevacizumab 15 mg/kg every 3 weeks. Patients then received carboplatin (AUC = 6), paclitaxel 200 mg/m2, and bevacizumab 15 mg/kg for 4 cycles in module B. Patients who did not have progressive disease in module A received maintenance erlotinib 150 mg daily and bevacizumab 15 mg/kg every 3 weeks in module C. Results: Forty-eight patients were enrolled in this multicenter phase II trial. Most patients were male (62.5%) and white (77.1%) with stage IV disease (93.8%) and adenocarcinoma histologic type (66.7%). The overall response rate in module A was 10.4%, in module B it was 15.1%, and in module C it was 5.5%. The study achieved its primary endpoint, with a nonprogression rate of 45.8% in module A. The median overall survival (OS) was 12.6 months. Conclusion: The novel systemic therapy regimen is feasible in patients with advanced NSCLC. However there is no further role for developing this regimen in unselected patients with NSCLC. Clinical Lung Cancer, Vol. 13, No. 2, 123-8 (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:123 / 128
页数:6
相关论文
共 50 条
  • [1] The SATURN trial: the value of maintenance erlotinib in patients with non-small-cell lung cancer
    Neal, Joel W.
    FUTURE ONCOLOGY, 2010, 6 (12) : 1827 - 1832
  • [2] A Phase II Trial of Erlotinib As Front-Line Treatment in Clinically Selected Patients With Non-Small-Cell Lung Cancer
    Pallis, Athanasios G.
    Voutsina, Alexandra
    Kentepozidis, Nikolaos
    Giassas, Stylianos
    Papakotoulas, Pavlos
    Agelaki, Sofia
    Tryfonidis, Kostas
    Kotsakis, Athanasios
    Vamvakas, Lambros
    Vardakis, Nikolaos
    Georgoulias, Vassilis
    CLINICAL LUNG CANCER, 2012, 13 (02) : 129 - 135
  • [3] A phase II trial of induction of erlotinib followed by cytotoxic chemotherapy for EGFR mutation-positive non-squamous non-small cell lung cancer patients
    Tani, Tetsuo
    Naoki, Katsuhiko
    Yasuda, Hiroyuki
    Arai, Daisuke
    Ishioka, Kota
    Ohgino, Keiko
    Yoda, Satoshi
    Nakayama, Sohei
    Satomi, Ryosuke
    Terai, Hideki
    Ikemura, Shinnosuke
    Sato, Takashi
    Soejima, Kenzo
    CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2019, 84 (05) : 1065 - 1071
  • [4] Phase II Trial of Carboplatin, Paclitaxel, Cetuximab, and Bevacizumab Followed by Cetuximab and Bevacizumab in Advanced Nonsquamous Non-Small-Cell Lung Cancer SWOG S0536
    Kim, Edward S.
    Moon, James
    Herbst, Roy S.
    Redman, Mary W.
    Dakhil, Shaker R.
    Velasco, Mario R., Jr.
    Hirsch, Fred R.
    Mack, Philip C.
    Kelly, Karen
    Heymach, John V.
    Gandara, David R.
    JOURNAL OF THORACIC ONCOLOGY, 2013, 8 (12) : 1519 - 1528
  • [5] Toxicity of Targeted Therapy in Non-Small-Cell Lung Cancer Management
    Ricciardi, Serena
    Tomao, Silverio
    de Marinis, Filippo
    CLINICAL LUNG CANCER, 2009, 10 (01) : 28 - 35
  • [6] Phase II trial of neoadjuvant chemotherapy using alternating doublets in non-small-cell lung cancer
    Martins, Renato G.
    Dienstmann, Rodrigo
    de Biasi, Paulo
    Dantas, Karina
    Santos, Valdelice
    Toscano, Edson
    Roriz, Walter
    Zaraboni, Mauro
    Sousa, Aureliano
    Small, Isabele A.
    Moreira, Denise
    Ferreira, Carlos G.
    Zukin, Mauro
    CLINICAL LUNG CANCER, 2007, 8 (04) : 257 - 263
  • [7] Efficacy of bevacizumab plus erlotinib versus erlotinib alone in advanced non-small-cell lung cancer after failure of standard first-line chemotherapy (BeTa): a double-blind, placebo-controlled, phase 3 trial
    Herbst, Roy S.
    Ansari, Rafat
    Bustin, Frederique
    Flynn, Patrick
    Hart, Lowell
    Otterson, Gregory A.
    Vlahovic, Gordana
    Soh, Chang-Heok
    O'Connor, Paula
    Hainsworth, John
    LANCET, 2011, 377 (9780) : 1846 - 1854
  • [8] A Randomized, Phase II, Biomarker-Selected Study Comparing Erlotinib to Erlotinib Intercalated With Chemotherapy in First-Line Therapy for Advanced Non-Small-Cell Lung Cancer
    Hirsch, Fred R.
    Kabbinavar, Fairooz
    Eisen, Tim
    Martins, Renato
    Schnell, Fredrick M.
    Dziadziuszko, Rafal
    Richardson, Katherine
    Richardson, Frank
    Wacker, Bret
    Sternberg, David W.
    Rusk, Jason
    Franklin, Wilbur A.
    Varella-Garcia, Marileila
    Bunn, Paul A., Jr.
    Camidge, D. Ross
    JOURNAL OF CLINICAL ONCOLOGY, 2011, 29 (26) : 3567 - 3573
  • [9] The eligibility of advanced non-small-cell lung cancer patients for targeted therapy clinical trials
    Clarey, J.
    Kao, S. C.
    Clarke, S. J.
    Vardy, J.
    ANNALS OF ONCOLOGY, 2012, 23 (05) : 1229 - 1233
  • [10] Randomized, Placebo-Controlled, Phase II Study of Sequential Erlotinib and Chemotherapy As First-Line Treatment for Advanced Non-Small-Cell Lung Cancer
    Mok, Tony S. K.
    Wu, Yi-Long
    Yu, Chong-Jen
    Zhou, Caicun
    Chen, Yuh-Min
    Zhang, Li
    Ignacio, Jorge
    Liao, Meilin
    Srimuninnimit, Vichien
    Boyer, Michael J.
    Chua-Tan, Marina
    Sriuranpong, Virote
    Sudoyo, Aru W.
    Jin, Kate
    Johnston, Michael
    Chui, Winsome
    Lee, Jin-Soo
    JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (30) : 5080 - 5087