Randomized Phase III Trial of Maintenance Bevacizumab With or Without Pemetrexed After First-Line Induction With Bevacizumab, Cisplatin, and Pemetrexed in Advanced Nonsquamous Non-Small-Cell Lung Cancer: AVAPERL (MO22089)

被引:297
作者
Barlesi, Fabrice [1 ,2 ]
Scherpereel, Arnaud [3 ]
Rittmeyer, Achim [4 ]
Pazzola, Antonio [5 ]
Tur, Neus Ferrer [6 ]
Kim, Joo-Hang [7 ]
Ahn, Myung-Ju [8 ]
Aerts, Joachim G. J. V. [9 ,10 ]
Gorbunova, Vera [12 ]
Vikstrom, Anders [13 ]
Wong, Elaine K. [14 ]
Perez-Moreno, Pablo [14 ]
Mitchell, Lada [14 ]
Groen, Harry J. M. [11 ]
机构
[1] Aix Marseille Univ, AP HM, Marseille, France
[2] Ctr Invest Clin, Marseille, France
[3] Ctr Hosp Reg Univ Lille, Hop A Calmette, Lille, France
[4] Lungenfachklin Immenhausen, Immenhausen, Germany
[5] Osped Civile Santissima, Sassari, Italy
[6] Hosp Son Llatzer, Palma De Mallorca, Spain
[7] Yonsei Univ, Coll Med, Seoul 120749, South Korea
[8] Sungkyunkwan Univ, Sch Med, Seoul, South Korea
[9] Amphia Hosp, Breda, Netherlands
[10] Erasmus MC, Rotterdam, Netherlands
[11] Univ Groningen, Univ Med Ctr Groningen, Groningen, Netherlands
[12] NN Blokhin Canc Res Ctr Russia, Moscow, Russia
[13] Lungkliniken, Linkoping, Sweden
[14] F Hoffmann Roche, Basel, Switzerland
关键词
EML4-ALK FUSION GENE; TREATMENT RATIONALE; PLUS GEMCITABINE; THERAPY; CARBOPLATIN; PLACEBO; DESIGN;
D O I
10.1200/JCO.2012.42.3749
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Purpose Maintenance therapy is associated with improved survival in patients with non-small-cell lung cancer (NSCLC), but few studies have compared active agents in this setting. AVAPERL evaluated the safety and efficacy of bevacizumab with or without pemetrexed as continuation maintenance treatment. Patients and Methods Patients with advanced nonsquamous NSCLC received first-line bevacizumab 7.5 mg/kg, cisplatin 75 mg/m(2), and pemetrexed 500 mg/m(2) once every 3 weeks for four cycles. Those achieving response or stable disease were randomly assigned at a ratio of 1: 1 to maintenance bevacizumab 7.5 mg/kg or bevacizumab 7.5 mg/kg plus pemetrexed 500 mg/m(2) once every 3 weeks until disease progression or unacceptable toxicity. The primary end point was progression-free survival (PFS) after random assignment. Results In total, 376 patients received induction treatment, 71.9% achieved disease control, and 67.3% were randomly assigned to maintenance therapy, with 125 and 128 receiving single-agent bevacizumab and bevacizumab plus pemetrexed treatment, respectively. At a median follow-up of 8.1 months, PFS from random assignment was significantly improved in the bevacizumab plus pemetrexed arm (median, 3.7 v 7.4 months; hazard ratio, 0.48; 95% CI, 0.35 to 0.66; P < .001) per a stratified model. The PFS benefit extended across age, performance status, smoking history, and induction response (stable disease v partial response) subgroups. Any grade, grade >= 3, and serious adverse events occurred more often with bevacizumab plus pemetrexed maintenance. No new safety signals were observed. Conclusion In an unselected population of patients with nonsquamous NSCLC who had achieved disease control with platinum-based chemotherapy plus bevacizumab, bevacizumab plus pemetrexed maintenance was associated with a significant PFS benefit compared with bevacizumab alone. The combination was well tolerated. (C) 2013 by American Society of Clinical Oncology
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页码:3004 / +
页数:10
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