A Randomized Phase II Trial of Pemetrexed/Gemcitabine/Bevacizumab or Pemetrexed/Carboplatin/Bevacizumab in the First-Line Treatment of Elderly Patients with Advanced Non-small Cell Lung Cancer

被引:26
|
作者
Spigel, David R. [1 ,2 ]
Hainsworth, John D. [1 ,2 ]
Shipley, Dianna L. [2 ]
Ervin, Thomas J. [3 ]
Kohler, Peter C. [4 ]
Lubiner, Eric T. [3 ]
Peyton, James D. [2 ]
Waterhouse, David M. [5 ]
Burris, Howard A., III [1 ,2 ]
Greco, F. Anthony [1 ,2 ]
机构
[1] Sarah Cannon Res Inst, Nashville, TN 37203 USA
[2] Tennessee Oncol PLLC, Nashville, TN USA
[3] Florida Canc Specialists, Ft Myers, FL USA
[4] Munson Med Ctr, Traverse City, MI USA
[5] Oncol Hematol Care Inc, Cincinnati, OH USA
关键词
Elderly; Pemetrexed; Bevacizumab; Non-small cell lung cancer; OLDER PATIENTS; CHEMOTHERAPY USE; GEMCITABINE; CARBOPLATIN; BEVACIZUMAB; AGE; EPIDEMIOLOGY; SURVEILLANCE; COMBINATION; PACLITAXEL;
D O I
10.1097/JTO.0b013e3182307efe
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To assess time to progression (TTP) in elderly patients with previously untreated nonsquamous non-small cell lung cancer treated with pemetrexed/gemcitabine/bevacizumab or pemetrexed/carboplatin/bevacizumab. Methods: Eligible patients were aged 70 years or older with newly diagnosed stage IIIB/IV nonsquamous non-small cell lung cancer; Eastern Cooperative Oncology Group performance status 0 to 1; adequate organ function; and no active central nervous system metastasis. Patients were randomized 1: 1 to cohort A (pemetrexed 500 mg/m(2) IV, gemcitabine 1500 mg/m2 IV, and bevacizumab 10 mg/kg IV; days 1 and 15 of 28-day cycles) or cohort B (pemetrexed 500 mg/m2 IV, carboplatin area under the concentration-time curve = 5 IV, and bevacizumab 15 mg/kg IV; day 1 of 21-day cycles). After six cycles, stable/responding patients continued bevacizumab until disease progression. Results: Between March 2007 and December 2009, 110 patients (median age, 76 years; 88% stage IV) were treated for medians of 2.5 cycles (cohort A) and 6 cycles (cohort B). Overall response rate was 35% in both cohorts, with stable disease rates of 33% (A) and 45% (B). TTP by cohort was 4.7 and 10.2 months with median OS 7.5 and 14.8 months, respectively. Severe toxicities included the following: neutropenia (A, 51% and B, 45%), fatigue (A, 36% and B, 18%), anemia (A, 22% and B, 7%), infection (A, 25% and B, 7%), thrombocytopenia (A, 11% and B, 31%), and thromboembolism (A, 7% and B, 7%). Three potential treatment-related deaths occurred in cohort A (sepsis, thrombocytopenia, and myocardial infarction) and two in B (sepsis and pulmonary hemorrhage). Conclusions: Treatment with pemetrexed/carboplatin/bevacizumab was associated with improved TTP and OS in this elderly population and should be further evaluated. Treatment-related toxicities were expected and usually manageable, although deaths occurred with both regimens.
引用
收藏
页码:196 / 202
页数:7
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