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首页> 外文期刊>Journal of thoracic oncology: official publication of the International Association for the Study of Lung Cancer >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.
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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.

机译:在一系列晚期非小细胞肺癌的老年患者的一线治疗中,培养基/吉西他滨/贝伐单抗或磷酸盐/卡铂/贝伐单抗的随机期II试验。

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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/m2 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.
机译:目的:评估患有先前未经处理的非催名非小细胞肺癌的老年人患者进展(TTP)的时间,用磷酸盐/吉西他滨/贝伐单抗或磷酸盐/卡铂/贝伐单抗治疗。方法:符合条件的患者年龄70岁或以上患者,新诊断术阶段IIIB / IV非小细胞肺癌;东方合作肿瘤学组性能状态0至1;适当的器官功能;并且没有活跃的中枢神经系统转移。患者将患者1:1进行坐α(聚氨基雷德500mg / m 2 IV,吉西他滨1500mg / m 2 IV,贝伐单抗10mg / kg IV;第1天和第28天循环的第1天和第15天)或队列B(Pemetrexed 500mg /在浓度 - 时间曲线下的M2 IV,卡铂面积= 5〜静脉,贝伐单抗15mg / kg IV; 21天循环的第1天)。经过六个循环,稳定/响应患者持续贝伐单抗直至疾病进展。结果:2007年3月和2009年12月,110名患者(中位年龄,76岁; 88%阶段IV)对2.5个循环(群组)和6个循环(COHORT B)的中位进行治疗。两个群组的整体反应率为35%,稳定的疾病率为33%(a)和45%(b)。 COHORT的TTP分别为4.7和10.2个月,分别为7.5和14.8个月。严重的毒性包括:中性粒细胞病(a,51%和b,45%),疲劳(a,36%和b,18%),贫血(a,22%和b,7%),感染(a,25 %和B,7%),血小板减少症(A,11%和B,31%)和血栓栓塞(A,7%和B,7%)。群组(脓毒症,血小板减少症和心肌梗死)和两种(败血症和肺出血)发生了三种潜在的治疗相关死亡。结论:用Pemetrexed / Carboplatin / Bevacizumab治疗与这种老年人人口的改善的TTP和OS相关,并应进一步评估。虽然两种方案发生死亡,但预期治疗有关的毒性并通常是可控的。

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