Phase 2 Study of Pemetrexed Plus Carboplatin, or Pemetrexed Plus Cisplatin with Concurrent Radiation Therapy Followed by Pemetrexed Consolidation in Patients with Favorable-Prognosis Inoperable Stage IIIA/B Non-Small-Cell Lung Cancer

被引:25
作者
Choy, Hak [1 ]
Schwartzberg, Lee S. [2 ,3 ]
Dakhil, Shaker R. [4 ]
Garon, Edward B. [5 ]
Gerber, David E. [1 ]
Choksi, Janak K. [6 ]
Govindan, Ramaswamy [7 ]
Peng, Guangbin [8 ]
Koustenis, Andrew [8 ]
Treat, Joseph [8 ]
Obasaju, Coleman [8 ]
机构
[1] Univ Texas Southwestern, Dallas, TX USA
[2] ACORN, Memphis, TN USA
[3] West Clin, Memphis, TN USA
[4] Canc Ctr Kansas, Wichita, KS USA
[5] Univ Calif Los Angeles, Translat Oncol Res Int Network, Los Angeles, CA USA
[6] Alamance Reg Med Ctr, Burlington, NC USA
[7] Washington Univ, St Louis, MO USA
[8] Lilly USA LLC, Indianapolis, IN USA
基金
美国国家卫生研究院;
关键词
Non-small-cell lung cancer; Pemetrexed; Cisplatin; Chemoradiotherapy; Stage III; LEUKEMIA GROUP-B; CHEST RADIATION; HOOSIER ONCOLOGY; US ONCOLOGY; IN-VITRO; CHEMOTHERAPY; TRIAL; RADIOTHERAPY; DOCETAXEL; ETOPOSIDE;
D O I
10.1097/JTO.0b013e3182a02546
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: There is no consensus chemotherapy regimen with concurrent radiotherapy (RT) for inoperable stage IIIA/B non-small-cell lung cancer. This trial evaluated pemetrexed with carboplatin (PCb) or cisplatin (PC) with concurrent RT followed by consolidation pemetrexed. Methods: In this open-label, noncomparative phase II trial, patients with inoperable stage IIIA/B non-small-cell lung cancer (initially all histologies, later restricted to nonsquamous) were randomized (1:1) to PCb or PC with concurrent RT (64-68 Gy over days 1-45). Consolidation pemetrexed monotherapy was administered every 21 days for three cycles. Primary endpoint was 2-year overall survival (OS) rate. Results: From June 2007 to November 2009, 98 patients were enrolled (PCb: 46; PC: 52). The 2-year OS rate was PCb: 45.4% (95% confidence interval [CI], 29.5-60.0%); PC: 58.4% (95% CI, 42.6-71.3%), and in nonsquamous patients was PCb: 48.0% (95% CI, 29.0-64.8%); PC: 55.8% (95% CI, 38.0-70.3%). Median time to disease progression was PCb: 8.8 months (95% CI, 6.0-12.6 months); PC: 13.1 months (95% CI, 8.3-not evaluable [NE]). Median OS (months) was PCb: 18.7 (95% CI, 12.9-NE); PC: 27.0 (95% CI, 23.2-NE). The objective response rates (ORRs) were PCb: 52.2%; PC: 46.2%. Grade 4 treatment-related toxicities (% PCb/% PC) were: anemia, 0/1.9; neutropenia, 6.5/3.8; thrombocytopenia, 4.3/1.9; and esophagitis, 0/1.9. Most patients completed scheduled chemotherapy and RT during induction and consolidation phases. No drug-related deaths were reported during chemoradiotherapy. Conclusions: Because of study design, efficacy comparisons cannot be made. However, both combinations with concurrent RT were active and well tolerated.
引用
收藏
页码:1308 / 1316
页数:9
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