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首页> 外文期刊>International Journal of Radiation Oncology, Biology, Physics >70 Gy thoracic radiotherapy is feasible concurrent with chemotherapy for limited-stage small-cell lung cancer: analysis of Cancer and Leukemia Group B study 39808.
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70 Gy thoracic radiotherapy is feasible concurrent with chemotherapy for limited-stage small-cell lung cancer: analysis of Cancer and Leukemia Group B study 39808.

机译:70 Gy胸腔放疗与化疗相结合可用于有限期小细胞肺癌:癌症和白血病B组研究39808的分析。

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PURPOSE: To prospectively evaluate the feasibility of delivering 70 Gy once-daily thoracic radiotherapy (TRT), concurrent with chemotherapy, in the treatment of limited-stage small-cell lung cancer (L-SCLC). MATERIALS AND METHODS: Eligible patients received two cycles of induction paclitaxel (175 mg/m(2) on Day 1) and topotecan (1 mg/m(2) on Days 1-5) with granulocyte colony stimulating factor support, followed by three cycles of carboplatin (area under the curve = 5 on Day 1) and etoposide (100 mg/m(2) on Days 1-3). TRT (70 Gy, 2 Gy/fx/7 weeks) was initiated with the first cycle of carboplatin and etoposide. Prophylactic cranial irradiation was offered to patients achieving a complete response or good partial response. RESULTS: Ninety percent of patients (57 of 63) proceeded to protocol TRT. There was one treatment-related fatality. Nonhematologic Grade 3/4 toxicities affecting more than 10% of patients, during or after TRT, were dysphagia (16%/5%) and febrile neutropenia (12%/4%). The response rate to all therapy was 92% and the median overall survival is 22.4 months (95% confidence interval 16.1, infinity ). Twenty-eight patients remain alive with a median follow-up of 24.7 months. CONCLUSION: 70 Gy once-daily TRT can be delivered safely in the cooperative group setting for patients with L-SCLC. Initial efficacy data are encouraging. The hypothesis that high-dose once-daily TRT results in comparable or improved survival compared with twice-daily accelerated TRT warrants testing in a Phase III trial.
机译:目的:前瞻性评估在有限期小细胞肺癌(L-SCLC)治疗中,每天进行70 Gy一次胸腔放疗(TRT)和化学疗法的可行性。材料与方法:符合条件的患者接受粒细胞集落刺激因子支持的两个周期的诱导性紫杉醇(第1天为175 mg / m(2))和托泊替康(第1-5天为1 mg / m(2))。卡铂(曲线下面积=第1天为5)和依托泊苷(第1-3天为100 mg / m(2))的周期。 TRT(70 Gy,2 Gy / fx / 7周)从卡铂和依托泊苷的第一个周期开始。为达到完全缓解或良好部分缓解的患者提供了预防性颅骨照射。结果:百分之九十的患者(63人中的57人)接受了方案TRT。有1例与治疗有关的死亡。在TRT期间或之后,影响超过10%的患者的非血液学3/4级毒性为吞咽困难(16%/ 5%)和发热性中性粒细胞减少症(12%/ 4%)。所有疗法的反应率为92%,中位总生存期为22.4个月(95%置信区间16.1,无穷大)。 28名患者仍然存活,中位随访24.7个月。结论:L-SCLC患者在合作组中每天可以安全地递送70 Gy的TRT。最初的疗效数据令人鼓舞。与每日两次加速TRT相比,大剂量每日一次TRT可导致相当或更高的生存率这一假设值得在III期试验中进行测试。

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