Study of paclitaxel, etoposide, and cisplatin chemotherapy combined with twice-daily thoracic radiotherapy for patients with limited-stage small-cell lung cancer: A Radiation Therapy Oncology Group 9609 phase II study

被引:43
|
作者
Ettinger, DS
Berkey, BA
Abrams, RA
Fontanesi, J
Machtay, M
Duncan, PJ
Curran, WJ
Movsas, B
Byhardt, RW
机构
[1] Johns Hopkins Univ, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD 21231 USA
[2] Radiat Therapy Oncol Grp, Philadelphia, PA USA
[3] Univ Penn, Med Ctr, Philadelphia, PA 19104 USA
[4] Thomas Jefferson Univ Hosp, Philadelphia, PA 19107 USA
[5] Fox Chase Canc Ctr, Philadelphia, PA 19111 USA
[6] Cedars Sinai Med Ctr, Los Angeles, CA 90048 USA
[7] Greater Dayton Canc Ctr, Kettering, OH USA
[8] Med Coll Wisconsin, Milwaukee, WI 53226 USA
关键词
D O I
10.1200/JCO.2005.00.414
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose To determine the response rate, progression-free survival and overall survival, and toxicity of paclitaxel, etoposide, and cisplatin combined with accelerated hyperfractionated thoracic radiotherapy in patients with limited-disease (LD) small-cell lung cancer (SCLC). Patients and Methods LD-SCLC patients with measurable disease, Karnofsky performance score of ? 70, and adequate organ function who were previously untreated were eligible for the study. Treatment was as follows. In cycle 1 of chemotherapy, concurrent thoracic radiation therapy was administered. In cycles 2 to 4, chemotherapy was administered alone. In cycle 1, chemotherapy consisted of paclitaxel 135 mg/m(2) intravenous over 3 hours on day 1, etoposide 60 mg/m2 intravenous on day 1 and 80 mg/m2 orally on days 2 and 3, and cisplatin 60 mg/m2 intravenous on day 1. In cycles 2 to 4, the paclitaxel dose was increased to 175 mg/m(2), with the etoposide and cisplatin doses remaining the same as in cycle 1. The thoracic radiation therapy consisted of 1.5 Gy in 30 fractions (total dose, 45 Gy) administered 5 days a week for 3 weeks. Results Fifty-five patients were enrolled onto the study, and 53 were assessable. The major toxicities included grade 3 and 4 acute neutropenia (32% and 43%, respectively) and grade 3 and 4 esophagitis (32% and 4%, respectively). Two patients died as a result of therapy (one died of acute respiratory distress syndrome, and one died of sepsis). There was one late fatal pulmonary toxicity. The median survival time was 24.7 months. The 2-year survival rate was 54.7%. The median progression-free survival time was 13 months, with a 2-year progression-free survival rate of 26.4%. Conclusion Although this therapeutic regimen is effective in the treatment of patients with LD-SCLC, it is unlikely that the three-drug combination with thoracic radiation therapy will improve the survival times compared with the etoposide plus cisplatin chemotherapy regimen with thoracic radiation therapy in LD-SCLC patients.
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收藏
页码:4991 / 4998
页数:8
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