4.7 Article

Induction chemotherapy followed by chemoradiotherapy compared with chemoradiotherapy alone for regionally advanced unresectable stage III non-small-cell lung cancer: Cancer and Leukemia Group B

期刊

JOURNAL OF CLINICAL ONCOLOGY
卷 25, 期 13, 页码 1698-1704

出版社

AMER SOC CLINICAL ONCOLOGY
DOI: 10.1200/JCO.2006.07.3569

关键词

-

类别

资金

  1. NCI NIH HHS [CA77658, CA12449, CA71323, CA47642, CA47559, CA21060, CA74811, CA08025, CA04326, CA45564, CA37135, CA77298, CA11028, CA77440, CA16450, CA07968, CA86726, CA35421, CA12046, CA29511, CA45808, CA45389, CA26806, U10 CA033601, CA03927, CA41287, CA29165, CA32291, CA47555, CA47577, CA02599, CA11789, CA04457, CA77597, CA33601] Funding Source: Medline

向作者/读者索取更多资源

Purpose Standard therapy for unresectable stage III non-small-cell lung cancer includes concomitant chemoradiotherapy. In Cancer and Leukemia Group B 39801, we evaluated whether induction chemotherapy before concurrent chemoradiotherapy would result in improved survival. Patients and Methods Between July 1998 and May 2002, 366 patients were randomly assigned to arm A, which involved immediate concurrent chemoradiotherapy with carboplatin area under the concentration-time curve (AUC) of 2 and paclitaxel 50 mg/m(2) given weekly during 66 Gy of chest radiotherapy, or arm B, which involved two cycles of carboplatin AUC 6 and paclitaxel 200 mg/m(2) administered every 21 days followed by identical chemoradiotherapy. The accrual goal was 360 patients. Results Thirty-four percent of patients were female, 66% were male, and the median age was 63 years. Grade 3 or 4 toxicities during induction chemotherapy on arm B consisted mainly of neutropenia (18% and 20%, respectively). During concurrent chemoradiotherapy, there was no difference in severity of in-field toxicities of esophagitis ( grade 3 and 4 were, respectively, 30% and 2% for arm A v 28% and 8% for arm B) and dyspnea ( grade 3 and 4 were, respectively, 11% and 3% for arm A v 15% and 4% for arm B). Survival differences were not statistically significant ( P =.3), with a median survival on arm A of 12 months (95% CI, 10 to 16 months) versus 14 months ( 95% CI, 11 to 16 months) on arm B and a 2-year survival of 29% ( 95% CI, 22% to 35%) and 31% ( 95% CI, 25% to 38%). Age, weight loss before therapy, and performance status were statistically significant predictive factors. Conclusion The addition of induction chemotherapy to concurrent chemoradiotherapy added toxicity and provided no survival benefit over concurrent chemoradiotherapy alone. The median survival achieved in each of the treatment groups is low, and the routine use of weekly carboplatin and paclitaxel with simultaneous radiotherapy should be re-examined.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据