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

被引:365
作者
Vokes, Everett E.
Herndon, James E., II
Kelley, Michael J.
Cicchetti, M. Giulia
Ramnath, Nithya
Neill, Harvey
Atkins, James N.
Watson, Dorothy M.
Akerley, Wallace
Green, Mark R.
机构
[1] Univ Chicago, Chicago, IL 60637 USA
[2] Duke Univ, Med Ctr, Canc & Leukemia Grp B, Ctr Stat, Durham, NC USA
[3] Wake Forest Univ, Bowman Gray Sch Med, Winston Salem, NC USA
[4] Roswell Pk Canc Inst, Buffalo, NY 14263 USA
[5] Univ Tennessee, Memphis, TN USA
[6] Univ Massachusetts, Sch Med, Worcester, MA USA
[7] Rhode Isl Hosp, Providence, RI USA
[8] Med Univ S Carolina, Charleston, SC 29425 USA
关键词
D O I
10.1200/JCO.2006.07.3569
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
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页码:1698 / 1704
页数:7
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