Results from a Single Institution Phase II Trial of Concurrent Docetaxel/Carboplatin/Radiotherapy Followed by Surgical Resection and Consolidation Docetaxel/Carboplatin in Stage III Non-Small-Cell Lung Cancer

被引:1
作者
Das, Millie [1 ]
Donington, Jessica S. [2 ]
Murphy, James [3 ]
Kozak, Margaret [3 ]
Eclov, Neville [3 ]
Whyte, Richard I. [4 ]
Hoang, Chuong D. [4 ]
Zhou, Lisa [1 ]
Le, Quynh-Thu [3 ]
Loo, Billy W., Jr. [3 ]
Wakelee, Heather [1 ]
机构
[1] Stanford Univ, Dept Med, Div Oncol, Stanford, CA 94305 USA
[2] NYU, Sch Med, Dept Cardiothorac Surg, New York, NY 10003 USA
[3] Stanford Univ, Dept Radiat Oncol, Stanford, CA 94305 USA
[4] Stanford Univ, Dept Cardiothorac Surg, Stanford, CA 94305 USA
关键词
NSCLC; Phase II; Stage III; Trimodality therapy; WEEKLY DOCETAXEL; RADIOTHERAPY; CHEMOTHERAPY; CARBOPLATIN; MORBIDITY; MORTALITY; SURVIVAL; SURGERY; THERAPY;
D O I
10.1016/j.cllc.2011.06.003
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The optimal treatment of locally advanced non-small-cell lung cancer (NSCLC) remains controversial. We hypothesized that using a trimodality approach in selected patients with stage IIIA/IIIB disease would be both feasible and efficacious with reasonable toxicity. Patients/Methods: We enrolled 13 patients with resectable stage III NSCLC on a prospective phase II trial of trimodality therapy. Induction treatment consisted of weekly docetaxel 20 mg/m(2) and weekly carboplatin at an area under curve (AUC) of 2 concurrent with 45 Gy thoracic radiotherapy. Resection was performed unless felt to be unsafe or if patients had progressive disease. Postoperative consolidation consisted of docetaxel 75 mg/m(2) and carboplatin at an AUC of 6 every 3 weeks for 3 cycles with growth factor support. Results: All patients responded to induction chemoradiotherapy as measured by total gross tumor volume reductions of 43% on average ( range, 27%-64%). Twelve patients underwent resection of the tumor and involved nodes, yielding a resectability rate of 92%. The primary endpoint of 2-year overall survival (OS) was 72% (95% confidence interval [CI], 36%-90%), and 2-year progression-free survival (PFS) was 36% (95% CI, 9%-64%). The maximal toxicity observed per patient was grade II in 5 patients (38%); grade III in 7 patients (54%); grade IV in 1 patient (8%); and grade V in none. Conclusion: This trimodality approach resulted in promising outcomes with reasonable toxicity in carefully selected patients with stage III NSCLC at a single institution.
引用
收藏
页码:280 / 285
页数:6
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