Department of Medicine, Division of Oncology, Stanford University, CA, USA.
Clin Lung Cancer. 2011 Sep;12(5):280-5. doi: 10.1016/j.cllc.2011.06.003. Epub 2011 Jul 14.
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.
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.
This trimodality approach resulted in promising outcomes with reasonable toxicity in carefully selected patients with stage III NSCLC at a single institution.
局部晚期非小细胞肺癌(NSCLC)的最佳治疗方法仍存在争议。我们假设在 IIIA/IIIB 期可切除的 NSCLC 患者中,采用三联疗法是可行且有效的,同时具有合理的毒性。
患者/方法:我们在一项三联疗法的前瞻性 II 期试验中纳入了 13 例可切除的 III 期 NSCLC 患者。诱导治疗包括每周 20mg/m²的多西他赛和每周 AUC 为 2 的卡铂,同时进行 45Gy 的胸部放疗。如果认为不安全或患者出现疾病进展,则进行手术切除。术后巩固治疗包括多西他赛 75mg/m²和 AUC 为 6 的卡铂,每 3 周一次,共 3 个周期,并使用生长因子支持。
所有患者对诱导放化疗均有反应,平均总肿瘤体积减少了 43%(范围为 27%-64%)。12 例患者接受了肿瘤和受累淋巴结的切除术,切除率为 92%。2 年总生存率(OS)的主要终点为 72%(95%置信区间[CI],36%-90%),2 年无进展生存率(PFS)为 36%(95% CI,9%-64%)。每个患者观察到的最大毒性为 5 例(38%)为 2 级;7 例(54%)为 3 级;1 例(8%)为 4 级;无 5 级。
在单一机构中,对精心选择的 III 期 NSCLC 患者采用这种三联疗法,结果令人鼓舞,毒性合理。