Instituto Nacional do Câncer - INCA, Brazilian National Cancer Institute - Rio de Janeiro, Brazil.
J Bras Pneumol. 2011 May-Jun;37(3):354-9. doi: 10.1590/s1806-37132011000300012.
Adjuvant chemotherapy is recommended for most patients submitted to resection due to non-small cell lung cancer (NSCLC) staged as II or IIIA. However, although various chemotherapy regimens that include cisplatin have been used in phase III trials, the best choice remains unclear. The objective of this study was to describe the experience of the Instituto Nacional do Câncer (INCA, Brazilian National Cancer Institute), located in the city of Rio de Janeiro, Brazil, with the use of the cisplatin-etoposide combination in such patients, with a special focus on survival data.
We retrospectively evaluated the medical charts of the patients receiving adjuvant therapy for NSCLC at the INCA between 2004 and 2008.
We included 51 patients, all of whom were treated with the cisplatin-etoposide combination. The median follow-up period was 31 months, and the median overall survival was 57 months. In the univariate analysis, median survival was lower in the patients submitted to chemotherapy plus radiotherapy than in those submitted to chemotherapy alone (19 vs. 57 months; p < 0.001), and there was a trend toward lower median survival in stage III patients than in stage I-II patients (34 vs. 57 months; p = 0.22). Overall survival was not significantly associated with gender (p = 0.70), histological pattern (p = 0.33), or cisplatin dose (p = 0.13).
Our results support the use of adjuvant chemotherapy, and our survival data are similar to those reported in major randomized clinical trials. However, long-term follow-up is warranted in this population.
对于非小细胞肺癌(NSCLC)II 期或 IIIA 期患者,推荐进行辅助化疗。然而,尽管在 III 期临床试验中使用了各种包含顺铂的化疗方案,但最佳选择仍不明确。本研究旨在描述巴西里约热内卢国家癌症研究所(INCA)在辅助治疗 NSCLC 患者中使用顺铂-依托泊苷联合方案的经验,特别关注生存数据。
我们回顾性评估了 2004 年至 2008 年在 INCA 接受辅助治疗的 NSCLC 患者的病历。
共纳入 51 例患者,均接受顺铂-依托泊苷联合方案治疗。中位随访时间为 31 个月,中位总生存期为 57 个月。单因素分析显示,化疗联合放疗的患者中位生存期短于单纯化疗患者(19 个月 vs. 57 个月;p < 0.001),且 III 期患者的中位生存期短于 I-II 期患者(34 个月 vs. 57 个月;p = 0.22)。总生存期与性别(p = 0.70)、组织学类型(p = 0.33)或顺铂剂量(p = 0.13)无关。
我们的结果支持使用辅助化疗,我们的生存数据与主要随机临床试验报告的结果相似。然而,仍需要对该人群进行长期随访。