Department of Obstetrics and Gynecology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Int J Radiat Oncol Biol Phys. 2011 Dec 1;81(5):1252-7. doi: 10.1016/j.ijrobp.2010.07.2006. Epub 2010 Nov 13.
The aim of this study was to compare the efficacy and toxicity of consolidation chemotherapy after concurrent chemoradiation (CCRT) and CCRT alone in patients with locally advanced cervical carcinoma.
Using medical records from January 2001 to December 2007, 39 patients treated with consolidation chemotherapy after CCRT (Group 1) were matched to 39 patients treated with CCRT alone (Group 2). Consolidation chemotherapy consisted of three additional cycles of chemotherapy with cisplatin 60 mg/m2 (Day 1) and 5-fluorouracil 1,000 mg/m2 per day (Days 1-5) given every 3 weeks. The primary endpoint was overall survival.
During a median follow-up period of 35 months (range, 8-96 months), 10 (25.6%) and 16 (41.0%) patients showed disease progression in Groups 1 and 2, respectively. Distant recurrence with or without locoregional/lymphogenous recurrence occurred more frequently in Group 2 than in Group 1 (23.1% vs. 7.7%, p=0.06). By contrast, there was no difference in locoregional or lymphogenous recurrence between the two groups. The rate of overall survival was higher in Group 1 than in Group 2 (92.7% vs. 69.9%, p=0.042), whereas the difference in progression-free survival between the groups was not statistically significant (70.1% vs. 55.1%, p=0.079). Although the difference was not statistically significant, neutropenia was more common in Group 1 than in Group 2 (10.9% vs. 4.7%, p=0.07).
Consolidation chemotherapy after CCRT may improve survival and reduce distant recurrence without additional toxicity compared to CCRT alone in patients with locally advanced cervical carcinoma.
本研究旨在比较局部晚期宫颈癌患者同步放化疗(CCRT)后巩固化疗与单纯 CCRT 的疗效和毒性。
通过查阅 2001 年 1 月至 2007 年 12 月的病历资料,我们将 39 例接受 CCRT 后巩固化疗的患者(1 组)与 39 例接受单纯 CCRT 的患者(2 组)进行匹配。巩固化疗采用顺铂 60mg/m2(第 1 天)和 5-氟尿嘧啶 1000mg/m2(第 1-5 天),每 3 周重复 3 个周期。主要终点为总生存。
在中位随访期 35 个月(范围 8-96 个月)内,1 组和 2 组分别有 10(25.6%)和 16(41.0%)例患者出现疾病进展。远处复发伴或不伴局部/淋巴结转移在 2 组更为常见(23.1% vs. 7.7%,p=0.06)。相反,两组局部或淋巴结复发无差异。1 组总生存率高于 2 组(92.7% vs. 69.9%,p=0.042),而两组无进展生存率差异无统计学意义(70.1% vs. 55.1%,p=0.079)。虽然差异无统计学意义,但 1 组中性粒细胞减少的发生率高于 2 组(10.9% vs. 4.7%,p=0.07)。
与单纯 CCRT 相比,CCRT 后巩固化疗可能提高局部晚期宫颈癌患者的生存率,降低远处复发率,且毒性无增加。