Department of Radiation Oncology, Selcuk University, Konya, Turkey
Department of Radiation Oncology, Selcuk University, Konya, Turkey.
Int J Gynecol Cancer. 2019 Jan;29(1):42-47. doi: 10.1136/ijgc-2018-000022.
Standard treatment for locally advanced cervical cancer (LACC) includes concomitant chemoradiotherapy (CRT) that typically controls localized disease. However, most patients develop distant metastasis, ultimately leading to death.
To determine the role of adjuvant carboplatin and paclitaxel for clinical outcomes in patients with LACC.
Between 2010 and 2017, 109 patients with LACC were retrospectively evaluated. All patients received cisplatin (40 mg/m) with concurrent external-beam radiotherapy (up to 50.4 Gy), followed by intra-cavitary brachytherapy. Forty-six of 109 patients received a median of six cycles (range 3-6 cycles) of adjuvant chemotherapy consisting of paclitaxel (175 mg/m) and carboplatin (CRT + chemotherapy group; area under the curve 5). The remaining 63 patients did not receive adjuvant chemotherapy (CRT group).
Disease-free survival and overall survival after a median follow-up of 24.5 months (range 2.6-94.75 months) were 93.5% and 95.7% and 69.8% and 82.5 % for the CRT + chemotherapy and CRT groups, respectively (p = 0.001, p = 0.012, respectively). No acute grade 3/4 gastrointestinal or genitourinary toxicities were seen during CRT. During adjuvant chemotherapy, the most troublesome side effects were hematologic and neurologic toxicities; however, most were manageable. No chronic grade 3/4 genitourinary toxicities were seen.
Adjuvant chemotherapy in patients with LACC significantly improved both disease-free survival and overall survival without increasing unmanageable toxicity. Future larger prospective trials are warranted to verify these findings.
局部晚期宫颈癌(LACC)的标准治疗包括同时进行放化疗(CRT),这通常可以控制局部疾病。然而,大多数患者会发展为远处转移,最终导致死亡。
确定辅助卡铂和紫杉醇在 LACC 患者临床结局中的作用。
回顾性评估了 2010 年至 2017 年期间的 109 例 LACC 患者。所有患者均接受顺铂(40mg/m)联合外照射放疗(最高 50.4Gy),随后行腔内近距离放疗。109 例患者中有 46 例接受了中位数为 6 个周期(范围 3-6 个周期)的辅助化疗,包括紫杉醇(175mg/m)和卡铂(CRT+化疗组;曲线下面积 5)。其余 63 例患者未接受辅助化疗(CRT 组)。
中位随访 24.5 个月(范围 2.6-94.75 个月)后,无病生存率和总生存率分别为 93.5%和 95.7%,以及 69.8%和 82.5%,CRT+化疗组和 CRT 组分别为(p=0.001,p=0.012)。CRT 期间未观察到急性 3/4 级胃肠道或泌尿生殖系统毒性。在辅助化疗期间,最麻烦的副作用是血液学和神经毒性;然而,大多数是可以控制的。未观察到慢性 3/4 级泌尿生殖系统毒性。
LACC 患者的辅助化疗显著提高了无病生存率和总生存率,且未增加不可管理的毒性。未来需要更大规模的前瞻性试验来验证这些发现。