Department of Obstetrics and Gynaecology, Erasmus Medical Centre Cancer Institute , Rotterdam .
Int J Hyperthermia. 2014 Feb;30(1):6-10. doi: 10.3109/02656736.2013.844366. Epub 2013 Oct 24.
Concomitant hyperthermia has been shown to improve response rate after cisplatin in recurrent cervical cancer in previously irradiated patients. It is unclear whether similar response rates can be obtained in patients with a recurrence after previous platinum-containing chemoradiation.
This study aimed to evaluate the outcome of cisplatin-based chemotherapy with concurrent hyperthermia in patients with recurrent cervical cancer after radiotherapy and cisplatin.
Patients with recurrent cervical cancer after cisplatin-based chemoradiation or neoadjuvant chemotherapy followed by surgery and radiotherapy who were treated with concurrent platinum-based chemotherapy and hyperthermia were eligible for this retrospective analysis. All patients received six or eight weekly platinum-based chemotherapy cycles in combination with six or eight weekly hyperthermia sessions. The time-to-event variables were estimated using Kaplan-Meier analysis. P-values less than 0.05 were considered significant.
All 38 evaluable patients were selected from the hyperthermia database in the Academic Medical Centre (Amsterdam) and the Erasmus Medical Centre (Rotterdam). Mean age at relapse was 45.7 years (range 27-74). Median time to recurrence after first-line treatment was 15 months. A total of 27 patients had a local and/or regional recurrence; 11 had disease beyond the pelvis. All planned courses of cisplatin chemotherapy and hyperthermia were administered in 17/38 patients. Median follow-up was 6.5 months. One patient died during treatment; response rate was 4/37 (14%), with one complete response. Overall survival was 23% at 12 months and 4% at 24 months. The incidence of grade 3-4 haematological complications did not exceed 10%.
In this retrospective study, concurrent cisplatin and hyperthermia after first-line cisplatin-containing chemoradiation showed poor response and survival. We do not recommend this treatment for recurrence of locally advanced cervical cancer.
在先前接受过放疗的复发性宫颈癌患者中,联合高热已被证明可提高顺铂治疗后的反应率。目前尚不清楚在先前接受含铂化疗放疗后复发的患者中是否能获得类似的反应率。
本研究旨在评估在接受顺铂为基础的放化疗后复发的宫颈癌患者中,顺铂联合高热进行化疗的疗效。
符合条件的患者为在接受以顺铂为基础的放化疗或新辅助化疗加手术和放疗后复发的宫颈癌患者,且接受了顺铂为基础的化疗联合高热的治疗。所有患者均接受 6 或 8 个周期的每周铂类化疗联合 6 或 8 个周期的每周高热治疗。采用 Kaplan-Meier 分析评估生存时间等时间相关变量。P 值小于 0.05 认为具有统计学意义。
所有 38 例可评估的患者均选自阿姆斯特丹学术医学中心(Academic Medical Centre)和鹿特丹伊拉斯谟医学中心(Erasmus Medical Centre)的高热数据库。复发时的平均年龄为 45.7 岁(27-74 岁)。首次治疗后复发的中位时间为 15 个月。27 例患者有局部和/或区域复发;11 例患者疾病超出骨盆范围。17/38 例患者接受了计划中的顺铂化疗和高热治疗。中位随访时间为 6.5 个月。1 例患者在治疗期间死亡;37 例患者中,客观缓解率为 4/37(14%),完全缓解 1 例。12 个月和 24 个月的总生存率分别为 23%和 4%。3-4 级血液学并发症的发生率未超过 10%。
在本回顾性研究中,在一线含铂化疗放疗后,顺铂联合高热治疗的反应率和生存率均较差。我们不建议将该方案用于局部晚期宫颈癌的复发。