Onishi H, Yamaguchi M, Kuriyama K, Tsukamoto T, Ishigame K, Ichikawa T, Aoki S, Yoshikawa T, Araki T, Nambu A, Araki T, Hashi A, Yasumizu T, Hoshi K, Ito H
Department of Radiology, Yamanashi Medical University, Nakakoma-gun, Japan.
Cancer J Sci Am. 2000 Jan-Feb;6(1):40-5.
The purpose of this study was to explore the effect of concurrent intra-arterial infusion of platinum drugs in patients with stage III or IV uterine cervical cancer treated with radical radiation therapy.
Thirty-three patients with advanced (stage IIIA, 2; IIIB, 28; IVA, 3) uterine cervical squamous cell carcinoma were randomized into a concurrent intra-arterial infusion of platinum drugs with radiation therapy (IAPRT) group (18 patients) and a radiation therapy alone group (15 patients). After altering intrapelvic blood flow by embolization of the superior and inferior gluteal arteries under pelvic angiography, intra-arterial infusion of platinum drug through catheters inserted into both internal iliac arteries was performed concurrently with radiation therapy. One-shot infusion of cisplatin (100 mg/m2) twice with a 2- to 3-week interval was performed in eight patients, weekly infusion of carboplatin (100 mg/m2) via a reservoir five to six times was performed in four patients, and daily shot of cisplatin (10 mg/body) or 21 days via a reservoir was performed in six patients. Radiation therapy consisted of external-beam irradiation of 50 Gy/25 fractions/5 weeks for the whole pelvis with midline block after 30 Gy and intracavitary high-dose-rate brachytherapy using tandem and ovoids of 24 Gy/4 fractions/4 weeks to point A.
The local complete response rate of the IAPRT group was 94% and was significantly higher than that of the radiation therapy group (67%). There were no significant differences in local response in the three drug delivery methods. Two- and 5-year overall survival rates were 54.5% and 44.4% in the IAPRT group, and 74.5% and 50.0% in the radiation therapy group, respectively. There was no significant difference between the two groups. In the IAPRT group, grade 3 or 4 acute bowel complications were seen in 33% of patients, grade 3 or 4 late bowel complications were seen 44%, and grade 3 or 4 myelosuppression was seen in 33%, and these complications were seen more in the IAPRT group than in the radiation therapy group and caused death in some patients.
IAPRT had a better local response than radiation therapy but showed no proof of control over recurrence and had a poorer survival than radiation therapy. There were many local recurrences and distant metastases, contrary to the better first response of the IAPRT group over the radiation therapy group. Complications of the IAPRT group were very severe and made the patient's performance status and prognosis worse than in the radiation therapy group. We need to design some methods to decrease these complications to make use of the good local response acquired with IAPRT. Furthermore, we should re-examine the indication of IAPRT in patients with a large tumor because local recurrence and distant metastasis would be inevitable.
本研究旨在探讨同步动脉内输注铂类药物对接受根治性放射治疗的III期或IV期子宫颈癌患者的影响。
33例晚期(IIIA期2例、IIIB期28例、IVA期3例)子宫颈鳞状细胞癌患者被随机分为同步动脉内输注铂类药物联合放射治疗(IAPRT)组(18例患者)和单纯放射治疗组(15例患者)。在盆腔血管造影下通过栓塞臀上动脉和臀下动脉改变盆腔内血流后,通过插入双侧髂内动脉的导管同步进行铂类药物的动脉内输注与放射治疗。8例患者每2至3周一次静脉推注顺铂(100mg/m²)两次,4例患者通过储液器每周输注卡铂(100mg/m²)5至6次,6例患者每日静脉推注顺铂(10mg/体)或通过储液器每21天一次。放射治疗包括全盆腔外照射50Gy/25次/5周,在30Gy后进行中线挡铅,以及使用串珠和卵圆体进行腔内高剂量率近距离放射治疗,给予A点24Gy/4次/4周。
IAPRT组的局部完全缓解率为94%,显著高于放射治疗组(67%)。三种给药方式的局部反应无显著差异。IAPRT组的2年和5年总生存率分别为54.5%和44.4%,放射治疗组分别为74.5%和50.0%。两组之间无显著差异。在IAPRT组中,33%的患者出现3级或4级急性肠道并发症,44%出现3级或4级晚期肠道并发症,33%出现3级或4级骨髓抑制,这些并发症在IAPRT组中比放射治疗组更常见,且导致部分患者死亡。
IAPRT的局部反应优于放射治疗,但未显示出对复发的控制效果,且生存率低于放射治疗。与IAPRT组优于放射治疗组的初始反应相反,存在许多局部复发和远处转移。IAPRT组的并发症非常严重,使患者的身体状况和预后比放射治疗组更差。我们需要设计一些方法来减少这些并发症,以利用IAPRT获得的良好局部反应。此外,对于肿瘤较大的患者,我们应重新审视IAPRT的适应证,因为局部复发和远处转移将不可避免。