Tropé C, Kaern J, Vergote I B, Kristensen G, Abeler V
Department of Gynecologic Oncology and Pathology, Norweigian Radium Hospital, Montebello, Oslo.
Gynecol Oncol. 1993 Nov;51(2):236-43. doi: 10.1006/gyno.1993.1279.
The optimal treatment of early-stage ovarian borderline tumors is controversial. Only a few randomized trials evaluating adjuvant treatment for this disease have been published. Between 1970 and 1988 four consecutive randomized trials, including patients with ovarian borderline tumors, were conducted at the Norwegian Radium Hospital. After surgery, 253 stage I-II borderline tumors without residual disease were randomly allocated to these protocols. The adjuvant treatment in the four trials consisted of [1] external irradiation (Ext) combined with intraperitoneal instillation of radioactive gold (198Au) or Ext alone, [2] intraperitoneal radioactive therapy followed by thio-TEPA or no further treatment, [3] thio-TEPA or no adjuvant therapy, and [4] cisplatin or 32P treatment. The patients were equally distributed according to prognostic variables within the eight randomization groups. The overall corrected and crude survival were 99 and 94%, respectively. In 83% of the patients a hysterectomy, bilateral salpingo-oophorectomy, and omentectomy was performed. None of the patients with less extensive surgery relapsed. Adjuvant therapy did not seem to improve the overall corrected survival. On the contrary, toxicity was added with small bowel complications after radiation therapy, neurotoxicity after cisplatin treatment, and bone marrow toxicity after thio-TEPA therapy. It is concluded that stage I borderline tumors should not receive any adjuvant treatment.
早期卵巢交界性肿瘤的最佳治疗方法存在争议。仅有少数评估该疾病辅助治疗的随机试验发表。1970年至1988年间,挪威镭医院连续进行了四项随机试验,纳入了卵巢交界性肿瘤患者。手术后,253例无残留病灶的Ⅰ - Ⅱ期交界性肿瘤被随机分配至这些方案中。四项试验中的辅助治疗包括:[1] 外照射(Ext)联合腹腔内注入放射性金(198Au)或单纯外照射;[2] 腹腔内放射治疗后给予噻替派或不再进行进一步治疗;[3] 噻替派或不进行辅助治疗;[4] 顺铂或32P治疗。患者根据预后变量在八个随机分组中平均分布。总体校正生存率和粗生存率分别为99%和94%。83%的患者接受了子宫切除术、双侧输卵管卵巢切除术和大网膜切除术。手术范围较小的患者均未复发。辅助治疗似乎并未改善总体校正生存率。相反,放疗后出现小肠并发症、顺铂治疗后出现神经毒性、噻替派治疗后出现骨髓毒性,增加了毒性反应。结论是Ⅰ期交界性肿瘤不应接受任何辅助治疗。