Peters W A, Rivkin S E, Smith M R, Tesh D E
Puget Sound Oncology Consortium, Seattle, Washington 98104.
Gynecol Oncol. 1989 Sep;34(3):323-7. doi: 10.1016/0090-8258(89)90166-2.
Twenty-eight patients with a uterine stromal sarcoma or mixed mesodermal tumor were treated with cisplatin 100 mg/m2 and Adriamycin 45-60 mg/m2, given with intravenous hydration every 3 to 4 weeks. Group I consists of 11 patients with measurable disease following initial surgery or with a recurrence. Eight of the eleven evaluable patients with measurable disease had a response (73%), and three of these patients have had a negative second-look procedure, and two are alive and disease free more than 24 months after initiation of treatment. Group II consists of 17 patients treated with adjuvant chemotherapy after primary surgery. The patients were selected for adjuvant therapy based on previous established poor prognostic features. Of the 17 patients in group II, 14 had invasion of the outer one-third of the myometrium and the other three had invasion to the middle one-third. Seven had documented positive pelvic and/or periaortic lymph nodes and five had positive peritoneal washings. With a median follow-up of 34 months, there have been only four recurrences in group II. Two of the recurrences occurred in patients who discontinued therapy after only two cycles of chemotherapy. There is a projected 5-year survival of 75% in these high-risk patients. Of the seven patients with documented nodal involvement, one patient died with a recurrence at 23 months, one patient died from a perforated diverticulum, and the other five are alive and disease free with a median follow-up of 36 months (34-90 months). Two patients with multiple positive nodes are disease free at more than 5 years. Combination chemotherapy with cisplatin and Adriamycin has a high response rate with advanced measurable disease and improves survival in high-risk patients who receive it as adjuvant therapy.
28例子宫间质肉瘤或混合性中胚叶肿瘤患者接受了顺铂100mg/m²和阿霉素45 - 60mg/m²治疗,每3至4周静脉补液一次。第一组由11例初次手术后有可测量病灶或复发的患者组成。11例可评估的有可测量病灶的患者中,8例有反应(73%),其中3例患者二次探查结果为阴性,2例患者在治疗开始后24个月以上仍存活且无疾病。第二组由17例初次手术后接受辅助化疗的患者组成。根据先前确定的不良预后特征选择患者进行辅助治疗。第二组的17例患者中,14例子宫肌层外三分之一受侵,另外3例肌层中三分之一受侵。7例有盆腔和/或腹主动脉旁淋巴结阳性记录,5例腹腔冲洗液阳性。中位随访34个月,第二组仅4例复发。其中2例复发发生在仅接受两个周期化疗后停药的患者。这些高危患者预计5年生存率为75%。7例有淋巴结受累记录的患者中,1例患者在23个月时因复发死亡,1例患者死于憩室穿孔,另外5例存活且无疾病,中位随访36个月(34 - 90个月)。2例有多个阳性淋巴结的患者5年以上无疾病。顺铂和阿霉素联合化疗对晚期可测量病灶有较高的反应率,并能提高接受辅助治疗的高危患者的生存率。