Hainsworth J D, Grosh W W, Burnett L S, Jones H W, Wolff S N, Greco F A
Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
Ann Intern Med. 1988 Feb;108(2):165-70. doi: 10.7326/0003-4819-108-2-165.
To determine the efficacy of a 6-month course of combination chemotherapy with hexamethylmelamine, cyclophosphamide, doxorubicin, and cisplatin (H-CAP) in the treatment of advanced ovarian carcinoma.
Prospective, non-randomized, single-institution trial with a 6-month course of chemotherapy, followed by second-look laparotomy for restaging. Minimum follow-up after completion of therapy is 83 months.
Fifty-five patients with advanced (stage III or IV), intermediate- or high-grade epithelial carcinoma of the ovary. Twenty patients had limited residual tumor (3 cm or less maximal tumor diameter) after initial cytoreductive surgery; 35 had extensive residual disease.
All patients received chemotherapy with hexamethylmelamine (150 mg/m2 body surface area orally on days 1 to 14), cyclophosphamide (350 mg/m2 intravenously on days 1 and 8), doxorubicin (20 mg/m2 intravenously on days 1 and 8), and cisplatin (60 mg/m2 intravenously on day 1). Courses were repeated at 4-week intervals; 41 patients (75%) received six courses; 10 patients received five courses, 3 patients received four courses, and 1 patients received three courses. Forty-seven patients underwent second-look laparotomy after completion of therapy; 8 had their disease restaged clinically.
Fifty-three of fifty-five patients (96%) had either partial or complete response to treatment. Nineteen of forty-seven patients who had a second-look laparotomy had a surgically documented complete response; 17 of these 19 patients began chemotherapy with limited residual tumor. Ten patients (18%) remain disease-free 83 to 108 months after therapy, whereas three additional patients died of other diseases without clinical evidence of recurrent ovarian cancer. Nine of twenty patients who began chemotherapy with limited residual tumor remain disease-free, as compared to only 1 of 35 patients with more extensive tumor (P less than 0.001). All long-term, disease-free survivors had surgically documented complete response at second-look laparotomy.
Treatment with cisplatin-based combination chemotherapy after aggressive cytoreductive surgery should be considered standard treatment for advanced ovarian carcinoma. Our intensive, 6-month course of treatment produced results comparable to those previously reported with prolonged treatment.
确定六甲蜜胺、环磷酰胺、阿霉素和顺铂联合化疗(H-CAP)6个月疗程治疗晚期卵巢癌的疗效。
前瞻性、非随机、单机构试验,采用6个月化疗疗程,随后进行二次剖腹探查以重新分期。治疗完成后的最短随访时间为83个月。
55例晚期(III期或IV期)中高级别卵巢上皮癌患者。20例患者在初次细胞减灭术后有局限性残留肿瘤(最大肿瘤直径3cm或更小);35例有广泛残留病灶。
所有患者接受六甲蜜胺(第1至14天口服150mg/m²体表面积)、环磷酰胺(第1天和第8天静脉注射350mg/m²)、阿霉素(第1天和第8天静脉注射20mg/m²)和顺铂(第1天静脉注射60mg/m²)联合化疗。疗程每4周重复一次;41例患者(75%)接受6个疗程;10例患者接受5个疗程,3例患者接受4个疗程,1例患者接受3个疗程。47例患者在治疗完成后接受了二次剖腹探查;8例患者进行了临床重新分期。
55例患者中有53例(96%)对治疗有部分或完全反应。47例接受二次剖腹探查的患者中有19例手术记录为完全缓解;这19例患者中有17例开始化疗时残留肿瘤局限。10例患者(18%)在治疗后83至108个月无疾病生存,另外3例患者死于其他疾病,无卵巢癌复发的临床证据。开始化疗时残留肿瘤局限的20例患者中有9例无疾病生存,而35例肿瘤更广泛的患者中只有1例无疾病生存(P<0.001)。所有长期无疾病生存者在二次剖腹探查时手术记录为完全缓解。
积极的细胞减灭术后以顺铂为基础的联合化疗应被视为晚期卵巢癌的标准治疗。我们强化的6个月疗程治疗产生的结果与先前报道的延长疗程治疗的结果相当。