Gemignani M L, Hensley M L, Cohen R, Venkatraman E, Saigo P E, Barakat R R
Department of Surgery, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, New York 10021, USA.
Gynecol Oncol. 2001 Jan;80(1):16-20. doi: 10.1006/gyno.2000.6012.
The objective of this study was to determine the clinical outcomes of patients with fallopian tube carcinoma treated with paclitaxel-based combination chemotherapy following primary cytoreductive surgery.
Twenty-four patients with the diagnosis of primary tubal adenocarcinoma treated between 1993 and 1998 were identified through the gynecology service database and the Memorial Sloan-Kettering Cancer Center tumor registry. Medical records were reviewed for information on age, stage, chemotherapy regimen, surgical intervention, relapse, and survival. All patients had their histologic material initially read or reviewed at Memorial Sloan-Kettering Cancer Center prior to treatment. The original slides were reviewed again by one of the authors (P.E.S.) to confirm the diagnosis of primary fallopian tube cancer.
The mean age of the patients was 63 years (range, 44-76). Distribution by stage was as follows: four patients (17%) were Stage I, three patients (12%) were Stage II, 16 patients (67%) were Stage III, one patient (4%) was Stage IV. Four patients had grade 2 tumors, 20 had grade 3. Sixteen patients (67%) had optimal cytoreduction at the time of initial surgery with residual disease less than 1 cm. Eight patients (33%) had suboptimal cytoreduction. Following initial surgery, all patients were treated with paclitaxel-based chemotherapy for a median of five cycles. Twenty-three patients received paclitaxel at the dose of 135-175 mg/m(2) in combination with carboplatin or cisplatin; the majority, 17 of 23 (74%), received carboplatin. One patient received paclitaxel alone. Median follow-up from time of initial surgery was 24 months (range, 1-73 months). Two patients are dead of disease. Overall survival for the entire group was 96% at 12 months by Kaplan-Meier analysis, and 90% at 3 years. The overall median progression-free survival was 27 months (range, 5-57 months) for the entire group. The median disease progression-free survival at 3 years was 67% (95% CI, 45-100) in the optimally debulked group as compared with 45% in the suboptimally debulked group (95% CI, 27-57). Twelve patients (50%) had evidence of recurrence or persistent disease. There were fewer recurrences in the optimally debulked group: 5 of the 16 patients (31%) versus 7 of the 8 patients (88%) with suboptimal cytoreduction.
Optimally cytoreduced patients with primary fallopian tube carcinoma treated with a paclitaxel-based chemotherapy regimen have an excellent possibility of survival.
本研究的目的是确定原发性细胞减灭术后接受以紫杉醇为基础的联合化疗的输卵管癌患者的临床结局。
通过妇科服务数据库和纪念斯隆凯特琳癌症中心肿瘤登记处,确定了1993年至1998年间诊断为原发性输卵管腺癌的24例患者。查阅病历以获取有关年龄、分期、化疗方案、手术干预、复发和生存的信息。所有患者在治疗前其组织学材料最初均在纪念斯隆凯特琳癌症中心进行阅读或复查。原始切片由作者之一(P.E.S.)再次复查以确诊原发性输卵管癌。
患者的平均年龄为63岁(范围44 - 76岁)。分期分布如下:4例患者(17%)为Ⅰ期,3例患者(12%)为Ⅱ期,16例患者(67%)为Ⅲ期,1例患者(4%)为Ⅳ期。4例患者为2级肿瘤,20例为3级。16例患者(67%)在初次手术时实现了最佳细胞减灭,残留病灶小于1 cm。8例患者(33%)细胞减灭未达最佳。初次手术后,所有患者均接受以紫杉醇为基础的化疗,中位疗程为5个周期。23例患者接受剂量为135 - 175 mg/m²的紫杉醇联合卡铂或顺铂治疗;其中大多数,23例中的17例(74%)接受了卡铂治疗。1例患者仅接受了紫杉醇治疗。自初次手术起的中位随访时间为24个月(范围1 - 73个月)。2例患者死于疾病。通过Kaplan-Meier分析,整个组在12个月时的总生存率为96%,3年时为90%。整个组的总中位无进展生存期为27个月(范围5 - 57个月)。最佳减瘤组在3年时的中位无病进展生存率为67%(95%可信区间,45 - 100),而减瘤未达最佳组为45%(95%可信区间,27 - 57)。12例患者(50%)有复发或疾病持续存在的证据。最佳减瘤组的复发较少:16例患者中的5例(31%),而减瘤未达最佳的8例患者中有7例(88%)。
接受以紫杉醇为基础的化疗方案治疗的原发性输卵管癌且细胞减灭最佳的患者有极佳的生存可能性。