Cascales-Campos Pedro Antonio, Gil J, Gil E, Feliciangeli E, González-Gil A, Parrilla J J, Parrilla P
Departamento De Cirugía General, Unidad De Cirugía De La Carcinomatosis Peritoneal, Virgen De La Arrixaca University Hospital, Murcia, Spain,
Ann Surg Oncol. 2014 Jul;21(7):2383-9. doi: 10.1245/s10434-014-3599-4. Epub 2014 Mar 6.
We analyze the efficacy of hyperthermic intraoperative intraperitoneal chemotherapy (HIPEC) for microscopic residual disease in patients with stage IIIC/IV ovarian cancer after a complete cytoreduction of their disease.
We analyzed the data of 87 consecutive patients diagnosed with stage IIIC/IV ovarian cancer operated between December 1998 and July 2011. In every patient it was possible to achieve a complete cytoreduction of their disease. (Since January 2008, our center has incorporated the use of HIPEC in patients with peritoneal surface malignancies, including patients with peritoneal dissemination of primary ovarian cancer.)
Of 87 patients, 52 were treated with HIPEC (paclitaxel 60 mg/m(2), 60 min, 42 °C). After a univariate analysis, factors associated with lower disease-free interval were: performing a gastrointestinal anastomosis, operative time greater than 270 min, poorly differentiated histology, and not being treated with HIPEC. After multivariate analysis, independent prognostic factors included not being treated with HIPEC [hazard ratio (HR) 8.77, 95 % CI 2.76-14.42, p < 0.01] and the presence of poorly differentiated tumors (HR 1.98, 95 % CI 1.45-8.56, p < 0.05). Disease-free survival at 1 and 3 years was 66 and 18 %, respectively, in patients without HIPEC and 81 and 63 %, respectively, in patients treated with HIPEC (p < 0.01). HIPEC administration did not alter the results obtained for disease-free survival in patients with undifferentiated tumors.
The treatment of the microscopic disease following complete cytoreduction with HIPEC in patients with advanced ovarian cancer is effective and can prolong disease-free survival. This survival benefit was not seen in undifferentiated tumors.
我们分析了热灌注术中腹腔内化疗(HIPEC)对IIIC/IV期卵巢癌患者在疾病完全细胞减灭术后微小残留病灶的疗效。
我们分析了1998年12月至2011年7月间连续87例诊断为IIIC/IV期卵巢癌并接受手术的患者的数据。每位患者均有可能实现疾病的完全细胞减灭。(自2008年1月起,我们中心将HIPEC应用于腹膜表面恶性肿瘤患者,包括原发性卵巢癌腹膜播散患者。)
87例患者中,52例接受了HIPEC治疗(紫杉醇60mg/m²,60分钟,42°C)。单因素分析后,与无病生存期较短相关的因素有:进行胃肠吻合术、手术时间超过270分钟、组织学分级差以及未接受HIPEC治疗。多因素分析后,独立预后因素包括未接受HIPEC治疗[风险比(HR)8.77,95%置信区间2.76 - 14.42,p < 0.01]和存在低分化肿瘤(HR 1.98,95%置信区间1.45 - 8.56,p < 0.05)。未接受HIPEC治疗的患者1年和3年无病生存率分别为66%和18%,接受HIPEC治疗的患者分别为81%和63%(p < 0.01)。HIPEC给药并未改变未分化肿瘤患者无病生存期的结果。
晚期卵巢癌患者在完全细胞减灭术后用HIPEC治疗微小病灶是有效的,且可延长无病生存期。在未分化肿瘤中未观察到这种生存获益。