Hepatobiliary and Surgical Oncology Unit, UNSW Department of Surgery, and the St George Clinical School, University of New South Wales, St George Hospital, Kogarah, NSW, Australia.
Cancer Manag Res. 2012;4:413-22. doi: 10.2147/CMAR.S31070. Epub 2012 Nov 23.
TO REVIEW THE TWO MAIN APPROACHES OF INTRAPERITONEAL (IP) CHEMOTHERAPY DELIVERY IN OVARIAN CANCER: postoperative adjuvant IP chemotherapy after cytoreductive surgery (CRS) and intraoperative hyperthermic intraperitoneal chemotherapy (HIPEC).
A literature search was conducted to identify studies that employed postoperative adjuvant IP chemotherapy after CRS or combined CRS and intraoperative HIPEC in patients with ovarian cancer. Data of interest included chemotherapy protocol, morbidity and mortality, and survival data.
Three large randomized controlled trials comprising 707 patients with advanced ovarian cancer who received postoperative adjuvant IP chemotherapy were reviewed. Morbidity rate ranged from 56% to 94% in IP chemotherapy, and mortality rate ranged from 1% to 2%. Median disease-free survival ranged from 24 to 28 months, and overall survival ranged from 49 to 66 months. Planned chemotherapy completion rates ranged from 42% to 71%. Twenty-four nonrandomized studies that reported HIPEC comprised 1167 patients with both advanced and recurrent ovarian cancer. In patients with advanced ovarian cancer, mortality ranged from 0% to 5%, minor morbidity ranged from 16% to 90%, and major morbidity ranged from 0% to 40%. Median disease-free survival ranged from 13 to 56 months, and overall survival ranged from 14 to 64 months. Survival at 5 years ranged from 35% to 70%. In patients with recurrent ovarian cancer, the mortality rate ranged from 0% to 10%, minor morbidity ranged from 7% to 90%, and major morbidity ranged from 0% to 49%. Median disease-free survival ranged from 13 to 24 months and overall survival from 23 to 49 months. Survival at 5 years ranged from 12% to 54%.
There is level-one evidence suggesting the benefit of postoperative adjuvant intraperitoneal chemotherapy for patients with advanced ovarian cancer after cytoreductive surgery, albeit catheter-related complications resulted after treatment discontinuation. Studies report the use of HIPEC predominantly in the setting of recurrent disease and have demonstrated encouraging results, which merits further investigation in future clinical trials.
综述卵巢癌腹腔内化疗的两种主要途径:细胞减灭术后辅助腹腔内化疗(IP 化疗)和术中腹腔内热灌注化疗(HIPEC)。
对采用细胞减灭术后辅助 IP 化疗或联合细胞减灭术和术中 HIPEC 治疗卵巢癌患者的研究进行了文献检索。有意义的数据包括化疗方案、发病率和死亡率以及生存数据。
对纳入的 707 例接受术后辅助 IP 化疗的晚期卵巢癌患者的 3 项大型随机对照试验进行了综述。IP 化疗的发病率为 56%至 94%,死亡率为 1%至 2%。无病生存期中位数为 24 至 28 个月,总生存期中位数为 49 至 66 个月。计划完成化疗的比例为 42%至 71%。24 项非随机研究报告了 HIPEC 治疗晚期和复发性卵巢癌患者,共纳入 1167 例患者。在晚期卵巢癌患者中,死亡率为 0%至 5%,轻度发病率为 16%至 90%,重度发病率为 0%至 40%。无病生存期中位数为 13 至 56 个月,总生存期中位数为 14 至 64 个月。5 年生存率为 35%至 70%。在复发性卵巢癌患者中,死亡率为 0%至 10%,轻度发病率为 7%至 90%,重度发病率为 0%至 49%。无病生存期中位数为 13 至 24 个月,总生存期中位数为 23 至 49 个月。5 年生存率为 12%至 54%。
有一级证据表明,对于接受细胞减灭术的晚期卵巢癌患者,术后辅助腹腔内化疗有益,尽管治疗中断后会出现与导管相关的并发症。研究报告主要在复发性疾病的情况下使用 HIPEC,并取得了令人鼓舞的结果,值得进一步在未来的临床试验中进行研究。