van der Vange N, van Goethem A R, Zoetmulder F A, Kaag M M, van de Vaart P J, ten Bokkel Huinink W W, Beijnen J H
Department of Gynaecological Oncology, The Netherlands Cancer Institute (Antoni van Leeuwenhoek Ziekenhuis), Amsterdam, The Netherlands.
Eur J Surg Oncol. 2000 Nov;26(7):663-8. doi: 10.1053/ejso.2000.0978.
The feasibility, morbidity and toxicity of an intensified surgical treatment strategy consisting of aggressive cytoreductive surgery, intra-operative intraperitoneal perfusion of cisplatin and hyperthermia were evaluated in women with recurrent ovarian cancer.
Five heavily pre-treated patients with extensive abdominal tumour bulk entered this pilot study. In all cases aggressive cytoreduction leaving tumour remnants <5 mm in diameter could be performed. This was followed intra-operatively by perfusion of the abdominal cavity with hyperthermic cisplatin 50-70 mg/m(2)for 90 min. During perfusion the intra-abdominal temperature was maintained at 40 degrees C. The median duration of surgery was 10 hours (range 9-11 hours).
No major intra- or post-operative complications emerged. Median post-operative ileus (resuming of soft diet) was 11 days (9-13 days). The mean period of hospitalization was 25 days (range 17-42). Toxicity due to i.p. cisplatin was mainly metabolic and of grade 1-2, while no nephrotoxicity was observed. The pharmacokinetics of cisplatin indicated that the maximum concentration of cisplatin measured in the perfusate was 15 times higher than in plasma.
We conclude that aggressive cytoreduction combined with hyperthermic intra-operative intraperitoneal cisplatin was feasible in a small group of heavily pre-treated ovarian cancer patients with extensive tumour bulk with acceptable morbidity and toxicity. Further studies are required in larger groups of patients to further establish the feasibility of this intensified treatment strategy. We stress that OVHIPEC is not a treatment modality on its own for advanced ovarian cancer. The effectiveness of OVHIPEC is likely to be dependent on the effectiveness of post-operative adjuvant chemotherapeutic regimens.
对复发性卵巢癌患者采用包括积极的细胞减灭术、术中腹腔内灌注顺铂和热疗的强化手术治疗策略的可行性、发病率和毒性进行评估。
五例经过大量前期治疗且腹部肿瘤体积较大的患者进入了这项前瞻性研究。在所有病例中,均可进行积极的细胞减灭术,使肿瘤残余直径<5毫米。随后在术中用50 - 70毫克/平方米的热顺铂对腹腔进行90分钟的灌注。灌注期间腹腔内温度维持在40摄氏度。手术中位持续时间为10小时(范围9 - 11小时)。
未出现重大的术中或术后并发症。术后中位肠梗阻(恢复软食)时间为11天(9 - 13天)。平均住院时间为25天(范围17 - 42天)。腹腔内顺铂引起的毒性主要为1 - 2级代谢性毒性,未观察到肾毒性。顺铂的药代动力学表明,灌注液中测得的顺铂最大浓度比血浆中高15倍。
我们得出结论,对于一小部分经过大量前期治疗、肿瘤体积较大的卵巢癌患者,积极的细胞减灭术联合术中腹腔内热灌注顺铂是可行的,其发病率和毒性可接受。需要在更大规模的患者群体中进行进一步研究,以进一步确定这种强化治疗策略的可行性。我们强调,腹腔内热灌注化疗本身并非晚期卵巢癌的一种治疗方式。腹腔内热灌注化疗的有效性可能取决于术后辅助化疗方案的有效性。