Intra-operative intra-peritoneal chemotherapy with cisplatin in patients with peritoneal carcinomatosis of ovarian cancer

被引:29
|
作者
Guardiola, Emmanuel [2 ]
Delroeux, Delphine [3 ]
Heyd, Bruno [3 ]
Combe, Marielle [4 ]
Lorgis, Veronique [2 ]
Demarchi, Martin [2 ]
Stein, Ulrich [2 ]
Royer, Bernard [1 ]
Chauffert, Bruno [5 ]
Pivot, Xavier [2 ]
机构
[1] Dept Pharmacol, F-25030 Besancon, France
[2] Univ Hosp Jean Minjoz, Dept Med Oncol, F-25030 Besancon, France
[3] Univ Hosp Jean Minjoz, CHU Jean Minjoz, Dept Surg, F-25030 Besancon, France
[4] Dept Anesthesia Intens Care, F-25030 Besancon, France
[5] Anticanc Ctr Georges Francois Leclerc, F-21000 Dijon, France
来源
关键词
GYNECOLOGIC-ONCOLOGY-GROUP; STAGE-III OVARIAN; INTRAPERITONEAL CISPLATIN; PHASE-III; CYTOREDUCTIVE SURGERY; CONSOLIDATION THERAPY; COMPLETE REMISSION; IP CISPLATIN; PACLITAXEL; TRIAL;
D O I
10.1186/1477-7819-7-14
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Intra-peritoneal (i.p.) chemotherapy is an encouraging treatment option for ovarian cancer with peritoneum involvement in addition with intravenous (i.v.) chemotherapy. Intraoperative i.p. chemotherapy is an interesting method of administration by enhancing the diffusion of chemotherapy. This study had assessed the feasibility of intra-operative i.p. chemotherapy in patients with peritoneal carcinoma of ovarian cancer. Methods: From January 2003 to February 2006, 47 patients with stage III ovarian cancer were treated with standard paclitaxel carboplatin intravenous chemotherapy and debulking surgery with intra-operative i.p. chemotherapy. After optimal cytoreductive surgery, defined by no unresectable residual disease > 1 cm, i.p. chemotherapy was performed during surgery. The peritoneal cavity was filled by 3 litres of isotonic saline pre-heated at 37 degrees and 90 mg of cisplatin. The sequence was repeated twice during 2 hours based on previous published studies which optimized the cisplatin dosage and exposure duration. Optimal diffusion was obtained by stirring by hands during the 2 hours. Results: Median age was 59.6 years. No severe haematological or non-haematological toxicity induced by intra operative i.p. chemotherapy was reported. No patient died due to the complications of surgery or the i.p. chemotherapy. No neurotoxicity occurred, and one patients had renal impairment. Conclusion: This study demonstrates the feasibility of intra-operative i.p. chemotherapy with cisplatin after optimal resection of peritoneal tumor nodules. Further randomized trials are planned to investigate the clinical benefit of this therapeutic modality.
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