Cytoreductive surgery and hyperthermic intraperitoneal chemotherapy as upfront therapy for advanced epithelial ovarian cancer: Multi-institutional phase-II trial

Abstract Objective. The primary end-point of this multi-institutional phase-II trial was to assess results in terms of overall survival after cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC) in treatment-naive epithelial ovarian cancer (EOC) with advanced peritoneal...

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Veröffentlicht in:Gynecologic oncology 2011-08, Vol.122 (2), p.215-220
Hauptverfasser: Deraco, Marcello, Kusamura, Shigeki, Virzì, Salvatore, Puccio, Francesco, Macrì, Antonio, Famulari, Ciro, Solazzo, Massimiliano, Bonomi, Serena, Iusco, Domenico Rosario, Baratti, Dario
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container_end_page 220
container_issue 2
container_start_page 215
container_title Gynecologic oncology
container_volume 122
creator Deraco, Marcello
Kusamura, Shigeki
Virzì, Salvatore
Puccio, Francesco
Macrì, Antonio
Famulari, Ciro
Solazzo, Massimiliano
Bonomi, Serena
Iusco, Domenico Rosario
Baratti, Dario
description Abstract Objective. The primary end-point of this multi-institutional phase-II trial was to assess results in terms of overall survival after cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC) in treatment-naive epithelial ovarian cancer (EOC) with advanced peritoneal involvement. Secondary end-points were treatment morbi-mortality and outcome effects of time to subsequent adjuvant systemic chemotherapy (TTC). Methods. Twenty-six women with stage III–IV EOC were prospectively enrolled in 4 Italian centers to undergo CRS and closed-abdomen HIPEC with cisplatin and doxorubicin. Then they received systemic chemotherapy with carboplatin (AUC 6) and paclitaxel (175 mg/m2 ) for 6 cycles. Results. Macroscopically complete cytoreduction was achieved in 15 patients; only minimal residual disease (≤ 2.5 mm) remained in 11. Major complications occurred in four patients and postoperative death in one. After a median follow-up of 25 months, 5-year overall survival was 60.7% and 5-year progression-free survival 15.2% (median 30 months). Excluding operative death, all the patients underwent systemic chemotherapy at a median of 46 days from combined treatment (range: 29–75). The median number of cycles per patient was 6 (range: 1–8). The time to chemotherapy did not affect the OS or PFS. Conclusions. In selected patients with advanced stage EOC, upfront CRS and HIPEC provided promising results in terms of outcome. Morbidity was comparable to aggressive cytoreduction without HIPEC. Postoperative recovery delayed the initiation of adjuvant systemic chemotherapy but not sufficiently to impact negatively on survival. These data warrant further evaluation in a randomized clinical trial.
doi_str_mv 10.1016/j.ygyno.2011.05.004
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The primary end-point of this multi-institutional phase-II trial was to assess results in terms of overall survival after cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC) in treatment-naive epithelial ovarian cancer (EOC) with advanced peritoneal involvement. Secondary end-points were treatment morbi-mortality and outcome effects of time to subsequent adjuvant systemic chemotherapy (TTC). Methods. Twenty-six women with stage III–IV EOC were prospectively enrolled in 4 Italian centers to undergo CRS and closed-abdomen HIPEC with cisplatin and doxorubicin. Then they received systemic chemotherapy with carboplatin (AUC 6) and paclitaxel (175 mg/m2 ) for 6 cycles. Results. Macroscopically complete cytoreduction was achieved in 15 patients; only minimal residual disease (≤ 2.5 mm) remained in 11. Major complications occurred in four patients and postoperative death in one. After a median follow-up of 25 months, 5-year overall survival was 60.7% and 5-year progression-free survival 15.2% (median 30 months). Excluding operative death, all the patients underwent systemic chemotherapy at a median of 46 days from combined treatment (range: 29–75). The median number of cycles per patient was 6 (range: 1–8). The time to chemotherapy did not affect the OS or PFS. Conclusions. In selected patients with advanced stage EOC, upfront CRS and HIPEC provided promising results in terms of outcome. Morbidity was comparable to aggressive cytoreduction without HIPEC. Postoperative recovery delayed the initiation of adjuvant systemic chemotherapy but not sufficiently to impact negatively on survival. These data warrant further evaluation in a randomized clinical trial.</description><identifier>ISSN: 0090-8258</identifier><identifier>EISSN: 1095-6859</identifier><identifier>DOI: 10.1016/j.ygyno.2011.05.004</identifier><identifier>PMID: 21665254</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adult ; Aged ; Antineoplastic Agents - administration &amp; dosage ; Antineoplastic Agents - therapeutic use ; Carcinoma, Ovarian Epithelial ; Combined Modality Therapy ; Cytoreductive surgery ; Epithelial ovarian cancer ; Female ; Hematology, Oncology and Palliative Medicine ; Humans ; Hyperthermia, Induced - methods ; Hyperthermic intraperitoneal chemotherapy ; Injections, Intraperitoneal ; Middle Aged ; Neoplasm Staging ; Neoplasms, Glandular and Epithelial - mortality ; Neoplasms, Glandular and Epithelial - pathology ; Neoplasms, Glandular and Epithelial - therapy ; Obstetrics and Gynecology ; Ovarian Neoplasms - mortality ; Ovarian Neoplasms - pathology ; Ovarian Neoplasms - therapy ; peritoneal carcinomatosis ; Peritoneal Neoplasms - mortality ; Peritoneal Neoplasms - secondary ; Peritoneal Neoplasms - therapy ; peritonectomy</subject><ispartof>Gynecologic oncology, 2011-08, Vol.122 (2), p.215-220</ispartof><rights>Elsevier Inc.</rights><rights>2011 Elsevier Inc.</rights><rights>Copyright © 2011 Elsevier Inc. 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The primary end-point of this multi-institutional phase-II trial was to assess results in terms of overall survival after cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC) in treatment-naive epithelial ovarian cancer (EOC) with advanced peritoneal involvement. Secondary end-points were treatment morbi-mortality and outcome effects of time to subsequent adjuvant systemic chemotherapy (TTC). Methods. Twenty-six women with stage III–IV EOC were prospectively enrolled in 4 Italian centers to undergo CRS and closed-abdomen HIPEC with cisplatin and doxorubicin. Then they received systemic chemotherapy with carboplatin (AUC 6) and paclitaxel (175 mg/m2 ) for 6 cycles. Results. Macroscopically complete cytoreduction was achieved in 15 patients; only minimal residual disease (≤ 2.5 mm) remained in 11. Major complications occurred in four patients and postoperative death in one. After a median follow-up of 25 months, 5-year overall survival was 60.7% and 5-year progression-free survival 15.2% (median 30 months). Excluding operative death, all the patients underwent systemic chemotherapy at a median of 46 days from combined treatment (range: 29–75). The median number of cycles per patient was 6 (range: 1–8). The time to chemotherapy did not affect the OS or PFS. Conclusions. In selected patients with advanced stage EOC, upfront CRS and HIPEC provided promising results in terms of outcome. Morbidity was comparable to aggressive cytoreduction without HIPEC. Postoperative recovery delayed the initiation of adjuvant systemic chemotherapy but not sufficiently to impact negatively on survival. 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The primary end-point of this multi-institutional phase-II trial was to assess results in terms of overall survival after cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC) in treatment-naive epithelial ovarian cancer (EOC) with advanced peritoneal involvement. Secondary end-points were treatment morbi-mortality and outcome effects of time to subsequent adjuvant systemic chemotherapy (TTC). Methods. Twenty-six women with stage III–IV EOC were prospectively enrolled in 4 Italian centers to undergo CRS and closed-abdomen HIPEC with cisplatin and doxorubicin. Then they received systemic chemotherapy with carboplatin (AUC 6) and paclitaxel (175 mg/m2 ) for 6 cycles. Results. Macroscopically complete cytoreduction was achieved in 15 patients; only minimal residual disease (≤ 2.5 mm) remained in 11. Major complications occurred in four patients and postoperative death in one. After a median follow-up of 25 months, 5-year overall survival was 60.7% and 5-year progression-free survival 15.2% (median 30 months). Excluding operative death, all the patients underwent systemic chemotherapy at a median of 46 days from combined treatment (range: 29–75). The median number of cycles per patient was 6 (range: 1–8). The time to chemotherapy did not affect the OS or PFS. Conclusions. In selected patients with advanced stage EOC, upfront CRS and HIPEC provided promising results in terms of outcome. Morbidity was comparable to aggressive cytoreduction without HIPEC. Postoperative recovery delayed the initiation of adjuvant systemic chemotherapy but not sufficiently to impact negatively on survival. These data warrant further evaluation in a randomized clinical trial.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>21665254</pmid><doi>10.1016/j.ygyno.2011.05.004</doi><tpages>6</tpages></addata></record>
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subjects Adult
Aged
Antineoplastic Agents - administration & dosage
Antineoplastic Agents - therapeutic use
Carcinoma, Ovarian Epithelial
Combined Modality Therapy
Cytoreductive surgery
Epithelial ovarian cancer
Female
Hematology, Oncology and Palliative Medicine
Humans
Hyperthermia, Induced - methods
Hyperthermic intraperitoneal chemotherapy
Injections, Intraperitoneal
Middle Aged
Neoplasm Staging
Neoplasms, Glandular and Epithelial - mortality
Neoplasms, Glandular and Epithelial - pathology
Neoplasms, Glandular and Epithelial - therapy
Obstetrics and Gynecology
Ovarian Neoplasms - mortality
Ovarian Neoplasms - pathology
Ovarian Neoplasms - therapy
peritoneal carcinomatosis
Peritoneal Neoplasms - mortality
Peritoneal Neoplasms - secondary
Peritoneal Neoplasms - therapy
peritonectomy
title Cytoreductive surgery and hyperthermic intraperitoneal chemotherapy as upfront therapy for advanced epithelial ovarian cancer: Multi-institutional phase-II trial
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