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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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 & 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. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c413t-fe499ae1fb6eeb4cc4e4a7b97427fe70ebe03d8151cb7defe6815aebbb0ae24b3</citedby><cites>FETCH-LOGICAL-c413t-fe499ae1fb6eeb4cc4e4a7b97427fe70ebe03d8151cb7defe6815aebbb0ae24b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ygyno.2011.05.004$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27923,27924,45994</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21665254$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Deraco, Marcello</creatorcontrib><creatorcontrib>Kusamura, Shigeki</creatorcontrib><creatorcontrib>Virzì, Salvatore</creatorcontrib><creatorcontrib>Puccio, Francesco</creatorcontrib><creatorcontrib>Macrì, Antonio</creatorcontrib><creatorcontrib>Famulari, Ciro</creatorcontrib><creatorcontrib>Solazzo, Massimiliano</creatorcontrib><creatorcontrib>Bonomi, Serena</creatorcontrib><creatorcontrib>Iusco, Domenico Rosario</creatorcontrib><creatorcontrib>Baratti, Dario</creatorcontrib><title>Cytoreductive surgery and hyperthermic intraperitoneal chemotherapy as upfront therapy for advanced epithelial ovarian cancer: Multi-institutional phase-II trial</title><title>Gynecologic oncology</title><addtitle>Gynecol Oncol</addtitle><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.</description><subject>Adult</subject><subject>Aged</subject><subject>Antineoplastic Agents - administration & dosage</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Carcinoma, Ovarian Epithelial</subject><subject>Combined Modality Therapy</subject><subject>Cytoreductive surgery</subject><subject>Epithelial ovarian cancer</subject><subject>Female</subject><subject>Hematology, Oncology and Palliative Medicine</subject><subject>Humans</subject><subject>Hyperthermia, Induced - methods</subject><subject>Hyperthermic intraperitoneal chemotherapy</subject><subject>Injections, Intraperitoneal</subject><subject>Middle Aged</subject><subject>Neoplasm Staging</subject><subject>Neoplasms, Glandular and Epithelial - mortality</subject><subject>Neoplasms, Glandular and Epithelial - pathology</subject><subject>Neoplasms, Glandular and Epithelial - therapy</subject><subject>Obstetrics and Gynecology</subject><subject>Ovarian Neoplasms - mortality</subject><subject>Ovarian Neoplasms - pathology</subject><subject>Ovarian Neoplasms - therapy</subject><subject>peritoneal carcinomatosis</subject><subject>Peritoneal Neoplasms - mortality</subject><subject>Peritoneal Neoplasms - secondary</subject><subject>Peritoneal Neoplasms - therapy</subject><subject>peritonectomy</subject><issn>0090-8258</issn><issn>1095-6859</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFksuO1DAQRS0EYpqBL0BC3rFKKCfOCwkk1OLR0iAWwNqyncq0m8QOttNSPoc_xaFnWLBhVXbVuWW5bhHynEHOgNWvTvl6u1qXF8BYDlUOwB-QHYOuyuq26h6SHUAHWVtU7RV5EsIJAEpgxWNyVbC6roqK78iv_Rqdx37R0ZyRhsXfol-ptD09rjP6eEQ_GU2NjV6mu4nOohypPuLktqKcEx3oMg_e2UjvU4PzVPZnaTX2FGeT8qNJOneW3khL9Vbxr-nnZYwmMzZEE5donE3MfJQBs8OBxoSOT8mjQY4Bn93Fa_L9w_tv-0_ZzZePh_27m0xzVsZsQN51EtmgakTFtebIZaO6hhfNgA2gQij7llVMq6bHAet0lqiUAokFV-U1eXnpO3v3c8EQxWSCxnGUFt0SRNu0UHRdxRNZXkjtXQgeBzF7M0m_CgZis0acxB9rxGaNgEoka5LqxV3_RU3Y_9Xce5GANxcA0y_PBr0I2uA2QONRR9E7858H3v6j16OxRsvxB64YTm7xabpBMBEKAeLrth3bcjCW9iKF8jfq3LzU</recordid><startdate>20110801</startdate><enddate>20110801</enddate><creator>Deraco, Marcello</creator><creator>Kusamura, Shigeki</creator><creator>Virzì, Salvatore</creator><creator>Puccio, Francesco</creator><creator>Macrì, Antonio</creator><creator>Famulari, Ciro</creator><creator>Solazzo, Massimiliano</creator><creator>Bonomi, Serena</creator><creator>Iusco, Domenico Rosario</creator><creator>Baratti, Dario</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20110801</creationdate><title>Cytoreductive surgery and hyperthermic intraperitoneal chemotherapy as upfront therapy for advanced epithelial ovarian cancer: Multi-institutional phase-II trial</title><author>Deraco, Marcello ; Kusamura, Shigeki ; Virzì, Salvatore ; Puccio, Francesco ; Macrì, Antonio ; Famulari, Ciro ; Solazzo, Massimiliano ; Bonomi, Serena ; Iusco, Domenico Rosario ; Baratti, Dario</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c413t-fe499ae1fb6eeb4cc4e4a7b97427fe70ebe03d8151cb7defe6815aebbb0ae24b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Antineoplastic Agents - administration & dosage</topic><topic>Antineoplastic Agents - therapeutic use</topic><topic>Carcinoma, Ovarian Epithelial</topic><topic>Combined Modality Therapy</topic><topic>Cytoreductive surgery</topic><topic>Epithelial ovarian cancer</topic><topic>Female</topic><topic>Hematology, Oncology and Palliative Medicine</topic><topic>Humans</topic><topic>Hyperthermia, Induced - methods</topic><topic>Hyperthermic intraperitoneal chemotherapy</topic><topic>Injections, Intraperitoneal</topic><topic>Middle Aged</topic><topic>Neoplasm Staging</topic><topic>Neoplasms, Glandular and Epithelial - mortality</topic><topic>Neoplasms, Glandular and Epithelial - pathology</topic><topic>Neoplasms, Glandular and Epithelial - therapy</topic><topic>Obstetrics and Gynecology</topic><topic>Ovarian Neoplasms - mortality</topic><topic>Ovarian Neoplasms - pathology</topic><topic>Ovarian Neoplasms - therapy</topic><topic>peritoneal carcinomatosis</topic><topic>Peritoneal Neoplasms - mortality</topic><topic>Peritoneal Neoplasms - secondary</topic><topic>Peritoneal Neoplasms - therapy</topic><topic>peritonectomy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Deraco, Marcello</creatorcontrib><creatorcontrib>Kusamura, Shigeki</creatorcontrib><creatorcontrib>Virzì, Salvatore</creatorcontrib><creatorcontrib>Puccio, Francesco</creatorcontrib><creatorcontrib>Macrì, Antonio</creatorcontrib><creatorcontrib>Famulari, Ciro</creatorcontrib><creatorcontrib>Solazzo, Massimiliano</creatorcontrib><creatorcontrib>Bonomi, Serena</creatorcontrib><creatorcontrib>Iusco, Domenico Rosario</creatorcontrib><creatorcontrib>Baratti, Dario</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Gynecologic oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Deraco, Marcello</au><au>Kusamura, Shigeki</au><au>Virzì, Salvatore</au><au>Puccio, Francesco</au><au>Macrì, Antonio</au><au>Famulari, Ciro</au><au>Solazzo, Massimiliano</au><au>Bonomi, Serena</au><au>Iusco, Domenico Rosario</au><au>Baratti, Dario</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cytoreductive surgery and hyperthermic intraperitoneal chemotherapy as upfront therapy for advanced epithelial ovarian cancer: Multi-institutional phase-II trial</atitle><jtitle>Gynecologic oncology</jtitle><addtitle>Gynecol Oncol</addtitle><date>2011-08-01</date><risdate>2011</risdate><volume>122</volume><issue>2</issue><spage>215</spage><epage>220</epage><pages>215-220</pages><issn>0090-8258</issn><eissn>1095-6859</eissn><abstract>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.</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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