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Peritoneal Sarcomatosis: Is There a Subset of Patients Who May Benefit from Cytoreductive Surgery and Hyperthermic Intraperitoneal Chemotherapy?
Background Unlike novel molecular-targeted therapies for metastatic gastrointestinal stromal tumors (GIST), conventional treatments for peritoneal sarcomatosis (PS) are mostly ineffective. As with carcinomatosis of epithelial origin, a rationale base supports an aggressive locoregional treatment of...
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Published in: | Annals of surgical oncology 2010-12, Vol.17 (12), p.3220-3228 |
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creator | Baratti, Dario Pennacchioli, Elisabetta Kusamura, Shigeki Fiore, Marco Balestra, Maria Rosaria Colombo, Chiara Mingrone, Elvira Alessanrdro, Gronchi Deraco, Marcello |
description | Background
Unlike novel molecular-targeted therapies for metastatic gastrointestinal stromal tumors (GIST), conventional treatments for peritoneal sarcomatosis (PS) are mostly ineffective. As with carcinomatosis of epithelial origin, a rationale base supports an aggressive locoregional treatment of PS, but the use of CRS and HIPEC in this setting is still controversial. We assessed the outcome of clinically and pathologically homogeneous subsets of patients with PS uniformly treated by cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC).
Methods
A prospective database of 37 patients who underwent CRS and close-abdomen HIPEC with cisplatin and doxorubicin or mitomycin-C was reviewed. PS originated from GIST (pre-imatinib era) in 8 patients, uterine leiomyosarcoma (ULS) in 11, retroperitoneal liposarcoma (RPLP) in 13, and other sarcoma in 5.
Results
CRS was macroscopically complete in 28 patients (75.7%). Operative mortality was 3.7% and morbidity 21.6%. After median follow-up of 104 (range, 1–131) months, peritoneal disease progression occurred in 16 patients, distant metastases in 5, and both in 13. For all patients, median overall survival was 26.2 months; 7 patients were alive at 46–130 months (ULS,
n
= 4; RPLP,
n
= 2; GIST,
n
= 1). RPLP had the best overall survival (median, 34 months) but 100% peritoneal relapse; GIST had dismal overall, local–regional-free and distant-free survival; ULS had the higher proportion of long survivors and best local–regional-free survival.
Conclusions
Overall, results of CRS and HIPEC did not compare favorably to those of conventional therapy. In a subgroup analysis, the combined approach did not change GIST and RPLS natural history. The interesting results with ULS may warrant further investigations. |
doi_str_mv | 10.1245/s10434-010-1178-x |
format | article |
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Unlike novel molecular-targeted therapies for metastatic gastrointestinal stromal tumors (GIST), conventional treatments for peritoneal sarcomatosis (PS) are mostly ineffective. As with carcinomatosis of epithelial origin, a rationale base supports an aggressive locoregional treatment of PS, but the use of CRS and HIPEC in this setting is still controversial. We assessed the outcome of clinically and pathologically homogeneous subsets of patients with PS uniformly treated by cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC).
Methods
A prospective database of 37 patients who underwent CRS and close-abdomen HIPEC with cisplatin and doxorubicin or mitomycin-C was reviewed. PS originated from GIST (pre-imatinib era) in 8 patients, uterine leiomyosarcoma (ULS) in 11, retroperitoneal liposarcoma (RPLP) in 13, and other sarcoma in 5.
Results
CRS was macroscopically complete in 28 patients (75.7%). Operative mortality was 3.7% and morbidity 21.6%. After median follow-up of 104 (range, 1–131) months, peritoneal disease progression occurred in 16 patients, distant metastases in 5, and both in 13. For all patients, median overall survival was 26.2 months; 7 patients were alive at 46–130 months (ULS,
n
= 4; RPLP,
n
= 2; GIST,
n
= 1). RPLP had the best overall survival (median, 34 months) but 100% peritoneal relapse; GIST had dismal overall, local–regional-free and distant-free survival; ULS had the higher proportion of long survivors and best local–regional-free survival.
Conclusions
Overall, results of CRS and HIPEC did not compare favorably to those of conventional therapy. In a subgroup analysis, the combined approach did not change GIST and RPLS natural history. The interesting results with ULS may warrant further investigations.</description><identifier>ISSN: 1068-9265</identifier><identifier>EISSN: 1534-4681</identifier><identifier>DOI: 10.1245/s10434-010-1178-x</identifier><identifier>PMID: 20585874</identifier><language>eng</language><publisher>New York: Springer-Verlag</publisher><subject>Adult ; Aged ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Bone and Soft Tissue Sarcomas ; Chemotherapy, Cancer, Regional Perfusion ; Cisplatin - administration & dosage ; Combined Modality Therapy ; Doxorubicin - administration & dosage ; Female ; Humans ; Hyperthermia, Induced ; Leiomyosarcoma - classification ; Leiomyosarcoma - pathology ; Leiomyosarcoma - therapy ; Liposarcoma - classification ; Liposarcoma - pathology ; Liposarcoma - therapy ; Male ; Medicine ; Medicine & Public Health ; Middle Aged ; Mitomycin - administration & dosage ; Neoplasm Staging ; Oncology ; Peritoneal Neoplasms - classification ; Peritoneal Neoplasms - pathology ; Peritoneal Neoplasms - therapy ; Prospective Studies ; Retroperitoneal Neoplasms - classification ; Retroperitoneal Neoplasms - pathology ; Retroperitoneal Neoplasms - therapy ; Surgery ; Surgical Oncology ; Survival Rate ; Treatment Outcome ; Uterine Neoplasms - classification ; Uterine Neoplasms - pathology ; Uterine Neoplasms - therapy ; Young Adult</subject><ispartof>Annals of surgical oncology, 2010-12, Vol.17 (12), p.3220-3228</ispartof><rights>Society of Surgical Oncology 2010</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c370t-6729cf485f76f1c65905ab007741d3f9ccb9fad7e234aa06b5927be98c1eca5f3</citedby><cites>FETCH-LOGICAL-c370t-6729cf485f76f1c65905ab007741d3f9ccb9fad7e234aa06b5927be98c1eca5f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20585874$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Baratti, Dario</creatorcontrib><creatorcontrib>Pennacchioli, Elisabetta</creatorcontrib><creatorcontrib>Kusamura, Shigeki</creatorcontrib><creatorcontrib>Fiore, Marco</creatorcontrib><creatorcontrib>Balestra, Maria Rosaria</creatorcontrib><creatorcontrib>Colombo, Chiara</creatorcontrib><creatorcontrib>Mingrone, Elvira</creatorcontrib><creatorcontrib>Alessanrdro, Gronchi</creatorcontrib><creatorcontrib>Deraco, Marcello</creatorcontrib><title>Peritoneal Sarcomatosis: Is There a Subset of Patients Who May Benefit from Cytoreductive Surgery and Hyperthermic Intraperitoneal Chemotherapy?</title><title>Annals of surgical oncology</title><addtitle>Ann Surg Oncol</addtitle><addtitle>Ann Surg Oncol</addtitle><description>Background
Unlike novel molecular-targeted therapies for metastatic gastrointestinal stromal tumors (GIST), conventional treatments for peritoneal sarcomatosis (PS) are mostly ineffective. As with carcinomatosis of epithelial origin, a rationale base supports an aggressive locoregional treatment of PS, but the use of CRS and HIPEC in this setting is still controversial. We assessed the outcome of clinically and pathologically homogeneous subsets of patients with PS uniformly treated by cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC).
Methods
A prospective database of 37 patients who underwent CRS and close-abdomen HIPEC with cisplatin and doxorubicin or mitomycin-C was reviewed. PS originated from GIST (pre-imatinib era) in 8 patients, uterine leiomyosarcoma (ULS) in 11, retroperitoneal liposarcoma (RPLP) in 13, and other sarcoma in 5.
Results
CRS was macroscopically complete in 28 patients (75.7%). Operative mortality was 3.7% and morbidity 21.6%. After median follow-up of 104 (range, 1–131) months, peritoneal disease progression occurred in 16 patients, distant metastases in 5, and both in 13. For all patients, median overall survival was 26.2 months; 7 patients were alive at 46–130 months (ULS,
n
= 4; RPLP,
n
= 2; GIST,
n
= 1). RPLP had the best overall survival (median, 34 months) but 100% peritoneal relapse; GIST had dismal overall, local–regional-free and distant-free survival; ULS had the higher proportion of long survivors and best local–regional-free survival.
Conclusions
Overall, results of CRS and HIPEC did not compare favorably to those of conventional therapy. In a subgroup analysis, the combined approach did not change GIST and RPLS natural history. The interesting results with ULS may warrant further investigations.</description><subject>Adult</subject><subject>Aged</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Bone and Soft Tissue Sarcomas</subject><subject>Chemotherapy, Cancer, Regional Perfusion</subject><subject>Cisplatin - administration & dosage</subject><subject>Combined Modality Therapy</subject><subject>Doxorubicin - administration & dosage</subject><subject>Female</subject><subject>Humans</subject><subject>Hyperthermia, Induced</subject><subject>Leiomyosarcoma - classification</subject><subject>Leiomyosarcoma - pathology</subject><subject>Leiomyosarcoma - therapy</subject><subject>Liposarcoma - classification</subject><subject>Liposarcoma - pathology</subject><subject>Liposarcoma - therapy</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Middle Aged</subject><subject>Mitomycin - administration & dosage</subject><subject>Neoplasm Staging</subject><subject>Oncology</subject><subject>Peritoneal Neoplasms - classification</subject><subject>Peritoneal Neoplasms - pathology</subject><subject>Peritoneal Neoplasms - therapy</subject><subject>Prospective Studies</subject><subject>Retroperitoneal Neoplasms - classification</subject><subject>Retroperitoneal Neoplasms - pathology</subject><subject>Retroperitoneal Neoplasms - therapy</subject><subject>Surgery</subject><subject>Surgical Oncology</subject><subject>Survival Rate</subject><subject>Treatment Outcome</subject><subject>Uterine Neoplasms - classification</subject><subject>Uterine Neoplasms - pathology</subject><subject>Uterine Neoplasms - therapy</subject><subject>Young Adult</subject><issn>1068-9265</issn><issn>1534-4681</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNp1kc1q3TAQhUVoaH7aB8imiG66cjuSLUvupiSXtLmQ0EASsjSyPOp1uLYcSS7xW_SRq8vNDwSykjTznTODDiFHDL4yXohvgUGRFxkwyBiTKnvYIftMpEpRKvYu3aFUWcVLsUcOQrgDYDIH8Z7scRBKKFnsk3-X6LvoBtRreqW9cb2OLnThO10Ger1Cj1TTq6kJGKmz9FLHDocY6O3K0Qs90xMc0HaRWu96upij89hOJnZ_Man8H_Qz1UNLz-YRfUx2fWfocohejy9zFyvs3aapx_nHB7Jr9Trgx8fzkNz8PL1enGXnv38tF8fnmcklxKyUvDK2UMLK0jJTigqEbgCkLFib28qYprK6lcjzQmsoG1Fx2WClDEOjhc0PyZet7-jd_YQh1n0XDK7XekA3hVoxUZWQ5zyRn1-Rd27yQ1puA3GVGEgQ20LGuxA82nr0Xa_9XDOoN2HV27Bq2LxTWPVD0nx6NJ6aHttnxVM6CeBbIKTWkD7zZfLbrv8Bbn-iTA</recordid><startdate>20101201</startdate><enddate>20101201</enddate><creator>Baratti, Dario</creator><creator>Pennacchioli, Elisabetta</creator><creator>Kusamura, Shigeki</creator><creator>Fiore, Marco</creator><creator>Balestra, Maria Rosaria</creator><creator>Colombo, Chiara</creator><creator>Mingrone, Elvira</creator><creator>Alessanrdro, Gronchi</creator><creator>Deraco, Marcello</creator><general>Springer-Verlag</general><general>Springer Nature B.V</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>3V.</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20101201</creationdate><title>Peritoneal Sarcomatosis: Is There a Subset of Patients Who May Benefit from Cytoreductive Surgery and Hyperthermic Intraperitoneal Chemotherapy?</title><author>Baratti, Dario ; Pennacchioli, Elisabetta ; Kusamura, Shigeki ; Fiore, Marco ; Balestra, Maria Rosaria ; Colombo, Chiara ; Mingrone, Elvira ; Alessanrdro, Gronchi ; Deraco, Marcello</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c370t-6729cf485f76f1c65905ab007741d3f9ccb9fad7e234aa06b5927be98c1eca5f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Bone and Soft Tissue Sarcomas</topic><topic>Chemotherapy, Cancer, Regional Perfusion</topic><topic>Cisplatin - administration & dosage</topic><topic>Combined Modality Therapy</topic><topic>Doxorubicin - administration & dosage</topic><topic>Female</topic><topic>Humans</topic><topic>Hyperthermia, Induced</topic><topic>Leiomyosarcoma - classification</topic><topic>Leiomyosarcoma - pathology</topic><topic>Leiomyosarcoma - therapy</topic><topic>Liposarcoma - classification</topic><topic>Liposarcoma - pathology</topic><topic>Liposarcoma - therapy</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Middle Aged</topic><topic>Mitomycin - administration & dosage</topic><topic>Neoplasm Staging</topic><topic>Oncology</topic><topic>Peritoneal Neoplasms - classification</topic><topic>Peritoneal Neoplasms - pathology</topic><topic>Peritoneal Neoplasms - therapy</topic><topic>Prospective Studies</topic><topic>Retroperitoneal Neoplasms - classification</topic><topic>Retroperitoneal Neoplasms - pathology</topic><topic>Retroperitoneal Neoplasms - therapy</topic><topic>Surgery</topic><topic>Surgical Oncology</topic><topic>Survival Rate</topic><topic>Treatment Outcome</topic><topic>Uterine Neoplasms - classification</topic><topic>Uterine Neoplasms - pathology</topic><topic>Uterine Neoplasms - therapy</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Baratti, Dario</creatorcontrib><creatorcontrib>Pennacchioli, Elisabetta</creatorcontrib><creatorcontrib>Kusamura, Shigeki</creatorcontrib><creatorcontrib>Fiore, Marco</creatorcontrib><creatorcontrib>Balestra, Maria Rosaria</creatorcontrib><creatorcontrib>Colombo, Chiara</creatorcontrib><creatorcontrib>Mingrone, Elvira</creatorcontrib><creatorcontrib>Alessanrdro, Gronchi</creatorcontrib><creatorcontrib>Deraco, Marcello</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Annals of surgical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Baratti, Dario</au><au>Pennacchioli, Elisabetta</au><au>Kusamura, Shigeki</au><au>Fiore, Marco</au><au>Balestra, Maria Rosaria</au><au>Colombo, Chiara</au><au>Mingrone, Elvira</au><au>Alessanrdro, Gronchi</au><au>Deraco, Marcello</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Peritoneal Sarcomatosis: Is There a Subset of Patients Who May Benefit from Cytoreductive Surgery and Hyperthermic Intraperitoneal Chemotherapy?</atitle><jtitle>Annals of surgical oncology</jtitle><stitle>Ann Surg Oncol</stitle><addtitle>Ann Surg Oncol</addtitle><date>2010-12-01</date><risdate>2010</risdate><volume>17</volume><issue>12</issue><spage>3220</spage><epage>3228</epage><pages>3220-3228</pages><issn>1068-9265</issn><eissn>1534-4681</eissn><abstract>Background
Unlike novel molecular-targeted therapies for metastatic gastrointestinal stromal tumors (GIST), conventional treatments for peritoneal sarcomatosis (PS) are mostly ineffective. As with carcinomatosis of epithelial origin, a rationale base supports an aggressive locoregional treatment of PS, but the use of CRS and HIPEC in this setting is still controversial. We assessed the outcome of clinically and pathologically homogeneous subsets of patients with PS uniformly treated by cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC).
Methods
A prospective database of 37 patients who underwent CRS and close-abdomen HIPEC with cisplatin and doxorubicin or mitomycin-C was reviewed. PS originated from GIST (pre-imatinib era) in 8 patients, uterine leiomyosarcoma (ULS) in 11, retroperitoneal liposarcoma (RPLP) in 13, and other sarcoma in 5.
Results
CRS was macroscopically complete in 28 patients (75.7%). Operative mortality was 3.7% and morbidity 21.6%. After median follow-up of 104 (range, 1–131) months, peritoneal disease progression occurred in 16 patients, distant metastases in 5, and both in 13. For all patients, median overall survival was 26.2 months; 7 patients were alive at 46–130 months (ULS,
n
= 4; RPLP,
n
= 2; GIST,
n
= 1). RPLP had the best overall survival (median, 34 months) but 100% peritoneal relapse; GIST had dismal overall, local–regional-free and distant-free survival; ULS had the higher proportion of long survivors and best local–regional-free survival.
Conclusions
Overall, results of CRS and HIPEC did not compare favorably to those of conventional therapy. In a subgroup analysis, the combined approach did not change GIST and RPLS natural history. The interesting results with ULS may warrant further investigations.</abstract><cop>New York</cop><pub>Springer-Verlag</pub><pmid>20585874</pmid><doi>10.1245/s10434-010-1178-x</doi><tpages>9</tpages></addata></record> |
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subjects | Adult Aged Antineoplastic Combined Chemotherapy Protocols - therapeutic use Bone and Soft Tissue Sarcomas Chemotherapy, Cancer, Regional Perfusion Cisplatin - administration & dosage Combined Modality Therapy Doxorubicin - administration & dosage Female Humans Hyperthermia, Induced Leiomyosarcoma - classification Leiomyosarcoma - pathology Leiomyosarcoma - therapy Liposarcoma - classification Liposarcoma - pathology Liposarcoma - therapy Male Medicine Medicine & Public Health Middle Aged Mitomycin - administration & dosage Neoplasm Staging Oncology Peritoneal Neoplasms - classification Peritoneal Neoplasms - pathology Peritoneal Neoplasms - therapy Prospective Studies Retroperitoneal Neoplasms - classification Retroperitoneal Neoplasms - pathology Retroperitoneal Neoplasms - therapy Surgery Surgical Oncology Survival Rate Treatment Outcome Uterine Neoplasms - classification Uterine Neoplasms - pathology Uterine Neoplasms - therapy Young Adult |
title | Peritoneal Sarcomatosis: Is There a Subset of Patients Who May Benefit from Cytoreductive Surgery and Hyperthermic Intraperitoneal Chemotherapy? |
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