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Impact of tumor viability at second-look procedures performed before completing treatment on the Intergroup Rhabdomyosarcoma Study Group protocol IRS-IV, 1991-1997: a report from the children's oncology group
Abstract Purposes The aims of the study were to compare results of clinical/radiographic studies before second-look procedures (SLP) with SLP specimens from patients with gross residual sarcoma at diagnosis and to relate tumor viability to outcome. Patients Seventy-three patients underwent SLP befor...
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Published in: | Journal of pediatric surgery 2010-11, Vol.45 (11), p.2160-2168 |
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container_title | Journal of pediatric surgery |
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creator | Raney, Beverly Stoner, Julie Anderson, James Andrassy, Richard Arndt, Carola Brown, Ken Crist, William Maurer, Harold Qualman, Stephen Wharam, Moody Wiener, Eugene Meyer, William Hayes-Jordan, Andrea |
description | Abstract Purposes The aims of the study were to compare results of clinical/radiographic studies before second-look procedures (SLP) with SLP specimens from patients with gross residual sarcoma at diagnosis and to relate tumor viability to outcome. Patients Seventy-three patients underwent SLP before completing chemotherapy, with (n = 59) or without (n = 14) radiotherapy. Tumor sites were bladder/prostate (n = 27), head/orbit/parameningeal (n = 22), extremity/trunk (n = 14), and retroperitoneum/pelvis (n = 10). Results Of 14 patients, 1 (7%) with clinical/radiographic complete response (CR) had viable tumor. Of 59 patients, 35 (59%) without CR had viable tumor. Five-year failure-free survival (FFS) rates were 81% in 37 patients without viable tumor and 53% in 36 patients with viable tumor (Cox proportional hazards adjusted P = .05). Five-year FFS rates were 67% in 15 patients with clear margins and 43% in 21 patients with tumor-involved margins (n = 18) or viable gross tumor (n = 3) (Cox proportional hazards adjusted P = .04). Five-year survival was 78% to 79% among 73 patients with and 333 patients without SLP during treatment. Conclusions Second-look procedures can show whether viable tumor is present and may be beneficial in selected patients with rhabdomyosarcoma. Disappearance of tumor (CR) usually correlated with no viable tumor at SLP. However, 41% of patients without CR had no viable tumor. Those without viable tumor had increased FFS but not survival compared to those with viable tumor. |
doi_str_mv | 10.1016/j.jpedsurg.2010.07.021 |
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Patients Seventy-three patients underwent SLP before completing chemotherapy, with (n = 59) or without (n = 14) radiotherapy. Tumor sites were bladder/prostate (n = 27), head/orbit/parameningeal (n = 22), extremity/trunk (n = 14), and retroperitoneum/pelvis (n = 10). Results Of 14 patients, 1 (7%) with clinical/radiographic complete response (CR) had viable tumor. Of 59 patients, 35 (59%) without CR had viable tumor. Five-year failure-free survival (FFS) rates were 81% in 37 patients without viable tumor and 53% in 36 patients with viable tumor (Cox proportional hazards adjusted P = .05). Five-year FFS rates were 67% in 15 patients with clear margins and 43% in 21 patients with tumor-involved margins (n = 18) or viable gross tumor (n = 3) (Cox proportional hazards adjusted P = .04). Five-year survival was 78% to 79% among 73 patients with and 333 patients without SLP during treatment. Conclusions Second-look procedures can show whether viable tumor is present and may be beneficial in selected patients with rhabdomyosarcoma. Disappearance of tumor (CR) usually correlated with no viable tumor at SLP. However, 41% of patients without CR had no viable tumor. Those without viable tumor had increased FFS but not survival compared to those with viable tumor.</description><identifier>ISSN: 0022-3468</identifier><identifier>EISSN: 1531-5037</identifier><identifier>DOI: 10.1016/j.jpedsurg.2010.07.021</identifier><identifier>PMID: 21034938</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Antineoplastic Agents - therapeutic use ; Child ; Childhood rhabdomyosarcoma ; Diagnostic Imaging - methods ; Disease-Free Survival ; Dose Fractionation ; Female ; Follow-Up Studies ; Humans ; IRS-IV protocol ; Male ; Neoplasm Staging ; Neoplasm, Residual ; Pediatrics ; Retrospective Studies ; Rhabdomyosarcoma - diagnosis ; Rhabdomyosarcoma - epidemiology ; Rhabdomyosarcoma - therapy ; Second-look procedures ; Second-Look Surgery - methods ; Surgery ; Survival Rate ; Time Factors ; Treatment Outcome ; United States - epidemiology</subject><ispartof>Journal of pediatric surgery, 2010-11, Vol.45 (11), p.2160-2168</ispartof><rights>2010</rights><rights>Copyright © 2010. Published by Elsevier Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c536t-13cc58a0c23dc3cb5fe5b2858ed50723ce27b3284406b0771439af32ec27203c3</citedby><cites>FETCH-LOGICAL-c536t-13cc58a0c23dc3cb5fe5b2858ed50723ce27b3284406b0771439af32ec27203c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27900,27901</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21034938$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Raney, Beverly</creatorcontrib><creatorcontrib>Stoner, Julie</creatorcontrib><creatorcontrib>Anderson, James</creatorcontrib><creatorcontrib>Andrassy, Richard</creatorcontrib><creatorcontrib>Arndt, Carola</creatorcontrib><creatorcontrib>Brown, Ken</creatorcontrib><creatorcontrib>Crist, William</creatorcontrib><creatorcontrib>Maurer, Harold</creatorcontrib><creatorcontrib>Qualman, Stephen</creatorcontrib><creatorcontrib>Wharam, Moody</creatorcontrib><creatorcontrib>Wiener, Eugene</creatorcontrib><creatorcontrib>Meyer, William</creatorcontrib><creatorcontrib>Hayes-Jordan, Andrea</creatorcontrib><creatorcontrib>For the Soft-Tissue Sarcoma Committee of the Children's Oncology Group, Arcadia, California, USA</creatorcontrib><creatorcontrib>Soft-Tissue Sarcoma Committee of the Children's Oncology Group</creatorcontrib><title>Impact of tumor viability at second-look procedures performed before completing treatment on the Intergroup Rhabdomyosarcoma Study Group protocol IRS-IV, 1991-1997: a report from the children's oncology group</title><title>Journal of pediatric surgery</title><addtitle>J Pediatr Surg</addtitle><description>Abstract Purposes The aims of the study were to compare results of clinical/radiographic studies before second-look procedures (SLP) with SLP specimens from patients with gross residual sarcoma at diagnosis and to relate tumor viability to outcome. Patients Seventy-three patients underwent SLP before completing chemotherapy, with (n = 59) or without (n = 14) radiotherapy. Tumor sites were bladder/prostate (n = 27), head/orbit/parameningeal (n = 22), extremity/trunk (n = 14), and retroperitoneum/pelvis (n = 10). Results Of 14 patients, 1 (7%) with clinical/radiographic complete response (CR) had viable tumor. Of 59 patients, 35 (59%) without CR had viable tumor. Five-year failure-free survival (FFS) rates were 81% in 37 patients without viable tumor and 53% in 36 patients with viable tumor (Cox proportional hazards adjusted P = .05). Five-year FFS rates were 67% in 15 patients with clear margins and 43% in 21 patients with tumor-involved margins (n = 18) or viable gross tumor (n = 3) (Cox proportional hazards adjusted P = .04). Five-year survival was 78% to 79% among 73 patients with and 333 patients without SLP during treatment. Conclusions Second-look procedures can show whether viable tumor is present and may be beneficial in selected patients with rhabdomyosarcoma. Disappearance of tumor (CR) usually correlated with no viable tumor at SLP. However, 41% of patients without CR had no viable tumor. Those without viable tumor had increased FFS but not survival compared to those with viable tumor.</description><subject>Antineoplastic Agents - therapeutic use</subject><subject>Child</subject><subject>Childhood rhabdomyosarcoma</subject><subject>Diagnostic Imaging - methods</subject><subject>Disease-Free Survival</subject><subject>Dose Fractionation</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>IRS-IV protocol</subject><subject>Male</subject><subject>Neoplasm Staging</subject><subject>Neoplasm, Residual</subject><subject>Pediatrics</subject><subject>Retrospective Studies</subject><subject>Rhabdomyosarcoma - diagnosis</subject><subject>Rhabdomyosarcoma - epidemiology</subject><subject>Rhabdomyosarcoma - therapy</subject><subject>Second-look procedures</subject><subject>Second-Look Surgery - methods</subject><subject>Surgery</subject><subject>Survival Rate</subject><subject>Time Factors</subject><subject>Treatment Outcome</subject><subject>United States - epidemiology</subject><issn>0022-3468</issn><issn>1531-5037</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNqFUs1u1DAQjhCIbguvUPnWC1n8k8RZDghU0RKpElIXuFqOM9l1msRh7FTKW_JIeHdbDly42Nb4-_H4myS5ZHTNKCved-tugsbPuFtzGotUrilnL5IVywVLcyrky2RFKeepyIryLDn3vqM0lil7nZxxRkW2EeUq-V0NkzaBuJaEeXBIHq2ubW_DQnQgHowbm7R37oFM6Aw0M4InE2DrcICG1BAPQIwbph6CHXckIOgwwBglRxL2QKoxAO7QzRO53-u6ccPivMZI0WQb5mYht8fLqB-ccT2p7rdp9fMdYZsNS-MiPxBNECaHgbTohqOq2du-QRivfPSJLLdbyNHkTfKq1b2Ht0_7RfLj5sv366_p3bfb6vrzXWpyUYSUCWPyUlPDRWOEqfMW8pqXeQlNTiUXBrisBS-zjBY1lZJlYqNbwcFwyakw4iK5OunGd_-awQc1WG-g7_UIbvZKFjyTjPMyIosT0qDzHqFVE9pB46IYVYcwVaeew1SHMBWVKoYZiZdPFnMdP_sv7Tm9CPh0AkBs9NECKm8sjDEmi2CCapz9v8fHfyRMb0drdP8AC_jOzTjGb1RMea6o2h5G6jBRLA5TXsbu_gAHT8ww</recordid><startdate>20101101</startdate><enddate>20101101</enddate><creator>Raney, Beverly</creator><creator>Stoner, Julie</creator><creator>Anderson, James</creator><creator>Andrassy, Richard</creator><creator>Arndt, Carola</creator><creator>Brown, Ken</creator><creator>Crist, William</creator><creator>Maurer, Harold</creator><creator>Qualman, Stephen</creator><creator>Wharam, Moody</creator><creator>Wiener, Eugene</creator><creator>Meyer, William</creator><creator>Hayes-Jordan, Andrea</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>20101101</creationdate><title>Impact of tumor viability at second-look procedures performed before completing treatment on the Intergroup Rhabdomyosarcoma Study Group protocol IRS-IV, 1991-1997: a report from the children's oncology group</title><author>Raney, Beverly ; Stoner, Julie ; Anderson, James ; Andrassy, Richard ; Arndt, Carola ; Brown, Ken ; Crist, William ; Maurer, Harold ; Qualman, Stephen ; Wharam, Moody ; Wiener, Eugene ; Meyer, William ; Hayes-Jordan, Andrea</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c536t-13cc58a0c23dc3cb5fe5b2858ed50723ce27b3284406b0771439af32ec27203c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Antineoplastic Agents - therapeutic use</topic><topic>Child</topic><topic>Childhood rhabdomyosarcoma</topic><topic>Diagnostic Imaging - methods</topic><topic>Disease-Free Survival</topic><topic>Dose Fractionation</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>IRS-IV protocol</topic><topic>Male</topic><topic>Neoplasm Staging</topic><topic>Neoplasm, Residual</topic><topic>Pediatrics</topic><topic>Retrospective Studies</topic><topic>Rhabdomyosarcoma - diagnosis</topic><topic>Rhabdomyosarcoma - epidemiology</topic><topic>Rhabdomyosarcoma - therapy</topic><topic>Second-look procedures</topic><topic>Second-Look Surgery - methods</topic><topic>Surgery</topic><topic>Survival Rate</topic><topic>Time Factors</topic><topic>Treatment Outcome</topic><topic>United States - epidemiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Raney, Beverly</creatorcontrib><creatorcontrib>Stoner, Julie</creatorcontrib><creatorcontrib>Anderson, James</creatorcontrib><creatorcontrib>Andrassy, Richard</creatorcontrib><creatorcontrib>Arndt, Carola</creatorcontrib><creatorcontrib>Brown, Ken</creatorcontrib><creatorcontrib>Crist, William</creatorcontrib><creatorcontrib>Maurer, Harold</creatorcontrib><creatorcontrib>Qualman, Stephen</creatorcontrib><creatorcontrib>Wharam, Moody</creatorcontrib><creatorcontrib>Wiener, Eugene</creatorcontrib><creatorcontrib>Meyer, William</creatorcontrib><creatorcontrib>Hayes-Jordan, Andrea</creatorcontrib><creatorcontrib>For the Soft-Tissue Sarcoma Committee of the Children's Oncology Group, Arcadia, California, USA</creatorcontrib><creatorcontrib>Soft-Tissue Sarcoma Committee of the Children's Oncology Group</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>Journal of pediatric surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Raney, Beverly</au><au>Stoner, Julie</au><au>Anderson, James</au><au>Andrassy, Richard</au><au>Arndt, Carola</au><au>Brown, Ken</au><au>Crist, William</au><au>Maurer, Harold</au><au>Qualman, Stephen</au><au>Wharam, Moody</au><au>Wiener, Eugene</au><au>Meyer, William</au><au>Hayes-Jordan, Andrea</au><aucorp>For the Soft-Tissue Sarcoma Committee of the Children's Oncology Group, Arcadia, California, USA</aucorp><aucorp>Soft-Tissue Sarcoma Committee of the Children's Oncology Group</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Impact of tumor viability at second-look procedures performed before completing treatment on the Intergroup Rhabdomyosarcoma Study Group protocol IRS-IV, 1991-1997: a report from the children's oncology group</atitle><jtitle>Journal of pediatric surgery</jtitle><addtitle>J Pediatr Surg</addtitle><date>2010-11-01</date><risdate>2010</risdate><volume>45</volume><issue>11</issue><spage>2160</spage><epage>2168</epage><pages>2160-2168</pages><issn>0022-3468</issn><eissn>1531-5037</eissn><abstract>Abstract Purposes The aims of the study were to compare results of clinical/radiographic studies before second-look procedures (SLP) with SLP specimens from patients with gross residual sarcoma at diagnosis and to relate tumor viability to outcome. Patients Seventy-three patients underwent SLP before completing chemotherapy, with (n = 59) or without (n = 14) radiotherapy. Tumor sites were bladder/prostate (n = 27), head/orbit/parameningeal (n = 22), extremity/trunk (n = 14), and retroperitoneum/pelvis (n = 10). Results Of 14 patients, 1 (7%) with clinical/radiographic complete response (CR) had viable tumor. Of 59 patients, 35 (59%) without CR had viable tumor. Five-year failure-free survival (FFS) rates were 81% in 37 patients without viable tumor and 53% in 36 patients with viable tumor (Cox proportional hazards adjusted P = .05). Five-year FFS rates were 67% in 15 patients with clear margins and 43% in 21 patients with tumor-involved margins (n = 18) or viable gross tumor (n = 3) (Cox proportional hazards adjusted P = .04). Five-year survival was 78% to 79% among 73 patients with and 333 patients without SLP during treatment. Conclusions Second-look procedures can show whether viable tumor is present and may be beneficial in selected patients with rhabdomyosarcoma. Disappearance of tumor (CR) usually correlated with no viable tumor at SLP. However, 41% of patients without CR had no viable tumor. Those without viable tumor had increased FFS but not survival compared to those with viable tumor.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>21034938</pmid><doi>10.1016/j.jpedsurg.2010.07.021</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antineoplastic Agents - therapeutic use Child Childhood rhabdomyosarcoma Diagnostic Imaging - methods Disease-Free Survival Dose Fractionation Female Follow-Up Studies Humans IRS-IV protocol Male Neoplasm Staging Neoplasm, Residual Pediatrics Retrospective Studies Rhabdomyosarcoma - diagnosis Rhabdomyosarcoma - epidemiology Rhabdomyosarcoma - therapy Second-look procedures Second-Look Surgery - methods Surgery Survival Rate Time Factors Treatment Outcome United States - epidemiology |
title | Impact of tumor viability at second-look procedures performed before completing treatment on the Intergroup Rhabdomyosarcoma Study Group protocol IRS-IV, 1991-1997: a report from the children's oncology group |
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