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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
Main Authors: 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
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cited_by cdi_FETCH-LOGICAL-c536t-13cc58a0c23dc3cb5fe5b2858ed50723ce27b3284406b0771439af32ec27203c3
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container_end_page 2168
container_issue 11
container_start_page 2160
container_title Journal of pediatric surgery
container_volume 45
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. 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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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