Prognostic significance of tumor response at the end of therapy in group III rhabdomyosarcoma: A report from the Children's Oncology Group Journal Article


Authors: Rodeberg, D. A.; Stoner, J. A.; Hayes-Jordan, A.; Kao, S. C.; Wolden, S. L.; Qualman, S. J.; Meyer, W. H.; Hawkins, D. S.
Article Title: Prognostic significance of tumor response at the end of therapy in group III rhabdomyosarcoma: A report from the Children's Oncology Group
Abstract: Purpose Some patients with rhabdomyosarcoma (RMS) achieve less than a complete response (CR) despite receiving all planned therapy. We assessed the impact of best response at the completion of all therapy on patient outcome. Patients and Methods We studied 419 clinical group III participants who completed all protocol therapy without developing progressive disease for Intergroup Rhabdomyosarcoma Study (IRS) IV. Response (complete resolution [CR], partial response [PR; >= 50% decrease], or no response [NR; >= 50% decrease and < 25% increase]) was determined by radiographic measurement and categorized by the best response. Results At the end of therapy, 341 participants (81%) achieved a best response of CR and 78 (19%) had a best response of PR/NR. Five-year failure-free survival was similar for participants achieving CR (80%) and PR/NR (78%). After adjustment for age, nodal status, primary site, and histology, there was no significant indication of lower risk of failure (hazard ratio [HR], 0.77; 95% CI, 0.46 to 1.27; P = .3) nor death (HR, 0.63; 95% CI, 0.36 to 1.09; P = .1) for CR versus PR/NR participants. Seventeen participants with a best response of PR/NR had surgical procedures; eight (50%) of 16 with available pathology reports had residual viable tumor and only three achieved a complete resection. Resection of residual masses was not associated with improved outcome. Conclusion CR status at the end of protocol therapy in clinical group III participants was not associated with a reduction of disease recurrence and death. Aggressive alternative therapy may not be warranted for RMS patients with a residual mass at the end of planned therapy. J Clin Oncol 27: 3705-3711. (C) 2009 by American Society of Clinical Oncology
Keywords: chemotherapy; ewing sarcoma; positron-emission-tomography; soft-tissue sarcoma; postchemotherapy residual masses; acute; lymphoblastic-leukemia; pediatric-oncology; study-iv; advanced seminoma; free survival
Journal Title: Journal of Clinical Oncology
Volume: 27
Issue: 22
ISSN: 0732-183X
Publisher: American Society of Clinical Oncology  
Date Published: 2009-08-01
Start Page: 3705
End Page: 3711
Language: English
ACCESSION: ISI:000268502500022
DOI: 10.1200/jco.2008.19.5933
PROVIDER: wos
PMCID: PMC3020959
PUBMED: 19470937
Notes: --- - Article - "Source: Wos"
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  1. Suzanne L Wolden
    560 Wolden