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               <dc:title>Localized incompletely resected standard risk rhabdomyosarcoma in children and adolescents: Results from the European Paediatric Soft Tissue Sarcoma Study Group RMS 2005 trial</dc:title>
               <dc:creator>Mandeville, Henry</dc:creator>
               <dc:creator>alaggio, rita</dc:creator>
               <dc:creator>Ben-Arush, Myriam</dc:creator>
               <dc:creator>Hladun Alvaro, Raquel</dc:creator>
               <dc:creator>Ramos Albiac, Monica</dc:creator>
               <dc:creator>Bisogno, Gianni</dc:creator>
               <dc:creator>Minard-Colin, Veronique</dc:creator>
               <dc:creator>Chargari, Cyrus</dc:creator>
               <dc:subject>Músculs - Càncer - Quimioteràpia</dc:subject>
               <dc:subject>Tumors de parts toves</dc:subject>
               <dc:subject>Músculs - Càncer - Radioteràpia</dc:subject>
               <dc:subject>Infants</dc:subject>
               <dc:subject>Quimioteràpia combinada</dc:subject>
               <dc:subject>DISEASES::Neoplasms::Neoplasms by Histologic Type::Neoplasms, Connective and Soft Tissue::Neoplasms, Muscle Tissue::Myosarcoma::Rhabdomyosarcoma</dc:subject>
               <dc:subject>Other subheadings::Other subheadings::Other subheadings::/drug therapy</dc:subject>
               <dc:subject>ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT::Therapeutics::Radiotherapy</dc:subject>
               <dc:subject>NAMED GROUPS::Persons::Age Groups::Child</dc:subject>
               <dc:subject>ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT::Therapeutics::Therapeutics::Drug Therapy::Antineoplastic Protocols::Therapeutics::Drug Therapy::Antineoplastic Combined Chemotherapy Protocols</dc:subject>
               <dc:subject>ENFERMEDADES::neoplasias::neoplasias por tipo histológico::neoplasias de tejido conjuntivo y de tejidos blandos::neoplasias de tejido muscular::miosarcoma::rabdomiosarcoma</dc:subject>
               <dc:subject>Otros calificadores::Otros calificadores::Otros calificadores::/farmacoterapia</dc:subject>
               <dc:subject>TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS::terapéutica::radioterapia</dc:subject>
               <dc:subject>DENOMINACIONES DE GRUPOS::personas::Grupos de Edad::niño</dc:subject>
               <dc:subject>TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS::terapéutica::terapéutica::farmacoterapia::protocolos antineoplásicos::terapéutica::farmacoterapia::protocolos de quimioterapia antineoplásica combinada</dc:subject>
               <dc:description>Alkylator chemotherapy; Radiotherapy; Rhabdomyosarcoma</dc:description>
               <dc:description>Quimioterapia alquilante; Radioterapia; Rabdomiosarcoma</dc:description>
               <dc:description>Quimioteràpia alquilant; Radioteràpia; Rabdomiosarcoma</dc:description>
               <dc:description>Background&#xd;
The authors report the prospective evaluation of reduced dose alkylator chemotherapy combined with radiotherapy for European Pediatric Soft Tissue Sarcoma Study Group (EpSSG) standard risk nonalveolar rhabdomyosarcoma (NA-RMS).&#xd;
Patients and Methods&#xd;
Localized node negative Intergroup Rhabdomyosarcoma Study (IRS) II/III NA-RMS at favorable sites (subgroup C), &lt;25 years old, received five cycles of ifosfamide, vincristine, and dactinomycin (IVA) chemotherapy (30 g/m2 ifosfamide) and four cycles of vincristine and dactinomycin (if receiving radiotherapy), or nine cycles of IVA (54 g/m2 ifosfamide) ± radiotherapy. Delayed primary tumor excision was considered for IRS III tumors. The primary end points were event-free survival (EFS) and overall survival (OS).&#xd;
Results&#xd;
From October 2005 to December 2016, 359 evaluable patients were recruited: orbit, 164 (45.7%); head and neck nonparameningeal, 77 (21.4%); and genitourinary non–bladder/prostate, 118 (32.9%). EFS and OS were 77.4% (95% confidence interval [CI], 72.5–81.6) and 93.5% (95% CI, 90.1–95.8), respectively. Lower dose alkylator chemotherapy and radiotherapy achieved 5-year OS of 93.7% but the difference with higher dose alkylator chemotherapy +/- radiotherapy was not significant (p = 0.8003). Adjuvant radiotherapy improved EFS with 5-year estimates of 84.7% versus 65.2% for nonirradiated (p &lt; .0001), but not OS (p = .9298). Omitting radiotherapy for orbital tumors reduced OS (5-year was 87.1% vs. 97.3% for irradiated, p = .0257). Following R0 resection (n = 60), radiotherapy did not significantly improve EFS or OS.&#xd;
Conclusions&#xd;
Radiotherapy for local tumor control allows for reduction of cumulative dose of alkylators in EpSSG standard risk subgroup C RMS patients. The omission of radiotherapy did not affect OS in all patients except those with orbital RMS and was associated with inferior EFS.</dc:description>
               <dc:date>2025-10-24T10:40:01Z</dc:date>
               <dc:date>2025-10-24T10:40:01Z</dc:date>
               <dc:date>2025-01-17T13:10:18Z</dc:date>
               <dc:date>2025-01-17T13:10:18Z</dc:date>
               <dc:date>2024-12-01</dc:date>
               <dc:type>info:eu-repo/semantics/article</dc:type>
               <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
               <dc:identifier>http://hdl.handle.net/11351/12435</dc:identifier>
               <dc:relation>Cancer;130(23)</dc:relation>
               <dc:relation>https://doi.org/10.1002/cncr.35497</dc:relation>
               <dc:rights>Attribution 4.0 International</dc:rights>
               <dc:rights>http://creativecommons.org/licenses/by/4.0/</dc:rights>
               <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
               <dc:publisher>Wiley</dc:publisher>
               <dc:source>Scientia</dc:source>
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