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The Impact of Radiation Therapy on Metastatic Rhabdomyosarcoma: Results From the EpSSG MTS 2008 Study.
Cameron, Alison L; Mandeville, Henry; Coppadoro, Beatrice; Periasamy, Manivannan; Davila Fajardo, Raquel; Ferrari, Andrea; Gaze, Mark N; Helfre, Sylvie; Magelssen, Henriette; Minard-Colin, Veronique; Ramos, Monica; Schoot, Reineke; Zanetti, Illaria; Bisogno, Gianni; Chisholm, Julia C; Merks, Johannes H M.
Affiliation
  • Cameron AL; Bristol Haematology and Oncology Centre, Universities Hospital Bristol and Weston NHS Foundation Trust, Bristol, United Kingdom. Electronic address: Alison.cameron@UHBW.nhs.uk.
  • Mandeville H; Department of Radiotherapy, The Royal Marsden Hospital and The Institute of Cancer Research, Sutton, United Kingdom.
  • Coppadoro B; Hematology Oncology Division, Department of Women's and Children's Health, University of Padova, Padova, Italy.
  • Periasamy M; Bristol Haematology and Oncology Centre, Universities Hospital Bristol and Weston NHS Foundation Trust, Bristol, United Kingdom.
  • Davila Fajardo R; Department of Radiation Oncology, University Medical Center Utrecht, Utrecht, the Netherlands; Princess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
  • Ferrari A; Paediatric Oncology Unit, Fondazione IRCCS Istituto Nazionale Tumori, Milano, Italy.
  • Gaze MN; Department of Oncology, University College London Hospitals NHS Foundation Trust, London, United Kingdom.
  • Helfre S; Department of Radiotherapy, Institut Curie, Paris, France.
  • Magelssen H; Oslo University Hospital, Department of Oncology, Oslo, Norway.
  • Minard-Colin V; Department of Pediatric and Adolescent Oncology, INSERM 1015, Gustave Roussy, Université Paris-Saclay, Villejuif, France.
  • Ramos M; Radiation Oncology Department, Hospital Universitari Vall d'Hebron, Barcelona, Spain.
  • Schoot R; Princess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
  • Zanetti I; Hematology Oncology Division, Department of Women's and Children's Health, University of Padova, Padova, Italy.
  • Bisogno G; Pediatric Hematology Oncology Division, Department of Women's and Children's Health, University of Padua, Padua, Italy.
  • Chisholm JC; Children and Young People's Unit, The Royal Marsden and Institute of Cancer Research, Sutton, United Kingdom.
  • Merks JHM; Princess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands; Division of Imaging and Oncology, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.
Article in En | MEDLINE | ID: mdl-39222824
ABSTRACT

PURPOSE:

Radiation oncologists use radiation variably for children with metastatic rhabdomyosarcoma (RMS). Data from the European paediatric Soft tissue sarcoma Study Group (EpSSG) MTS 2008 study were retrospectively analyzed to validate the previous observation that the use of radiation is associated with improved outcomes and guide future recommendations on radiation use in this patient group. METHODS AND MATERIALS The radiation delivered to 216 patients aged 0 to 21 years with metastatic RMS was retrospectively reviewed and classified as radical (all sites of disease irradiated within the protocol parameters), partial (some sites irradiated within the protocol parameters), and none (no radiation or delivered outside the protocol parameters). Landmark analysis excluded those with an event before day 221. Overall survival (OS) and progression-free survival were modeled using the Kaplan-Meier method to investigate the impact of radiation. The joint effect of treatment and known prognostic factors was examined using the Cox regression model.

RESULTS:

Overall, 56 patients received radical, 104 partial, and 56 no radiation therapy per protocol. Owing to nonrandomized data, the groups were heterogeneous, particularly fewer sites of metatatic disease and less with bone metatases in those receiving radical radiation. The 3-year progression-free survival was 62.0% (95% CI, 47.9-73.4), 39.5% (95% CI, 29.8-49.1), 30.1% (95% CI, 18.7-42.3) for radical, partial, and no radiation therapy groups (P = .002), respectively, and the 3-year OS was 70.1% (95% CI, 55.8-80.6), 53.1% (95% CI, 42.6-62.5), and 52.3% (95% CI, 38.3-64.5; P = .019), respectively. Multivariable analysis confirmed incremental improvement in OS with additional radiation, with hazard ratio of 1, 1.8, and 2.4 (P = .022) for radical, partial, and no radiation therapy per protocol, respectively.

CONCLUSIONS:

Radiation to all sites of disease seems to improve outcomes for children with metastatic RMS and should be considered when feasible. If not feasible, radiation is still recommended to the primary site and involved regional lymphadenopathy. Randomized clinical trials are required to confirm these findings, given the heterogeneity between the groups and potential confounding factors in this analysis.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Int J Radiat Oncol Biol Phys / Int. j. radiat. oncol. biol. phys / International journal of radiation oncology, biology and physic Year: 2024 Document type: Article Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Int J Radiat Oncol Biol Phys / Int. j. radiat. oncol. biol. phys / International journal of radiation oncology, biology and physic Year: 2024 Document type: Article Country of publication: United States