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Radiation Therapy Dose Escalation in Unresectable Ewing Sarcoma: Final Results of a Phase 3 Randomized Controlled Trial.
Laskar, Siddhartha; Sinha, Shwetabh; Chatterjee, Abhishek; Khanna, Nehal; Manjali, Jifmi Jose; Puri, Ajay; Gulia, Ashish; Nayak, Prakash; Vora, Tushar; Chinnaswamy, Girish; Prasad, Maya; Bajpai, Jyoti; Juvekar, Shashikant; Desai, Subhash; Janu, Amit; Rangarajan, Venkatesh; Purandare, Nilendu; Shah, Sneha; Rekhi, Bharat; Jambhekar, Nirmala; Muckaden, Mary Ann; Kurkure, Purna.
Afiliação
  • Laskar S; Department of Radiation Oncology, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India. Electronic address: laskars2000@yahoo.com.
  • Sinha S; Department of Radiation Oncology, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.
  • Chatterjee A; Department of Radiation Oncology, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.
  • Khanna N; Department of Radiation Oncology, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.
  • Manjali JJ; Department of Radiation Oncology, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.
  • Puri A; Department of Orthopedic Oncology, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.
  • Gulia A; Department of Orthopedic Oncology, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.
  • Nayak P; Department of Orthopedic Oncology, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.
  • Vora T; Department of Pediatric Oncology, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.
  • Chinnaswamy G; Department of Pediatric Oncology, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.
  • Prasad M; Department of Pediatric Oncology, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.
  • Bajpai J; Department of Medical Oncology, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.
  • Juvekar S; Department of Radiodiagnosis, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.
  • Desai S; Department of Radiodiagnosis, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.
  • Janu A; Department of Radiodiagnosis, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.
  • Rangarajan V; Department of Nuclear Medicine & Molecular Imaging, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.
  • Purandare N; Department of Nuclear Medicine & Molecular Imaging, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.
  • Shah S; Department of Nuclear Medicine & Molecular Imaging, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.
  • Rekhi B; Department of Pathology, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.
  • Jambhekar N; Department of Pathology, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.
  • Muckaden MA; Department of Radiation Oncology, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.
  • Kurkure P; Department of Pediatric Oncology, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.
Int J Radiat Oncol Biol Phys ; 113(5): 996-1002, 2022 08 01.
Article em En | MEDLINE | ID: mdl-35568246
ABSTRACT

PURPOSE:

Our aim was to assess the effect of radiation therapy (RT) dose escalation on outcomes in surgically unresectable Ewing sarcoma (ES)/primitive neuroectodermal tumor (PNET). METHODS AND MATERIALS Patients with nonmetastatic unresectable ES/PNET (excluding intracranial/chest wall) receiving vincristine, doxorubicin, cyclophosphamide, ifosfamide, and etoposide chemotherapy, planned for definitive RT, were accrued in this single-institution, open-label, phase 3 randomized controlled trial. Randomization was between standard dose RT (SDRT; 55.8 Gy/31 fractions/5 days a week) versus escalated dose RT (EDRT; 70.2 Gy/39 fractions/5 days a week) with a primary objective of improving local control (LC) by 17% (65%-82%). Secondary outcomes included disease-free survival (DFS), overall survival (OS), and functional outcomes by Musculoskeletal Tumor Society score.

RESULTS:

Between April 2005 and December 2015, 95 patients (SDRT 47 and EDRT 48) with a median age of 17 years (interquartile range, 13-23 years) were accrued. The majority of patients were male (59%). Pelvis was the most common site of primary disease (n = 60; 63%). The median largest tumor dimension (9.7 cm) and the median maximum standardized uptake value (8.2) on pretreatment fluorodeoxyglucose positron emission tomography-computed tomography were similar. At a median follow-up of 67 months, the 5-year LC, DFS, and OS for the entire cohort was 62.4%, 41.3%, and 51.9%, respectively. The 5-year LC was significantly better in EDRT compared with SDRT (76.4% vs 49.4%; P = .02). The differences in DFS and OS at 5 years (for EDRT vs SDRT) did not achieve statistical significance (DFS 46.7% vs 31.8%; P = .22 and OS 58.8% vs 45.4%; P = .08). There was a higher incidence of Radiation Therapy Oncology Group grade >2 skin toxic effects (acute) in the EDRT arm (10.4% vs 2.1%; P = .08) with excellent functional outcomes (median Musculoskeletal Tumor Society score = 29) in both arms.

CONCLUSIONS:

EDRT results in improved LC with good functional outcomes without a significant increase in toxic effects. Radiation dose escalation should be considered for surgically unresectable nonmetastatic ES/PNET.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sarcoma de Ewing / Tumores Neuroectodérmicos Primitivos Tipo de estudo: Clinical_trials Limite: Adolescent / Adult / Female / Humans / Male Idioma: En Revista: Int J Radiat Oncol Biol Phys Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sarcoma de Ewing / Tumores Neuroectodérmicos Primitivos Tipo de estudo: Clinical_trials Limite: Adolescent / Adult / Female / Humans / Male Idioma: En Revista: Int J Radiat Oncol Biol Phys Ano de publicação: 2022 Tipo de documento: Article