Total Body Irradiation or Chemotherapy Conditioning in Childhood ALL: A Multinational, Randomized, Noninferiority Phase III Study

Christina Peters(St Anna Children's Hospital), Jean‐Hugues Dalle(Université Paris Cité), Franco Locatelli(Bambino Gesù Children's Hospital), Ulrike Pöetschger(St Anna Children's Hospital), Petr Sedláček(University Hospital in Motol), Jochen Buechner(Oslo University Hospital), Peter J. Shaw(Children's Hospital at Westmead), Raquel Staciuk, Marianne Ifversen(Copenhagen University Hospital), Herbert Pichler(St Anna Children's Hospital), Kim Vettenranta(University of Helsinki), Peter Švec(National Institute of Cardiovascular Diseases), Olga Aleinikova(Belarusian Research Center For Pediatric Oncology and Hematology), Jerry Stein(Tel Aviv University), Tayfun Güngör(University Children's Hospital Zurich), Jacek Toporski(Skåne University Hospital), Tony H. Truong(Alberta Children's Hospital), Cristina Díaz de Heredia(Vall d'Hebron Hospital Universitari), Marc Bierings(Princess Máxima Center), Hany Ariffin(University of Malaya), Mohammed Al Essa(King Saud bin Abdulaziz University for Health Sciences), Birgit Burkhardt(University Hospital Münster), Kirk R. Schultz(University of British Columbia), Roland Meisel(Heinrich Heine University Düsseldorf), Arjan Lankester(Willem-Alexander Kinderziekenhuis), Marc Ansari(University Hospital of Geneva), Martin Schrappe(University Hospital Schleswig-Holstein), on behalf of the IBFM Study Group;(Charité - Universitätsmedizin Berlin), Arend von Stackelberg(University of Milan), on behalf of the IntReALL Study Group(University Hospital Regensburg), Adriana Balduzzi(Goethe University Frankfurt), on behalf of the I-BFM SCT Study Group, Selim Corbacioglu(University Hospital Regensburg), on behalf of the EBMT Paediatric Diseases Working Party, Peter Bader(Goethe University Frankfurt)
Journal of Clinical Oncology
December 17, 2020
Cited by 324Open Access
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Abstract

PURPOSE Total body irradiation (TBI) before allogeneic hematopoietic stem cell transplantation (HSCT) in pediatric patients with acute lymphoblastic leukemia (ALL) is efficacious, but long-term side effects are concerning. We investigated whether preparative combination chemotherapy could replace TBI in such patients. PATIENTS AND METHODS FORUM is a randomized, controlled, open-label, international, multicenter, phase III, noninferiority study. Patients ≤ 18 years at diagnosis, 4-21 years at HSCT, in complete remission pre-HSCT, and with an HLA-compatible related or unrelated donor were randomly assigned to myeloablative conditioning with fractionated 12 Gy TBI and etoposide versus fludarabine, thiotepa, and either busulfan or treosulfan. The noninferiority margin was 8%. With 1,000 patients randomly assigned in 5 years, 2-year minimum follow-up, and one-sided alpha of 5%, 80% power was calculated. A futility stopping rule would halt random assignment if chemoconditioning was significantly inferior to TBI (EudraCT: 2012-003032-22; ClinicalTrials.gov: NCT01949129 ). RESULTS Between April 2013 and December 2018, 543 patients were screened, 417 were randomly assigned, 212 received TBI, and 201 received chemoconditioning. The stopping rule was applied on March 31, 2019. The median follow-up was 2.1 years. In the intention-to-treat population, 2-year overall survival (OS) was significantly higher following TBI (0.91; 95% CI, 0.86 to 0.95; P < .0001) versus chemoconditioning (0.75; 95% CI, 0.67 to 0.81). Two-year cumulative incidence of relapse and treatment-related mortality were 0.12 (95% CI, 0.08 to 0.17; P < .0001) and 0.02 (95% CI, < 0.01 to 0.05; P = .0269) following TBI and 0.33 (95% CI, 0.25 to 0.40) and 0.09 (95% CI, 0.05 to 0.14) following chemoconditioning, respectively. CONCLUSION Improved OS and lower relapse risk were observed following TBI plus etoposide compared with chemoconditioning. We therefore recommend TBI plus etoposide for patients > 4 years old with high-risk ALL undergoing allogeneic HSCT.


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