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


Journal

Journal of clinical oncology : official journal of the American Society of Clinical Oncology
ISSN: 1527-7755
Titre abrégé: J Clin Oncol
Pays: United States
ID NLM: 8309333

Informations de publication

Date de publication:
01 02 2021
Historique:
pubmed: 18 12 2020
medline: 28 8 2021
entrez: 17 12 2020
Statut: ppublish

Résumé

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. 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). 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; 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.

Identifiants

pubmed: 33332189
doi: 10.1200/JCO.20.02529
pmc: PMC8078415
doi:

Substances chimiques

Etoposide 6PLQ3CP4P3
Thiotepa 905Z5W3GKH
treosulfan CO61ER3EPI
Vidarabine FA2DM6879K
Busulfan G1LN9045DK
fludarabine P2K93U8740

Banques de données

ClinicalTrials.gov
['NCT01949129']
EudraCT
['2012-003032-22']

Types de publication

Clinical Trial, Phase III Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

295-307

Commentaires et corrections

Type : CommentIn
Type : CommentIn

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Auteurs

Christina Peters (C)

St. Anna Children's Hospital, Children's Cancer Research Institute, University Vienna, Vienna, Austria.

Jean-Hugues Dalle (JH)

Hôpital Robert Debré, GH APHP-Nord Université de Paris, Paris, France.

Franco Locatelli (F)

Department of Pediatric Hematology and Oncology, IRCCS Ospedale Pediatrico Bambino Gesù, Sapienza University of Rome, Rome, Italy.

Ulrike Poetschger (U)

Children's Cancer Research Institute, Vienna, Austria.

Petr Sedlacek (P)

Department of Pediatric Hematology and Oncology, Motol University Hospital, Prague, Czech Republic.

Jochen Buechner (J)

Department of Pediatric Hematology and Oncology, Oslo University Hospital, Oslo, Norway.

Peter J Shaw (PJ)

The Children`s Hospital at Westmead, Sydney, Australia.

Raquel Staciuk (R)

Hospital de Pediatría, Buenos Aires, Argentina.

Marianne Ifversen (M)

Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.

Herbert Pichler (H)

St. Anna Children's Hospital, Children's Cancer Research Institute, University Vienna, Vienna, Austria.

Kim Vettenranta (K)

Children's Hospital, University of Helsinki, Helsinki, Finland.

Peter Svec (P)

National Institute of Children's Diseases, Bratislava, Slovakia.

Olga Aleinikova (O)

Belarusian Research Center for Pediatric Oncology, Hematology and Immunology, Borovlyani, Belarus.

Jerry Stein (J)

Schneider Children's Medical Center of Israel, Sackler Faculty of Medicine, Tel Aviv University, Petach-Tikva, Israel.

Tayfun Güngör (T)

Universitäts-Kinderspital, Zurich, Switzerland.

Jacek Toporski (J)

Skåne University Hospital, Lund, Sweden.

Tony H Truong (TH)

Alberta Children's Hospital Calgary, Calgary, Alberta, Canada.

Cristina Diaz-de-Heredia (C)

Hospital Universitari Vall d'Hebron, Barcelona, Spain.

Marc Bierings (M)

Princess Máxima Center for Pediatric Oncology, Bilthoven, the Netherlands.

Hany Ariffin (H)

University of Malaya, Kuala Lumpur, Malaysia.

Mohammed Essa (M)

King Abdullah Specialist Children's Hospital, King Abdullah International Medical Research Center, King Saud Bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.

Birgit Burkhardt (B)

Children's University Hospital Münster, Münster, Germany.

Kirk Schultz (K)

University of British Columbia, Vancouver, British Columbia, Canada.

Roland Meisel (R)

Division of Pediatric Stem Cell Therapy, Department of Pediatric Oncology, Hematology and Clinical Immunology, Medical Faculty, Heinrich-Heine-University, Duesseldorf, Germany.

Arjan Lankester (A)

Willem-Alexander Children's Hospital, Leiden, the Netherlands.

Marc Ansari (M)

Geneva University Hospital, Geneva, Switzerland.

Martin Schrappe (M)

Universitätsklinikum Schleswig-Holstein, Kiel, Germany.

Arend von Stackelberg (A)

Charité University Hospital Berlin, Berlin, Germany.

Adriana Balduzzi (A)

Università degli Studi di Milano-Fondazione MBBM, Monza, Italy.

Selim Corbacioglu (S)

Universitätsklinikum Regensburg, Regensburg, Germany.

Peter Bader (P)

Goethe University, University Hospital Frankfurt, Department for Children and Adolescents, Division for Stem Cell Transplantation, Immunology and Intensive Care Medicine, Frankfurt am Main, Germany.

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Classifications MeSH