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

Author:

Peters Christina1,Dalle Jean-Hugues2,Locatelli Franco3,Poetschger Ulrike4,Sedlacek Petr5,Buechner Jochen6,Shaw Peter J.7,Staciuk Raquel8,Ifversen Marianne9,Pichler Herbert1,Vettenranta Kim10,Svec Peter11,Aleinikova Olga12,Stein Jerry13,Güngör Tayfun14,Toporski Jacek15,Truong Tony H.16,Diaz-de-Heredia Cristina17,Bierings Marc18,Ariffin Hany19,Essa Mohammed20,Burkhardt Birgit21,Schultz Kirk22,Meisel Roland23,Lankester Arjan24,Ansari Marc25,Schrappe Martin26,von Stackelberg Arend27,Balduzzi Adriana28,Corbacioglu Selim29,Bader Peter30, , , ,

Affiliation:

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

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

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

4. Children's Cancer Research Institute, Vienna, Austria

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

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

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

8. Hospital de Pediatría, Buenos Aires, Argentina

9. Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark

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

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

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

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

14. Universitäts-Kinderspital, Zurich, Switzerland

15. Skåne University Hospital, Lund, Sweden

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

17. Hospital Universitari Vall d’Hebron, Barcelona, Spain

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

19. University of Malaya, Kuala Lumpur, Malaysia

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

21. Children's University Hospital Münster, Münster, Germany

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

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

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

25. Geneva University Hospital, Geneva, Switzerland

26. Universitätsklinikum Schleswig-Holstein, Kiel, Germany

27. Charité University Hospital Berlin, Berlin, Germany

28. Università degli Studi di Milano—Fondazione MBBM, Monza, Italy

29. Universitätsklinikum Regensburg, Regensburg, Germany

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

Abstract

PURPOSETotal 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 METHODSFORUM 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 ).RESULTSBetween 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.CONCLUSIONImproved 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.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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