Comparing transplant outcomes in ALL patients after haploidentical with PTCy or matched unrelated donor transplantation

Author:

Al Malki Monzr M.1ORCID,Yang Dongyun2ORCID,Labopin Myriam3,Afanasyev Boris4,Angelucci Emanuele5ORCID,Bashey Asad6,Socié Gérard7,Karduss-Urueta Amado8,Helbig Grzegorz9ORCID,Bornhauser Martin10,Niittyvuopio Riitta11,Ganser Arnold12,Ciceri Fabio13,Brecht Arne14,Koc Yener15,Bejanyan Nelli16,Ferraro Francesca17,Kebriaei Partow18,Mokhtari Sally19,Ghobadi Armin17,Nakamura Ryotaro1ORCID,Forman Stephen J.1,Champlin Richard18ORCID,Mohty Mohamad3,Ciurea Stefan O.18,Nagler Arnon32021

Affiliation:

1. Department of Hematology and Hematopoietic Cell Transplantation and

2. Department of Computational Quantitative Medicine–Beckman Research Institute, City of Hope National Medical Center, Duarte, CA;

3. Department of Hematology, European Society for Blood and Marrow Transplantation (EBMT) Paris Study Office/Centros de Referência em Saúde do Trabalhador, Hôpital Saint Antoine, INSERM, Paris, France;

4. Raisa Gorbacheva Memorial Institute of Children Oncology, Hematology and Transplantation, St. Petersburg, Russia;

5. Ematologia e Centro Trapianti, Istituto di Ricovero e Cura a Carattere Scientifico Ospedale Policlinico San Martino, Genoa, Italy;

6. The Blood and Marrow Transplant Program, Northside Hospital, Atlanta, GA;

7. Department of Hematology–Bone Marrow Transplantation (BMT), Hospital St. Louis, Paris, France;

8. Bone Marrow Transplant Program, Instituto de Cancerologia–Clinica Las Americas, Medellin, Colombia;

9. Department of Hematology and Bone Marrow Transplantation, School of Medicine in Katowice, Medical University of Silesia, Katowice, Poland;

10. University Hospital Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany;

11. Stem Cell Transplantation Unit, Comprehensive Cancer Center, Helsinki University Hospital, Helsinki, Finland;

12. Department of Hematology, Hemostasis, Oncology, and Stem Cell Transplantation, Hannover Medical School, Hannover, Germany;

13. Hematology and BMT Unit, San Raffaele Scientific Institute, Milan, Italy;

14. Helios Dr. Horst Schmidt Kliniken Wiesbaden, Wiesbaden, Germany;

15. Stem Cell Transplant Unit, Medical Park Hospitals, Antalya, Turkey;

16. Division of Hematology, Oncology and Transplantation, University of Minnesota Medical Center, Minneapolis, MN;

17. Division of Oncology, Department of Internal Medicine, School of Medicine, Washington University in St. Louis, St. Louis, MO;

18. Department of Stem Cell Transplantation and Cellular Therapy, MD Anderson Cancer Center, Houston, TX;

19. Department of Clinical Translational Project Development, City of Hope National Medical Center, Duarte, CA;

20. Hematology Division, BMT Department, Chaim Sheba Medical Center, Tel Hashomer, Israel; and

21. Acute Leukaemia Working Party, EBMT, Paris, France

Abstract

Abstract We compared outcomes of 1461 adult patients with acute lymphoblastic leukemia (ALL) receiving hematopoietic cell transplantation (HCT) from a haploidentical (n = 487) or matched unrelated donor (MUD; n = 974) between January 2005 and June 2018. Graft-versus-host disease (GVHD) prophylaxis was posttransplant cyclophosphamide (PTCy), calcineurin inhibitor (CNI), and mycophenolate mofetil (MMF) for haploidentical, and CNI with MMF or methotrexate with/without antithymoglobulin for MUDs. Haploidentical recipients were matched (1:2 ratio) with MUD controls for sex, conditioning intensity, disease stage, Philadelphia-chromosome status, and cytogenetic risk. In the myeloablative setting, day +28 neutrophil recovery was similar between haploidentical (87%) and MUD (88%) (P = .11). Corresponding rates after reduced-intensity conditioning (RIC) were 84% and 88% (P = .47). The 3-month incidence of grade II-IV acute GVHD (aGVHD) and 3-year chronic GVHD (cGVHD) was similar after haploidentical compared with MUD: myeloablative conditioning, 33% vs 34% (P = .46) for aGVHD and 29% vs 31% for cGVHD (P = .58); RIC, 31% vs 30% (P = .06) for aGVHD and 24% vs 29% for cGVHD (P = .86). Among patients receiving myeloablative regimens, 3-year probabilities of overall survival were 44% and 51% with haploidentical and MUD (P = .56). Corresponding rates after RIC were 43% and 42% (P = .6). In this large multicenter case-matched retrospective analysis, despite the limitations of a registry-based study (ie, unavailability of key elements such as minimal residual disease testing), our analysis indicated that outcomes of patients with ALL undergoing HCT from a haploidentical donor were comparable with 8 of 8 MUD transplantations.

Publisher

American Society of Hematology

Subject

Hematology

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