A survey of fully haploidentical hematopoietic stem cell transplantation in adults with high-risk acute leukemia: a risk factor analysis of outcomes for patients in remission at transplantation

Author:

Ciceri Fabio1,Labopin Myriam2,Aversa Franco3,Rowe Jakob M.4,Bunjes Donald5,Lewalle Philippe6,Nagler Arnon7,Di Bartolomeo Paolo8,Lacerda João F.9,Lupo Stanghellini Maria Teresa1,Polge Emmanuelle2,Frassoni Francesco10,Martelli Massimo F.3,Rocha Vanderson211

Affiliation:

1. Hematology and BMT Unit, San Raffaele Scientific Institute, Milano, Italy;

2. ALWP, EBMT-Paris Office, Hôpital Saint Antoine Assistance Publique-Hôpitaux de Paris (AP-HP), Université Pierre et Marie Curie Paris 6, Paris, France;

3. Hematology, University of Perugia, Perugia, Italy;

4. Rambam Medical Centre Technion, Israel Institute of Technology, Haifa, Israel;

5. University of Ulm, Ulm, Germany;

6. Institut Bordet, Universite libre de Bruxelles, Bruxelles, Belgium;

7. Chaim Sheba Medical Center, Tel Hashomer, Israel;

8. Ospedale Civile, Pescara, Italy;

9. Hospital de Santa Maria, University of Lisbon, Lisbon, Portugal;

10. Hematology, H San Martino Genova, Genova, Italy; and

11. Hôpital Saint-Louis, Paris, France

Abstract

Haploidentical hematopoietic stem cell transplantation (haplo-HSCT) is an alternative treatment to patients with high-risk acute leukemia lacking a human leukocyte antigen-matched donor. We analyzed 173 adults with acute myeloid leukemia (AML) and 93 with acute lymphoblastic leukemia (ALL) who received a haplo-HSCT in Europe. All grafts were T cell–depleted peripheral blood progenitor cells from a direct family or other related donor. At transplantation, there were 25 patients with AML in CR1 (complete remission 1), 61 in more than or equal to CR2, and 87 in nonremission, and 24 with ALL in CR1, 37 in more than or equal to CR2, and 32 in nonremission. Median follow-up was 47 months in AML and 29 months in the ALL groups. Engraftment was observed in 91% of the patients. Leukemia-free survival at 2 years was 48% plus or minus 10%, 21% plus or minus 5%, and 1% for patients with AML undergoing transplantation in CR1, more than or equal to CR2, and nonremission, and 13% plus or minus 7%, 30% plus or minus 8%, and 7% plus or minus 5% in ALL patients, respectively. In conclusion, haplo-HSCT can be an alternative option for the treatment of high-risk acute leukemia patients in remission, lacking a human leukocyte antigen-matched donor.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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