Is a matched unrelated donor search needed for all allogeneic transplant candidates?

Stefan O. Ciurea, Maria Cecilia Borges Bittencourt, Denái R. Milton, Kai Cao, Piyanuch Kongtim, Gabriela Rondon, Julianne Chen, Marina Konopleva, Jorge M. Ramos Perez, Mohammed F. El Shazly, Majdi Aljadayeh, Michele Alvarez, Jin Im, Gheath Al-Atrash, Rohtesh Mehta, Uday Popat, Qaiser Bashir, Betul Oran, Chitra M. Hosing, Issa F. KhouriPartow Kebriaei, Richard E. Champlin

Research output: Contribution to journalArticlepeer-review

23 Scopus citations

Abstract

Donor availability for allogeneic transplantation remains an important factor in determining outcomes of a successful transplant. We examined outcomes of 242 patients treated over 3 years who had a matched unrelated donor (MUD) search at our institution. One hundred sixty patients (66%) had a 10 of 10 MUD identified, and 85 (53%) proceeded to MUD transplantation. White patients and those with common haplotypes were more likely to have a MUD identified (odds ratio [OR], 7.4 [P, .0001]; OR, 41.6 [P, .0001]), and were more likely to proceed to transplantation with a MUD (OR, 11.2 [P, .0001]; OR, 85.1 [P 5 .002]). In addition, patients who were newly diagnosed/in remission at the time of MUD search had a higher probability of receiving a transplant (OR, 2.01 [P 5 .013]) and better progression-free survival (PFS; P, .0001). In multivariate analysis for patients who received a transplant, donor type did not influence PFS at 3 years, which was 40% for MUD and 57% for haploidentical transplants, respectively (hazard ratio, 1.2 [P 5 .50]). In conclusion, race, haplotype frequency, and disease status at the time of MUD search influence the probability of identifying a MUD and receiving a transplant. Patients with a low likelihood of receiving a MUD transplant may proceed to a haploidentical transplant as soon as indicated, as this approach does not appear to compromise transplant outcomes.

Original languageEnglish (US)
Pages (from-to)2254-2261
Number of pages8
JournalBlood Advances
Volume2
Issue number17
DOIs
StatePublished - Sep 11 2018

ASJC Scopus subject areas

  • Hematology

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