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Author Notes:

Correspondence: Michael A. Pulsipher, MD, Children’s Hospital Los Angeles, 4650 Sunset Blvd., Mailstop #62, Los Angeles, CA 90027, mpulsipher@chla.usc.edu, Phone: (323) 361-2546

Author contributions: MAP, PA, DLC, RJD, MMH, SFL, BRL, JPM, JDR, GES, MLR, JWV designed the trial. MAP, WN, BES, HK, RMB, RJD oversaw and conducted the study. MAP, BES, BRL, PC, DMK analyzed and interpreted the data and wrote the manuscript.

MAP, MLR, AAM, IAA, LPA, ASA, EDB, RLB, CB, BJB, ERB, NJB, DD, KD, CCD, TEH, AEH, PNH, BHL, DJ, AAJ, KAK, HL, JLL, ML, MRL, WL, MMS, JMM, JM, SM, VP, VKP, MLR, SDR, WBR, IS, JS, GBS, PJS, SS, TS, WT, JPU, MV, EKW, DJW, GAY enrolled related donors. The final manuscript was reviewed and approved by all authors.

Disclosures: None of the authors has any conflict of interest to declare.

Subjects:

Research Funding:

This study was funded by R01 HL085707 through the NHLBI. Additional funding for MAP was provided by 2UG1HL069254 (NHLBI/NCI) and the Johnny Crisstopher Children’s Charitable Foundation St. Baldrick’s Consortium Grant.

The CIBMTR is supported primarily by Public Health Service Grant/Cooperative Agreement 5U24CA076518 from the National Cancer Institute (NCI), the National Heart, Lung and Blood Institute (NHLBI) and the National Institute of Allergy and Infectious Diseases (NIAID);

a Grant/Cooperative Agreement 1U24HL138660 from NHLBI and NCI; a contract HHSH250201700006C with Health Resources and Services Administration (HRSA/DHHS);

three Grants N00014-17-1-2388, N00014-17-1-2850 and N00014-18-1-2045 from the Office of Naval Research; and grants from Adaptive Biotechnologies; *Amgen, Inc.;

Anonymous donation to the Medical College of Wisconsin; Astellas Pharma US; Atara Biotherapeutics, Inc.; Be the Match Foundation; *bluebird bio, Inc.;

Bristol Myers Squibb Oncology; *Celgene Corporation; *Chimerix, Inc.; *CytoSen Therapeutics, Inc.;

Fred Hutchinson Cancer Research Center; Gamida Cell Ltd.; Gilead Sciences, Inc.; HistoGenetics, Inc.; Immucor;

*Incyte Corporation; Janssen Scientific Affairs, LLC; *Jazz Pharmaceuticals, Inc.; Karius, Inc.; Karyopharm Therapeutics, Inc.;

*Kite Pharma, Inc.; Medac, GmbH; *Mediware; The Medical College of Wisconsin; *Merck & Co, Inc.;

*Mesoblast; MesoScale Diagnostics, Inc.; Millennium, the Takeda Oncology Co.; *Miltenyi Biotec, Inc.;

Mundipharma EDO; National Marrow Donor Program; Novartis Pharmaceuticals Corporation; PCORI;

*Pfizer, Inc; *Pharmacyclics, LLC; PIRCHE AG; *Sanofi Genzyme; *Seattle Genetics; Shire; Spectrum Pharmaceuticals, Inc.; St. Baldrick’s Foundation;

Swedish Orphan Biovitrum, Inc.; *Takeda Oncology; and University of Minnesota.

Keywords:

  • Science & Technology
  • Life Sciences & Biomedicine
  • Hematology
  • Immunology
  • Transplantation
  • Stem cell transplantation
  • BM collection toxicities
  • Donor safety
  • PBSC collection toxicities
  • Quality of life
  • Bone marrow
  • Retrospective analysis
  • Prospective trial
  • Adverse events
  • Healthy donors
  • Family donors
  • Mobilization
  • Collection
  • PBSC

Effect of Aging and Predonation Comorbidities on the Related Peripheral Blood Stem Cell Donor Experience: Report from the Related Donor Safety Study

Tools:

Journal Title:

Biology of Blood and Marrow Transplantation

Volume:

Volume 25, Number 4

Publisher:

, Pages 699-711

Type of Work:

Article | Post-print: After Peer Review

Abstract:

The development of reduced-intensity approaches for allogeneic hematopoietic cell transplantation has resulted in growing numbers of older related donors (RDs) of peripheral blood stem cells (PBSCs). The effects of age on donation efficacy, toxicity, and long-term recovery in RDs are poorly understood. To address this we analyzed hematologic variables, pain, donation-related symptoms, and recovery in 1211 PBSC RDs aged 18 to 79 enrolled in the Related Donor Safety Study. RDs aged > 60 had a lower median CD34 + level before apheresis compared with younger RDs (age > 60, 59 × 10 6 /L; age 41 to 60, 81 × 10 6 /L; age 18 to 40, 121 × 10 6 /L; P <.001). This resulted in older donors undergoing more apheresis procedures (49% versus 30% ≥ 2 collections, P <.001) and higher collection volumes (52% versus 32% > 24 L, P <.001), leading to high percentages of donors aged > 60 with postcollection thrombocytopenia <50 × 10 9 /L (26% and 57% after 2 and 3days of collection, respectively). RDs aged 18 to 40 had a higher risk of grades 2 to 4 pain and symptoms pericollection, but donors over age 40 had more persistent pain at 1, 6, and 12 months (odds ratio [OR], 1.7; P = 0.02) and a higher rate of nonrecovery to predonation levels (OR, 1.7; P =.01). Donors reporting comorbidities increased significantly with age, and those with comorbidities that would have led to deferral by National Marrow Donor Program unrelated donor standards had an increased risk for persistent grades 2 to 4 pain (OR, 2.41; P <.001) and failure to recover to predonation baseline for other symptoms (OR, 2.34; P =.004). This information should be used in counseling RDs regarding risk and can assist in developing practice approaches aimed at improving the RD experience for high-risk individuals.

Copyright information:

© 2018 American Society for Blood and Marrow Transplantation.

This is an Open Access work distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/).
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