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Hematopoietic Cell Transplantation and Outcomes Related to Human Papillomavirus Disease in GATA2 Deficiency

  1. Author:
    Parta,Mark
    Cole, Kristen
    Avila, Daniele
    Duncan, Lisa
    Baird, Kristin
    Schuver, Bazetta Blacklock
    Wilder,Jennifer
    Palmer, Cindy
    Daub, Janine
    Hsu, Amy P.
    Zerbe, Christa S.
    Marciano, Beatriz E.
    Cuellar-Rodriguez, Jennifer M.
    Bauer, Thomas R.
    Nason, Martha
    Calvo, Katherine R.
    Merideth, Melissa
    Stratton, Pamela
    DeCherney, Alan
    Shah, Nirali N.
    Holland, Steven M.
    Hickstein, Dennis D.
  2. Author Address

    Frederick Natl Lab Canc Res, Leidos Biomed Res, Clin Res Directorate, Frederick, MD USA.NIH, Nursing Dept, Clin Ctr, Bldg 10, Bethesda, MD 20892 USA.NCI, Immune Deficiency Cellular Therapy Program, NIH, Bethesda, MD 20892 USA.NCI, Pediat Oncol Branch, NIH, Bethesda, MD 20892 USA.NCI, Off Clin Director, NIH, Bethesda, MD 20892 USA.NIAID, Lab Clin Immunol & Microbiol, NIH, 9000 Rockville Pike, Bethesda, MD 20892 USA.NIAID, Biostat Res Branch, Div Clin Res, Bethesda, MD 20892 USA.NIH, Dept Lab Med, Clin Ctr, Bldg 10, Bethesda, MD 20892 USA.NHGRI, NIH, Bethesda, MD 20892 USA.NINDS, Off Clin Director, NIH, Bldg 36,Rm 4D04, Bethesda, MD 20892 USA.NICHD, NIH, Bethesda, MD USA.
    1. Year: 2021
    2. Date: May
    3. Epub Date: 2021 01 03
  1. Journal: Transplantation and Cellular Therapy
  2. ELSEVIER SCIENCE INC,
    1. 27
    2. 5
    3. Pages: 435.e1-435.e11
  3. Type of Article: Article
  4. ISSN: 2666-6375
  1. Abstract:

    GATA2 deficiency is a bone marrow failure syndrome effectively treated with hematopoietic cell transplantation (HCT), which also addresses the predisposition to many infections (prominently mycobacterial). However, many GATA2-deficient persons who come to HCT also have prevalent and refractory human papilloma virus disease (HPVD), which can be a precursor to cancer. We analyzed 75 HCT recipients for the presence of HPVD to identify patient characteristics and transplantation results that influence HPVD outcomes. We assessed the impact of cellular recovery and iatrogenic post-transplantation immunosuppression, as per protocol (PP) or intensified/prolonged (IP) graft-versus-host disease (GVHD) prophylaxis or treatment, on the persistence or resolution of HPVD. Our experience with 75 HCT recipients showed a prevalence of 49% with anogenital HPVD, which was either a contributing or primary factor in the decision to proceed to HCT. Of 24 recipients with sufficient follow-up, 13 had resolution of HPVD, including 8 with IP and 5 with PP. Eleven recipients had persistent HPVD, including 5 with IP and 6 with PP immunosuppression. No plausible cellular recovery group (natural killer cells or T cells) showed a significant difference in HPV outcomes. One recipient died of metastatic squamous cell carcinoma, presumably of anogenital origin, at 33 months post-transplantation after prolonged immunosuppression for chronic GVHD. Individual cases demonstrate the need for continued aggressive monitoring, especially in the context of disease prevalent at transplantation or prior malignancy. HCT proved curative in many cases in which HPVD was refractory and recurrent prior to transplantation, supporting a recommendation that HPVD should be considered an indication rather than contraindication to HCT, but post-transplantation monitoring should be prolonged with a high level of vigilance for new or recurrent HPVD. (C) 2021 The American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. All rights reserved.

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External Sources

  1. DOI: 10.1016/j.jtct.2020.12.028
  2. PMID: 33965189
  3. WOS: 000648721800027

Library Notes

  1. Fiscal Year: FY2020-2021
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