International recommendations for screening and preventative practices for long-term survivors of transplantation and cellular therapy: a 2023 update
- PMID: 38413823
- PMCID: PMC11809468
- DOI: 10.1038/s41409-023-02190-2
International recommendations for screening and preventative practices for long-term survivors of transplantation and cellular therapy: a 2023 update
Abstract
As hematopoietic cell transplantation (HCT) and cellular therapy expand to new indications and international access improves, the volume of HCT performed annually continues to rise. Parallel improvements in HCT techniques and supportive care entails more patients surviving long-term, creating further emphasis on survivorship needs. Survivors are at risk for developing late complications secondary to pre-, peri- and post-transplant exposures and other underlying risk-factors. Guidelines for screening and preventive practices for HCT survivors were originally published in 2006 and updated in 2012. To review contemporary literature and update the recommendations while considering the changing practice of HCT and cellular therapy, an international group of experts was again convened. This review provides updated pediatric and adult survivorship guidelines for HCT and cellular therapy. The contributory role of chronic graft-versus-host disease (cGVHD) to the development of late effects is discussed but cGVHD management is not covered in detail. These guidelines emphasize special needs of patients with distinct underlying HCT indications or comorbidities (e.g., hemoglobinopathies, older adults) but do not replace more detailed group, disease, or condition specific guidelines. Although these recommendations should be applicable to the vast majority of HCT recipients, resource constraints may limit their implementation in some settings.
© 2024. The Author(s).
Conflict of interest statement
COMPETING INTERESTS
The authors report no conflicts of interest relevant to this work. The authors report the following financial relationships. YA: Lecture fee: Otsuka Pharmaceutical Co., Ltd; CHUGAI PHARMACEUTICAL CO., LTD.; Novartis Pharma KK; AbbVie GK; Honorarium: Meiji Seika Pharma Co, Ltd.; Consultant fee: JCR Pharmaceuticals Co., Ltd.; Kyowa Kirin Co., Ltd. GG: Principal Investigator of Project Sickle Cure, a Sickle Cell Transplant Advocacy and Research Alliance Study partially funded by bluebirdbio. I serve on the steering committee of a STAR clinical trial for which Bristol Myers Squibb has provided funding. NM: Consultant for Anthem, Inc; Stock in HCA Healthcare. Rachel Phelan: Bluebirdbio: advisory board. Amgen: research funding. SR: Medical Monitor for Resource for Clinical Investigation in Blood and Marrow Transplantation (RCI BMT). HS: personal fees: Incyte, Janssen, Novartis, Sanofi and from the Belgian Hematological Society (BHS); research grants from Novartis and the BHS. non-financial support from Gilead, Pfizer, the EBMT (European Society for Blood and Marrow transplantation) and the CIBMTR (Center for International Bone Marrow Transplantation Research). AS: consultant fee from Spotlight Therapeutics, Medexus Inc., Vertex Pharmaceuticals, Sangamo Therapeutics and Editas Medicine. Medical Monitor for Resource for Clinical Investigation in Blood and Marrow Transplantation (RCI BMT). Research funding from CRISPR Therapeutics and honoraria from Vindico Medical Education. AS is the St. Jude Children’s Research Hospital site principal investigator of clinical trials for genome editing of sickle cell disease sponsored by Vertex Pharmaceuticals/CRISPR Therapeutics (
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References
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