Secondary solid cancer screening following hematopoietic cell transplantation

Hematopoietic stem cell transplant (HCT) recipients have a substantial risk of developing secondary solid cancers, particularly beyond 5 years after HCT and without reaching a plateau overtime. A working group was established through the Center for International Blood and Marrow Transplant Research...

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Published inBone marrow transplantation (Basingstoke) Vol. 50; no. 8; pp. 1013 - 1023
Main Authors Inamoto, Y, Shah, N N, Savani, B N, Shaw, B E, Abraham, A A, Ahmed, I A, Akpek, G, Atsuta, Y, Baker, K S, Basak, G W, Bitan, M, DeFilipp, Z, Gregory, T K, Greinix, H T, Hamadani, M, Hamilton, B K, Hayashi, R J, Jacobsohn, D A, Kamble, R T, Kasow, K A, Khera, N, Lazarus, H M, Malone, A K, Lupo-Stanghellini, M T, Margossian, S P, Muffly, L S, Norkin, M, Ramanathan, M, Salooja, N, Schoemans, H, Wingard, J R, Wirk, B, Wood, W A, Yong, A, Duncan, C N, Flowers, M E D, Majhail, N S
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 01.08.2015
Nature Publishing Group
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Summary:Hematopoietic stem cell transplant (HCT) recipients have a substantial risk of developing secondary solid cancers, particularly beyond 5 years after HCT and without reaching a plateau overtime. A working group was established through the Center for International Blood and Marrow Transplant Research and the European Group for Blood and Marrow Transplantation with the goal to facilitate implementation of cancer screening appropriate to HCT recipients. The working group reviewed guidelines and methods for cancer screening applicable to the general population and reviewed the incidence and risk factors for secondary cancers after HCT. A consensus approach was used to establish recommendations for individual secondary cancers. The most common sites include oral cavity, skin, breast and thyroid. Risks of cancers are increased after HCT compared with the general population in skin, thyroid, oral cavity, esophagus, liver, nervous system, bone and connective tissues. Myeloablative TBI, young age at HCT, chronic GVHD and prolonged immunosuppressive treatment beyond 24 months were well-documented risk factors for many types of secondary cancers. All HCT recipients should be advised of the risks of secondary cancers annually and encouraged to undergo recommended screening based on their predisposition. Here we propose guidelines to help clinicians in providing screening and preventive care for secondary cancers among HCT recipients.
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These authors are co-first authors and contributed equally to this work.
ISSN:0268-3369
1476-5365
DOI:10.1038/bmt.2015.63