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Comment
. 2020 Nov 24;4(22):5631-5634.
doi: 10.1182/bloodadvances.2020003168.

Malignant progression of donor-engrafted clonal hematopoiesis in sibling recipients after stem cell transplantation

Affiliations
Comment

Malignant progression of donor-engrafted clonal hematopoiesis in sibling recipients after stem cell transplantation

Louis Nevejan et al. Blood Adv. .
No abstract available

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Conflict of interest statement

Conflict-of-interest disclosure: The authors declare no competing financial interests.

Figures

Figure 1.
Figure 1.
Evolution of JAK2 p.(V617F) mutational burden (%) in peripheral blood from donor and recipient as described in case 1. Donor, blue dashed line (Δ); MDS-EB2, MDS with excess blasts-2; PV, polycythemia vera; recipient,  red full line (•); sWGS, shallow whole-genome sequencing; Tx, transplantation.
Figure 2.
Figure 2.
Sequencing data of both donor and recipient after allogeneic hematopoietic stem cell transplantation at time of diagnosis of DCHN. NGS was performed by using a panel of 21 genes relevant to myeloid malignancies. Shallow whole-genome sequencing (sWGS) was performed only of both donor and recipient samples as described in case 1 (details are provided in the supplemental Data). Definitions of hematologic neoplasms are according to the updated (2016) World Health Organization classification and to Valent et al. AML-M2, acute myeloid leukemia with maturation; AML-M5, acute monoblastic leukemia; Dx, diagnosis; CHIP, CH of indeterminate potential; MDS-MLD, MDS with multilineage dysplasia; MDS-RS-MLD, MDS with ring sideroblasts and multilineage dysplasia; yo, years old.

Comment on

References

    1. Boettcher S, Wilk CM, Singer J, et al. . Clonal hematopoiesis in donors and long-term survivors of related allogeneic hematopoietic stem cell transplantation. Blood. 2020;135(18):1548-1559. - PubMed
    1. Van Pelt K, Nollet F, Selleslag D, et al. . The JAK2V617F mutation can occur in a hematopoietic stem cell that exhibits no proliferative advantage: a case of human allogeneic transplantation. Blood. 2008;112(3):921-922. - PubMed
    1. Valent P, Orazi A, Steensma DP, et al. . Proposed minimal diagnostic criteria for myelodysplastic syndromes (MDS) and potential pre-MDS conditions. Oncotarget. 2017;8(43):73483-73500. - PMC - PubMed
    1. Gondek LP, Zheng G, Ghiaur G, et al. . Donor cell leukemia arising from clonal hematopoiesis after bone marrow transplantation. Leukemia. 2016;30(9):1916-1920. - PMC - PubMed
    1. Engel N, Rovo A, Badoglio M, et al. ; Transplant Complications Working Party of the European Society for Blood and Marrow Transplantation . European experience and risk factor analysis of donor cell-derived leukaemias/MDS following haematopoietic cell transplantation. Leukemia. 2019;33(2):508-517. - PubMed