The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
Increased incidence of hematologic malignancies in SCD after HCT in adults with graft failure and mixed chimerism
Abstract
Lawal et al report on a 45-fold increase in secondary hematologic malignancy in 120 patients following hematopoietic stem cell transplantation (HSCT) for sickle cell disease (SCD), comparable to what has been reported following gene therapy. Notably, the cohort is enriched for older patients and for haploidentical transplant recipients with mixed chimerism following HSCT. These data further support the idea that pre-existing premalignant myeloid clones undergo clonal selection in the setting of nonmyeloablative HSCT and contribute to secondary malignancy.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“This may also be relevant to other transplantation settings as blood cancers have also been reported in patients with SCD treated with HCT48–54.”
From Clonal selection of hematopoietic stem cells after gene therapy for sickle cell disease (2023) · cites this paper as [54]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Role of TP53 mutations in the origin and evolution of therapy-related acute myeloid leukaemia
Wong, T. N., Ramsingh, G., Young, A. L., Miller, C. A., Touma, W., Welch, J. S., Lamprecht, T. L., Shen, D., Hundal, J., Fulton, R. S., et al. (2015) · Nature · doi:10.1038/nature13968 · Cited by 892
Research works printed but not linked: 22
- Seminog, 2016, Risk of individual malignant neoplasms in patients with sickle cell disease: English national record linkage study, J R Soc Med, 109, 303, 10.1177/0141076816651037 · DOI · Paper page
- Brunson, 2017, Increased risk of leukemia among sickle cell disease patients in California, Blood, 130, 1597, 10.1182/blood-2017-05-783233 · DOI · Paper page
- Hsieh, 2014, Nonmyeloablative hla-matched sibling allogeneic hematopoietic stem cell transplantation for severe sickle cell phenotype, JAMA, 312, 48, 10.1001/jama.2014.7192 · DOI
- Alzahrani, 2021, Non-myeloablative human leukocyte antigen-matched related donor transplantation in sickle cell disease: outcomes from three independent centres, Br J Haematol, 192, 761, 10.1111/bjh.17311 · DOI · Paper page
- Walters, 1996, Barriers to bone marrow transplantation for sickle cell anemia, Biol Blood Marrow Transplant, 2, 100
- Fitzhugh, 2017, Cyclophosphamide improves engraftment in patients with SCD and severe organ damage who undergo haploidentical peripheral blood stem cell transplantation, Blood Adv, 1, 652, 10.1182/bloodadvances.2016002972 · DOI
- Fitzhugh, 2017, At least 20% donor myeloid chimerism is necessary to reverse the sickle phenotype after allogeneic hematopoietic stem cell transplantation, Blood, 130, 1946, 10.1182/blood-2017-03-772392 · DOI
- Abraham, 2017, Relationship between mixed donor-recipient chimerism and disease recurrence following hematopoietic stem cell transplantation for sickle cell disease, Biol Blood Marrow Transplant, 23, 2178, 10.1016/j.bbmt.2017.08.038 · DOI
- Jones, 2021, Leukemia after gene therapy for sickle cell disease: insertional mutagenesis, busulfan, both, or neither, Blood, 138, 942, 10.1182/blood.2021011488 · DOI
- Hsieh, 2020, Myelodysplastic syndrome unrelated to lentiviral vector in a patient treated with gene therapy for sickle cell disease, Blood Adv, 4, 2058, 10.1182/bloodadvances.2019001330 · DOI · Paper page
- Goyal, 2022, Acute myeloid leukemia case after gene therapy for sickle cell disease, N Engl J Med, 386, 138, 10.1056/NEJMoa2109167 · DOI · Paper page
- Eapen, 2019, Effect of donor type and conditioning regimen intensity on allogeneic transplantation outcomes in patients with sickle cell disease: a retrospective multicentre, cohort study, Lancet Haematol, 6, e585, 10.1016/S2352-3026(19)30154-1 · DOI · Paper page
- Bernaudin, 2020, Long-term event-free survival, chimerism and fertility outcomes in 234 patients with sickle-cell anemia younger than 30 years after myeloablative conditioning and matched-sibling transplantation in France, Haematologica, 105, 91, 10.3324/haematol.2018.213207 · DOI
- Li, 2019, Myeloid neoplasms in the setting of sickle cell disease: an intrinsic association with the underlying condition rather than a coincidence; report of 4 cases and review of the literature, Mod Pathol, 32, 1712, 10.1038/s41379-019-0325-6 · DOI · Paper page
- Janakiram, 2018, Accelerated leukemic transformation after haplo-identical transplantation for hydroxyurea-treated sickle cell disease, Leuk Lymphoma, 59, 241, 10.1080/10428194.2017.1324158 · DOI · Paper page
- Coombs, 2017, Therapy-related clonal hematopoiesis in patients with non-hematologic cancers is common and associated with adverse clinical outcomes, Cell Stem Cell, 21, 374, 10.1016/j.stem.2017.07.010 · DOI · Paper page
- Bolton, 2020, Cancer therapy shapes the fitness landscape of clonal hematopoiesis, Nat Genet, 52, 1219, 10.1038/s41588-020-00710-0 · DOI · Paper page
- Friedberg, 1999, Outcome in patients with myelodysplastic syndrome after autologous bone marrow transplantation for non-Hodgkin's lymphoma, J Clin Oncol, 17, 3128, 10.1200/JCO.1999.17.10.3128 · DOI
- Sevilla, 2002, Secondary acute myeloid leukemia and myelodysplasia after autologous peripheral blood progenitor cell transplantation, Ann Hematol, 81, 11, 10.1007/s00277-001-0400-0 · DOI
- Gibson, 2017, Clonal hematopoiesis associated with adverse outcomes after autologous stem-cell transplantation for lymphoma, J Clin Oncol, 35, 1598, 10.1200/JCO.2016.71.6712 · DOI · Paper page
- Mouhieddine, 2020, Clonal hematopoiesis is associated with adverse outcomes in multiple myeloma patients undergoing transplant, Nat Commun, 11, 2996, 10.1038/s41467-020-16805-5 · DOI
- Ghannam, 2020, Baseline TP53 mutations in adults with SCD developing myeloid malignancy following hematopoietic cell transplantation, Blood, 135, 1185
Cited by
Clonal selection of hematopoietic stem cells after gene therapy for sickle cell disease
Spencer Chapman, M., Cull, A. H., Ciuculescu, M. F., Esrick, E. B., Mitchell, E., Jung, H., O’Neill, L., Roberts, K., Fabre, M. A., Williams, N., et al. (2023) · Nature Medicine · doi:10.1038/s41591-023-02636-6 · Cited by 67
Metadata
- Authors
- Lawal, R. A., Mukherjee, D., Limerick, E. M., Coles, W., Hsieh, M. M., Dillon, L. W., Hourigan, C. S., & Fitzhugh, C. D.
- Venue
- Blood
- Publisher
- American Society of Hematology
- Published
- 2022-12-08
- Volume
- 140
- Issue
- 23
- Pages
- 2514-2518
- ISSN
- 0006-4971
- 1528-0020
- Cited by
- 49
- References
- 1
- Language
- en
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Increased incidence of hematologic malignancies in SCD after HCT in adults with graft failure and mixed chimerism. https://app.cochat.ai/papers/10.1182/blood.2022017960
- The paper
- Lawal, R. A., Mukherjee, D., Limerick, E. M., Coles, W., Hsieh, M. M., Dillon, L. W., Hourigan, C. S., & Fitzhugh, C. D. (2022). Increased incidence of hematologic malignancies in SCD after HCT in adults with graft failure and mixed chimerism. Blood. https://doi.org/10.1182/blood.2022017960