Role of donor clonal hematopoiesis in allogeneic hematopoietic stem-cell transplantation
Abstract
PURPOSE: Clonal hematopoiesis of indeterminate potential (CHIP) occurs in the blood of approximately 20% of older persons. CHIP is linked to an increased risk of hematologic malignancies and of all-cause mortality; thus, the eligibility of stem-cell donors with CHIP is questionable. We comprehensively investigated how donor CHIP affects outcome of allogeneic hematopoietic stem-cell transplantation (HSCT). METHODS: We collected blood samples from 500 healthy, related HSCT donors (age ≥ 55 years) at the time of stem-cell donation for targeted sequencing with a 66-gene panel. The effect of donor CHIP was assessed on recipient outcomes, including graft-versus-host disease (GVHD), cumulative incidence of relapse/progression (CIR/P), and overall survival (OS). RESULTS: A total of 92 clonal mutations with a median variant allele frequency of 5.9% were identified in 80 (16.0%) of 500 donors. CHIP prevalence was higher in donors related to patients with myeloid compared with lymphoid malignancies (19.2% v 6.3%; P ≤ .001). In recipients allografted with donor CHIP, we found a high cumulative incidence of chronic GVHD (cGVHD; hazard ratio [HR], 1.73; 95% CI, 1.21 to 2.49; P = .003) and lower CIR/P (univariate: HR, 0.62; 95% CI, 0.40 to 0.97; P = .027; multivariate: HR, 0.63; 95% CI, 0.41 to 0.98; P = .042) but no effect on nonrelapse mortality. Serial quantification of 25 mutations showed engraftment of 24 of 25 clones and disproportionate expansion in half of them. Donor-cell leukemia was observed in two recipients. OS was not affected by donor CHIP status (HR, 0.88; 95% CI, 0.65 to 1.321; P = .434). CONCLUSION: Allogeneic HSCT from donors with CHIP seems safe and results in similar survival in the setting of older, related donors. Future studies in younger and unrelated donors are warranted to extend these results. Confirmatory studies and mechanistic experiments are warranted to challenge the hypothesis that donor CHIP might foster cGVHD development and reduce relapse/progression risk.
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One possible explanation for the higher graft-versus-host disease and reduced relapse rates is that donor cells harboring the mutations were capable of mounting stronger immune responses against both normal host tissues and the tumor.
“One possible explanation for this finding is that the donor cells harboring the mutations were capable of mounting stronger immune responses against both normal host tissues and the tumor.”
From Clonal hematopoiesis in human aging and disease (2019) · cites this paper as [95]
Bone marrow transplant recipients with hematological malignancies who received donor marrow from carriers of CHIP had higher rates of graft-versus-host disease and reduced relapse rates.
“Bone marrow transplant recipients with hematological malignancies who received donor marrow from carriers of CHIP had higher rates of graft-versus-host disease and reduced relapse rates 95.”
From Clonal hematopoiesis in human aging and disease (2019) · cites this paper as [95]
Cites
Signatures of mutational processes in human cancer
Initiative, A. P. C. G., Alexandrov, L. B., ICGC Breast Cancer Consortium, ICGC MMML-Seq Consortium, PedBrain, I., Nik-Zainal, S., Wedge, D. C., Aparicio, S. A. J. R., Behjati, S., Biankin, A. V., et al. (2013) · Nature · doi:10.1038/nature12477 · Cited by 9,660 · see citing works
Age-related clonal hematopoiesis associated with adverse outcomes
Jaiswal, S., Fontanillas, P., Flannick, J., Manning, A., Grauman, P. V., Mar, B. G., Lindsley, R. C., Mermel, C. H., Burtt, N., Chavez, A., et al. (2014) · New England Journal of Medicine · doi:10.1056/nejmoa1408617 · Cited by 4,841 · see citing works
Filipovich, A. H., Weisdorf, D. J., Pavletic, S. Z., Socié, G., Wingard, J. R., Lee, S. J., Martin, P. J., Chien, J. W., Przepiorka, D., Couriel, D. R., et al. (2005) · Transplantation and Cellular Therapy · doi:10.1016/j.bbmt.2005.09.004 · Cited by 3,554 · see citing works
Self-citationClonal hematopoiesis and blood-cancer risk inferred from blood DNA sequence
Genovese, G., Kähler, A. K., Handsaker, R. E., Lindberg, J., Rose, S. A., Bakhoum, S. F., Chambert, K., Mick, E., Neale, B. M., Fromer, M., et al. (2014) · New England Journal of Medicine · doi:10.1056/nejmoa1409405 · Cited by 3,531 · see citing works
Szer, J. (1999) · The Medical Journal of Australia · doi:10.5694/j.1326-5377.1999.tb127745.x · Cited by 3,376 · see citing works
Clonal hematopoiesis and risk of atherosclerotic cardiovascular disease
Jaiswal, S., Natarajan, P., Silver, A. J., Gibson, C. J., Bick, A. G., Shvartz, E., McConkey, M., Gupta, N., Gabriel, S., Ardissino, D., et al. (2017) · New England Journal of Medicine · doi:10.1056/nejmoa1701719 · Cited by 2,683 · see citing works
Frequent pathway mutations of splicing machinery in myelodysplasia
Yoshida, K., Sanada, M., Shiraishi, Y., Nowak, D., Nagata, Y., Yamamoto, R., Sato, Y., Sato-Otsubo, A., Kon, A., Nagasaki, M., et al. (2011) · Nature · doi:10.1038/nature10496 · Cited by 2,029 · see citing works
Self-citation<i>DNMT3A</i> Mutations in Acute Myeloid Leukemia
Ley, T. J., Ding, L., Walter, M. J., McLellan, M. D., Lamprecht, T., Larson, D. E., Kandoth, C., Payton, J. E., Baty, J., Welch, J., et al. (2010) · New England Journal of Medicine · doi:10.1056/nejmoa1005143 · Cited by 1,983 · see citing works
Clonal hematopoiesis of indeterminate potential and its distinction from myelodysplastic syndromes
Steensma, D. P., Bejar, R., Jaiswal, S., Lindsley, R. C., Sekeres, M. A., Hasserjian, R. P., & Ebert, B. L. (2015) · Blood · doi:10.1182/blood-2015-03-631747 · Cited by 1,971 · see citing works
Age-related mutations associated with clonal hematopoietic expansion and malignancies
Xie, M., Lu, C., Wang, J., McLellan, M. D., Johnson, K. J., Wendl, M. C., McMichael, J. F., Schmidt, H. K., Yellapantula, V., Miller, C. A., et al. (2014) · Nature Medicine · doi:10.1038/nm.3733 · Cited by 1,874 · see citing works
Mutation in <i>TET2</i> in Myeloid Cancers
Delhommeau, F., Dupont, S., Valle, V. D., James, C., Trannoy, S., Massé, A., Kosmider, O., Le Couedic, J.-P., Robert, F., Alberdi, A., et al. (2009) · New England Journal of Medicine · doi:10.1056/nejmoa0810069 · Cited by 1,776 · see citing works
Clonal hematopoiesis associated with TET2 deficiency accelerates atherosclerosis development in mice
Fuster, J. J., MacLauchlan, S., Zuriaga, M. A., Polackal, M. N., Ostriker, A. C., Chakraborty, R., Wu, C.-L., Sano, S., Muralidharan, S., Rius, C., et al. (2017) · Science · doi:10.1126/science.aag1381 · Cited by 1,536 · see citing works
Identification of pre-leukaemic haematopoietic stem cells in acute leukaemia
Shlush, L. I., Zandi, S., Mitchell, A., Chen, W. C., Brandwein, J. M., Gupta, V., Kennedy, J. A., Schimmer, A. D., Schuh, A. C., Yee, K. W., et al. (2014) · Nature · doi:10.1038/nature13038 · Cited by 1,443 · see citing works
Dnmt3a is essential for hematopoietic stem cell differentiation
Challen, G. A., Sun, D., Jeong, M., Luo, M., Jelinek, J., Berg, J. S., Bock, C., Vasanthakumar, A., Gu, H., Xi, Y., et al. (2012) · Nature Genetics · doi:10.1038/ng.1009 · Cited by 1,122 · see citing works
Quivoron, C., Couronné, L., Della Valle, V., Lopez, C. K., Plo, I., Wagner-Ballon, O., Do Cruzeiro, M., Delhommeau, F., Arnulf, B., Stern, M.-H., et al. (2011) · Cancer Cell · doi:10.1016/j.ccr.2011.06.003 · Cited by 924 · see citing works
Pathophysiology of Chronic Graft-versus-Host Disease and Therapeutic Targets
Zeiser, R., & Blazar, B. R. (2017) · New England Journal of Medicine · doi:10.1056/nejmra1703472 · Cited by 750 · see citing works
Clonal haematopoiesis harbouring AML-associated mutations is ubiquitous in healthy adults
Young, A. L., Challen, G. A., Birmann, B. M., & Druley, T. E. (2016) · Nature Communications · doi:10.1038/ncomms12484 · Cited by 692 · see citing works
Somatic Mutations and Clonal Hematopoiesis in Aplastic Anemia
Yoshizato, T., Dumitriu, B., Hosokawa, K., Makishima, H., Yoshida, K., Townsley, D., Sato-Otsubo, A., Sato, Y., Liu, D., Suzuki, H., et al. (2015) · New England Journal of Medicine · doi:10.1056/nejmoa1414799 · Cited by 646 · see citing works
Self-citationGelsi‐Boyer, V., Trouplin, V., Adélaı̈de, J., Bonansea, J., Cervera, N., Carbuccia, N., Lagarde, A., Prébet, T., Nezri, M., Sainty, D., et al. (2009) · British Journal of Haematology · doi:10.1111/j.1365-2141.2009.07697.x · Cited by 563 · see citing works
Leukemia-associated somatic mutations drive distinct patterns of age-related clonal hemopoiesis
McKerrell, T., Park, N., Moreno, T., Grove, C. S., Ponstingl, H., Stephens, J., Crawley, C., Craig, J., Scott, M. A., Hodkinson, C., et al. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.02.005 · Cited by 534 · see citing works
Gibson, C. J., Lindsley, R. C., Tchekmedyian, V., Mar, B. G., Shi, J., Jaiswal, S., Bosworth, A., Francisco, L., He, J., Bansal, A., et al. (2017) · Journal of Clinical Oncology · doi:10.1200/jco.2016.71.6712 · Cited by 480 · see citing works
JAK2 haplotype is a major risk factor for the development of myeloproliferative neoplasms
Jones, A., Chase, A., Silver, R., Oscier, D., Zoi, K., Wang, Y. L., Cario, H., Pahl, H., Collins, A., Reiter, A., et al. (2009) · Nature Genetics · doi:10.1038/ng.334 · Cited by 407 · see citing works
Preleukaemic clonal haemopoiesis and risk of therapy-related myeloid neoplasms: a case-control study
Takahashi, K., Wang, F., Kantarjian, H., Doss, D., Khanna, K., Thompson, E., Zhao, L., Patel, K., Neelapu, S., Gumbs, C., et al. (2017) · The Lancet Oncology · doi:10.1016/s1470-2045(16)30626-x · Cited by 399 · see citing works
Buscarlet, M., Provost, S., Zada, Y. F., Barhdadi, A., Bourgoin, V., Lépine, G., Mollica, L., Szuber, N., Dubé, M.-P., & Busque, L. (2017) · Blood · doi:10.1182/blood-2017-04-777029 · Cited by 383 · see citing works
Myelodysplastic Syndromes Are Propagated by Rare and Distinct Human Cancer Stem Cells In Vivo
Woll, P. S., Kjällquist, U., Chowdhury, O., Doolittle, H., Wedge, D. C., Thongjuea, S., Erlandsson, R., Ngara, M., Anderson, K., Deng, Q., et al. (2014) · Cancer Cell · doi:10.1016/j.ccr.2014.03.036 · Cited by 317 · see citing works
Gillis, N. K., Ball, M., Zhang, Q., Ma, Z., Zhao, Y., Yoder, S. J., Balasis, M. E., Mesa, T. E., Sallman, D. A., Lancet, J. E., et al. (2017) · The Lancet Oncology · doi:10.1016/s1470-2045(16)30627-1 · Cited by 317 · see citing works
Acquired Initiating Mutations in Early Hematopoietic Cells of CLL Patients
Damm, F., Mylonas, E., Cosson, A., Yoshida, K., Della-Valle, V., Mouly, E., Diop, M. K., Scourzic, L., Shiraishi, Y., Chiba, K., et al. (2014) · Cancer Discovery · doi:10.1158/2159-8290.cd-14-0104 · Cited by 266 · see citing works
Self-citationThe Nlrp3 inflammasome regulates acute graft-versus-host disease
Jankovic, D. L., Ganesan, J., Bscheider, M., Stickel, N., Weber, F. C., Guarda, G., Follo, M., Pfeifer, D., Tardivel, A., Ludigs, K., et al. (2013) · The Journal of Experimental Medicine · doi:10.1084/jem.20130084 · Cited by 236 · see citing works
Damm, F., Kosmider, O., Gelsi‐Boyer, V., Renneville, A., Carbuccia, N., Hidalgo-Curtis, C., Della-Valle, V., Couronné, L., Scourzic, L., Chesnais, V., et al. (2012) · Blood · doi:10.1182/blood-2011-12-400994 · Cited by 232 · see citing works
Self-citationBCOR and BCORL1 mutations in myelodysplastic syndromes and related disorders
Damm, F., Chesnais, V., Nagata, Y., Yoshida, K., Scourzic, L., Okuno, Y., Itzykson, R., Sanada, M., Shiraishi, Y., Gelsi‐Boyer, V., et al. (2013) · Blood · doi:10.1182/blood-2012-11-469619 · Cited by 217 · see citing works
Self-citationHematopoietic lineage distribution and evolutionary dynamics of clonal hematopoiesis
Arends, C. M., Galan-Sousa, J., Hoyer, K., Chan, W., Jäger, M., Yoshida, K., Seemann, R., Noerenberg, D., Waldhueter, N., Fleischer-Notter, H., et al. (2018) · Leukemia · doi:10.1038/s41375-018-0047-7 · Cited by 194 · see citing works
Self-citationHow I diagnose and manage individuals at risk for inherited myeloid malignancies
The University of Chicago Hematopoietic Malignancies Cancer Risk Team (2016) · Blood · doi:10.1182/blood-2016-05-670240 · Cited by 181 · see citing works
Schmidt, M., Rinke, J., Schäfer, V., Schnittger, S., Kohlmann, A., Obstfelder, E., Kunert, C., Ziermann, J., Winkelmann, N., Eigendorff, E., et al. (2014) · Leukemia · doi:10.1038/leu.2014.272 · Cited by 143 · see citing works
Gamper, C. J., Agoston, A. T., Nelson, W. G., & Powell, J. D. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0802960 · Cited by 107 · see citing works
Altieri, A., Bermejo, J. L., & Hemminki, K. (2005) · Blood · doi:10.1182/blood-2005-01-0140 · Cited by 99 · see citing works
Frequent NFKBIE deletions are associated with poor outcome in primary mediastinal B-cell lymphoma
Mansouri, L., Noerenberg, D., Young, E., Mylonas, E., Abdulla, M., Frick, M., Asmar, F., Ljungström, V., Schneider, M., Yoshida, K., et al. (2016) · Blood · doi:10.1182/blood-2016-03-704528 · Cited by 93 · see citing works
Self-citationYu, Q., Zhou, B., Zhang, Y., Nguyen, E., Du, J., Glosson, N. L., & Kaplan, M. H. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1103803109 · Cited by 91 · see citing works
Donor-engrafted CHIP is common among stem cell transplant recipients with unexplained cytopenias
Gibson, C. J., Kennedy, J. A., Nikiforow, S., Kuo, F. C., Alyea, E. P., Ho, V. T., Ritz, J., Soiffer, R. J., Antin, J. H., & Lindsley, R. C. (2017) · Blood · doi:10.1182/blood-2017-01-764951 · Cited by 91 · see citing works
Donor cell leukemia arising from clonal hematopoiesis after bone marrow transplantation
Gondek, L. P., Zheng, G., Ghiaur, G., Dezern, A. E., Matsui, W. H., Yegnasubramanian, S., Lin, M.-T., Levis, M. J., Eshleman, J. R., Varadhan, R., et al. (2016) · Leukemia · doi:10.1038/leu.2016.63 · Cited by 90 · see citing works
Kato, M., Yamashita, T., Suzuki, R., Matsumoto, K., Nishimori, H., Takahashi, S., Iwato, K., Nakaseko, C., Kondo, T., Imada, K., et al. (2016) · Leukemia · doi:10.1038/leu.2016.23 · Cited by 60 · see citing works
EGR2 mutations define a new clinically aggressive subgroup of chronic lymphocytic leukemia
Young, E., Noerenberg, D., Mansouri, L., Ljungström, V., Frick, M., Sutton, L.-A., Blakemore, S. J., Galan-Sousa, J., Plevová, K., Baliakas, P., et al. (2016) · Leukemia · doi:10.1038/leu.2016.359 · Cited by 52 · see citing works
Self-citationHerold, S., Kühn, M., Bonin, M. V., Stange, T., Platzbecker, U., Radke, J., Lange, T., Sockel, K., Gutsche, K., Schetelig, J., et al. (2017) · Leukemia · doi:10.1038/leu.2017.104 · Cited by 37 · see citing works
Self-citationA tale of two siblings: two cases of AML arising from a single pre-leukemic DNMT3A mutant clone
Hahn, C. N., Ross, D. M., Feng, J., Beligaswatte, A. M., Hiwase, D., Parker, W. T., Ho, M., Zawitkowski, M., Ambler, K., Cheetham, G., et al. (2015) · Leukemia · doi:10.1038/leu.2015.67 · Cited by 33 · see citing works
Process of allogeneic hematopoietic cell transplantation decision making for older adults
Randall, J., Keven, K., Atlı, T., & Ustun, C. (2015) · Bone Marrow Transplantation · doi:10.1038/bmt.2015.241 · Cited by 31 · see citing works
Damm, F., Markus, B., Thol, F. R., Morgan, M. A., Göhring, G., Schlegelberger, B., Krauter, J., Heuser, M., Bernard, O., & Ganser, A. (2014) · Genes Chromosomes and Cancer · doi:10.1002/gcc.22191 · Cited by 28 · see citing works
Self-citationTall, A. R., & Levine, R. L. (2017) · Nature · doi:10.1038/nature21505 · Cited by 24 · see citing works
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de Latour, R. P., Kulasekararaj, A. G., Iacobelli, S., Terwel, S. R., Cook, R., Griffin, M., Halkes, C. J. M., Récher, C., Barraco, F., Forcade, É., et al. (2022) · New England Journal of Medicine · doi:10.1056/nejmoa2109965 · Cited by 308 · see citing works
Self-citationClonal hematopoiesis and non-hematologic disorders
Jaiswal, S. (2020) · Blood · doi:10.1182/blood.2019000989 · Cited by 182 · see citing works
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Weeks, L. D., & Ebert, B. L. (2023) · Blood · doi:10.1182/blood.2023022222 · Cited by 169 · see citing works
Donor Clonal Hematopoiesis and Recipient Outcomes After Transplantation
Gibson, C. J., Kim, H. T., Zhao, L., Murdock, H. M., Hambley, B., Ogata, A., Madero-Marroquin, R., Wang, S., Green, L., Fleharty, M., et al. (2022) · Journal of Clinical Oncology · doi:10.1200/jco.21.02286 · Cited by 168 · see citing works
Somatic Mutations in “Benign” Disease
Mustjoki, S. M., & Young, N. S. (2021) · New England Journal of Medicine · doi:10.1056/nejmra2101920 · Cited by 160 · see citing works
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Belizaire, R., Wong, W. J., Robinette, M. L., & Ebert, B. L. (2023) · Nature Reviews Immunology · doi:10.1038/s41577-023-00843-3 · Cited by 161 · see citing works
CD123 as a Therapeutic Target in the Treatment of Hematological Malignancies
Testa, U., Pelosi, E., & Castelli, G. (2019) · Cancers · doi:10.3390/cancers11091358 · Cited by 158 · see citing works
Christen, F., Hoyer, K., Yoshida, K., Hou, H., Waldhüter, N., Heuser, M., Hills, R. K., Chan, W., Hablesreiter, R., Blau, O., et al. (2019) · Blood · doi:10.1182/blood-2018-05-852822 · Cited by 140 · see citing works
Self-citationNam, A. S., Dusaj, N., Izzo, F., Murali, R., Myers, R. M., Mouhieddine, T. H., Sotelo, J., Benbarche, S., Waarts, M., Gaiti, F., et al. (2022) · Nature Genetics · doi:10.1038/s41588-022-01179-9 · Cited by 140 · see citing works
Clonal Hematopoiesis: Mechanisms Driving Dominance of Stem Cell Clones
Challen, G., & Goodell, M. A. (2020) · Blood · doi:10.1182/blood.2020006510 · Cited by 131 · see citing works
Clonal hematopoiesis: Mutation-specific adaptation to environmental change
Florez, M. A., Tran, B. T., Wathan, T. K., DeGregori, J., Pietras, E. M., & King, K. Y. (2022) · Cell Stem Cell · doi:10.1016/j.stem.2022.05.006 · Cited by 129 · see citing works
Loke, J. C. T., Malladi, R. K., Moss, P. A. H., & Craddock, C. (2019) · British Journal of Haematology · doi:10.1111/bjh.16355 · Cited by 120 · see citing works
Rautenberg, C., Germing, U., Haas, R. R., Kobbe, G., & Schroeder, T. A. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20010228 · Cited by 112 · see citing works
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Dharan, N. J., Yeh, P., Bloch, M., Yeung, M. M., Baker, D., Guinto, J., Roth, N., Ftouni, S., Ognenovska, K., Smith, D., et al. (2021) · Nature Medicine · doi:10.1038/s41591-021-01357-y · Cited by 108 · see citing works
Clonal hematopoiesis, somatic mosaicism, and age-associated disease
Evans, M. A., & Walsh, K. (2022) · Physiological Reviews · doi:10.1152/physrev.00004.2022 · Cited by 105 · see citing works
Hecker, J. S., Hartmann, L., Rivière, J., Buck, M. C., van der Garde, M., Rothenberg‐Thurley, M., Fischer, L., Winter, S., Ksienzyk, B., Ziemann, F., et al. (2021) · Blood · doi:10.1182/blood.2020010163 · Cited by 98 · see citing works
Arends, C. M., Liman, T. G., Strzelecka, P. M., Kufner, A., Löwe, P., Huo, S., Stein, C. M., Piper, S. K., Tilgner, M., Sperber, P. S., et al. (2023) · Blood · doi:10.1182/blood.2022017661 · Cited by 99 · see citing works
Self-citationClonal hematopoiesis and associated diseases: A review of recent findings
Asada, S., & Kitamura, T. (2021) · Cancer Science · doi:10.1111/cas.15094 · Cited by 97 · see citing works
Dholaria, B., Savani, B. N., Hamilton, B. K., Oran, B., Liu, H. D., Tallman, M. S., Ciurea, S. O., Holtzman, N. G., Phillips, G. L., Devine, S. M., et al. (2020) · Transplantation and Cellular Therapy · doi:10.1016/j.bbmt.2020.09.020 · Cited by 89 · see citing works
Chang, Y., Pei, X., & Huang, X. (2022) · The Lancet Haematology · doi:10.1016/s2352-3026(22)00293-9 · Cited by 92 · see citing works
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Arends, C. M., Weiß, M., Christen, F., Eulenberg-Gustavus, C., Rousselle, A., Kettritz, R., Eckardt, K., Chan, W., Hoyer, K., Frick, M., et al. (2019) · Haematologica · doi:10.3324/haematol.2019.223305 · Cited by 87 · see citing works
Self-citationRotz, S. J., Bhatt, N. S., Hamilton, B. K., Duncan, C., Aljurf, M. D., Atsuta, Y., Beebe, K. L., Buchbinder, D. K., Burkhard, P., Carpenter, P. A., et al. (2024) · Transplantation and Cellular Therapy · doi:10.1016/j.jtct.2023.12.001 · Cited by 86 · see citing works
Saini, N. Y., Swoboda, D. M., Greenbaum, U., Ma, J., Patel, R. D., Devashish, K., Das, K., Tanner, M. R., Strati, P., Nair, R. K., et al. (2022) · Blood Cancer Discovery · doi:10.1158/2643-3230.bcd-21-0177 · Cited by 82 · see citing works
Boettcher, S., Wilk, C. M., Singer, J., Beier, F., Burcklen, E., Beisel, C., Ferreira, M. S. V., Gourri, E., Gassner, C., Frey, B. M., et al. (2020) · Blood · doi:10.1182/blood.2019003079 · Cited by 79 · see citing works
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Lundgren, S., Keränen, M. A. I., Kankainen, M., Huuhtanen, J., Walldin, G., Kerr, C. M., Clemente, M. J., Ebeling, F. T., Rajala, H. L. M., Brück, O. E., et al. (2021) · Leukemia · doi:10.1038/s41375-021-01231-3 · Cited by 61 · see citing works
Self-citationClonal dynamics after allogeneic haematopoietic cell transplantation
Spencer Chapman, M., Wilk, C. M., Boettcher, S., Mitchell, E., Dawson, K., Williams, N., Müller, J., Kovtonyuk, L., Jung, H., Caiado, F., et al. (2024) · Nature · doi:10.1038/s41586-024-08128-y · Cited by 60 · see citing works
Ortmann, C. A., Dorsheimer, L., Abou‐El‐Ardat, K., Hoffrichter, J., Aßmus, B., Bonig, H. B., Scholz, A., Pfeifer, H., Martin, H., Schmid, T., et al. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.04.064 · Cited by 60 · see citing works
Clonal Hematopoiesis: From Mechanisms to Clinical Intervention
Köhnke, T., & Majeti, R. (2021) · Cancer Discovery · doi:10.1158/2159-8290.cd-21-0901 · Cited by 59 · see citing works
Arends, C. M., Dimitriou, S., Stahler, A., Hablesreiter, R., Strzelecka, P. M., Stein, C. M., Tilgner, M., Saiki, R., Ogawa, S., Bullinger, L., et al. (2021) · Blood · doi:10.1182/blood.2021014108 · Cited by 57 · see citing works
Self-citationWong, W., Bhatt, S. T., Trinkaus, K. M., Pusic, I., Elliott, K., Mahajan, N., Wan, F., Switzer, G. E., Confer, D. L., DiPersio, J. F., et al. (2020) · Science Translational Medicine · doi:10.1126/scitranslmed.aax6249 · Cited by 52 · see citing works
Clonal hematopoiesis in elderly twins: concordance, discordance, and mortality
Hansen, J. W., Pedersen, D. A., Larsen, L. A., Husby, S., Clemmensen, S. B., Hjelmborg, J., Favero, F., Weischenfeldt, J., Christensen, K., & Grønbæk, K. (2019) · Blood · doi:10.1182/blood.2019001793 · Cited by 53 · see citing works
How I Treat AML in 2023 Incorporating the Updated Classifications and Guidelines
Chaer, F. E., Hourigan, C. S., & Zeidan, A. M. (2023) · Blood · doi:10.1182/blood.2022017808 · Cited by 51 · see citing works
Clonal hematopoiesis and its emerging effects on cellular therapies
Bonin, M. V., Jambor, H. K., Teipel, R., Stölzel, F., Thiede, C., Damm, F., Kroschinsky, F., Schetelig, J., Chavakis, T., & Bornhäuser, M. (2021) · Leukemia · doi:10.1038/s41375-021-01337-8 · Cited by 46 · see citing works
Self-citationRotz, S. J., Ryan, T. D., & Hayek, S. S. (2020) · Journal of Thrombosis and Thrombolysis · doi:10.1007/s11239-020-02344-9 · Cited by 46 · see citing works
What To Tell Your Patient With Clonal Hematopoiesis And Why: Insights From Two Specialized Clinics
Steensma, D. P., & Bolton, K. L. (2020) · Blood · doi:10.1182/blood.2019004291 · Cited by 43 · see citing works
Concordance for clonal hematopoiesis is limited in elderly twins
Fabre, M. A., McKerrell, T., Zwiebel, M., Vijayabaskar, M. S., Park, N., Wells, P. M., Rad, R., Deloukas, P., Small, K. S., Steves, C. J., et al. (2019) · Blood · doi:10.1182/blood.2019001807 · Cited by 43 · see citing works
Tumor-Based Genetic Testing and Familial Cancer RiskPreprint
Forman, A. D., & Sotelo, J. (2019) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a036590 · Cited by 42 · see citing works
Lee, J.-M., Kim, Y., Park, S., Han, E., Kim, M., & Kim, M. (2019) · Journal of Clinical Medicine · doi:10.3390/jcm8122077 · Cited by 41 · see citing works
Stem cell donors should be screened for CHIP
Dezern, A. E., & Gondek, L. P. (2020) · Blood Advances · doi:10.1182/bloodadvances.2019000394 · Cited by 41 · see citing works
Clonal hematopoiesis: Molecular and clinical implications
Kusne, Y. N., Xie, Z., & Patnaik, M. M. (2022) · Leukemia Research · doi:10.1016/j.leukres.2022.106787 · Cited by 41 · see citing works
Lymphoid clonal hematopoiesis: implications for malignancy, immunity, and treatment
von Beck, K., von Beck, T. A., Ferrell, P. B., Bick, A. G., & Kishtagari, A. (2023) · Blood Cancer Journal · doi:10.1038/s41408-022-00773-8 · Cited by 42 · see citing works
Clinical Implications and Dynamics of Clonal Hematopoiesis in Anti-CD19 CAR T-cell Treated Patients
Panagiota, V., Kerschbaum, J. F., Penack, O., Stein, C. M., Arends, C. M., Koenecke, C., Strzelecka, P. M., Kloos, A., Wiegand, L., Lasch, A., et al. (2023) · HemaSphere · doi:10.1097/hs9.0000000000000957 · Cited by 40 · see citing works
Self-citationDynamics of clonal hematopoiesis under DNA-damaging treatment in patients with ovarian cancer
Arends, C. M., Kopp, K., Hablesreiter, R., Estrada, N., Christen, F., Moll, U. M., Zeillinger, R., Schmitt, W., Sehouli, J., Kulbe, H., et al. (2024) · Leukemia · doi:10.1038/s41375-024-02253-3 · Cited by 39 · see citing works
Self-citationClonal hematopoiesis and preleukemia—Genetics, biology, and clinical implications
Hartmann, L., & Metzeler, K. H. (2019) · Genes Chromosomes and Cancer · doi:10.1002/gcc.22756 · Cited by 37 · see citing works
Shin, T., Zhou, Y., Chen, S., Cordes, S., Grice, M. Z., Fan, X., Lee, B., Aljanahi, A. A., Hong, S. G., Vaughan, K. L., et al. (2022) · Blood · doi:10.1182/blood.2021014875 · Cited by 38 · see citing works
Spyridonidis, A. (2020) · Blood · doi:10.1182/blood.2019003566 · Cited by 38 · see citing works
Bewersdorf, J. P., Ardasheva, A., Podoltsev, N. A., Singh, A., Biancon, G., Halene, S., & Zeidan, A. M. (2019) · Blood Reviews · doi:10.1016/j.blre.2019.100587 · Cited by 36 · see citing works
Kennedy, V. E., & Olin, R. L. (2021) · The Lancet Haematology · doi:10.1016/s2352-3026(21)00231-3 · Cited by 36 · see citing works
Okamura, R., Piccioni, D. E., Boichard, A., Lee, S., Jimenez, R. E., Sicklick, J. K., Kato, S., & Kurzrock, R. (2021) · International Journal of Cancer · doi:10.1002/ijc.33481 · Cited by 35 · see citing works
Stem cell donors should not be screened for clonal hematopoiesis
Gibson, C. J., & Lindsley, R. C. (2020) · Blood Advances · doi:10.1182/bloodadvances.2019000395 · Cited by 34 · see citing works
Oran, B., Champlin, R. E., Wang, F., Tanaka, T. N., Saliba, R. M., Alatrash, G., Garcia‐Manero, G., Kantarjian, H. M., Cao, K., Shpall, E. J., et al. (2021) · Leukemia · doi:10.1038/s41375-021-01312-3 · Cited by 34 · see citing works
Williams, L. S., Williams, K. M., Gillis, N., Bolton, K. L., Damm, F., Deuitch, N. T., Farhadfar, N., Gergis, U. S., Keel, S., Michelis, F. V., et al. (2023) · Transplantation and Cellular Therapy · doi:10.1016/j.jtct.2023.10.018 · Cited by 33 · see citing works
Self-citationWorel, N., Aljurf, M. D., Anthias, C., Buser, A. S., Cody, M. R., Fechter, M., Galeano, S., Greinix, H. T., Kisch, A. M., Koh, M., et al. (2022) · The Lancet Haematology · doi:10.1016/s2352-3026(22)00184-3 · Cited by 33 · see citing works
Genetics of donor cell leukemia in acute myelogenous leukemia and myelodysplastic syndrome
Williams, L. S., Doucette, K., Karp, J. E., & Lai, C. (2021) · Bone Marrow Transplantation · doi:10.1038/s41409-021-01214-z · Cited by 32 · see citing works
Hematology 2022—what is complete HLA match in 2022?
Spellman, S. R. (2022) · Hematology · doi:10.1182/hematology.2022000326 · Cited by 32 · see citing works
Newell, L. F., Williams, T. P., Liu, J., Yu, Y., Chen, Y., Booth, G. C., Knight, R. J., Goslee, K., Cook, R. J., Leonard, J. T., et al. (2021) · Transplantation and Cellular Therapy · doi:10.1016/j.jtct.2021.04.014 · Cited by 31 · see citing works
Inflammageing and clonal haematopoiesis interplay and their impact on human disease
Hajishengallis, G., & Chavakis, T. (2026) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-025-00936-y · Cited by 35 · see citing works
Somatic mutations in autoinflammatory and autoimmune disease
Torreggiani, S., Castellan, F. S., Aksentijevich, I. A., & Beck, D. B. (2024) · Nature Reviews Rheumatology · doi:10.1038/s41584-024-01168-8 · Cited by 29 · see citing works
Decreasing chronic graft-versus-host disease rates in all populations
Carpenter, P. A., Gooley, T. A., Boiko, J. R., Lee, C. J., Burroughs, L. M., Mehta, R. S., Salit, R. B., Bhatt, N. S., Krakow, E. F., Dahlberg, A. E., et al. (2024) · Blood Advances · doi:10.1182/bloodadvances.2024012722 · Cited by 27 · see citing works
Nowakowska, M. K., Kim, T., Thompson, M. T., Bolton, K. L., Deswal, A., Lin, S. H., Scheet, P., Wehner, M. R., & Nead, K. T. (2022) · American Journal of Hematology · doi:10.1002/ajh.26465 · Cited by 27 · see citing works
Clonal Hematopoiesis and therapy related MDS/AML
Desai, P. M., & Roboz, G. J. (2019) · Best Practice & Research Clinical Haematology · doi:10.1016/j.beha.2019.02.006 · Cited by 27 · see citing works
Novel Biomarkers for Outcome After Allogeneic Hematopoietic Stem Cell Transplantation
Chen, S., & Zeiser, R. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.01854 · Cited by 25 · see citing works
Awada, H. K., Thapa, B., & Visconte, V. (2020) · Cells · doi:10.3390/cells9112512 · Cited by 24 · see citing works
The clinical implications of clonal hematopoiesis in hematopoietic cell transplantation
Nawas, M. T., Schetelig, J., Damm, F., Levine, R. L., Perales, M., Giralt, S. A., van den Brink, M. R. M., Arcila, M. E., Zehir, A., Papaemmanuil, E., et al. (2020) · Blood Reviews · doi:10.1016/j.blre.2020.100744 · Cited by 24 · see citing works
Self-citationClonal hematopoiesis in men living with HIV and association with subclinical atherosclerosis
Wang, S., Paşca, S., Post, W. S., Langan, S. J., Pallavajjalla, A., Haley, L. M., Gocke, C. D., Budoff, M. J., Haberlen, S., Brown, T. T., et al. (2022) · AIDS · doi:10.1097/qad.0000000000003280 · Cited by 24 · see citing works
Optimizing Donor Choice and GVHD Prophylaxis in Allogeneic Hematopoietic Cell Transplantation
Holtan, S. G., Versluis, J., Weisdorf, D. J., & Cornelissen, J. J. (2021) · Journal of Clinical Oncology · doi:10.1200/jco.20.01771 · Cited by 23 · see citing works
Loke, J. C. T., Vyas, H., & Craddock, C. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.666091 · Cited by 22 · see citing works
CHIPing away the progression potential of CHIP: A new reality in the making
Xie, Z., & Zeidan, A. M. (2022) · Blood Reviews · doi:10.1016/j.blre.2022.101001 · Cited by 21 · see citing works
Clonal hematopoiesis and bone marrow failure syndromes
Paşca, S., & Gondek, L. P. (2021) · Best Practice & Research Clinical Haematology · doi:10.1016/j.beha.2021.101273 · Cited by 21 · see citing works
Somatic Mosaicism in Biology and Disease
Ogawa, H., Horitani, K., Izumiya, Y., & Sano, S. (2021) · Annual Review of Physiology · doi:10.1146/annurev-physiol-061121-040048 · Cited by 20 · see citing works
Modeling clonal hematopoiesis in umbilical cord blood cells by CRISPR/Cas9
Christen, F., Hablesreiter, R., Hoyer, K., Hennch, C., Maluck-Böttcher, A., Segler, A., Madadi, A., Frick, M., Bullinger, L., Briest, F., et al. (2021) · Leukemia · doi:10.1038/s41375-021-01469-x · Cited by 21 · see citing works
Self-citationTo portray clonal evolution in blood cancer, count your stem cells
Lyne, A.-M., Laplane, L., & Perié, L. (2020) · Blood · doi:10.1182/blood.2020008407 · Cited by 22 · see citing works
Papo, M., Friedrich, C., Delaval, L., de BOYSSON, H., Viallard, J., Bachmeyer, C., Sené, T., Humbert, S., Duffau, P., Contis, A., et al. (2021) · Lara D. Veeken · doi:10.1093/rheumatology/keab337 · Cited by 21 · see citing works
Natural Barcodes for Longitudinal Single Cell Tracking of Leukemic and Immune Cell Dynamics
Penter, L., Gohil, S. H., & Wu, C. J. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2021.788891 · Cited by 20 · see citing works
Mangaonkar, A. A., & Patnaik, M. M. (2023) · American Journal of Hematology · doi:10.1002/ajh.26915 · Cited by 20 · see citing works
Rotz, S. J., Bhatt, N. S., Hamilton, B. K., Duncan, C., Aljurf, M. D., Atsuta, Y., Beebe, K. L., Buchbinder, D. K., Burkhard, P., Carpenter, P. A., et al. (2024) · Bone Marrow Transplantation · doi:10.1038/s41409-023-02190-2 · Cited by 20 · see citing works
CHIP: is clonal hematopoiesis a surrogate for aging and other disease?
Gondek, L. P. (2021) · Hematology · doi:10.1182/hematology.2021000270 · Cited by 20 · see citing works
Refining AML Treatment: The Role of Genetics in Response and Resistance Evaluation to New Agents
Halik, A., Arends, C. M., Bullinger, L., Damm, F., & Frick, M. (2022) · Cancers · doi:10.3390/cancers14071689 · Cited by 19 · see citing works
Self-citationGu, W., Zhang, Y., Sun, T., Ju, M., Liu, X. F., Xue, F., Chen, Y., Liu, W., Li, H., Wang, W., et al. (2023) · Research and Practice in Thrombosis and Haemostasis · doi:10.1016/j.rpth.2023.100132 · Cited by 19 · see citing works
Kim, K. H., Kim, T., Novitzky‐Basso, I., Lee, H., Yoo, Y., Ahn, J., Pašić, I., Law, A., Lam, W., Michelis, F. V., et al. (2023) · Haematologica · doi:10.3324/haematol.2022.281806 · Cited by 18 · see citing works
Self-citationMoving toward a conceptualization of measurable residual disease in myelodysplastic syndromes
Schulz, E., Aplan, P. D., Freeman, S. D., & Pavletic, S. Z. (2023) · Blood Advances · doi:10.1182/bloodadvances.2023010098 · Cited by 17 · see citing works
Clonal Hematopoiesis of Indeterminate Potential as a Novel Risk Factor for Donor-Derived Leukemia
Burns, S. S., & Kapur, R. (2020) · Stem Cell Reports · doi:10.1016/j.stemcr.2020.07.008 · Cited by 18 · see citing works
Newell, L. F., Dunlap, J. B., Gatter, K. M., Bagby, G. C., Press, R. D., Cook, R. J., Fletcher, L. B., Leonard, J. T., Leong, K., Bubalo, J. S., et al. (2021) · American Journal of Transplantation · doi:10.1111/ajt.16635 · Cited by 17 · see citing works
Single-cell genomics in acquired bone marrow failure syndromes
Wu, Z., & Young, N. S. (2023) · Blood · doi:10.1182/blood.2022018581 · Cited by 16 · see citing works
Significance of targeting DNMT3A mutations in AML
Huang, G., Cai, X., & Li, D. (2024) · Annals of Hematology · doi:10.1007/s00277-024-05885-8 · Cited by 18 · see citing works
Ktena, Y. P., Koldobskiy, M. A., Barbato, M. I., Fu, H.-H., Luznik, L., Llosa, N. J., Haile, A., Klein, O. R., Liu, C., Gamper, C. J., et al. (2022) · Journal of Clinical Investigation · doi:10.1172/jci158047 · Cited by 17 · see citing works
Clonal Hematopoiesis of Indeterminate Potential: Current Understanding and Future Directions
Singh, I., & Singh, A. (2023) · Current Oncology Reports · doi:10.1007/s11912-023-01382-9 · Cited by 16 · see citing works
Clones assemble! The clonal complexity of blood during ontogeny and disease
Ganuza, M., Hall, T., Obeng, E. A., & McKinney‐Freeman, S. (2020) · Experimental Hematology · doi:10.1016/j.exphem.2020.01.009 · Cited by 16 · see citing works
Feldkamp, J. D., Vetter, V. M., Arends, C. M., Lang, T. J. L., Bullinger, L., Damm, F., Demuth, I., & Frick, M. (2022) · Haematologica · doi:10.3324/haematol.2021.280021 · Cited by 16 · see citing works
Self-citationClonal haematopoiesis to clonal cytopenias: unravelling disease evolution over time
Kirschner, K., Kusne, Y. N., Cargo, C. A., & Patnaik, M. M. (2025) · The Lancet Haematology · doi:10.1016/s2352-3026(25)00137-1 · Cited by 16 · see citing works
CAR T-cell Therapy Meets Clonal Hematopoiesis
Uslu, U., & June, C. H. (2022) · Blood Cancer Discovery · doi:10.1158/2643-3230.bcd-22-0067 · Cited by 15 · see citing works
Ueda, M., Higgins, J. E., Jenkins, I., Randolph, T. W., Smith, T. H., Valentine, C. C., Salk, J. J., Yeung, C. C. S., Beppu, L. W., Campbell, J., et al. (2024) · Science Translational Medicine · doi:10.1126/scitranslmed.ado5108 · Cited by 14 · see citing works
In MDS, is higher risk higher reward?
Sanz, G. F. (2019) · Hematology · doi:10.1182/hematology.2019000042 · Cited by 15 · see citing works
Neuendorff, N. R., Khan, A., Ullrich, F., Yates, S. J., Devarakonda, S. S., Lin, R. J., von Tresckow, B., Córdoba, R., Artz, A. S., & Rosko, A. E. (2024) · Journal of Geriatric Oncology · doi:10.1016/j.jgo.2024.101734 · Cited by 13 · see citing works
Donor derived leukemia in allogeneic transplantation
Aldoss, I. T., Clark, M. C., Marcucci, G., & Forman, S. J. (2021) · Leukemia & lymphoma/Leukemia and lymphoma · doi:10.1080/10428194.2021.1929966 · Cited by 13 · see citing works
- Authors
- Frick, M., Chan, W., Arends, C. M., Hablesreiter, R., Halik, A., Heuser, M., Michonneau, D., Blau, O., Hoyer, K., Christen, F., Galan-Sousa, J., Noerenberg, D., Wais, V., Stadler, M., Yoshida, K., Schetelig, J., Schuler, E., Thol, F., Clappier, E., Christopeit, M., Ayuk, F., Bornhäuser, M., Blau, I. W., Ogawa, S., Zemojtel, T., Gerbitz, A., Wagner, E. M., Spriewald, B. M., Schrezenmeier, H., Kuchenbauer, F., Kobbe, G., Wiesneth, M., Koldehoff, M., Socié, G., Kroeger, N., Bullinger, L., Thiede, C., & Damm, F.
- Affiliations
- Humboldt-Universität zu Berlin (DE)
- Medizinische Hochschule Hannover (DE)
- Inserm (FR)
- University Hospital Ulm (DE)
- Kyoto University (JP)
- University Hospital Carl Gustav Carus (DE)
- Heinrich Heine University Düsseldorf (DE)
- Hôpital Saint-Louis (FR)
- Universität Hamburg (DE)
- Berlin Institute of Health (BIH) Core Genomics Facility, Charité, University Medical Center, Berlin, Germany
- Johannes Gutenberg University Mainz (DE)
- Friedrich-Alexander-Universität Erlangen-Nürnberg (DE)
- German Red Cross (DE)
- Essen University Hospital (DE)
- David Michonneau and Gérard Socié, INSERM U1160, Institut Universitaire d’Hematologie, Paris/University Paris Diderot, Paris, France
- University Hospital Eppendorf, Hamburg, Germany
- German Cancer Research Center (DE)
- Charité - University Medical Center Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, Berlin, Germany
- ORCID
- Frick, Mareike
- Arends, Christopher Maximilian
- Hablesreiter, Raphael
- Halik, Adriane
- Heuser, Michael
- Michonneau, David
- Blau, Olga
- Hoyer, Kaja
- Christen, Friederike
- Noerenberg, Daniel
- Yoshida, Kenichi
- Schetelig, Johannes
- Schuler, Esther
- Thol, Felicitas
- Clappier, Emmanuelle
- Christopeit, Maximilian
- Ayuk, Francis
- Bornhäuser, Martin
- Blau, Igor Wolfgang
- Ogawa, Seishi
- Gerbitz, Armin
- Wagner, Eva M.
- Schrezenmeier, Hubert
- Kuchenbauer, Florian
- Kobbe, Guido
- Koldehoff, Michael
- Bullinger, Lars
- Thiede, Christian
- Venue
- Journal of Clinical Oncology
- Published
- 2019-02-10
- Volume
- 37
- Issue
- 5
- Pages
- 375-385
- ISSN
- 0732-183X (ISSN-L)
- 1527-7755
- OpenAlex
- W2899711966
- Cited by
- 223
- References
- 46
- Citations by year
- 2026: 12 · 2025: 14 · 2024: 31 · 2023: 28 · 2022: 38 · 2021: 39 · 2020: 36 · 2019: 23 · 2018: 1 · 2012: 1
- FWCI
- 17.77
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Clinical Oncology (publishedVersion)
- PubMed (publishedVersion)
- MDC Repository (Max-Delbrueck-Center for Molecular Medicine) (submittedVersion)
- Funders
- Japan Society for the Promotion of Science (19H05656, 15H05909)
- Topics
- Health Sciences › Medicine › Hematology › Hematopoietic Stem Cell Transplantation
- Health Sciences › Medicine › Hematology › Acute Myeloid Leukemia Research
- Health Sciences › Medicine › Surgery › Transplantation: Methods and Outcomes
- Keywords
- clonal hematopoiesis of indeterminate potential, allogeneic hematopoietic stem cell transplantation, donor eligibility, chronic graft-versus-host disease, relapse and progression, clonal mutations, clonal expansion, donor cell leukemia, overall survival
- MeSH terms
- Age Factors, Aged, Female, Gene Frequency, Graft vs Host Disease, Hematopoiesis, Hematopoietic Stem Cells, Humans, Male, Middle Aged, Mutation, Retrospective Studies, Transplantation, Homologous, Treatment Outcome, Hematopoietic Stem Cell Transplantation, Hematologic Neoplasms, Unrelated Donors
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