Abstract
We conducted a nationwide retrospective study to evaluate the prognostic influence of +1, der(1;7)(q10;p10) [hereafter der(1;7)] and −7/del(7q) after allogeneic hematopoietic stem cell transplantation (allo-HSCT) for de novo myelodysplastic syndromes (MDS). In this database, 69 MDS patients with der(1;7), 75 with −7/del(7q), and 511 with normal karyotype (NK) underwent allo-HSCT at advanced disease status. The 3-year overall survival (OS) and cumulative incidence of relapse (CIR) were 50.4 and 19.4% for those with der(1;7), 36.2 and 38.4% for −7/del(7q), and 51.1 and 20.7% for NK, respectively. In the multivariate analysis, the presence of −7/del(7q) correlated with a significantly shorter OS (HR [95% CI], 1.38 [1.00–1.89]; P = 0.048) and higher CIR (HR, 2.11 [1.36–3.28]; P = 0.001) than those with NK. There were 23 patients with der(1;7), 29 with −7/del(7q), and 347 with NK who underwent allo-HSCT at early disease status. The 3-year OS and CIR were as follows: 47.3 and 9.5% for the der(1;7) group, 70.5 and 13.8% for −7/del(7q), and 70.9 and 5.6% for NK, respectively. No significant differences were observed in OS and CIR among three groups. The impact of the loss of chromosome 7q on OS and CIR may differ based on its type and disease status after allo-HSCT for MDS.
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Acknowledgements
This work was supported in part by the Practical Research Project for Allergic Diseases and Immunology (Research Technology of Medical Transplantation) from the Japan Agency for Medical Research and Development, AMED. The authors would like to thank all the physicians and data managers at the various institutes who contributed valuable data on transplantation to the Japan Society for Hematopoietic Cell Transplantation (JSHCT) and all the members of the data management committees of JSHCT; a complete membership list of the “Adult Myelodysplastic Syndrome Working Group of the JSHCT” appears in the “Appendix”.
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HI and YM designed the research, organized the project, analyzed the data, and wrote the manuscript. HI, KA, JA, TI, KI, and YM collected data from TRUMP. HI, KA, JA, TI, KI, NU, TF, YO, SO, NU, TE, KI, YO, MT, TI, YA, and YM interpreted data and reviewed and approved the final manuscript.
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Appendix
The following institutions and hematologists contributed to this study: Nagasaki University: Dr. H. Itonaga and Dr. Y. Miyazaki; Kyoto University: Dr. A. Takeda and Dr. K. Aoki; Kanagawa Cancer Center: Dr. J. Aoki, Dr. M. Tanaka, and Dr. T Takahana; Kanazawa University Hospital: Dr. K. Ishiyama; Kobe City Medical General Hospital: Dr. Y. Shimomura and Dr. T. Ishikawa; Keio University School of Medicine: Drs. J. Kato and S. Okamoto; Japanese Red Cross Nagoya First Hospital: Dr. Y. Ozawa; Tokyo Metropolitan Cancer and Infectious Disease Centre Komagome Hospital: Drs. K. Kakizoe and N. Doki; JA Aichi Konan Kosei Hospital: Dr. A. Kohno; Toranomon Hospital: Dr. S. Takagi; Aichi Medical University: Dr. A. Takami; Hyogo College of Medicine: Dr. H. Tamaki; Akita University Hospital: Dr. M. Hirokawa; Mishuku Hospital: Dr. K. Masuoka; Niigata University: Dr. M. Masuko; Kinki University: Dr. K. Ashizawa and Dr. T. Ashida; NTT Medical Center Tokyo: Dr. R. Kida and Dr. K. Usuki; Hamanomachi Hospital: Dr. T. Eto; Sapporo Hokuyu Hospital: Dr. K. Minauchi and Dr. S. Ohta; Tohoku University Hospital: Dr. Y. Onishi; Kanazawa University Graduate School of Medical Sciences: Dr. S. Nakao; Shizuoka Cancer Center: Dr. T. Enami and Dr. T. Ikeda; Kansai Medical University Hirakata Hospital: Dr. K. Ishii; Tokyo Metropolitan Geriatric Hospital: Dr. S. Kobayashi; Tokai University School of Medicine: Dr. S. Machida; Osaka City University: Dr. H. Koh; National Cancer Center Hospital: Dr. T. Suzuki; The University of Tokyo: Dr. T. Konuma; Nagoya University Graduate School of Medicine: Dr. K. Miyao and Dr. T. Morishita; Tokyo Women’s Medical University: Dr. K. Yoshinaga; Ishikawa Prefectural Central Hospital: Dr. Y. Mizumaki and Dr. C. Sugimori; Kokura Memorial Hospital: Dr. A. Yonezawa; Okawama University Hospital: Dr S. Fujii.
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Itonaga, H., Ishiyama, K., Aoki, K. et al. Clinical impact of the loss of chromosome 7q on outcomes of patients with myelodysplastic syndromes treated with allogeneic hematopoietic stem cell transplantation. Bone Marrow Transplant 54, 1471–1481 (2019). https://doi.org/10.1038/s41409-019-0469-5
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DOI: https://doi.org/10.1038/s41409-019-0469-5
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