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Late effects after ablative allogeneic stem cell transplantation for adolescent and young adult acute myeloid leukemia.
Lee, Catherine J; Kim, Soyoung; Tecca, Heather R; Bo-Subait, Stephanie; Phelan, Rachel; Brazauskas, Ruta; Buchbinder, David; Hamilton, Betty K; Battiwalla, Minoo; Majhail, Navneet S; Lazarus, Hillard M; Shaw, Peter J; Marks, David I; Litzow, Mark R; Chhabra, Saurabh; Inamoto, Yoshihiro; DeFilipp, Zachariah; Hildebrandt, Gerhard C; Olsson, Richard F; Kasow, Kimberly A; Liesveld, Jane L; Rotz, Seth J; Badawy, Sherif M; Bhatt, Neel S; Yared, Jean A; Page, Kristin M; Arellano, Martha L; Kent, Michael; Farhadfar, Nosha; Seo, Sachiko; Hematti, Peiman; Freytes, César O; Rovó, Alicia; Ganguly, Siddhartha; Nathan, Sunita; Burns, Linda; Shaw, Bronwen E; Muffly, Lori S.
Afiliação
  • Lee CJ; Utah Blood and Marrow Transplant Program, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT.
  • Kim S; Center for International Blood and Marrow Transplant Research (CIBMTR), Department of Medicine, and.
  • Tecca HR; Division of Biostatics, Institute for Heath and Equity, Medical College of Wisconsin, Milwaukee, WI.
  • Bo-Subait S; Center for International Blood and Marrow Transplant Research (CIBMTR), Department of Medicine, and.
  • Phelan R; CIBMTR, National Marrow Donor Program/Be The Match, Minneapolis, MN.
  • Brazauskas R; Center for International Blood and Marrow Transplant Research (CIBMTR), Department of Medicine, and.
  • Buchbinder D; Center for International Blood and Marrow Transplant Research (CIBMTR), Department of Medicine, and.
  • Hamilton BK; Division of Biostatics, Institute for Heath and Equity, Medical College of Wisconsin, Milwaukee, WI.
  • Battiwalla M; Division of Pediatric Hematology, Children's Hospital of Orange County, Orange, CA.
  • Majhail NS; Blood and Marrow Transplant Program, Cleveland Clinic Taussig Cancer Institute, Cleveland, OH.
  • Lazarus HM; Hematology Branch, Sarah Cannon Bone Marrow Transplant Program, Nashville, TN.
  • Shaw PJ; Blood and Marrow Transplant Program, Cleveland Clinic Taussig Cancer Institute, Cleveland, OH.
  • Marks DI; Blood and Marrow Transplant Program, University Hospitals Case Medical Center, Case Western Reserve University, Cleveland, OH.
  • Litzow MR; The Children's Hospital of Westmead, Westmead, Australia.
  • Chhabra S; Adult Bone Marrow Transplant, University Hospitals Bristol National Health Service Trust, Bristol, United Kingdom.
  • Inamoto Y; Division of Hematology and Transplant Center, Mayo Clinic Rochester, Rochester, MN.
  • DeFilipp Z; Center for International Blood and Marrow Transplant Research (CIBMTR), Department of Medicine, and.
  • Hildebrandt GC; Division of Hematopoietic Stem Cell Transplantation, National Cancer Center Hospital, Tokyo, Japan.
  • Olsson RF; Blood and Marrow Transplant Program, Massachusetts General Hospital, Boston, MA.
  • Kasow KA; Markey Cancer Center, University of Kentucky, Lexington, KY.
  • Liesveld JL; Department of Laboratory Medicine, Karolinska Institutet, Stockholm, Sweden.
  • Rotz SJ; Centre for Clinical Research Sormland, Uppsala University, Uppsala, Sweden.
  • Badawy SM; Pediatric Hematology Oncology and Bone Marrow and Stem Cell Transplantation Program, University of North Carolina, Chapel Hill, NC.
  • Bhatt NS; Department of Medicine, University of Rochester Medical Center, Rochester, NY.
  • Yared JA; Department of Pediatric Hematology, Oncology, and Blood and Marrow Transplantation, Cleveland Clinic Children's Hospital, Cleveland, OH.
  • Page KM; Division of Hematology, Oncology and Stem Cell Transplant, Ann and Robert H. Lurie Children's Hospital of Chicago, Chicago, IL.
  • Arellano ML; Department of Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, IL.
  • Kent M; Fred Hutchinson Cancer Research Center, Seattle, WA.
  • Farhadfar N; Blood and Marrow Transplantation Program, Division of Hematology/Oncology, Department of Medicine, Greenebaum Comprehensive Cancer Center, University of Maryland, Baltimore, MD.
  • Seo S; Division of Pediatric Blood and Marrow Transplantation, Duke University Medical Center, Durham, NC.
  • Hematti P; Winship Cancer Institute, Emory University, Atlanta, GA.
  • Freytes CO; Levine Children's Hospital, Charlotte, NC.
  • Rovó A; Division of Hematology/Oncology, University of Florida College of Medicine, Gainesville, FL.
  • Ganguly S; Department of Haematology and Oncology, Dokkyo Medical University, Tochigi, Japan.
  • Nathan S; Division of Hematology/Oncology/Bone Marrow Transplantation, Department of Medicine, University of Wisconsin, Madison, WI.
  • Burns L; Texas Transplant Institute, San Antonio, TX.
  • Shaw BE; Inselspital, Universitatsspital Bern, Bern, Switzerland.
  • Muffly LS; Division of Hematological Malignancy and Cellular Therapeutics, University of Kansas Health System, Kansas City, KS.
Blood Adv ; 4(6): 983-992, 2020 03 24.
Article em En | MEDLINE | ID: mdl-32168378
ABSTRACT
There is marked paucity of data regarding late effects in adolescents and young adults (AYAs) who undergo myeloablative conditioning (MAC) allogeneic hematopoietic cell transplantation (HCT) for acute myeloid leukemia (AML). We evaluated late effects and survival in 826 1-year disease-free survivors of MAC HCT for AYA AML, with an additional focus on comparing late effects based upon MAC type (total body irradiation [TBI] vs high-dose chemotherapy only). The estimated 10-year cumulative incidence of subsequent neoplasms was 4% (95% confidence interval [CI], 2%-6%); 10-year cumulative incidence of nonmalignant late effects included gonadal dysfunction (10%; 95% CI, 8%-13%), cataracts (10%; 95% CI, 7%-13%), avascular necrosis (8%; 95% CI, 5%-10%), diabetes mellitus (5%; 95% CI, 3%-7%), and hypothyroidism (3%; 95% CI, 2%-5%). Receipt of TBI was independently associated with a higher risk of cataracts only (hazard ratio [HR], 4.98; P < .0001) whereas chronic graft-versus-host disease (cGVHD) was associated with an increased risk of cataracts (HR, 3.22; P = .0006), avascular necrosis (HR, 2.49; P = .006), and diabetes mellitus (HR, 3.36; P = .03). Estimated 10-year overall survival and leukemia-free survival were 73% and 70%, respectively, and did not differ on the basis of conditioning type. In conclusion, late effects among survivors of MAC HCT for AYA AML are frequent and are more closely linked to cGVHD than type of conditioning.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Leucemia Mieloide Aguda / Transplante de Células-Tronco Hematopoéticas / Doença Enxerto-Hospedeiro Tipo de estudo: Etiology_studies Limite: Adolescent / Adult / Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Leucemia Mieloide Aguda / Transplante de Células-Tronco Hematopoéticas / Doença Enxerto-Hospedeiro Tipo de estudo: Etiology_studies Limite: Adolescent / Adult / Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article