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Age no bar: A CIBMTR analysis of elderly patients undergoing autologous hematopoietic cell transplantation for multiple myeloma.
Munshi, Pashna N; Vesole, David; Jurczyszyn, Artur; Zaucha, Jan Maciej; St Martin, Andrew; Davila, Omar; Agrawal, Vaibhav; Badawy, Sherif M; Battiwalla, Minoo; Chhabra, Saurabh; Copelan, Edward; Kharfan-Dabaja, Mohamed A; Farhadfar, Nosha; Ganguly, Siddhartha; Hashmi, Shahrukh; Krem, Maxwell M; Lazarus, Hillard M; Malek, Ehsan; Meehan, Kenneth; Murthy, Hemant S; Nishihori, Taiga; Olin, Rebecca L; Olsson, Richard F; Schriber, Jeffrey; Seo, Sachiko; Shah, Gunjan; Solh, Melhem; Tay, Jason; Kumar, Shaji; Qazilbash, Muzaffar H; Shah, Nina; Hari, Parameswaran N; D'Souza, Anita.
Afiliação
  • Munshi PN; MedStar Georgetown University Hospital, Washington, DC.
  • Vesole D; John Theurer Cancer Center, Hackensack University Medical Center, Hackensack, New Jersey.
  • Jurczyszyn A; Medicini Department of Hematology, Jagiellonian University Medical College, Krakow, Poland.
  • Zaucha JM; Krakow Branch Polish Society of Haematology and Blood Transfusion, Krakow, Poland.
  • St Martin A; Department of Hematology and Transplantology, Medical University of Gdansk, Gdansk, Poland.
  • Davila O; Center for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee, Wisconsin.
  • Agrawal V; Center for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee, Wisconsin.
  • Badawy SM; Division of Hematology-Oncology, Indiana University School of Medicine, Indianapolis, Indiana.
  • Battiwalla M; Division of Hematology, Oncology and Stem Cell Transplant, Ann and Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois.
  • Chhabra S; Department of Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
  • Copelan E; Sarah Cannon Blood Cancer Network, Nashville, Tennessee.
  • Kharfan-Dabaja MA; Center for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee, Wisconsin.
  • Farhadfar N; Division of Hematology/Oncology, Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.
  • Ganguly S; Department of Hematologic Oncology and Blood Disorders, Levine Cancer Institute, Atrium Health, Charlotte, North Carolina.
  • Hashmi S; Division of Hematology-Oncology, Blood and Marrow Transplantation Program, Mayo Clinic, Jacksonville, Florida.
  • Krem MM; Division of Hematology/Oncology, University of Florida College of Medicine, Gainesville, Florida.
  • Lazarus HM; Division of Hematological Malignancy and Cellular Therapeutics, University of Kansas Health System, Kansas City, Kansas.
  • Malek E; Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota.
  • Meehan K; Oncology Center, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Murthy HS; Markey Cancer Center, University of Kentucky College of Medicine, Lexington, Kentucky.
  • Nishihori T; University Hospitals Cleveland Medical Center, Case Western Reserve University, Cleveland, Ohio.
  • Olin RL; Seidman Cancer Center, University Hospitals Cleveland Medical Center, Cleveland, Ohio.
  • Olsson RF; Norris Cotton Cancer Center, Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire.
  • Schriber J; Division of Hematology-Oncology, Blood and Marrow Transplantation Program, Mayo Clinic, Jacksonville, Florida.
  • Seo S; Department of Blood and Marrow Transplant and Cellular Immunotherapy, Moffitt Cancer Center, Tampa, Florida.
  • Shah G; University of California at San Francisco, San Francisco, California.
  • Solh M; Department of Laboratory Medicine, Karolinska Institute, Stockholm, Sweden.
  • Tay J; Centre for Clinical Research Sormland, Uppsala University, Uppsala, Sweden.
  • Kumar S; Cancer Transplant Institute, Virginia G. Piper Cancer Center, Scottsdale, Arizona.
  • Qazilbash MH; Arizona Oncology, Scottsdale, Arizona.
  • Shah N; Department of Hematology and Oncology, Dokkyo Medical University, Tochigi, Japan.
  • Hari PN; Department of Medicine, Adult Bone Marrow Transplantation Service, Memorial Sloan Kettering Cancer Center, New York, New York.
  • D'Souza A; The Blood and Marrow Transplant Group of Georgia, Northside Hospital, Atlanta, Georgia.
Cancer ; 126(23): 5077-5087, 2020 12 01.
Article em En | MEDLINE | ID: mdl-32965680
ABSTRACT

BACKGROUND:

Upfront autologous hematopoietic stem cell transplantation (AHCT) remains an important therapy in the management of patients with multiple myeloma (MM), a disease of older adults.

METHODS:

The authors investigated the outcomes of AHCT in patients with MM who were aged ≥70 years. The Center for International Blood and Marrow Transplant Research (CIBMTR) database registered 15,999 patients with MM in the United States within 12 months of diagnosis during 2013 through 2017; a total of 2092 patients were aged ≥70 years. Nonrecurrence mortality (NRM), disease recurrence and/or progression (relapse; REL), progression-free survival (PFS), and overall survival (OS) were modeled using Cox proportional hazards models with age at transplantation as the main effect. Because of the large sample size, a P value <.01 was considered to be statistically significant a priori.

RESULTS:

An increase in AHCT was noted in 2017 (28%) compared with 2013 (15%) among patients aged ≥70 years. Although approximately 82% of patients received melphalan (Mel) at a dose of 200 mg/m2 overall, 58% of the patients aged ≥70 years received Mel at a dose of 140 mg/m2 . On multivariate analysis, patients aged ≥70 years demonstrated no difference with regard to NRM (hazard ratio [HR] 1.3; 99% confidence interval [99% CI], 1-1.7 [P = .06]), REL (HR, 1.03; 99% CI, 0.9-1.1 [P = 0.6]), PFS (HR, 1.06; 99% CI, 1-1.2 [P = 0.2]), and OS (HR, 1.2; 99% CI, 1-1.4 [P = .02]) compared with the reference group (those aged 60-69 years). In patients aged ≥70 years, Mel administered at a dose of 140 mg/m2 was found to be associated with worse outcomes compared with Mel administered at a dose of 200 mg/m2 , including day 100 NRM (1% [95% CI, 1%-2%] vs 0% [95% CI, 0%-1%]; P = .003]), 2-year PFS (64% [95% CI, 60%-67%] vs 69% [95% CI, 66%-73%]; P = .003), and 2-year OS (85% [95% CI, 82%-87%] vs 89% [95% CI, 86%-91%]; P = .01]), likely representing frailty.

CONCLUSIONS:

The results of the current study demonstrated that AHCT remains an effective consolidation therapy among patients with MM across all age groups.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transplante de Células-Tronco Hematopoéticas / Mieloma Múltiplo Limite: Aged / Aged80 / Female / Humans / Male / Middle aged País como assunto: America do norte Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transplante de Células-Tronco Hematopoéticas / Mieloma Múltiplo Limite: Aged / Aged80 / Female / Humans / Male / Middle aged País como assunto: America do norte Idioma: En Ano de publicação: 2020 Tipo de documento: Article