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Effect of time to relapse on overall survival in patients with mantle cell lymphoma following autologous haematopoietic cell transplantation.
Riedell, Peter A; Hamadani, Mehdi; Ahn, Kwang W; Litovich, Carlos; Brunstein, Claudio G; Cashen, Amanda F; Cohen, Jonathon B; Epperla, Narendranath; Hill, Brian T; Im, Annie; Inwards, David J; Lister, John; McCarty, John M; Ravi Kiran Pingali, Sai; Shadman, Mazyar; Shaughnessy, Paul; Solh, Melhem; Stiff, Patrick J; Vose, Julie M; Kharfan-Dabaja, Mohamed A; Herrera, Alex F; Sauter, Craig S; Smith, Sonali M.
Afiliação
  • Riedell PA; Division of Hematology and Oncology, University of Chicago Medicine, Chicago, IL, USA.
  • Hamadani M; Department of Medicine, CIBMTR® (Center for International Blood and Marrow Transplant Research), Medical College of Wisconsin, Milwaukee, WI, USA.
  • Ahn KW; BMT & Cellular Therapy Program, Department of Medicine, Medical College of Wisconsin, Milwaukee, WI, USA.
  • Litovich C; Department of Medicine, CIBMTR® (Center for International Blood and Marrow Transplant Research), Medical College of Wisconsin, Milwaukee, WI, USA.
  • Brunstein CG; Division of Biostatistics, Institute for Health and Equity, Medical College of Wisconsin, Milwaukee, WI, USA.
  • Cashen AF; Department of Medicine, CIBMTR® (Center for International Blood and Marrow Transplant Research), Medical College of Wisconsin, Milwaukee, WI, USA.
  • Cohen JB; Department of Medicine, Adult Blood and Marrow Transplant Program, University of Minnesota, Minneapolis, MN, USA.
  • Epperla N; Division of Oncology, Washington University School of Medicine, Saint Louis, MO, USA.
  • Hill BT; Department of Hematology and Medical Oncology, Winship Cancer Institute, Emory University School of Medicine, Atlanta, GA, USA.
  • Im A; Division of Hematology, Department of Medicine, The James Cancer Hospital and Solove Research Institute, The Ohio State University, Columbus, OH, USA.
  • Inwards DJ; Department of Hematology and Medical Oncology, Taussig Cancer Institute, Cleveland Clinic, Cleveland, OH, USA.
  • Lister J; Division of Hematology/Oncology, University of Pittsburgh, UPMC Hillman Cancer Center, Pittsburgh, PA, USA.
  • McCarty JM; Division of Hematology, Mayo Clinic, Rochester, MN, USA.
  • Ravi Kiran Pingali S; Division of Hematology and Cellular Therapy, Allegheny Health Network Cancer Institute, Pittsburgh, PA, USA.
  • Shadman M; Bone Marrow Transplant Program, Department of Internal Medicine, Virginia Commonwealth University, Richmond, VA, USA.
  • Shaughnessy P; Houston Methodist Cancer Center, Houston, TX, USA.
  • Solh M; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
  • Stiff PJ; Medical Oncology Division, University of Washington, Seattle, WA, USA.
  • Vose JM; Sarah Cannon Transplant and Cellular Therapy Program Methodist Hospital, San Antonio, TX, USA.
  • Kharfan-Dabaja MA; The Blood and Marrow Transplant Group of Georgia, Northside Hospital, Atlanta, GA, USA.
  • Herrera AF; Department of Medicine, Loyola University Medical Center, Maywood, IL, USA.
  • Sauter CS; Division of Hematology/Oncology, University of Nebraska Medical Center, Omaha, NE, USA.
  • Smith SM; Division of Hematology-Oncology, Blood and Marrow Transplantation Program, Mayo Clinic, Jacksonville, FL, USA.
Br J Haematol ; 195(5): 757-763, 2021 12.
Article em En | MEDLINE | ID: mdl-34581433
ABSTRACT
In young and fit patients with mantle cell lymphoma (MCL), intensive induction therapy followed by a consolidative autologous haematopoietic cell transplant (autoHCT) is the standard of care in the front-line setting. Recently, time-to-event analysis has emerged as an important risk assessment tool in lymphoma, though its impact in MCL is not well defined. We utilized the Center for International Blood and Marrow Transplant Research database to evaluate the effect of post-autoHCT time to relapse on overall survival (OS) over time in 461 patients who underwent autoHCT within 12 months of MCL diagnosis. On multivariate analysis, the impact of relapse on OS was greatest at the six-month [hazard ratio (HR) = 7·68], 12-month (HR = 6·68), and 18-month (HR = 5·81) landmark timepoints. Using a dynamic landmark model we demonstrate that adjusted OS at five years following each landmark timepoint improved with time for relapsing and non-relapsing patients. Furthermore, early relapse (<18 months) following autoHCT defines a high-risk group with inferior post-relapse OS. This retrospective analysis highlights the impact of time to relapse on OS in MCL patients undergoing up-front autoHCT and emphasizes the need to consider novel therapeutic approaches for patients suffering early relapse.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article