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Autologous Transplantation in Follicular Lymphoma with Early Therapy Failure: A National LymphoCare Study and Center for International Blood and Marrow Transplant Research Analysis.
Casulo, Carla; Friedberg, Jonathan W; Ahn, Kwang W; Flowers, Christopher; DiGilio, Alyssa; Smith, Sonali M; Ahmed, Sairah; Inwards, David; Aljurf, Mahmoud; Chen, Andy I; Choe, Hannah; Cohen, Jonathon; Copelan, Edward; Farooq, Umar; Fenske, Timothy S; Freytes, Cesar; Gaballa, Sameh; Ganguly, Siddhartha; Jethava, Yogesh; Kamble, Rammurti T; Kenkre, Vaishalee P; Lazarus, Hillard; Lazaryan, Aleksandr; Olsson, Richard F; Rezvani, Andrew R; Rizzieri, David; Seo, Sachiko; Shah, Gunjan L; Shah, Nina; Solh, Melham; Sureda, Anna; William, Basem; Cumpston, Aaron; Zelenetz, Andrew D; Link, Brian K; Hamadani, Mehdi.
Afiliação
  • Casulo C; Wilmot Cancer Institute, University of Rochester, Rochester, New York.
  • Friedberg JW; Wilmot Cancer Institute, University of Rochester, Rochester, New York.
  • Ahn KW; Center for International Blood and Marrow Transplant Research, Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin; Division of Biostatistics, Institute for Health and Society, Medical College of Wisconsin, Milwaukee, Wisconsin.
  • Flowers C; Department of Hematology and Medical Oncology, Winship Cancer Institute, Emory University School of Medicine, Atlanta, Georgia.
  • DiGilio A; Center for International Blood and Marrow Transplant Research, Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.
  • Smith SM; Section of Hematology/Oncology, The University of Chicago, Chicago, Illinois.
  • Ahmed S; Department of Stem Cell Transplantation, Division of Cancer Medicine, The University of MD Anderson Cancer Center, Houston, Texas.
  • Inwards D; Division of Hematology, Mayo Clinic, Rochester, Minnesota.
  • Aljurf M; Department of Oncology, King Faisal Specialist Hospital Center & Research, Riydah, Saudi Arabia.
  • Chen AI; Blood and Marrow Transplant Program, Oregon Health and Science University, Portland, Oregon.
  • Choe H; Blood and Marrow Transplant Program, Weill Cornell Medical College, New York, New York.
  • Cohen J; Department of Hematology and Medical Oncology, Winship Cancer Institute, Emory University School of Medicine, Atlanta, Georgia.
  • Copelan E; Department of Hematologic Oncology and Blood Disorders, Levine Cancer Institute, Carolinas HealthCare System, Charlotte, North Carolina.
  • Farooq U; Department of Medicine, University of Iowa, Iowa City, Iowa.
  • Fenske TS; Division of Hematology and Oncology, Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.
  • Freytes C; Blood and Marrow Transplant Program, Texas Transplant Institute, San Antonio, Texas.
  • Gaballa S; Blood and Marrow Transplant Program, Thomas Jefferson University Hospital, Philadelphia, Pennsylvania.
  • Ganguly S; Division of Hematologic Malignancies and Cellular Therapeutics, University of Kansas Medical Center, Kansas City, Kansas.
  • Jethava Y; Blood and Marrow Transplant Program, University of Arkansas for Medical Sciences, Little Rock, Arkansas.
  • Kamble RT; Division of Hematology and Oncology, Center for Cell and Gene Therapy, Baylor College of Medicine, Houston, Texas.
  • Kenkre VP; Division of Hematology and Oncology, University of Wisconsin, Madison, Wisconsin.
  • Lazarus H; Seidman Cancer Center, University Hospitals Cleveland Medical Center, Cleveland, Ohio.
  • Lazaryan A; Blood and Marrow Transplant Program, University of Minnesota, Minneapolis, Minnesota.
  • Olsson RF; Division of Therapeutic Immunology, Department of Laboratory Medicine, Karolinska Institutet, Stockholm, Sweden; Centre for Clinical Research Sormland, Uppsala University, Uppsala, Sweden.
  • Rezvani AR; Blood and Marrow Transplant Program, Stanford Health Care, Stanford, California.
  • Rizzieri D; Division of Hematologic Malignancies and Cellular Therapy, Duke University, Durham, North Carolina.
  • Seo S; National Cancer Research Center, East Hospital, Chiba, Japan.
  • Shah GL; Blood and Marrow Transplant Program, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Shah N; Department of Stem Cell Transplantation, Division of Cancer Medicine, The University of MD Anderson Cancer Center, Houston, Texas.
  • Solh M; The Blood and Marrow Transplant Group of Georgia, Northside Hospital, Atlanta, Georgia.
  • Sureda A; Hematology Department, Institut Català d'Oncologia-Hospitalet, Barcelona, Spain.
  • William B; James Cancer Center, Ohio State Medical Center, Columbus, Ohio.
  • Cumpston A; Blood and Marrow Transplant Program, West Virginia University Hospitals, Morgantown, West Virginia.
  • Zelenetz AD; Blood and Marrow Transplant Program, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Link BK; Division of Hematology and Oncology, Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.
  • Hamadani M; Center for International Blood and Marrow Transplant Research, Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin. Electronic address: mhamadani@mcw.edu.
Biol Blood Marrow Transplant ; 24(6): 1163-1171, 2018 06.
Article em En | MEDLINE | ID: mdl-29242111
ABSTRACT
Patients with follicular lymphoma (FL) experiencing early therapy failure (ETF) within 2 years of frontline chemoimmunotherapy have poor overall survival (OS). We analyzed data from the Center for International Blood and Marrow Transplant Research (CIBMTR) and the National LymphoCare Study (NLCS) to determine whether autologous hematopoietic cell transplant (autoHCT) can improve outcomes in this high-risk FL subgroup. ETF was defined as failure to achieve at least partial response after frontline chemoimmunotherapy or lymphoma progression within 2 years of frontline chemoimmunotherapy. We identified 2 groups the non-autoHCT cohort (patients from the NLCS with ETF not undergoing autoHCT) and the autoHCT cohort (CIBMTR patients with ETF undergoing autoHCT). All patients received rituximab-based chemotherapy as frontline treatment; 174 non-autoHCT patients and 175 autoHCT patients were identified and analyzed. There was no difference in 5-year OS between the 2 groups (60% versus 67%, respectively; P = .16). A planned subgroup analysis showed that patients with ETF receiving autoHCT soon after treatment failure (≤1 year of ETF; n = 123) had higher 5-year OS than those without autoHCT (73% versus 60%, P = .05). On multivariate analysis, early use of autoHCT was associated with significantly reduced mortality (hazard ratio, .63; 95% confidence interval, .42 to .94; P = .02). Patients with FL experiencing ETF after frontline chemoimmunotherapy lack optimal therapy. We demonstrate improved OS when receiving autoHCT within 1 year of treatment failure. Results from this unique collaboration between the NLCS and CIBMTR support consideration of early consolidation with autoHCT in select FL patients experiencing ETF.
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Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 2_ODS3 / 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Assunto principal: Transplante Autólogo / Linfoma Folicular / Transplante de Células-Tronco Hematopoéticas / Rejeição de Enxerto Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Biol Blood Marrow Transplant Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 2_ODS3 / 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Assunto principal: Transplante Autólogo / Linfoma Folicular / Transplante de Células-Tronco Hematopoéticas / Rejeição de Enxerto Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Biol Blood Marrow Transplant Ano de publicação: 2018 Tipo de documento: Article