Proceedings from the National Cancer Institute's Second International Workshop on the Biology, Prevention, and Treatment of Relapse After Hematopoietic Stem Cell Transplantation: part III. Prevention and treatment of relapse after allogeneic transplantation. Conference Paper uri icon

Overview

abstract

  • In the Second Annual National Cancer Institute's Workshop on the Biology, Prevention, and Treatment of Relapse after Hematopoietic Stem Cell Transplantation, the Scientific/Educational Session on the Prevention and Treatment of Relapse after Allogeneic Transplantation highlighted progress in developing new therapeutic approaches since the first relapse workshop. Recent insights that might provide a basis for the development of novel, practical clinical trials were emphasized, including utilization of newer agents, optimization of donor lymphocyte infusion (DLI), and investigation of novel cellular therapies. Dr. de Lima discussed pre-emptive and maintenance strategies to prevent relapse after transplantation, for example, recent promising results suggestive of enhanced graft-versus-tumor activity with hypomethylating agents. Dr. Schmid provided an overview of adjunctive strategies to improve cell therapy for relapse, including cytoreduction before DLI, combination of targeted agents with DLI, and considerations in use of second transplantations. Dr. Porter addressed strategies to enhance T cell function, including ex vivo activated T cells and T cell engineering, and immunomodulatory approaches to enhance T cell function in vivo, including exogenous cytokines and modulation of costimulatory pathways.

publication date

  • September 7, 2013

Research

keywords

  • Antineoplastic Agents
  • Graft vs Tumor Effect
  • Hematologic Neoplasms
  • Hematopoietic Stem Cell Transplantation
  • Myeloablative Agonists
  • Transplantation Conditioning

Identity

PubMed Central ID

  • PMC3938421

Scopus Document Identifier

  • 84890904878

Digital Object Identifier (DOI)

  • 10.1016/j.bbmt.2013.08.012

PubMed ID

  • 24018392

Additional Document Info

volume

  • 20

issue

  • 1