Revised adult T-cell leukemia-lymphoma international consensus meeting report

  • Lucy B. Cook
  • , Shigeo Fuji
  • , Olivier Hermine
  • , Ali Bazarbachi
  • , Juan Carlos Ramos
  • , Lee Ratner
  • , Steve Horwitz
  • , Paul Fields
  • , Alina Tanase
  • , Horia Bumbea
  • , Kate Cwynarski
  • , Graham Taylor
  • , Thomas A. Waldmann
  • , Achilea Bittencourt
  • , Ambroise Marcais
  • , Felipe Suarez
  • , David Sibon
  • , Adrienne Phillips
  • , Matthew Lunning
  • , Reza Farid
  • Yoshitaka Imaizumi, Ilseung Choi, Takashi Ishida, Kenji Ishitsuka, Takuya Fukushima, Kaoru Uchimaru, Akifumi Takaori-Kondo, Yoshiki Tokura, Atae Utsunomiya, Masao Matsuoka, Kunihiro Tsukasaki, Toshiki Watanabe

Research output: Contribution to journalArticlepeer-review

Abstract

PURPOSE Adult T-cell leukemia-lymphoma (ATL) is a distinct mature T-cell malignancy caused by chronic infection with human T-lymphotropic virus type 1 with diverse clinical features and prognosis. ATL remains a challenging disease as a result of its diverse clinical features, multidrug resistance of malignant cells, frequent large tumor burden, hypercalcemia, and/or frequent opportunistic infection. In 2009, we published a consensus report to define prognostic factors, clinical subclassifications, treatment strategies, and response criteria. The 2009 consensus report has become the standard reference for clinical trials in ATL and a guide for clinical management. Since the last consensus there has been progress in the understanding of the molecular pathophysiology of ATL and risk-adapted treatment approaches. METHODS Reflecting these advances, ATL researchers and clinicians joined together at the 18th International Conference on Human Retrovirology—Human T-Lymphotropic Virus and Related Retroviruses—in Tokyo, Japan, March, 2017, to review evidence for current clinical practice and to update the consensus with a new focus on the subtype classification of cutaneous ATL, CNS lesions in aggressive ATL, management of elderly or transplantation-ineligible patients, and treatment strategies that incorporate up-front allogeneic hematopoietic stem-cell transplantation and novel agents. RESULTS As a result of lower-quality clinical evidence, a best practice approach was adopted and consensus statements agreed on by coauthors (. 90% agreement).

Original languageEnglish
Pages (from-to)677-687
Number of pages11
JournalJournal of Clinical Oncology
Volume37
Issue number8
DOIs
StatePublished - Mar 10 2019

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