TY - JOUR
T1 - Revised adult T-cell leukemia-lymphoma international consensus meeting report
AU - Cook, Lucy B.
AU - Fuji, Shigeo
AU - Hermine, Olivier
AU - Bazarbachi, Ali
AU - Ramos, Juan Carlos
AU - Ratner, Lee
AU - Horwitz, Steve
AU - Fields, Paul
AU - Tanase, Alina
AU - Bumbea, Horia
AU - Cwynarski, Kate
AU - Taylor, Graham
AU - Waldmann, Thomas A.
AU - Bittencourt, Achilea
AU - Marcais, Ambroise
AU - Suarez, Felipe
AU - Sibon, David
AU - Phillips, Adrienne
AU - Lunning, Matthew
AU - Farid, Reza
AU - Imaizumi, Yoshitaka
AU - Choi, Ilseung
AU - Ishida, Takashi
AU - Ishitsuka, Kenji
AU - Fukushima, Takuya
AU - Uchimaru, Kaoru
AU - Takaori-Kondo, Akifumi
AU - Tokura, Yoshiki
AU - Utsunomiya, Atae
AU - Matsuoka, Masao
AU - Tsukasaki, Kunihiro
AU - Watanabe, Toshiki
N1 - Publisher Copyright:
Copyright © 2019 American Society of Clinical Oncology. All rights reserved.
PY - 2019/3/10
Y1 - 2019/3/10
N2 - 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).
AB - 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).
UR - http://www.scopus.com/inward/record.url?scp=85062623443&partnerID=8YFLogxK
U2 - 10.1200/JCO.18.00501
DO - 10.1200/JCO.18.00501
M3 - Article
C2 - 30657736
AN - SCOPUS:85062623443
SN - 0732-183X
VL - 37
SP - 677
EP - 687
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
IS - 8
ER -