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 - Funding Information:
Supported in part by the National Institute for Health Research Imperial Biomedical Research Centre (L.B.C. and G.T.), core facility Grant No. P30-CA008748 from the National Institutes of Health, National Cancer Institute (S.H.), and the Japan Agency for Medical Research and Development under Grants No. JP18ak0101086h0001 and JP18ck0106338 (T.W. and K.T.).
Funding Information:
Supported in part by the National Institute for Health Research Imperial Biomedical Research Centre (L.B.C. and G.T.), core facility Grant No. P30-CA008748 from the National Institutes of Health, National Cancer Institute (S.H.), and the Japan Agency for Medical Research and Development under Grants No. JP18ak0101086h0001 and JP18ck0106338 (T.W. and K.T.). All participants of the ATL workshop held during the 18th International Conference on Human Retrovirology: HTLV and Related Viruses, March 7-10, Tokyo, Japan, 2017.
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 -