Cited by 1,608T-cell and Retrovirus StudiesViral-associated cancers and disordersCutaneous lymphoproliferative disorders research

Diagnostic criteria and classification of clinical subtypes of adult T‐cell leukaemia‐lymphoma: A REPORT FROM THE LYMPHOMA STUDY GROUP (1984–87)

Shimoyama, M., members of The Lymphoma Study Group (1984–87)·1991·British Journal of Haematology

Abstract

The following diagnostic criteria are proposed to classify four clinical subtypes of HTLV‐1 associated adult T‐cell leukaemia‐lymphoma (ATL): (1) Smouldering type, 5% or more abnormal lymphocytes of T‐cell nature in PB, normal lymphocyte level (< 4 × 10 9/1), no hypercalcaemia (corrected calcium level < 2·74 mmol/1), lactate dehydrogenase (LDH) value of up to 1·5 × the normal upper limit, no lymphadenopathy, no involvement of liver, spleen, central nervous system (CNS), bone and gastrointestinal tract, and neither ascites nor pleural effusion. Skin and pulmonary lesion(s) may be present. In case of less than 5% abnormal T‐lymphocytes in PB, at least one of histologically‐proven skin and pulmonary lesions should be present. (2) Chronic type, absolute lymphocytosis (4 × 10 9/1 or more) with T‐lymphocytosis more than 3·5 × 10 9/1. LDH value up to twice the normal upper limit, no hypercalcaemia, no involvement of CNS, bone and gastrointestinal tract, and neither ascites nor pleural effusion. Lymphadenopathy and involvement of liver, spleen, skin, and lung may be present, and 5% or more abnormal T‐lymphocytes are seen in PB in most cases. (3) Lymphoma type, no lymphocytosis, 1% or less abnormal T‐lymphocytes, and histologically‐proven lymphadenopathy with or without extranodal lesions. (4) Acute type, remaining ATL patients who have usually leukaemic manifestation and tumour lesions, but are not classified as any of the three other types. A total of 818 ATL patients with a mean age of 57 years, newly diagnosed from 1983 to 1987, were analysed by this criteria. There were 448 males and 370 females, and 253 were still alive with a median follow‐up time of 13·3 months from diagnosis, while 565 were dead with a median survival time (MST) of 5·4 months. MST was 6·2 months for acute type, 10·2 months for lymphoma type, 24·3 months for chronic type, and not yet reached for smouldering type. Projected 2‐ and 4‐year survival rates were 16·7% and 5·0% for acute type, 21·3% and 5·7% for lymphoma type, 52·4% and 26 × 9% for chronic type, 77·7% and 62·8% for smouldering type, respectively. Distinct clinical features and laboratory findings of each clinical subtype are described.

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Crossref · 10.1111/j.1365-2141.1991.tb08051.x

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  • The prevalence of ATL amongst HTLV-1 carriers is 5%.

    “with the prevalence of 5% amongst carriers [11,12]”

    From Current State of Therapeutics for HTLV-1 (2024) · cites this paper as [12]

  • ATL therapeutic strategies for patients are determined largely by clinical subtype (acute, lymphoma, chronic, and smouldering).

    “ATL therapeutic strategies for patients are determined largely by clinical subtype (acute, lymphoma, chronic, and smouldering) [12,193].”

    From Current State of Therapeutics for HTLV-1 (2024) · cites this paper as [12]

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Authors
Shimoyama, M., & members of The Lymphoma Study Group (1984–87)
Affiliations
National Cancer Center Hospital (JP)
Corresponding author
Shimoyama, M.
Venue
British Journal of Haematology
Publisher
Wiley
Published
1991-11
Volume
79
Issue
3
Pages
428-437
ISSN
  • 0007-1048 (ISSN-L)
  • 1365-2141
OpenAlex
W2009621572
Cited by
1,608
References
1
Citations by year
2026: 30 · 2025: 64 · 2024: 45 · 2023: 49 · 2022: 55 · 2021: 66 · 2020: 85 · 2019: 57 · 2018: 63 · 2017: 77 · 2016: 59 · 2015: 61 · 2014: 59 · 2013: 50 · 2012: 61
FWCI
6.96
Type
journal article
Language
en
Open access
closed
Locations
  • British Journal of Haematology (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Immunology and Microbiology › Immunology › T-cell and Retrovirus Studies
  • Health Sciences › Medicine › Oncology › Viral-associated cancers and disorders
  • Health Sciences › Medicine › Dermatology › Cutaneous lymphoproliferative disorders research
Keywords
adult T-cell leukemia/lymphoma, HTLV-1, diagnostic criteria, survival, prognostic factors, hypercalcemia, lactate dehydrogenase, lymphocytosis, extranodal involvement, lymphadenopathy, prognostic scoring
MeSH terms
Adult, Aged, Aged, 80 and over, Female, Follow-Up Studies, Humans, Male, Middle Aged, Opportunistic Infections, Prognosis, Leukemia-Lymphoma, Adult T-Cell

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