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ATLの臨床病型に基づいた治療法選択のアルゴリズム(高齢者:70歳以上)

出典
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1: 日本血液学会編. 造血器腫瘍診療ガイドライン 2023年版, 2023; 金原出版, p337.

ATL臨床病型の診断基準

出典
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1: Diagnostic criteria and classification of clinical subtypes of adult T-cell leukaemia-lymphoma. A report from the Lymphoma Study Group (1984-87).
著者: Shimoyama M.
雑誌名: Br J Haematol. 1991 Nov;79(3):428-37. doi: 10.1111/j.1365-2141.1991.tb08051.x.
Abstract/Text: 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 (less than 4 x 10(9)/l), no hypercalcaemia (corrected calcium level less than 2.74 mmol/l), lactate dehydrogenase (LDH) value of up to 1.5 x 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 x 10(9)/l or more) with T-lymphocytosis more than 3.5 x 10(9)/l, 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.
Br J Haematol. 1991 Nov;79(3):428-37. doi: 10.1111/j.1365-2141.1991.tb...

ATL臨床病型ごとの全生存曲線

出典
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1: Diagnostic criteria and classification of clinical subtypes of adult T-cell leukaemia-lymphoma. A report from the Lymphoma Study Group (1984-87).
著者: Shimoyama M.
雑誌名: Br J Haematol. 1991 Nov;79(3):428-37. doi: 10.1111/j.1365-2141.1991.tb08051.x.
Abstract/Text: 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 (less than 4 x 10(9)/l), no hypercalcaemia (corrected calcium level less than 2.74 mmol/l), lactate dehydrogenase (LDH) value of up to 1.5 x 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 x 10(9)/l or more) with T-lymphocytosis more than 3.5 x 10(9)/l, 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.
Br J Haematol. 1991 Nov;79(3):428-37. doi: 10.1111/j.1365-2141.1991.tb...

末梢血中のATL細胞(急性型)

フラワーセルとよばれる
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1: 著者提供

皮膚病変の肉眼像

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1: 著者提供

頸部リンパ節病変のCT像

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1: 著者提供

中枢神経病変のMRI像

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1: 著者提供

胃病変の内視鏡像

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1: 著者提供

併発したpneumocystis jiroveci肺炎の単純XP像

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1: 著者提供

VCAP療法

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1: 著者提供

AMP療法

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1: 著者提供

VECP療法

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1: 著者提供

中枢神経浸潤予防

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1: 著者提供

開始延期の規準

回復したら、使用量を変更せず再開する。
血小板数が<70,000 /uLの場合、他の基準を満たせば髄注はスキップして全身化学療法を行う。
 
出典
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1: 飛内賢正, 木下朝博, 塚崎邦弘(監), 永井宏和, 山口素子, 丸山大(編). 悪性リンパ腫治療マニュアル 改訂第5版. 金原出版, 2020.

薬剤使用量減量の規準

出典
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1: 飛内賢正, 木下朝博, 塚崎邦弘(監), 永井宏和, 山口素子, 丸山大(編). 悪性リンパ腫治療マニュアル 改訂第5版. 金原出版, 2020.

Ccr値によるCBDCAの使用量の変更規定

出典
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1: 著者提供

ATLの臨床病型に基づいた治療法選択のアルゴリズム(若年者:70歳未満)

出典
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1: 日本血液学会編. 造血器腫瘍診療ガイドライン 2023年版, 2023; 金原出版, p337.

ATLの臨床病型に基づいた治療法選択のアルゴリズム(高齢者:70歳以上)

出典
img
1: 日本血液学会編. 造血器腫瘍診療ガイドライン 2023年版, 2023; 金原出版, p337.

ATL臨床病型の診断基準

出典
imgimg
1: Diagnostic criteria and classification of clinical subtypes of adult T-cell leukaemia-lymphoma. A report from the Lymphoma Study Group (1984-87).
著者: Shimoyama M.
雑誌名: Br J Haematol. 1991 Nov;79(3):428-37. doi: 10.1111/j.1365-2141.1991.tb08051.x.
Abstract/Text: 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 (less than 4 x 10(9)/l), no hypercalcaemia (corrected calcium level less than 2.74 mmol/l), lactate dehydrogenase (LDH) value of up to 1.5 x 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 x 10(9)/l or more) with T-lymphocytosis more than 3.5 x 10(9)/l, 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.
Br J Haematol. 1991 Nov;79(3):428-37. doi: 10.1111/j.1365-2141.1991.tb...