Volume 110, Issue 2 pp. 370-378

Significance of lung resistance-related protein in the clinical outcome of acute leukaemic patients with reference to P-glycoprotein

Kazue Tsuji

Kazue Tsuji

Department of Medicine, St. Marianna Medical University,

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Toshiko Motoji

Toshiko Motoji

Department of Haematology, Tokyo Women's Medical University,

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Isamu Sugawara

Isamu Sugawara

Department of Pathology, The Research Institute of Tuberculosis,

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Hiroko Shiozaki

Hiroko Shiozaki

Department of Medicine, Saiseikai Maebashi Hospital,

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Yan-Hua Wang

Yan-Hua Wang

Department of Haematology, Tokyo Women's Medical University,

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Sayuri Motomura

Sayuri Motomura

Department of Haematology, Tokyo Women's Medical University,

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Michiko Okada

Michiko Okada

Chromosome Laboratory, Shiseikai Dai-ni Hospital,

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Takeshi Yasunami

Takeshi Yasunami

Department of Haematology, Tokyo Women's Medical University,

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Fumiaki Sano

Fumiaki Sano

Department of Medicine, St. Marianna Medical University,

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Masatomo Takahashi

Masatomo Takahashi

Department of Medicine, St. Marianna Medical University,

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Hiroshi Kawada

Hiroshi Kawada

Department of Haematology, Tokai University,

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Nobuo Maseki

Nobuo Maseki

Department of Medicine, Saitama Cancer Centre, and

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Shigeru Hoshino

Shigeru Hoshino

Department of Medicine, Omiya Red Cross Hospital, Tokyo, Japan

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Masashi Ishida

Masashi Ishida

Department of Medicine, St. Marianna Medical University,

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Hideaki Mizoguchi

Hideaki Mizoguchi

Department of Haematology, Tokyo Women's Medical University,

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First published: 24 December 2001
Citations: 15
Toshiko Motoji, Department of Haematology, Tokyo Women's Medical University, 8-1, Kawada-cho, Shinjuku-ku, Tokyo 162-8666, Japan. E-mail: [email protected]

Abstract

Lung resistance-related protein (LRP) overexpression in leukaemic blast cells from acute leukaemia patients and the effect of LRP or P-glycoprotein (P-gp) on the clinical outcome of acute leukaemia were investigated individually by dividing patients into four groups. The complete remission rate of group I (LRP and P-gp both negative) was 81·7%, group II (only LRP positive) 87·5%, group III (only P-gp positive) 87·1% and group IV (LRP and P-gp both positive) 40·0%. There were no statistical differences between group I and groups II or III, but a significant difference was observed between groups I, II or III and group IV. Median overall survival in group IV was significantly shorter (4·6 months) than in groups I, II or III, although no significant differences were observed between group I and groups II or III (18·9, 20·5 and 31·8 months). There was a tendency for disease-free survival in group III to be longer than that in groups I, II or IV. The reasons for these findings are discussed. Our present results indicate that the co-existence of LRP and P-gp strongly influenced the effectiveness of induction chemotherapy and long-term prognosis, whereas the isolated presence of LRP or P-gp did not.

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