Volume 114, Issue 1 pp. 111-113

A phase II trial of pirfenidone (5-methyl-1-phenyl-2-[1H]-pyridone), a novel anti-fibrosing agent, in myelofibrosis with myeloid metaplasia

Ruben A. Mesa

Ruben A. Mesa

Division of Hematology and Internal Medicine,

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Ayalew Tefferi

Ayalew Tefferi

Division of Hematology and Internal Medicine,

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Michelle A. Elliott

Michelle A. Elliott

Division of Hematology and Internal Medicine,

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H. Clark Hoagland

H. Clark Hoagland

Division of Hematology and Internal Medicine,

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Timothy G. Call

Timothy G. Call

Division of Hematology and Internal Medicine,

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Georgene S. Schroeder

Georgene S. Schroeder

Cancer Center Statistics Unit, and

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Soo-Young Yoon

Soo-Young Yoon

Division of Hematopathology, Mayo Clinic, Rochester, MN, and

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Chin-Yang Li

Chin-Yang Li

Division of Hematopathology, Mayo Clinic, Rochester, MN, and

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Leigh A. Gray

Leigh A. Gray

Division of Hematology and Internal Medicine,

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S. Margolin

S. Margolin

Marnac Inc., Dallas, TX, USA

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C. Christopher Hook

C. Christopher Hook

Division of Hematology and Internal Medicine,

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First published: 12 January 2002
Citations: 37
Dr C. Christopher Hook, Division of Hematology and Internal Medicine, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA. E-mail: [email protected]

Abstract

The anti-fibrotic and cytokine modulatory properties of pirfenidone suggest its usefulness in the treatment of myelofibrosis with myeloid metaplasia (MMM). In a prospective study, 28 patients with MMM were treated with oral pirfenidone. Twelve patients completed 1 year of therapy; 13 were withdrawn because of disease progression and three because of drug intolerance. Only one patient experienced a clinically relevant benefit with respect to anaemia and splenomegaly. The overall lack of clinical benefit correlated with no significant improvement in the bone marrow morphological features of the disease. We conclude that pirfenidone has no significant clinical or biological activity in MMM.

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