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Treatment of anaemia in myelodysplastic syndromes with prolonged administration of recombinant human granulocyte colony‐stimulating factor and erythropoietin
Author(s) -
Mantovani Luisa,
Lentini Giuseppe,
Hentschel Bettina,
Wickramanayake Premaratne Dias,
Loeffler Markus,
Diehl Volker,
Tesch Hans
Publication year - 2000
Publication title -
british journal of haematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.907
H-Index - 186
eISSN - 1365-2141
pISSN - 0007-1048
DOI - 10.1046/j.1365-2141.2000.02016.x
Subject(s) - erythropoietin , medicine , granulocyte colony stimulating factor , myelodysplastic syndromes , granulocyte , gastroenterology , anemia , cytokine , bone marrow , refractory (planetary science) , immunology , chemotherapy , biology , astrobiology
Treatment with recombinant human erythropoietin (rhEPO) improves anaemia in ≈ 20% of the patients with myelodysplastic syndromes (MDS). Recent reports suggest that a combination treatment with rhEPO plus recombinant human granulocyte colony‐stimulating factor (rhG‐CSF) given for up to 18 weeks may result in a higher erythroid response rate than with rhEPO alone. We investigated the potential advantage of an even more prolonged schedule of combined rhG‐CSF and rhEPO treatment to obtain and maintain stable responses. In a phase II study, 33 patients with MDS [17 with refractory anaemia (RA), eight with RA with ringed sideroblasts (RARS), eight with RA with excess blasts (RAEB) with bone marrow blast counts less than 20%] were scheduled to receive at least 36 weeks of combined therapy with rhG‐CSF and rhEPO. Seventeen of 28 evaluable patients demonstrated an erythroid response [61%; 95% confidence interval (CI) 41–78] after 12 weeks of treatment. The erythroid response rate was 80% (20 of 25 evaluable patients; 95% CI 59–93) after 36 weeks. Seven of these responses developed between week 12 and week 36, whereas two initially responding patients became refractory. The cytokine therapy was generally well tolerated. Nineteen of the 20 patients responding after 36 weeks continued to be treated with both cytokines. After 1 year and 2 years of continuous combined treatment, 50% of the initially included patients showed a continuing response. Our results suggest that a prolonged combination treatment with rhG‐CSF and rhEPO is highly effective in achieving a stable and long‐lasting erythroid response in many patients with MDS and low blast count.