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Randomized clinical study comparing aggressive chemotherapy with or without G‐CSF support for high‐risk myelodysplastic syndromes or secondary acute myeloid leukaemia evolving from MDS
Author(s) -
Bernasconi Carlo,
Alessandrino E. Paolo,
Bernasconi Paolo,
Bonfichi Maurizio,
Lazzarino Mario,
Canevari Angelo,
Castelli Guglielmo,
Brusamolino Ercole,
Pagnucco Guido,
Castagnola Carlo
Publication year - 1998
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.1365-2141.1998.00816.x
Subject(s) - medicine , neutropenia , etoposide , chemotherapy , gastroenterology , myelodysplastic syndromes , myeloid leukaemia , surgery , bone marrow
One hundred and five consecutive primary high‐risk myelodysplastic syndromes (MDS) or secondary acute myeloid leukaemia (sAML) evolving from MDS (performance status 0–3, ECOG) entered this study. Induction chemotherapy (CT) consisted of idarubicine 12 mg/m 2 i.v. on days 1 and 2, etoposide 60 mg/m 2 /12 h i.v. for 5 d, Ara‐C 120 mg/m 2 /12 h i.v. for 5 d (one or two courses). Patients were randomized to receive or not G‐CSF (5 μg/kg/d subcutaneously 48 h after the end of CT). 52 cases underwent CT alone and 53 CT+G‐CSF. The CT + G‐CSF patients had a significantly shorter duration of neutropenia (8 v 16 d) with a lower incidence of infections and significantly better responses (CR+PR: 74% v 52%, P < 0.05). 40 patients entered CR: 17 with CT and 23 with CT+G‐CSF. Responders underwent two consolidation courses with the same CT, followed by high‐dose Ara‐C (2 g/m 2 every 12 h for 3 d). Most CRs were clonal. At present 21 responders have relapsed (median relapse‐free survival 4.5 months). Eight responders received an allo‐BMT, six are alive in CR 7–57 months post‐transplant. Therefore allo‐BMT only increases the chance of a long survival and possible cure. In conclusion, CT+G‐CSF did not prolong either CR duration or survival; the growth factor support, however, increased the number of allo‐transplantable cases by inducing higher remission rates and improving clinical conditions.