Jl. Steegmann et al., Interferon alpha for chronic myeloid leukemia relapsing after allogeneic bone marrow transplantation, BONE MAR TR, 23(5), 1999, pp. 483-488
Citations number
32
Categorie Soggetti
Hematology,"Medical Research Diagnosis & Treatment
Interferon alpha (IFN alpha) induces cytogenetic responses in patients with
chronic myeloid leukemia (CML) who relapse after allogeneic bone marrow tr
ansplantation (BMT). The purpose of this study was to analyze the therapeut
ic role of IFN alpha in this setting. The experience of a single institutio
n and the published results on this topic were evaluated, We have included
patients who received IFN alpha as a single agent, excluding those patients
who received previous or simultaneous donor leukocyte infusions, The outco
mes of 11 patients treated in our center and those of 108 previously report
ed patients have been analyzed. Five out of 11 patients treated in our inst
itution obtained a complete cytogenetic response (CGR). Two patients contin
ue in complete cytogenetic response 3.5 and 8.2 years later, and the qualit
ative RT-PCR is negative for bcr-abl RNA. The CGR has been transient in one
patient, and follow-up is short in the other two. Secondary effects have b
een acceptable, with myelosuppression as the main toxic effect, Graft-versu
s-host disease did not occur. The literature review identified 108 patients
treated with IFN alpha as sole therapy for relapsed CML, Cytogenetic respo
nse and CGR seem to be better in patients with cytogenetic relapse, as comp
ared to patients with hematologic relapse (61% vs 45% and 45% vs 28%, respe
ctively). Several patients remained in CGR for more than 5 years. This over
view also suggests that CGR is more frequent when IFN alpha is used in pati
ents relapsing after non T-depleted BMT, IFN alpha induces complete cytogen
etic response in nearly half of the patients with CML who relapse after all
ogeneic BMT, with acceptable toxicity, We believe that these results using
IFN alpha as a front-line therapy for CML relapsing after BMT warrant a ran
domized comparison with donor lymphocyte infusions.