The majority of patients with acute promyelocytic leukemia (APL) possess ei
ther a bcr1 or a bcr3 type fusion between PML and RAR alpha genes. The junc
tion sequences may possibly be a target for immune response and influence s
usceptibility to the disease. In this case, HLA class I allele frequencies
would be different between bcr1 and bcr3 patients, To test this hypothesis,
we typed 102 APL patients for HLA-A, -B and -Cw alleles. The A*1, A*30, B*
51, B*41, Cw*0602, and Cw*1701 alleles showed a different distribution betw
een bcr1 and bcr3 patients, but in no case was this statistically significa
nt after correction for the number of comparisons or was confirmed in an in
dependent panel. Moreover, no difference was detected between bcr1 and bcr3
when HLA alleles were grouped according to their peptide binding specifici
ties. Comparing HLA frequencies, clinical features at diagnosis and clinica
l outcome of the 64 patients homogeneously treated with all-trans retinoic
acid and idarubicin (AIDA protocol) we observed a statistically significant
association between HLA-B*13 and risk of relapse by univariate and multiva
riate regression analysis. Should this finding be confirmed in larger futur
e studies, this observation would be of outmost importance in identifying p
atients at high risk of relapse in which more aggressive consolidation ther
apies should be used.