Purpose
To compare the efficacy of rituximab, dose-adjusted etoposide, prednisone, vincristine, cyclophosphamide, and doxorubicin (R-DA-EPOCH) with traditional rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) regimens in double-hit lymphoma (DHL) and gene copy number gain (CNG) lymphoma and to contrast the prognosis of these two disease types.
Methods
We retrospectively examined 127 cases of newly diagnosed diffuse large B-cell lymphoma (DLBCL), and used fluorescence in situ hybridization (FISH) to detect genetic abnormalities in
MYC, BCL2,
and
BCL6
.
Results
In the two schemes, the 2-year progression-free survival (PFS) was higher for R-DA-EPOCH group than for R-CHOP (79.8% vs 57.5%,
P
=0.002), this advantage was also reflected in 2-year overall survival (OS) (81.6% vs 58.5%,
P
=0.002). In double CNG patients, R-DA-EPOCH regimen was significantly better than R-CHOP (
P
=0.007 for PFS,
P
=0.010 for OS), and R-DA-EPOCH has the same advantage in DHL patients (
P
=0.001 for PFS,
P
=0.047 for OS). For the two disease types, the PFS for DHL was inferior to that for double CNG (52.9% vs 72.4%,
P
=0.008), while the OS was not significantly different (
P
=0.050). Subgroup analysis showed that the PFS for double CNG with
MYC
and
BCL2
was superior to that for DHL with
MYC
and
BCL2
(
P
=0.043), this trend is also seen in double CNG and DHL with
MYC
and
BCL6
(
P
=0.036). However, the OS was not significantly different between the two subgroups. Multivariate analyses showed that in DLBCL patients with genetic abnormality detected by FISH, the treatment and disease types were independent prognostic factors. The adverse reaction rates were similar in R-DA-EPOCH and R-CHOP (
P
>0.05).
Conclusion
Our retrospective study shows that DHL has a poorer prognosis than double CNG. Based on its improved lifetime and good tolerance, R-DA-EPOCH is a promising regimen for DHL or double CNG, which is expected to become the first-line treatment for high-risk DLBCL types based on more clinical research.