Low absolute peripheral blood CD4+ T-cell count predicts poor prognosis in R-CHOP-treated patients with diffuse large
Y Kusano1, M Yokoyama1, Y Terui1
1Department of Hematology Oncology, Hematology Oncology, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.
Blood Cancer Journal
|April 22, 2017
Summary
A low absolute CD4+ T-cell count (ACD4C) at diagnosis is a poor prognostic marker for diffuse large B-cell lymphoma (DLBCL) patients treated with R-CHOP. This finding helps predict patient outcomes and inform treatment strategies.
Area of Science:
- Oncology
- Immunology
- Hematology
Background:
- The absolute peripheral blood lymphocyte count is a prognostic factor in diffuse large B-cell lymphoma (DLBCL) patients treated with R-CHOP.
- The specific lymphocyte population reflecting DLBCL prognosis remains unclear.
Purpose of the Study:
- To investigate the prognostic significance of peripheral blood lymphocyte populations in DLBCL patients treated with R-CHOP.
- To determine if absolute CD4+ T-cell count (ACD4C) is an independent prognostic marker in DLBCL.
Main Methods:
- Analysis of 355 DLBCL patients treated with R-CHOP between 2006 and 2013.
- Correlation of absolute CD4+ T-cell count (ACD4C) at diagnosis with response rates and survival outcomes.
- Multivariate analysis to assess ACD4C as an independent prognostic marker.
Main Results:
- A low ACD4C at diagnosis negatively correlated with overall response rate and complete response rate (P<0.00001).
- ACD4C < 343 × 10^6/l significantly impacted 5-year progression-free survival and overall survival (P<0.00001 and P<0.00000001, respectively).
- Multivariate analysis identified ACD4C as an independent prognostic marker (hazard ratio=2.2, P<0.01).
Conclusions:
- A low absolute CD4+ T-cell count (ACD4C) at diagnosis is an independent poor prognostic marker in DLBCL patients.
- ACD4C can aid in predicting outcomes for DLBCL patients undergoing R-CHOP treatment.
- This finding may inform risk stratification and treatment decisions for DLBCL.


