» Articles » PMID: 19381687

Serum Soluble Fas Level Determines Clinical Outcome of Patients with Diffuse Large B-cell Lymphoma Treated with CHOP and R-CHOP

Abstract

Introduction: We previously reported that serum concentrations of soluble Fas (sFas) predict the clinical outcome of patients with diffuse large B cell lymphoma (DLBCL) after treatment with CHOP but without rituximab (R). Here, we investigated whether the role of sFas as a prognostic factor remains valid in the R-CHOP era.

Patients: We treated 132 patients with DLBCL between October 1995 and September 2002 (group A: without rituximab), and 75 between December 2002 and March 2007 (group B: with rituximab). The patients received eight cycles of CHOP or THP (tetrahydropyranyl-adriamycin)-COP before September 2002, and R-CHOP or R-THP-COP after October 2002. The distribution of patients according to the International Prognostic Index did not significantly differ between the groups.

Results: The 5-year overall survival (OS) rates for patients with sFas levels of > or = 3.0 and <3.0 ng/ml in group A were 19.8 and 61.9% (P < 0.0001), whereas the 3-year OS rates in group B were 54.7 and 92.2% (P < 0.01), respectively. Multivariate analysis using the proportional hazards model revealed that sFas most significantly correlated with overall survival (P < 0.05).

Conclusion: Serum sFas is thus a useful tool for selecting the appropriate therapeutic strategy for DLBCL.

Citing Articles

Clinical significance of oxidative stress for untreated patients with diffuse large B-cell lymphoma.

Nakamura H, Hara T, Mabuchi R, Matsumoto T, Nakamura N, Ninomiya S Mol Clin Oncol. 2021; 16(1):4.

PMID: 34824844 PMC: 8609529. DOI: 10.3892/mco.2021.2437.


Hide or defend, the two strategies of lymphoma immune evasion: potential implications for immunotherapy.

de Charette M, Houot R Haematologica. 2018; 103(8):1256-1268.

PMID: 30006449 PMC: 6068015. DOI: 10.3324/haematol.2017.184192.


Rationale for Adjunctive Therapies for Pediatric Sepsis Induced Multiple Organ Failure.

Podd B, Simon D, Lopez S, Nowalk A, Aneja R, Carcillo J Pediatr Clin North Am. 2017; 64(5):1071-1088.

PMID: 28941536 PMC: 5663307. DOI: 10.1016/j.pcl.2017.06.007.


Microenvironment abnormalities and lymphomagenesis: Immunological aspects.

Taylor J, Gribben J Semin Cancer Biol. 2015; 34:36-45.

PMID: 26232774 PMC: 4592463. DOI: 10.1016/j.semcancer.2015.07.004.


Multiparameter analysis of homogeneously R-CHOP-treated diffuse large B cell lymphomas identifies CD5 and FOXP1 as relevant prognostic biomarkers: report of the prospective SAKK 38/07 study.

Tzankov A, Leu N, Muenst S, Juskevicius D, Klingbiel D, Mamot C J Hematol Oncol. 2015; 8:70.

PMID: 26071053 PMC: 4472251. DOI: 10.1186/s13045-015-0168-7.


References
1.
Cheng J, Zhou T, Liu C, Shapiro J, BRAUER M, Kiefer M . Protection from Fas-mediated apoptosis by a soluble form of the Fas molecule. Science. 1994; 263(5154):1759-62. DOI: 10.1126/science.7510905. View

2.
Suda T, Takahashi T, Golstein P, Nagata S . Molecular cloning and expression of the Fas ligand, a novel member of the tumor necrosis factor family. Cell. 1993; 75(6):1169-78. DOI: 10.1016/0092-8674(93)90326-l. View

3.
Cheson B, Horning S, Coiffier B, Shipp M, Fisher R, Connors J . Report of an international workshop to standardize response criteria for non-Hodgkin's lymphomas. NCI Sponsored International Working Group. J Clin Oncol. 1999; 17(4):1244. DOI: 10.1200/JCO.1999.17.4.1244. View

4.
Griffith T, Brunner T, Fletcher S, Green D, Ferguson T . Fas ligand-induced apoptosis as a mechanism of immune privilege. Science. 1995; 270(5239):1189-92. DOI: 10.1126/science.270.5239.1189. View

5.
. National Cancer Institute sponsored study of classifications of non-Hodgkin's lymphomas: summary and description of a working formulation for clinical usage. The Non-Hodgkin's Lymphoma Pathologic Classification Project. Cancer. 1982; 49(10):2112-35. DOI: 10.1002/1097-0142(19820515)49:10<2112::aid-cncr2820491024>3.0.co;2-2. View