The Effect of FcγRIIIA Gene Polymorphism on the Treatment of Diffuse Large B-cell Non-Hodgkin Lymphoma: A Multicenter Prospective Observational Study

被引:4
作者
Buyukkurt, Nurhilal [1 ]
Ozcan, Mehmet Ali [2 ]
Ergene, Ulku [3 ]
Payzin, Bahriye [4 ]
Tunah, Sunay [2 ]
Demirkan, Fatih [2 ]
Ozsan, Hayri [2 ]
Piskin, Ozden [2 ]
Undar, Bulent [2 ]
机构
[1] Baskent Univ, Fac Med, Adana Educ & Res Ctr, Clin Hematol, Adana, Turkey
[2] Dokuz Eylul Univ, Fac Med, Dept Hematol, Izmir, Turkey
[3] Celal Bayar Univ, Fac Med, Dept Hematol, Manisa, Turkey
[4] Ataturk Training & Res Hosp, Clin Hematol, Izmir, Turkey
关键词
Fc gamma RIIIA; Diffuse large B-cell lymphoma; Rituximab; ANTI-CD20; MONOCLONAL-ANTIBODY; RITUXIMAB THERAPY; CHOP; EXPRESSION;
D O I
10.4274/tjh.2013.0367
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: The curative treatment approach for diffuse large B-cell lymphoma (DLBCL) is controversial even in the rituximab (R) era. The aim of this study was to examine the Fc gamma RIIIA gene polymorphism distribution of DLBCL patients who had been treated with R-CHOP (cyclophosphamide, doxorubicin, vincristine, and prednisone) chemotherapy. Furthermore, we investigated the impact of Fc gamma RIIIA gene polymorphism on the overall response rate (ORR) and overall survival (OS). Materials and Methods: Patients from 3 centers in the Aegean region of Turkey who had newly diagnosed CD20-positive DLBCL were enrolled in the study. The single nucleotide polymorphisms of the Fc gamma RIIIA gene were analyzed by real time-PCR. The response to treatment was determined in the middle and at the end of the protocol. During 2 years of follow-up, the patients were clinically and radiologically evaluated for disease status every 3 months. Results: Thirty-six patients were included in the study and the distributions of F/F, V/F, and V/V types of alleles of Fc gamma RIIIA were 25%, 50%, and 25%, respectively. Twenty-seven patients were considered as evaluable according to ORR and OS. The patients' ORR was 87.5%, 100%, and 50% in the F/F, V/F, and V/V allele groups, respectively. We did not establish any statistically significant differences among the 3 alleles groups in respect to ORR (p=0.93). The OS within 2 years in the F/F, V/F, and V/V allele groups was 62.5%, 100%, and 100%, respectively. The OS in the F/F allele group was found to be lower than in the other 2 allele groups (p=0.01). Conclusion: The distribution of gene polymorphisms in our study group was similar to those of previous studies. While ORR was similar between the groups, our results highlight a lower OS in F/F patients compared to other allele groups of Fc gamma RIIIA.
引用
收藏
页码:152 / 157
页数:6
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