Prognostic Value of High Thymidine Kinase Activity in Previously Untreated Diffuse Large B-Cell Lymphoma Treated by R-CHOP

Blood ◽  
2012 ◽  
Vol 120 (21) ◽  
pp. 1541-1541
Author(s):  
Kazuhito Suzuki ◽  
Yasuhito Terui ◽  
Noriko Nishimura ◽  
Yuko Mishima ◽  
Sakura Sakajiri ◽  
...  

Abstract Abstract 1541 Introduction Thymidine kinase (TK) activity has been investigated as a prognostic factor in hematological malignancies, and several studies have demonstrated that a high TK activity correlates with the disease stage and provides prognostic information on overall survival (OS) and progression free survival (PFS). However, the prognostic significance of TK activity for patients with diffuse large B-cell lymphoma (DLBCL) treated with R-CHOP has not been investigated yet. The purpose of this retrospective study was to investigate the prognostic value of high TK activity compared with other laboratory findings in evaluating OS in patients undergoing R-CHOP for previously untreated DLBCL. Methods We retrospectively analyzed patients treated with R-CHOP for previously untreated DLBCL from September 2003 to October 2008 in our institute. We evaluated serum TK activity, C-reactive protein (CRP), lactate dehydrogenase (LDH), and hemoglobin (Hb) before R-CHOP. The cut-off for TK activity was defined as 14 IU/L. The cut-offs for CRP and LDH were defined as the upper normal limits, and the cut-off for Hb was defined as the lower normal limit. The primary endpoint was OS. The OS and PFS were analyzed by the Kaplan-Meier method, and biological prognostic factors for OS were evaluated by Cox regression analysis. Second, complete response (CR) rate was assessed by the chi square test and Fisher's exact test, comparing patients with and without the prognostic factors. All p-values reported were two-sided, and statistical significance was defined as p < 0.05. Results The clinical records of 242 patients with previously untreated DLBCL were analyzed in this study. The median age of the patients was 65.2 years old (range, 23.2 – 88.1). The median levels of TK activity, CRP, LDH, and Hb were 14.0 IU/L (range, 3.0 – 1100), 0.3 IU/L (range, 0.1 – 21.2), 254.5 IU/L (range, 111.0 – 44432), and 13.1 g/dL (range, 7.7 – 17.0), respectively. Median follow-up time for all patients was 53.0 months. Median OS was 82.3 months (95% CI, 78.6 – 86.0). The OS was significantly worse in patients with high TK activity (p =.001) and anemia (p =.006) by univariate analysis. Median OS in the high and low TK activity groups was 71.7 months (95% CI 63.9 – 79.4) and 85.9 months (95% CI 81.8 – 89.9). In multivariate analysis, the OS was significantly worse in patients with high TK activity (HR 2.640, 95% CI 1.018 – 6.881; p =.046) and anemia (HR 2.228, 95% CI 1.000 – 4.967; p =.050). Median PFS was 73.9 months (95% CI, 69.4 – 78.4). The PFS was significantly worse in patients with high TK activity (p =.000), anemia (p =.005), and high LDH level (p =.010) by univariate analysis. Median PFS in the high and low TK activity groups was 57.3 months (95% CI 48.7 – 66.0) and 80.9 months (95% CI 75.5 – 86.2). In multivariate analysis, PFS was significantly worse in patients with high TK activity (HR 2.809, 95% CI 1.375 – 5.737; p =.005) and anemia (HR 1.902, 95% CI 1.033 – 3.504; p =.039). The CR and overall response rates were 81.4% and 93.0%, respectively. The OS was significantly better in patients who achieved CR than those with partial response or less. Median OS in the CR and non-CR groups was 86.1 months (95% CI 82.7 – 89.5) and 66.0 months (95% CI 53.6 – 78.3), respectively (p <.001). According to the chi square test and Fisher's exact test, the CR rates of patients with high TK activity (p <.001), high CRP (p =.004), and high LDH (p =.019) were significantly worse. The CR rates in the high and low TK activity groups were 68.9% and 92.5%, respectively. The OS for patients with high TK activity who did not achieve CR was even significantly worse than that of both low TK activity patients who did not achieve CR and high TK activity patients who achieved CR (p =.047 and <.001). However, the OS was similar in high and low TK activity group patients who achieved CR (p =.171, Figure 1). Conclusion High TK activity significantly worsened OS and PFS among patients with previously untreated DLBCL who had undergone R-CHOP. While we commonly perform R-CHOP for DLBCL as an initial treatment, our findings show that the OS becomes significantly worse in patients who do not achieve CR by R-CHOP. The OS in patients with high TK activity who did not achieve CR was significantly worse than that with both low TK activity patients who did not achieve CR and high TK activity patients who achieved CR. Our findings suggest that novel treatment strategies for previously untreated DLBCL patients with high TK activity are certainly necessary. Disclosures: No relevant conflicts of interest to declare.

Blood ◽  
2005 ◽  
Vol 106 (11) ◽  
pp. 2085-2085 ◽  
Author(s):  
John Kuruvilla ◽  
Tracy Nagy ◽  
Melania Pintilie ◽  
Armand Keating ◽  
Michael Crump

Abstract INTRODUCTION: PMLCL is an aggressive subtype of non-Hodgkin’s lymphoma with a distinct clinical and gene expression profile. While the results of primary therapy for PMLCL have been shown to be superior to those of DLBCL, the outcomes of salvage chemotherapy and autologous stem cell transplantation (ASCT) for relapsed or refractory disease are not well characterized. We studied the overall response rate (ORR) of this group of patients (pts) to second-line chemotherapy and compared their progression-free (PFS) and overall survival (OS) to a group of pts with DLBCL. METHODS: We retrospectively reviewed our computerized database and charts between Jan 1st 1995 until Dec 31st 2004 and identified 37 pts with PMLCL who underwent salvage chemotherapy. 143 consecutive pts with DLBCL that received salvage chemotherapy between Jan 1st 1999 and Dec 31st 2004 were also identified to serve as a cohort for comparison. All pts had disease that did not respond to or relapsed after initial anthracycline-based chemotherapy. Responses have been retrospectively assessed using International Workshop Criteria. Pts typically received 2–3 cycles of platinum-based salvage therapy to assess chemotherapy sensitivity; responding pts proceeded to PBSC mobilization and subsequent ASCT. The conditioning regimen consisted of high-dose VP16 60 mg/kg day −4 and melphalan 160 mg/m2 day −3 with PBSC infusion day 0. Pts with bulk disease at relapse (> 5cm) received involved field radiation post-ASCT. RESULTS: The median age at the time of salvage chemotherapy was 34 (range 21–64) in the PMLCL group vs. 50 (18–64) in the DLBCL group (P < 0.0001, Wilcoxon test). Advanced stage disease at salvage was found in 46% of PMLCL pts. vs. 49% of DLBCL pts (p=0.74 chi-square test). The distribution of primary refractory (57% PMLCL, 44% DLBCL) and relapsed pts (43% PMLCL, 56% DLBCL) was similar (p=0.17). The ORR to first line salvage chemotherapy was 25% in PMLCL pts vs. 48% in DLBCL pts (p=0.01, chi-square test). 22% of PMLCL and 50% of DLBCL pts were able to proceed to ASCT after all salvage chemotherapy and PBSC mobilization (p=0.002, chi-square). At two years post diagnosis of relapsed or refractory disease, the OS of the PMLCL pts was 31% vs. 50% in DLBCL pts (p=0.03). For pts undergoing ASCT, the 2-year post-ASCT OS (67% PMLCL vs. 59% DLBCL, p=0.99) and PFS (57% PMLCL vs. 36% DLBCL, p=0.64) were similar. Multivariate analysis to determine predictors of survival after progression found that ECOG performance status (2–3 vs. 0, HR=2.9,p=0.01) and primary refractory disease (HR=2, p=0.003) were predictive of OS. Survival was not significantly different between PMLCL and DLBCL types (p=0.18). Multivariate analysis to determine predictors of ORR to salvage chemotherapy showed that ECOG (1 vs. 0, OR=2.6, 2–3 vs. 0, OR=2.6, p=0.05), primary refractory lymphoma (OR= 6.1, p<0.0001) and PMLCL type (OR =2.5, p=0.05) were predictive of lack of response to salvage chemotherapy. CONCLUSIONS: In this “intent to transplant” analysis, relapsed or refractory PMLCL had an inferior ORR and survival from time of progression when compared to DLBCL. PMLCL pts who have chemosensitive disease have an OS and PFS post-ASCT that is similar to pts with DLBCL. Strategies for PMLCL should focus on improved salvage therapies for refractory and relapsed disease.


2021 ◽  
Vol 39 (S2) ◽  
Author(s):  
J.M. Raya ◽  
P. López‐García ◽  
C. D. Reyes ◽  
M.J. Rodríguez‐Salazar ◽  
C. De Bonis ◽  
...  

2012 ◽  
Vol 2012 ◽  
pp. 1-7 ◽  
Author(s):  
Ying Huang ◽  
Sheng Ye ◽  
Yabing Cao ◽  
Zhiming Li ◽  
Jiajia Huang ◽  
...  

Diffuse large B-cell lymphoma (DLBCL) can be molecularly subtyped as either germinal center B-cell (GCB) or non-GCB. The role of rituximab(R) in these two groups remains unclear. We studied 204 patients with de novo DLBCL (107 treated with first-line CHOP; 97 treated with first-line R-CHOP), patients being stratified into GCB and non-GCB on the basis of BCL-6, CD10, and MUM1 protein expression. The relationships between clinical characteristics, survival data, and immunophenotype (IHC) were studied. The 5-year overall survival (OS) in the CHOP and R-CHOP groups was 50.4% and 66.6% (P=0.031), respectively. GCB patients had a better 5-year OS than non-GCB patients whether treated with CHOP or not (65.0% versus 40.9%;P=0.011). In contrast, there is no difference in the 5-year OS for the GCB and non-GCB with R-CHOP (76.5% versus 61.3%;P=0.141). In non-GCB subtype, additional rituximab improved survival better than CHOP (61.3% versus 40.9%;P=0.0303). These results indicated that addition of rituximab to standard chemotherapy eliminates the prognostic value of IHC-defined GCB and non-GCB phenotypes in DLBCL by improving the prognostic value of non-GCB subtype of DLBCL.


2016 ◽  
Vol 71 (3) ◽  
pp. 280-286 ◽  
Author(s):  
S.H. Kwon ◽  
D.R. Kang ◽  
J. Kim ◽  
J.-K. Yoon ◽  
S.J. Lee ◽  
...  

2018 ◽  
Vol 60 (2) ◽  
pp. 358-366 ◽  
Author(s):  
Wenqiong Qin ◽  
Qiang Yuan ◽  
Jingkui Wu ◽  
Haonan Yu ◽  
Ying Wang ◽  
...  

2018 ◽  
Vol 2018 ◽  
pp. 1-8 ◽  
Author(s):  
Siqian Wang ◽  
Yongyong Ma ◽  
Lan Sun ◽  
Yifen Shi ◽  
Songfu Jiang ◽  
...  

It is generally believed that there is correlation between cancer prognosis and pretreatment PLR and NLR. However, there are limited data about their role in diffuse large B cell lymphoma (DLBCL). This study aims to determine the prognostic value of pretreatment PLR and NLR for patients who have DLBCL. The associations between clinical characteristics and NLR and PLR were evaluated among 182 DLBCL patients from January 2005 to June 2016. The optimal cutoff values for high PLR (⩾150) and NLR (⩾2.32) in prognosis prediction were determined. The effect of NLR and PLR on survival was evaluated through multivariate Cox regression analysis, univariate analysis, and log-rank test. According to the evaluation results, patients with high NLR and PLR had significantly shorter OS (P=0.026 and P=0.035) and PFS (P=0.024 and P=0.022) compared with those who have low PLR and NLR. On multivariate analyses, IPI>2, elevated LDH, and PLR⩾2.32 were prognostic factors for OS and PFS in DLBCL patients. Therefore, we demonstrated that high PLR and NLR predicted adverse prognostic factors in DLBCL patients.


2020 ◽  
Vol 20 (1) ◽  
Author(s):  
Chunyan Luan ◽  
Fei Wang ◽  
Ning Wei ◽  
Baoan Chen

Abstract Background Some studies have investigated the prognostic value exhibited by the Prognostic Nutritional Index (PNI) in patients suffering diffuse large B-cell lymphoma (DLBCL), but varying results were obtained. In order to determine the specific prognostic value more accurately, a meta-analysis was conducted in this study. Methods Literatures were searched from the China National Knowledge Infrastructure (CNKI), Wanfang, PubMed, Embase, the Cochrane Library, and Web of Science. Pooled hazard ratio (HR) and the 95% confidence interval (CI) were calculated to assess the association between PNI and the overall survival (OS) and the progression-free survival (PFS) of patients with DLBCL. Results Based on seven studies with a total number of 1311 patients, our meta-analysis revealed that low PNI may meant poor OS (HR = 2.14, 95% CI 1.66–2.75, p < 0.001) and poor PFS (HR = 1.75, 95% CI 1.36–2.25, p = 0.438). Subgroup analysis showed that, in Asians, low PNI was correlated to poor OS (pooled HR = 2.06 95% CI 1.59–2.66) and poor PFS (pooled HR = 1.66, 95% CI 1.28–2.15). Similar results were obtained from one European study, which is the only study performed outside of Asia from our literature search. Conclusion For patients with DLBCL, low PNI may be interpreted as adverse prognosis. More data from European patients are required in this study to avoid analysis bias.


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