Blood Res 2017; 52(3): 200-206
Platelet to lymphocyte ratio (PLR) retains independent prognostic significance in advanced stage marginal zone lymphoma patients treated with rituximab, cyclophosphamide, vincristine, and prednisone combination chemotherapy (R-CVP): Consortium for Improving Survival of Lymphoma trial
Jeongkuk Seo1, Won Seog Kim2, Jin Seok Kim3, Seok Jin Kim2, Jae Hoon Lee4, Jun Shik Hong4, Gyeong-Won Lee5, Sung Yong Oh1*, Ji-Hyun Lee1, Dok Hyun Yoon6, Won-Sik Lee7, Hyo Jung Kim8, Jae-Yong Kwak9, Hye Jin Kang10, Jae-Cheol Jo11, Yong Park12, Ho Sup Lee13, Hyo-Jin Kim1, and Cheolwon Suh6*

1Department of Internal Medicine, Dong-A University Hospital, Busan, Korea.

2Department of Medicine, Samsung Medical Center, Sunkyunkwan University School of Medicine, Seoul, Korea.

3Division of Hematology, Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea.

4Division of Hematology and Oncology, Department of Internal Medicine, Gachon University Gil Hospital, Incheon, Korea.

5Division of Hematology-Oncology, Department of Internal Medicine, Gyeongsang National University Hospital, Gyeongsang National University College of Medicine, Jinju, Korea.

6Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.

7Department of Hemato/Oncology, Busan Paik Hospital, College of Medicine, Inje University, Busan, Korea.

8Department of Internal Medicine, Hallym Medical Center, Hallym University College of Medicine, Anyang, Korea.

9Division of Hematology, Department of Internal Medicine, Chonbuk National University Medical School, Jeonju, Korea.

10Division of Hematology/Oncology, Department of Internal Medicine, Korea Cancer Center Hospital, Korea Institute of Radiological and Medical Sciences, Seoul, Korea.

11Department of Hematology and Oncology, Ulsan University Hospital, University of Ulsan College of Medicine, Ulsan, Korea.

12Department of Internal Medicine, Korea University College of Medicine, Seoul, Korea.

13Department of Internal Medicine, Kosin University College of Medicine, Busan, Korea.

Correspondence to: Cheolwon Suh, M.D., Ph.D. Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, 88 Olympic-ro 43-gil, Songpa-gu, Seoul 05505, Korea.
Received: April 29, 2017; Revised: May 28, 2017; Accepted: July 7, 2017; Published online: September 25, 2017.
© The Korean Journal of Hematology. All rights reserved.



Rituximab plus cyclophosphamide, vincristine, and prednisone (R-CVP) is one of the effective chemotherapeutic regimens for patients with advanced stage marginal zone lymphoma (MZL). However, prognostic factors that affect the outcome of treatment for MZL are not well understood.


Between August 2006 and June 2013, patients with newly diagnosed stage III and IV MZL treated with R-CVP as a first-line therapy from 15 institutions were retrospectively analyzed. Patients' clinical and laboratory data at diagnosis were collected by review of medical records.


A total of 80 patients were analyzed. Bone marrow involvement was observed in 30% cases. Twelve patients (15%) had nodal MZL, and 41.3% patients exhibited multiple mucosa-associated lymphoma tissue sites. Overall response rate was 91.3%, including 73.8% achieving complete response. Advanced MZL patients treated with R-CVP showed a 3-year progression-free survival (PFS) rate of 69.6%. Prognostic markers significantly affecting PFS in univariate analysis were platelet to lymphocyte ratio (PLR, <95 vs. ≥95, P=0.014), serum albumin (≤3.9 vs. >3.9 g/dL, P=0.008), and the International Prognostic Index (IPI) score (1 vs. 2–4, P=0.032). In multivariate analysis, only PLR (<95 vs. ≥95, HR 0.367, 95% CI, 0.139–0.971, P=0.043) was an independent risk factor for PFS.


PLR ≥95 at diagnosis is an independent prognostic marker for PFS in advanced stage MZL patients treated with R-CVP. This marker may aid clinicians in predicting the response to R-CVP chemotherapy in stage III and IV MZL patients.

Keywords: Marginal zone lymphoma, R-CVP, Prognosis, PLR

Marginal zone lymphoma (MZL) is a distinct subgroup of non-Hodgkin's lymphoma (NHL) that typically follows an indolent clinical course and has a long survival period [1]. In Korea, MZL accounts for 20.4% of all NHL, and is the second most frequent histological subtype after diffuse large B-cell lymphoma (DLBCL) [2].

For MZL with localized stage, regardless of subtype, it is well known that local modalities (such as radiotherapy or surgery) can be used to achieve good disease control. However, local therapy is inadequate in disseminated disease, which comprises at least a quarter of cases, leading to investigations for effective chemotherapy regimens [3].

After the introduction of rituximab, a chimeric monoclonal antibody directed against the B-cell-specific antigen CD20, into regimens targeted against MZL, rituximab in combination with other chemotherapeutic agents has shown promising results compared to conventional chemotherapy alone [45]. Among the studied regimens, chemotherapy comprised of rituximab plus cyclophosphamide, vincristine, and prednisone (R-CVP) has demonstrated comparable overall response rates (ORR), complete remission (CR) rates, and survival compared to other regimens containing rituximab [6].

The International Prognostic Index (IPI), although originally intended for use in patients with aggressive lymphoma [7], has been extensively applied, even in indolent lymphomas. However, it appears to have limited discriminating power, as the majority of patients are allocated to the favorable risk group [8]. Other prognostic indexes, such as the Follicular Lymphoma International Prognostic Index (FLIPI); Glasgow Prognostic Score (GPS), an inflammationbased prognostic score; or Marginal Zone Lymphoma Prognostic Index (MZLPI), have been proposed by different international groups that have mainly focused on indolent-nature lymphomas [91011].

Still, the prognostic factors that affect the outcome of MZL patients are not well understood. And after the introduction of rituximab, the relevance of previously recognized prognostic factors in other hematologic cancers has undergone reassessment [12]. Studies in various cancers have demonstrated that an elevation of neutrophils, platelets, monocytes, neutrophil to lymphocyte ratio (NLR), or platelet to lymphocyte ratio (PLR), or the decrease of serum albumin (SA) was associated with some unfavorable clinico-pathologic features [131415]. The relationship of poor prognosis and the elevation of white blood cells, platelets, or associated ratios may be explained through an inflammatory process elicited by cancer cells [101617]. Studies on platelets have shown that they might play an essential role in tumor spreading and growth [18]. Protective effects of lymphocytes as part of the immune surveillance system have also been investigated [19].

In this study, we aim to demonstrate whether the pretreatment levels of various inflammatory markers and/or conventional prognostic markers, can be prognostic indicators in patients treated with R-CVP for MZL.


After obtaining approval from the Institutional Review Board (IRB) of Dong-A University Hospital, patients with the diagnosis of advanced stage MZL from 15 different institutions in Korea between August 2006 and June 2013 were retrospectively evaluated. The IRB granted a waiver of informed consent based on the design of the study (retrospective data analysis study only, with no interactions with subjects/patients). Inclusion criteria comprised biopsy- confirmed diagnosis of MZL with advanced stage (Ann Arbor stage III/IV) and treatment with at least one cycle of R-CVP therapy with curative intent. Patients were excluded if they had prior chemotherapy other than R-CVP, were on rituximab maintenance therapy after R-CVP, or if they had incomplete clinical data.

Demographic and clinical data

Patient demographics, including age and sex, were collected from medical records. Clinical data included initial laboratory data within 7 days before the start of first cycle of chemotherapy, including complete blood count (CBC), NLR, PLR, absolute neutrophil count (ANC), absolute lymphocyte count (ALC), absolute monocyte count (AMC), SA, serum lactate dehydrogenase (LDH), date of diagnosis, nodal involvement, bone marrow (BM) findings, presence of B symptoms, Eastern Cooperative Oncology Group (ECOG) performance status, presence of bulky disease, Ann Arbor stage, and IPI. Each component of CBC was counted per microliter, and PLR was calculated by the ratio of platelet count (per microliter) divided by absolute lymphocyte count (per microliter).

Treatment data

Treatment consisted of rituximab (375 mg/m2), cyclophosphamide (750 mg/m2) and vincristine (1.4 mg/m2; maximum 2.0 mg), given intravenously on day 1, and oral prednisone 100 mg on days 1–5. The treatment was repeated every 3 weeks and continued for six or eight cycles.

Primary clinical outcome variables

The response evaluation was in accordance with the International Workshop for the Standardized Response Criteria for NHL. Overall survival (OS) was defined as date of diagnosis to date of death or date of last contact for those censored. Progression-free survival (PFS) was defined as the time from the date of diagnosis to the date of relapse, progression, or death from any cause.

Statistical analysis

For the numerical variables, a receiver operating characteristic (ROC) curve was performed to estimate the optimal point for sensitivity/specificity towards the progression of MZL. Time-to-event data was estimated using the Kaplan-Meier method, and the groups were compared using the log-rank test. The Cox proportional hazards model was used to estimate the hazard ratio (HR) and the corresponding 95% confidence interval (95% CI) in regard to the low risk group. Significant variables from univariate models at an alpha level of 5% were included in the multivariable Cox proportional hazards model. All reported P-values were two-sided, and a P-value <0.05 was considered significant. All analyses were conducted using Statistical Package for Social Sciences (SPSS) Version 20.0 for Windows.


In total, 80 patients who met the inclusion criteria were evaluated. Table 1 shows the clinical characteristics of the patients included in this analysis. The median age of the evaluated 80 patients (44 males and 36 females) was 55 (range, 16–81) years. All patients were diagnosed with advanced clinical stage (Ann Arbor stage III or IV) lymphoma with 19 (23.8%) at stage III and 61 (76.2%) at stage IV. Ten (12.5%) patients had a performance status of ≥2. Elevated LDH was identified in 12 (16.9%) patients. B symptoms (fever, night sweats, and weight loss) were observed in 8 (10%) patients. The distributions of IPI were: 1 in 23 (28.8%); 2 in 35 (43.8%); 3 in 16 (20%), and 4 in 6 (7.5%) patients. Twelve (15%) of the 80 patients had nodal MZL and 68 (85%) had MALT lymphoma. Among patients with MALT lymphoma, 33 (41.3%) patients had multiple MALT site involvement. BM involvement was observed in 24 (30%) patients.

Response and survival

Fifty-nine patients (73.8%) achieved a complete remission (CR) and 14 (17.5%) a partial remission (PR), while stable disease (SD) was observed in 4 (5%) patients and progressive disease in 2 (2.5%) patients. One patient was not evaluable for response, making the ORR 91.3% (95% CI, 85.0–96.3%). At a median follow-up of 24.9 months (range, 0.8–75.4), 17 patients (21.3%) had progression or relapse, and none died during the investigation period. Information regarding the treatment after disease relapse or progression was available for 15 patients. Thirteen patients received chemotherapy alone after relapse or progression, and two received chemotherapy followed with hematopoietic progenitor stem-cell transplantation (HPSCT). There was one patient who was lost to follow-up after only 1 cycle of R-CVP chemotherapy; therefore her data on treatment and response was not available. Median OS and PFS were not reached at the last follow-up, and PFS at 3 years was 69.6%, with the 3-year OS rate at 100% (Fig. 1).

Analysis of potential prognostic markers

To identify the optimal prognostic marker according to its sensitivity and specificity towards the relapse of MZL, a Receiver Operation Characteristic (ROC) curve analysis was performed for numerical variables (Table 2). Among the potential prognostic markers, only SA and PLR showed enough sensitivity/specificity to be put to survival rate analysis. For the SA, a cut-off value of 3.9 g/dL was generated according to the ROC analysis (sensitivity 71.0% and specificity 66.6%; AUC values 0.656, 95% CI 0.517–0.795, P=0.044). From the ROC curve, PLR value of 95 yielded the most optimal value to predict the relapse or recurrence of MZL (sensitivity 82.3% and specificity 55.6%; AUC values 0.623, 95% CI 0.448–0.799, P=0.113).

Univariate analysis of potential prognostic markers is shown in Table 3. An SA level ≥3.9 g/dL was shown to be a significant predictor of PFS (HR=0.243, 95% CI 0.086–0.691, P=0.004) (Fig. 2A). PLR was also significantly prognostic for PFS when evaluated for values <95 (HR=0.298, 95% CI 0.114–0.779, P=0.009) (Fig. 2B). Additionally, IPI, when categorized by a score of 1 versus 2–4, had prognostic significance for PFS (HR=0.444, 95% CI 0.211–0.933, P=0.017) (Fig. 2C). Other candidate factors, such as age, performance status, Ann Arbor stage, elevation of LDH, presence of B symptoms, extranodal MZL, and BM involvement were not prognostic in our population.

Multivariable analysis results for PFS are shown in Table 4. PLR continued to be an independent prognostic marker, with the hazard of progression for patients with PLR <95 shown to be about 36.7% (95% CI 13.9–97.1) of the hazard for those patients with PLR ≥95, when controlling for SA and IPI. The SA and IPI were not prognostic for PFS in our multivariate analysis.


In our review of 80 patients with advanced stage MZL, we found that a PLR value of ≥95 may have prognostic significance in those treated with R-CVP. Among other candidates for prognostic markers of MZL, a serum albumin lower than 3.9 g/dL and an IPI of 2 or higher had prognostic value when analyzed with univariate analysis, but did not have enough statistical significance when applied to multivariate analyses.

In 1993, the International Prognostic Index (IPI) was published [7]. Since then, IPI has been widely applied for the prediction of prognosis of NHLs. However, as IPI is designed for aggressive lymphoma and cases of indolent lymphoma such as MZL, as well as taking into account that the addition of rituximab to conventional chemotherapy has led to significant improvements in OS and PFS in patients with MZL, previously studied prognostic algorithms for such patients, including the IPI, had to be reconstructed [9].

Other prognostic indexes, such as FLIPI used for follicular lymphomas, or GPS, an inflammation-based prognostic index, or MZLPI, have been proposed as alternatives for more indolent lymphomas [91011]. But as our concern was focused on advanced stage MZL (which usually had disseminated disease, and hence, was a prerequisite for systemic chemotherapy), we did not consider prognostic indexes with Ann Arbor staging as a constituent.

The measurement of serum markers, such as CBC or serum albumin, is a simple step that could easily be employed in regular practice. Along with the serum markers, association of systemic inflammatory components with tumor survival, or the pathogenesis of neoplasm itself, has been proposed [2021]. The inflammatory parameters, namely, the ANC, AMC, ALC, platelet counts, NLR, PLR, CRP, serum albumin, and so forth are studied in many cancers for their correlation with prognosis [131415162223]. For solid tumors, a positive relationship between high PLR with worse prognosis of epithelial ovarian cancer was identified [1316].

For the hematologic malignancies, similar investigations on the connection of inflammatory markers and the outcome of disease have been carried out. For patients with non-Hodgkin's lymphoma, prognosis of DLBCL has been correlated with hypoalbuminemia, low ALC, AMC, increased NLR and PLR, AMC/ALC score, and GPS [152425262728]. Extranodal natural killer/T-cell lymphoma, nasal type, has also been shown to be related with GPS and PLR [10]. Outcomes of other hematologic malignancies, such as primary mediastinal large B-cell lymphoma, myelodysplastic syndromes, multiple myeloma, and acute myelogenous leukemia have also been related to systemic inflammatory markers [293031].

Studies regarding the correlation of inflammatory markers with the outcome of MZL were difficult to obtain. Four retrospective studies have been made regarding the prognostic factors of MZL. Two studies, during their research, commonly deduced the result that the discriminating powers of formerly used prognostic scoring systems, the IPI and the FLIPI, are limited, if not misleading [32]. One of those studies by Oh et al. [9] analyzed 205 patients with nongastric MZL with presumed prognostic factors, PFS and OS. The MZLPI was constructed via the summation of speculated prognostic factors: nodal MZL, ECOG performance ≥2, and advanced stage. The PFS and OS curves were both more discriminating than those of IPI or FLIPI. Another study on the prognostic factors of nongastric MZL by Arcaini et al. [33] demonstrated that disease dissemination to lymph nodes and BM is associated with a poorer outcome. Arcaini et al. [34] also showed that in splenic MZL patients, low hemoglobin levels (<12 g/dL), LDH levels higher than normal, and albumin levels less than 3.5 g/dL were predictors of higher risk.

A study by Mazloom et al. [32] analyzed 275 patients with MZL by dividing them into three groups based on three types: extranodal, nodal, and splenic. The results showed that an elevated serum β2-microglobulin level, B symptoms, and male gender were found to be correlated with decreased recurrence-free survival (RFS). Using these three variables, they formulated a 3-tier prognostic scoring system for extranodal MZL, which had statistically reasonable discriminating power (P=0.01 for RFS, P<0.0001 for OS). Their study also showed that IPI and FLIPI did not have statistical significance regarding OS of MZL.

None of the above-mentioned studies regarding the prognosis of MZL considered the previously emphasized role of inflammatory markers on malignancy development and progression. Groundwork investigations on the roles of platelets in tumor spreading and growth have shown that platelets mediate tumor cell growth, dissemination, and angiogenesis [18]. Investigators have suggested that platelets play a role in the homing of circulating tumor cells to distant organs and that platelet interactions with tumor cells lead to rolling and tethering of tumor cell aggregates, resulting in extravasation through the endothelial wall and immune protection [35]. Platelets have also been shown to promote the spread of tumors through multiple mechanisms, including selectin and integrin interactions with tumor cells [36]. In addition to their function in hemostasis, platelets are also involved in inflammatory disease and cancer [37].

In contrast to platelets, lymphocytes are considered a significant blood parameter related to immune surveillance. High lymphocytic infiltrate is associated with improved survival and superior response to systemic therapy [38], whereas low peripheral blood lymphocyte counts are related to poor cancer prognoses [39].

Our findings provide a new approach in predicting outcomes in MZL patients. Prediction of disease progression not only utilizing clinical or histopathological factors (e.g., tumor grade, tumor size, and tumor site), but also with host-response factors, such as systemic inflammatory markers, may have more clinical significance. Furthermore, the PLR can easily be assessed from peripheral blood tests that are available without additional expenditure, thus providing lower cost and greater convenience for predicting prognosis.

However, this study has some limitations, including the few deaths caused by MZL, the relatively small size of the analysis group, and the inherent bias that exists in a retrospective study. To verify the results of this study, a collective effort by way of a multi-institutional prospective study with longer follow-up will be needed. However, given the lack of prospective data, this retrospective study provides evidence to support the role of these prognostic factors and provides novel insight into predicting outcomes in MZL patients.

In conclusion, our study is the first to show that PLR is an independent prognostic marker in patients with MZL treated with R-CVP chemo-immunotherapy.

Fig. 1.

Kaplan-Meier graph depicting progression-free survival (PFS) of patients with advanced stage marginal zone lymphoma (MZL) treated with R-CVP chemotherapy (PFS at 3 years was 69.6%).

Fig. 2.

Kaplan-Meier survival plots; (A) Serum albumin level ≥3.9 g/dL was shown to be a significant predictor of progression free survival (PFS) (HR=0.243, 95% CI 0.086–0.691, P=0.004); (B) PLR was also significantly prognostic for PFS when evaluated for values of <95 (HR=0.298, 95% CI 0.114–0.779, P=0.009); (C) IPI, when categorized by a score of 1 versus 2–4, had prognostic significance for PFS (HR=0.444, 95% CI 0.211–0.933, P=0.017).

Table 1

Demographic and clinical characteristics.

a)Bone, bronchus, esophagus, nasopharynx, paranasal sinus, peritoneum, soft tissue, thymus, thyroid (1 case of each).

Abbreviations: BM, bone marrow; ECOG, Eastern Cooperative Oncology Group; IPI, international prognostic index; LDH, lactate dehydrogenase; MALT, mucosa associated lymphoid tissue; MZL, marginal zone lymphoma.

Table 2

Area under the curve values of prognostic marker candidates.

a)Under the nonparametric assumption. b)Null hypothesis: true area=0.5.

Abbreviations: ALC, absolute lymphocyte count; AMC, absolute monocyte count; ANC, absolute neutrophil count; CI, confidence interval; NLR, neutrophil to lymphocyte count; PLR, platelet to lymphocyte count.

Table 3

Univariate analysis of prognostic factors for time-to-progression.

a)P-value by log rank test. b)Number of patients initially evaluated with LDH were 71.

Abbreviations: CI, confidence interval; HR, hazard ratio; IPI, international prognostic index; LDH, lactate dehydrogenase; MZL, marginal zone lymphoma; PFS, progression free survival; PLR, platelet to lymphocyte ratio; SA, serum albumin.

Table 4

Multivariate analysis of prognostic factors for progression free survival.

a)P-value by Cox regression.

Abbreviations: CI, confidence interval; HR, hazard ratio; IPI, international prognostic index; PFS, progression free survival; PLR, platelet to lymphocyte ratio; SA, serum albumin.

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