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. 2019 Mar 27;19:273. doi: 10.1186/s12885-019-5466-y

The prognostic and clinicopathological significance of PD-L1 expression in patients with diffuse large B-cell lymphoma: a meta-analysis

Liping Qiu 1, Hanlu Zheng 1, Xiaoying Zhao 1,✉
PMCID: PMC6437873  PMID: 30917792

Abstract

Background

Programmed cell death receptor 1 ligand 1 (PD-L1) expression in various tumors, including hematologic malignancies, has recently become a research topic of great interest. We performed a meta-analysis to evaluate the prognostic and clinicopathological value of PD-L1 expressed in tumor cells of patients with diffuse large B-cell lymphoma (DLBCL).

Methods

Relevant studies were identified from PubMed, EMBASE, Web of Science and the Cochrane Library. The hazard ratio (HR) and 95% confidence interval (95% CI) were used for analyzing survival outcomes, and the odds ratio (OR) was used for analyzing clinicopathological parameters.

Results

Pooled results showed that tumor cell PD-L1 expression is associated with poor overall survival (OS) (HR = 2.128, 95% CI: 1.341–3.378, P = 0.001), the non-germinal center B-cell-like subtype (OR = 2.891, 95% CI: 2.087–4.003, P < 0.000), high international prognostic index score (3–5) (OR = 1.552, 95% CI: 1.111–2.169, P = 0.010), B symptoms (OR = 1.495, 95% Cl: 1.109–2.015, P = 0.008), positive MUM1 expression (OR = 3.365, 95% Cl: 1.578–7.175, P = 0.002) and negative BCL6 expression (OR = 0.414, 95% Cl: 0.217–0.792, P = 0.008). Sensitivity analysis showed that there was no publication bias among these studies.

Conclusions

Our meta-analysis supported the idea that tumor cell PD-L1 expression may represent a promising biomarker for predicting poor prognosis and is associated with adverse clinicopathologic features in DLBCL patients.

Keywords: Diffuse large B-cell lymphoma, Programmed cell death receptor 1 ligand 1 (PD-L1), Prognosis, Meta-analysis

Background

Diffuse large B-cell lymphoma (DLBCL) is the most common subtype of non-Hodgkin lymphoma (NHL), accounting for approximately 30–40% of newly diagnosed NHL cases [1]. Due to its highly heterogeneous features, approximately 35% of DLBCL cases cannot benefit from rituximab (R) combined with anthracycline-based chemotherapies and eventually experience relapsed/refractory disease [2]. Therefore, it is critical to identify additional biomarkers and new therapeutic targets for DLBCL.

The programmed cell death receptor 1/programmed cell death receptor 1 ligand 1 (PD-1/PD-L1) pathway regulates effector T-cell responses and protects tissues from immune-mediated damage [3]. However, mounting evidence shows that activation of the PD-1/PD-L1 pathway allows tumors to elude host immune surveillance [2, 4]. PD-L1 is a member of the B7 family, which is expressed on the surface of antigen-presenting cells and tumor cells [3]. Evidence has suggested that aberrant PD-L1 expression is associated with poor prognosis. Monoclonal antibody blockade of the PD-1/PD-L1 pathway demonstrated clinical activity in several types of cancers, such as non-small cell lung cancer [5, 6], melanoma [7], renal cell carcinoma [8, 9], and hematological malignancies including relapsed/refractory classic Hodgkin lymphoma (HL) [10]. However, the prognostic role of PD-L1 expression in DLBCL remains elusive. Different research targets such as tumor cells, tumor-infiltrating nonmalignant cells [11] or soluble PD-L1 [12] produce different results. Accordingly, we conducted a meta-analysis to explore whether the tumor cell expression of PD-L1 correlates with the clinicopathological features and prognosis of patients with DLBCL.

Methods

Search strategy

This meta-analysis was reported according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses statement [13]. We searched PubMed, EMBASE, Web of Science and the Cochrane Library databases for articles published before December 31, 2018. The terms employed for our search included “PD-L1”, “PDL1”, “B7-H1”, “CD274”, “programmed death ligand 1”, “diffuse large B-cell lymphoma” and “DLBCL”. The language of publications was restricted to English. To identify additional studies, review of the reference lists of relevant articles was also performed.

Selection criteria

Studies were selected if they met the following requirements: (1) Patients were diagnosed with histologically confirmed DLBCL; (2) Studies used immunohistochemistry (IHC) as a measurement technique and had a definite cutoff for determination of PD-L1 positivity; (3) Studies provided the associations of PD-L1 expression with overall survival (OS)/ progression-free survival (PFS) and clinicopathological features of DLBCL; and (4) The hazard ratio (HR) and its 95% confidence interval (CI) were provided in terms of direct extraction, the Kaplan-Meier Curve from which the HR was calculated or the P values and the numbers of the outcomes using Parmar’s method [14]. The exclusion criteria included the following: (1) The study was an animal study or cell line study, or the publication was a letter, conference abstract, expert opinion, review or included results with unavailable full text; (2) Studies did not evaluate PD-L1 expression in DLBCL patients; (3) Targets were restricted to tumor-infiltrating nonmalignant cells or soluble PD-L1 expression in DLBCL patients; (4) The data for estimating the HR and 95% CI were insufficient; (5) Patients had received anti-PD-1/PD-L1 therapy; (6) The cutoff value of positive PD-L1 expression was not reported or reported only as inaccurate data; or (7) The Newcastle–Ottawa quality assessment scale was less than 6 [15].

Data extraction and statistics

Two reviewers independently examined the included studies and extracted the relevant data. The following data were extracted: the name of the first author, the year of publication, country of origin, cut-off value used, antibodies used, the number of positive or negative cases, follow-up time, HRs and their 95% CIs of OS or PFS and clinicopathological parameters.

We pooled HRs and their 95% CIs to analyze the prognostic significance of PD-L1 expression on the survival outcome of DLBCL. If the HRs and their 95% CIs were not reported directly, data were extracted from the Kaplan-Meier survival curves published in the article and estimated using Engauge Digitizer version 4.1(http://markummitchell.github.io/engauge-digitizer/) or the P values and the numbers from the outcomes. In addition, we pooled odds ratios (ORs) and their 95% CIs to analyze the association between PD-L1 expression and clinicopathological parameters. Statistical heterogeneity was evaluated by a chi-squared test and I2. Significant heterogeneity was defined as I2 > 50% or P value< 0.1. If heterogeneity was observed, we used a random-effects model to calculate the combined effect sizes. If not, a fixed-effects model was employed. Sensitivity analyses were performed to estimate whether any individual study influenced the pooled HRs or ORs. Publication bias was assessed by Egger’s and Begg’s tests. All statistical analyses were performed using STATA version 12.0 (Stata Corporation, College Station, Texas, USA). All statistical tests were two-sided, and P < 0.05 was considered indicative of statistical significance.

Results

Search results

After a search with the abovementioned retrieval strategy and removal of duplicates, a total of 286 potentially relevant articles were initially identified. After reviewing the titles and/or abstracts, 33 articles remained. According to the inclusion and exclusion criteria, 13 studies with 1613 cases of DLBCL were ultimately included in our meta-analysis [11, 16–27] (Fig. 1). Among these 13 articles, 12 studies provided HRs and 95% CIs of overall survival, while 6 studies provided HRs and 95% CIs of PFS. All studies were retrospective study designs and used immunohistochemistry to detect PD-L1 expression in tumor cells. The specific characteristics of the included studies are shown in Table 1. Cutoff was defined as the percent PD-L1 expression in tumor cells among the total cells from the pathological tissue. Five studies [16, 18, 24, 25, 27] evaluated PD-L1 positive expression as the proportion of tumor cells showing only membranous staining or only cytoplasmic staining, while others focused on membranous and/or cytoplasmic staining. Five studies [16, 20, 21, 26, 27] provided the association between PD-L1 and pathologic features. Xing et al. [16] and Shi et al. [27] adopted cutoff values for the high expression of Ki-67, MYC, BCL2 and BCL6 of 80, 40, 30 and 30%, respectively. However, Hu et al. [21] chose 90% as the cutoff value for increased levels of Ki-67 expression. Bledsoe et al. [20] and Kwon et al. [26] did not provide the definite cutoff values.

Fig. 1.

Fig. 1

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Flow chart of the selection procedure for relevant studies

Table 1.

Characteristics of enrolled studies in diffuse large B-cell lymphoma

author country year cut-off cases antibody Follow-up (month) therapeutic regimen HR (95%CI) of OS HR (95%CI) of PFS
PD-L1+/− clone dilution source
Kiyasu J Japan 2015 0.3 34/239 EPR1161 1:200 Dako 60 80%RCHOP/CHOP-like 1.809
(1.051–3.112)		 NA
Xing W America 2016 0.3 14/72 E1L3N NA Cell Signaling 21
(0.067–175)		 RCHOP 2.418
(1.031–5.670)		 2.130
(1.050–4.330)
Kwon D Korea 2016 0.1 77/49 E1L3N NA Cell Signaling 52
(16–165)		 RCHOP 0.430
(0.152–1.217)		 NA
Dong L China 2016 0.05 54/46 ab153991 1:200 NA 52.4
(1.5–89.1)		 CHOP/CHOP-like+ 39%R 4.740
(1.097–20.477)		 NA
Four M France 2016 0.05 12/20 SP142 NA Ventana 17
(1–78)		 chemotherapy and/or radiotherapy 7.7
(1.6–37.2)		 1.7
(0.67–4.28)
Bledsoe JR America 2016 0.25 20/26 E1L3N 1:200 Cell Signaling 78 RCHOP 0.29
(0.06–1.25)		 0.19
(0.04–0.83)
Hu LY China 2017 0.05 100/104 NA 1:50 Cell Signaling 52
(1–114)		 RCHOP+ 26.7%RT 4.055
(1.610–10.230)		 1.584
(1.000–2.510)
Fang X China 2017 0.1 20/54 SP142 ready to use ZSGB-BIO 2.4–86.4 CHOP/CHOP-like+ 55.2%R 2.547
(0.964–6.730)		 NA
Liu Y China 2018 0.3 11/81 SP142 NA NA 58
(1–78)		 RCHOP 4.63
(1.53–13.99)		 NA
Ishikawa E Japan 2018 0.05 3/48 SP142 NA NA 42
(3.5–150)		 86.4%RCHOP 5.72
(1.50–21.8)		 NA
Sun C China 2018 0.5 34/253 22C3 NA Dako 76 CHOP/CHOP-like+ 53.7%R 1.494
(0.868–2.571)		 NA
Kwon HJ Korea 2018 0.3 23/84 E1L3N 1:100 Cell Signaling NA 86.9%RCHOP/CHOP-like 1.21
(0.15–9.98)		 2.21
(0.59–8.27)
Shi YF China 2018 0.3 21/104 SP142 1:100 Ventana 25.7
(0.8–131.1)		 58.1%RCHOP/CHOP-like;29.7%surgery NA 0.379
(0.149–0.962)
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NA not available; RCHOP rituximab, cyclophosphamide, doxorubicin, vincristine and prednisone; RT radiotherapy;HR hazard ratio;CI confidence interval;OS overall

survival; PFS progression-free survival

Association between PD-L1 expression and OS

We enrolled 12 studies to investigate the association between PD-L1 expression and OS in 1478 patients with DLBCL [11, 16–26]. Strong heterogeneity was observed (I2 = 60.0%, P = 0.004). Therefore, we used a random effects model and discovered that positive PD-L1 expression was associated with shorter OS compared with that of negative expression (HR = 2.128, 95% CI: 1.341–3.378, P = 0.001) (Fig. 2). Sensitivity analysis showed that the pooled HRs were not significantly affected by any single study (Fig. 3). For further evaluation, we performed a subgroup analysis of the cutoff value and region. The pooled subgroup results showed that studies using ≥30% (HR = 2.128, 95% CI: 1.341–3.378, P<0.000; I2 = 0, P = 0.44) as the cutoff value for predicting prognosis showed increased significance compares with those using<30% (HR =2.195, 95% CI: 0.884–5.446, P = 0.090; I2 = 74.5%, P = 0.001) (Table 2). Moreover, the predictive effects of PD-L1 became stronger when the studies were limited to Asian populations (HR =2.195, 95% CI: 1.352–9.980, P = 0.001; I2 = 56.2%, P = 0.019) or to Chinses populations (HR =2.729, 95% CI: 1.618–4.605, P<0.000; I2 = 37.1%, P = 0.174) (Table 2).

Fig. 2.

Fig. 2

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Forest plot describing the association between PD-L1 expression and OS with DLBCL

Fig. 3.

Fig. 3

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Sensitivity analysis of the relationship between PD-L1 expression and OS

Table 2.

Subgroup analysis of pooled hazard ratios for DLBCL with positive PD-L1 expression

Stratified analysis No. of studies No. of patients HR 95%CI P Heterogeneity
I 2 P
cutoff
 <0.3 7 633 2.195 0.884–5.446 0.009 74.50% 0.001
  ≥ 0.3 5 845 2.128 1.341–3.378 0 0 0.440
region I
 Asian region 9 1314 2.195 1.352–9.980 0.001 56.20% 0.019
 Non-Asian region 3 164 1.779 0.356–8.896 0.483 78.30% 0.010
region II
 China 7 757 2.729 1.618–4.605 0 37.10% 0.174
 Others 5 721 1.620 0.755–3.479 0.216 69.10% 0.004
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HR hazard ratio;CI confidence interval

Association between PD-L1 expression and PFS

Only 6 out of 13 studies including 600 patients with DLBCL provided information about PFS [16, 19–21, 26, 27]. We extracted HRs from the Kaplan-Meier survival curves in two of these studies [16, 26]. Significant heterogeneity was observed (I2 = 69.5%, P = 0.006), and a random effects model was used for the meta-analysis (Fig. 4). The pooled HR was 1.109, revealing that the patients with positive PD-L1 expression had a shorter PFS compared to those with negative PD-L1 expression; however, this difference was not statistically significant (95% CI: 0.581–2.117; P = 0.754).

Fig. 4.

Fig. 4

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Forest plot describing the association between PD-L1 expression and PFS with DLBCL

Association between PD-L1 expression and clinicopathological parameters

Related studies were enrolled to analyze the association between PD-L1 expression and clinicopathological parameters. The results are listed in Table 3. DLBCL is divided into germinal center B-cell-like (GCB) and non-GCB subtypes according to the cell of origin [28]. Pooled ORs suggested that increased PD-L1 expression was significantly associated with the non-GCB subtype (OR = 2.891, 95% CI: 2.087–4.003, P<0.00; I2 = 4.0%, P = 0.404) [11, 16–18, 20, 21, 23, 25–27], negative expression of Bcl-6 (OR = 0.414, 95% Cl: 0.217–0.792, P = 0.008; I2 = 24.5%, P = 0.266) and positive expression of MUM1(OR = 3.365, 95% Cl: 1.578–7.175, P = 0.002; I2 = 22.8%, P = 0.274) [16, 20, 26] (Fig. 5a-c). For clinical parameters, 7 out of 13 articles showed that positive PD-L1 expression was more common with international prognostic index (IPI) scores of 3–5 in DLBCL patients (OR = 1.552, 95% CI: 1.111–2.169, P = 0.010; I2 = 12.40%, P = 0.335) [11, 17, 18, 21, 22, 26, 27]. Using a fixed effects model, a pooled OR from nine studies demonstrated that PD-L1 overexpression was related to B symptoms (OR = 1.495, 95% Cl: 1.109–2.015, P = 0.008; I2 = 48.3%, P = 0.051 [11, 16, 17, 21–23, 25–27]. (Fig. 6a-b).

Table 3.

Association between PD-L1 expression and clinicopathological features

Clinicopathological parameters No. of studies No. of patients Model Pooled OR 95%CI P Heterogeneity
I 2 P
Age ≤60 vs. >60 12 1582 Fixed 0.887 0.675–1.166 0.390 0 0.744
Sex female vs. male 11 1457 Fixed 1.068 0.819–1.392 0.626 9.50% 0.353
Pathology GCB vs. non-GCB 10 1413 Fixed 2.891 2.087–4.003 0 4.00% 0.404
Stage I-II vs. III-IV 9 1336 Fixed 1.209 0.915–1.599 0.182 26.40% 0.209
IPI 3–5 vs. 0–2 7 993 Fixed 1.552 1.111–2.169 0.010 12.40% 0.335
ECOG ≤1 vs. >1 7 1048 Random 1.006 0.445–2.274 0.988 64.40% 0.010
B symptom no vs. yes 9 1345 Fixed 1.495 1.109–2.015 0.008 48.30% 0.051
CR no vs. yes 5 632 Random 1.109 0.552–2.230 0.771 54.80% 0.065
LDH normal vs. elevated 7 827 Fixed 1.341 0.939–1.915 0.107 25.50% 0.234
EB no vs. yes 5 860 Random 2.180 0.485–9.799 0.309 72.20% 0.006
BCL-2 negative vs. positive 4 357 Fixed 1.510 0.857–2.661 0.154 0 0.776
BCL-6 negative vs. positive 3 232 Fixed 2.414 1.263–4.612 0.008 24.50% 0.266
CD10 negative vs. positive 3 233 Fixed 4.367 1.626–11.729 0.003 36.70% 0.206
MUM1 negative vs. positive 3 233 Fixed 3.365 1.578–7.175 0.002 22.80% 0.274
MYC negative vs. positive 3 244 Fixed 1.252 0.647–2.420 0.504 0 0.627
ki-67% low vs. high 4 397 Fixed 0.876 0.535–1.433 0.598 0 0.987
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IPI international prognostic index; ECOG Eastern Cooperative Oncology Group; GCB germinal center B-cell-like; OR odd ratio; LDH Lactic dehydrogenase; CR complete remission

Fig. 5.

Fig. 5

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Forest plot describing the association between PD-L1 expression and pathological features. a. Pathological subtypes (t: non-GCB; c: GCB); b.BCL-6 (t: positive; c: negative); c.MUM-1 (t: positive; c: negative). event: positive PD-L1 expression; nevent: negative PD-L1 expression

Fig. 6.

Fig. 6

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Forest plot describing the association between PD-L1 expression and clinical parameter features. a. B symptoms (t: yes; c: no). b. IPI score (t: 3–5; c: 1–2). event: positive PD-L1 expression; nevent: negative PD-L1 expression

However, the associations were not significant between PD-L1 expression and age (≤60 vs.>60: OR = 0.887, 95% CI: 0.675–1.166, P = 0.39), gender (female vs. male: OR = 1.068, 95% CI: 0.819–1.392, P = 0.626), Ann Arbor stage(I-II vs. III-IV: OR = 1.209, 95% CI: 0.915–1.599, P = 0.182), Eastern Cooperative Oncology Group (ECOG) score (≤1 vs. > 1: OR = 1.006, 95% CI: 0.445–2.274, P = 0.988), lactic dehydrogenase (LDH) (normal vs. elevated: OR = 1.341, 95% CI: 0.939–1.915, P = 0.107), complete remission(CR)(no vs. yes: OR = 1.109, 95% CI: 0.552–2.230, P = 0.771), EB virus (EBV) in situ hybridization (negative vs. positive: OR = 2.180, 95% CI: 0.485–9.799, P = 0.309), Ki-67% (low vs. high: OR = 0.876, 95% CI: 0.535–1.433, P = 0.598), BCL2 (negative vs. positive: OR = 1.510, 95% CI: 0.857–2.661, P = 0.154) or MYC (negative vs. positive: OR = 1.252, 95% CI: 0.647–2.420, P = 0.504) (Table 3).

Publication bias

Begg’s test (P = 0.537) and Egger’s test (P = 0.586) demonstrated that there was no publication bias for positive PD-L1 expression regarding the HR of OS. Funnel plots revealed no publication bias for OS (Fig. 7).

Fig. 7.

Fig. 7

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Funnel plot was constructed to visualize potential publication bias for D-L1 expression and OS

Discussion

Recently, investigators have focused more attention on PD-L1 expression in relation to the prognosis of various cancers. Structural variations disrupting the 3′ region of the PD-L1 gene and carcinogenic signal induction are potential mechanisms of elevated PD-L1 expression in many cancers, including DLBCL [4]. The number of studies researching the prognostic value of PD-L1 expression in DLBCL is limited, and the conclusions have been controversial. Many previous studies found that PD-L1 expression was related to worsened prognosis [11, 16, 18, 21, 22, 24, 25]. However, while some investigators found no prognostic significance of PD-L1 [19, 23, 26, 27], others demonstrated that PD-L1 was a favorable prognostic in DLBCL [17, 20]. This meta-analysis provided evidence to estimate the value of PD-L1 detection in tumor cells of DLBCL by pooling all related studies.

Our meta-analysis indicated that positive PD-L1 expression is significantly associated with inferior OS in DLBCL patients. The subgroup analyses demonstrated that PD-L1 expression was an indicator of poor prognosis in Asian populations, especially in Chinese individuals. One reason for these differences might be the genetic diversity among different ethnicities. In addition, we found that the prognostic role of PD-L1 in DLBCL demonstrated increased significance when the cutoff value was equal to or greater than 30%. This cutoff value could be beneficial for precisely stratifying a group of DLBCL patients with poorer outcomes. However, further research based on a large sample size is needed to confirm these speculations.

Most patients enrolled in our analysis received CHOP (cyclophosphamide, doxorubicin, vincristine and prednisone) or CHOP-like therapy, and more than half of them received rituximab at the same time. Three [11, 18, 25] of the included studies indicated that PD-L1 expression induced poor OS regardless of the use of rituximab. Hence, DLBCL patients with PD-L1 overexpression are unable to gain an increased benefit from the first-line therapy. Recently, an in vitro study of DLBCL cells (CRL2631) showed that the therapeutic effect of CHOP on decreasing the cell survival rate and increasing apoptosis was impaired when the PD-1/PD-L1 pathway was activated. However, this impairment would not occur without PD-L1 expression [29]. Therefore, one possible reason for the poor outcome in DLBCL with positive PD-L1 expression is that PD-L1 expression may contribute to chemotherapeutic resistance. A novel applicable strategy based on underlying molecular oncogenic mechanisms is necessary to treat these patients.

Our meta-analysis supports that PD-L1 could be a biomarker for poor outcome in DLBCL patients and is a highly promising therapeutic target. A phase Ib study including 11 relapsed/refractory DLBCL patients showed that an anti-PD-1 monoclonal antibody (nivolumab) could improve the objective response with a median follow-up time of 22.7 weeks [30]. In a phase II study, 66 DLBCL patients who received pidilizumab (anti-PD-L1) after autologous hematopoietic stem-cell transplantation (16-month PFS: 0.72) compared favorably with those not receiving pidilizumab after transplantation (18-month PFS: 0.52) from the same population [31].

However, in our study, positive PD-L1 expression in tumor cells had no significant impact on PFS. Possible reasons were that the number of studies about PFS was limited and that the HRs of PFS were extracted from the Kaplan-Meier curve in two studies [16, 26], which may compromise the precision of the data.

The relationship between PD-L1 expression and clinicopathological features was also assessed. We demonstrated support for a significant association between positive PD-L1 expression and non-GCB, which was aligned with previous researchers’ viewpoints [32, 33]. In addition, we found that positive PD-L1 expression was significantly associated both with positive MUM1 expression and negative BCL6 expression. The latter two expressive states were common in non-GCB based on the Hans classification. A possible mechanism of this tendency was that 9p24.1 amplification, leading to PD-L1 overexpression and JAK/STAT3 signaling activation, commonly occurred in non-GCB [34, 35]. Thus, anti-PD-1/PD-L1 may be more appropriate for patients with this aggressive subtype.

Our study also revealed that increased PD-L1 expression was more frequently observed with unfavorable clinical manifestations, including IPI score 3–5 and B symptoms. These results supported that positive PD-L1 expression might be beneficial for the identification of DLBCL patients with a higher risk of disease progression. However, more clinical trials are needed to demonstrate the adverse effects of PD-L1 expression in DLBCL.

Several studies have suggested that PD-L1 expression was associated with EBV infection [36, 37]. Chen et al. [32] included 16 EBV + DLBCL cases and all of them displayed positive PD-L1 expression, using a cutoff value of 0.05. A possible mechanism is that EBV-encoded latent membrane protein 1, or inflammatory factors, promote AP1- signaling and JAK/STAT signaling to activate PD-L1 enhancer and promoter regions [32, 38]. Despite this evidence, we found that the association between PD-L1 expression and EBV was not statistically significant, which might be due to limited data. This relationship needs to be further clarified.

Recently, considerable attention has been devoted to studies on DLBCL displaying various pathological features. Higher Ki-67 expression was regarded as indicative of higher proliferative activity of the lymphoma and as a robust predictor of poor prognosis in DLBCL patients with or without rituximab treatment [39]. The overexpression of MYC caused uncontrolled cell proliferation, while the antiapoptotic factor BCL2 was associated with drug resistance. It has been documented that MYC/BCL2 coexpression in DLBCL occurred more frequently in the non-GCB subtype and was associated with an aggressive clinical course [40]. However, our limited data demonstrated no significant association between these adverse prognostic biomarkers and PD-L1 expression, inferring that these biomarkers might affect disease processes through different signaling pathways. Further studies are needed to determine the interaction between PD-L1 and other pathological characteristics.

Several limitations should be acknowledged. First, the number of patients in the enrolled studies was relatively small, and most studies were performed in Asian populations. Thus, larger well-designed studies, especially in Western countries, are required to confirm these results. Second, the cutoff values defined by IHC varied in the included studies, which might cause increased heterogeneity in the final results. Therefore, establishing standardized definitions of positive PD-L1 expression using unified antibodies and detecting PD-L1 with other markers will likely enhance the reliability of the conclusion.

Conclusion

Our meta-analysis supported that tumor cell PD-L1 expression in DLBCL patients was significantly associated with B symptoms, high IPI score (3–5), non-GCB subtype, positive MUM1 expression, negative BCL-6 expression and poor OS, which might be valuable for individual prognostic evaluations. Moreover, the results indicated that PD-1/PD-L1 might be a potential therapeutic target in DLBCL patients, especially for relapse/refractory cases. Further large-scale studies are warranted to clarify these findings and to assess the efficacy and safety of anti-PD-1 or PD-L1 therapy in DLBCL patients.

Acknowledgments

The authors thank the study participants for their involvement in each of the individual studies.

Funding

No specific funding.

Availability of data and materials

All data generated or analyzed during this study are included in this published article.

Abbreviations

CHOP

cyclophosphamide, doxorubicin, vincristine and prednisone

CI

confidence interval

CR

complete remission

DLBCL

diffuse large B-cell lymphoma

EBV

EB virus

ECOG

Eastern Cooperative Oncology Group

GCB

germinal center B-cell-like

HL

Hodgkin lymphoma

HR

hazard ratio

IHC

immunohistochemistry

IPI

international prognostic index

LDH

lactic dehydrogenase

NA

not available

NHL

non-Hodgkin lymphoma

OR

odds ratio

OS

overall survival

PD-1/PD-L1

programmed cell death receptor 1 /ligand 1

PFS

progression-free survival

R

rituximab

RT

radiotherapy

Authors’ contributions

LPQ and XYZ designed the study. LPQ and HLZ collected and analyzed the data. LPQ and XYZ wrote the main manuscript. All authors reviewed and approved the final version of the manuscript.

Ethics approval and consent to participate

All analyses were based on previously published studies; thus, no ethical approval or patient consent were required.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Contributor Information

Liping Qiu, Email: 21618174@zju.edu.cn.

Hanlu Zheng, Email: 21718221@zju.edu.cn.

Xiaoying Zhao, Email: zrxz@zju.edu.cn.

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