Prognostic Value of Programmed Death Ligand-1 Expression on Tumor-Infiltrating Immune Cells in Patients Treated with Cisplatin-Based Combination Adjuvant Chemotherapy Following Radical Cystectomy for Muscle-Invasive Bladder Cancer: A Retrospective Cohort Study.

PURPOSE: To investigate the prognostic value of programmed death ligand-1 (PD-L1) expression in tumor-infiltrating immune cells (ICs) in men treated with adjuvant chemotherapy (AC) following radical cystectomy (RC) for muscle-invasive bladder cancer (MIBC).
MATERIALS AND METHODS: We retrospectively reviewed 219 "high-risk" (≥pT3a and/or pN+) patients who underwent RC and received cisplatin-based AC for MIBC between March 2015 and September 2019. PD-L1 expression was measured using the VENTANA (SP-142) immunohistochemistry assay and categorized into the three groups according to the percentage of the tumor area covered by PD-L1 expression on ICs: IC0 (<1%), IC1 (≥1% and <5%), and IC2/3 (≥5%). Positive PD-L1 expression was defined as IC2/3 (≥5%). Kaplan-Meier survival analysis was used to assess recurrence-free survival (RFS), and Cox proportional hazard models were applied to identify factors predicting tumor recurrence.
RESULTS: In the entire cohort, the overall prevalence of PD-L1 IC0, IC1, and IC2/3 was 13.2%, 27.4%, and 59.4%, respectively. During the mean follow-up of 32.5 months, tumor recurrence was detected in 115 (52.5%) patients. On multivariable analysis, tumor stage (≥pT3; P=0.032), positive lymph nodes (P=0.001), and positive PD-L1 on ICs (P=0.005) were independent predictors of tumor recurrence. The 3 year RFS was 54.7% in patients with negative PD-L1 and 31.7% in patients with positive PD-L1.
CONCLUSION: PD-L1 is widely expressed in ICs. Positive PD-L1 on ICs was significantly associated with shorter RFS in patients treated with cisplatin-based AC following RC. The present results support the use of adjuvant immunotherapy in "high-risk" patients with PD-L1-expressing ICs.

Introduction

Radical cystectomy (RC) with pelvic lymph node dissection is the standard, potentially curative treatment option for muscle-invasive bladder cancer (MIBC).1,2 However, patients with locally advanced bladder cancer (BCa) following RC have a poor prognosis, with 5 year disease-free survival (DFS) rates ranging from 11.2% to 56.9%, depending on stage and lymph node (LN) status.3–5 Recent guidelines recommend cisplatin-based combination adjuvant chemotherapy (AC) in patients with pT3/4 and/or pN+ disease after RC who did not receive neoadjuvant chemotherapy.1 The main advantage of AC after local treatment is that there is no delay in the definite treatment, and the pathologic stage can be accurately identified.6 In addition, recent meta-analyses show that AC has some benefit in terms of overall survival (OS; hazard ratio [HR] = 0.77, P = 0.049) and DFS (HR = 0.66, P = 0.014).7 However, at least 30% of patients do not respond to AC and experience treatment-related adverse events without benefits.8 Therefore, identifying a biomarker that can predict the success of AC in an individual patient would be beneficial.

Tumor-host immune interactions are important for an effective response to chemotherapy.9,10 BCa is considered an immunogenic tumor because of its relatively high tumor mutational burden,11,12 and inhibition of programmed death-1 (PD-1)/programmed death ligand-1 (PD-L1) interaction has shown positive results in BCa by restoring T-cell mediated immune responses.13–15 However, the association between immune checkpoint molecules and outcomes of AC in MIBC remains unclear.

The identification of biomarkers for predicting the response to treatment and prognosis is necessary to select patients who may benefit from AC and to design follow-up strategies. Therefore, in this study, we investigated the prognostic value of PD-L1 expression on tumor-infiltrating immune cells (ICs) in patients treated with cisplatin-based AC following RC for MIBC.

Materials and Methods

Study Population

This retrospective study was approved by the Institutional Review Board of Ewha Womans University Mokdong Hospital (IRB No. 2019–04-032), and the requirement for written informed consent was waived due to the study design. All study protocols were carried out in accordance with the Declaration of Helsinki and all patient data complied with relevant data protection and privacy regulations. A prospectively maintained database of 530 patients who underwent RC for BCa between March 2015 and September 2019 by a single urologic oncology surgeon was retrospectively reviewed. In the entire cohort, patients who received intravesical instillation of Bacillus Calmette-Guerin (BCG) and chemotherapy and/or radiotherapy prior to RC (n = 61) were pathologically diagnosed with pT0-2N0 BCa (n = 160), and patients who did not receive AC following RC (n = 90) were excluded from the analysis. Ultimately, 219 patients with “high-risk” (≥pT3a and/or pN+) BCa treated with cisplatin-based AC following RC were analyzed in this study (Figure 1). All patients were staged cM0 preoperatively.

Figure 1

Flow chart.

All RCs were performed as open procedures and included removal of the prostate and seminal vesicle in men, and removal of the uterus and ovaries in women. Standard bilateral pelvic lymphadenectomy was performed in all patients.16 AC was performed approximately 1 month following RC, and patients received three to six courses of a combined gemcitabine/cisplatin (GC) regimen (1,000 mg/m2 gemcitabine on days 1 and 8, and 15 and 70 mg/m2 cisplatin on day 2) every 4 weeks.

Data Collection

Clinical and pathological characteristics of patients, including age at surgery, gender, pathologic tumor stage and LN involvement at RC, number of resected LNs, concomitant carcinoma in situ (CIS), lymphovascular invasion (LVI), surgical margin status, type of urinary diversion, and underlying histology, were obtained from medical records at the time of surgery.

Disease recurrence was defined as high-grade, upper tract primary tumors, local recurrence at the surgical bed or regional LNs and/or distant metastasis.17 Recurrence-free survival (RFS) was measured from the date of RC to the date of the first documented recurrence or the date of the last follow-up when the patient had not yet experienced disease recurrence.

Histologic Assessment

RC specimens were processed on formalin-fixed, paraffin-embedded sections and reviewed by an experienced pathologist specialized in genitourinary cancer. Pathologic staging and tumor grading were determined according to the 2010 TNM classification from the American Joint Committee on Cancer (AJCC)18 and the 2004 World Health Organization (WHO)/International Society of Urologic Pathology consensus classification.19

Immunohistochemistry (IHC) Assay for PD-L1 Expression and Quantification

The VENTANA PD-L1 (SP142) rabbit monoclonal primary antibody (Ventana Medical Systems, Tucson, AZ, USA) was used as a fully automated IHC assay on the BenchMark ULTRA (Ventana Medical Systems) staining platform to measure PD-L1 expression on tumor-infiltrating ICs following routine protocols and specific manufacturer instructions. This assay was optimized for the detection of PD-L1 expression in urothelial carcinoma, where IC is predictive.20 The results were analyzed by a pathologist specialized in genitourinary cancer who was blinded to the clinicopathologic and survival data. PD-L1 expression level was categorized into the following three groups based on the percentage of the tumor area covered by PD-L1 expression on ICs: IC0 (<1%), IC1 (≥1% and <5%), and IC2/3 (≥5%).21,22 In addition, PD-L1 expression was dichotomized as positive (≥5%) or negative (<5%) using a 5% cutoff value. Representative images of PD-L1 expression on ICs are shown in Figure 2.

Figure 2

Representative images showing immunohistochemical staining of programmed death ligand-1 on tumor-infiltrating immune cells in radical cystectomy specimens. (A) IC0 (×200), (B) IC1 (×200), (C) IC2 (×200), and (D) IC3 (×200) (bar scale 100 μm).

Follow-Up

Each patient was followed up according to the institutional protocol and recommendations. In general, after RC, patients were scheduled for a follow-up at 1 month postoperatively and then every 3 months for the first 2 years, every 6 months for the next 3 years, and annually thereafter. During the follow-up period, a physical examination with laboratory tests, urine analysis with cytology, chest radiography, and radiologic evaluation including computed tomography (CT) or magnetic resonance imaging (MRI) of the chest, abdomen, and pelvis were performed at every visit to identify local recurrence and/or distant metastasis. A bone scintigraphy scan was performed when clinically indicated. In cases of orthotopic urinary diversion, cystoscopy was performed in patients showing abnormal findings in urine cytology or when symptoms (irritative voiding or hematuria) were present.

Statistical Analysis

Descriptive statistics were obtained for demographic variables. Quantitative variables are presented as median (range) or mean (standard deviation, SD), and qualitative variables are presented as an absolute value (percentage). An independent t-test was used to compare continuous variables, and Pearson’s chi-square test was used to compare categorical clinicopathologic characteristics. Kaplan–Meier survival analysis was used to estimate RFS, and differences were assessed with the Log rank test. Cox proportional hazard models were used to identify predictive factors associated with tumor recurrence. All statistical analyses were performed using IBM SPSS statistics for Windows, version 23.0 (IBM Corp. Armonk, NY, USA). Two-sided P-values <0.05 were considered statistically significant.

Results

Patient Characteristics

The baseline clinicopathologic characteristics of the 219 “high-risk” patients who underwent cisplatin-based combination AC following RC for BCa are summarized in Table 1. In the entire cohort, the median (range) age at RC was 65.0 (37.0–74.0) years, and the male:female ratio was 4.2:1. Pure urothelial carcinoma was identified in 76.3% (167/219) of patients, and 190 (86.8%) patients had a locally advanced tumor stage (≥pT3) at RC. The median (range) number of resected LNs was 20.0 (3.0–52.0), and pathologic analysis demonstrated LN involvement in 117 (53.4%) patients. The overall prevalence of PD-L1 IC0, IC1, and IC2/3 on ICs was 13.2%, 27.4%, and 59.4%, respectively. After dividing patients into two groups according to tumor recurrence (Yes vs No), there were significant differences in pathologic T and N stages, number of resected LNs (22.0 vs 18.0), number of AC (4.0 vs 3.0), and PD-L1 score on ICs (each P < 0.05). However, there were no significant differences in age at surgery, gender, concomitant CIS, LVI, surgical margin status, type of urinary diversion, and histologic subtype between the groups.

Table 1

Clinicopathologic Characteristics of 219 “High-Risk” Patients Treated with Cisplatin-Based Combination Adjuvant Chemotherapy Following Radical Cystectomy

Parameters	Total	Recurrence		P
		Yes	No
No. of patients	219 (100.0)	115 (52.5)	104 (47.5)
Age at surgery, years				0.504
Median (range)	65.0 (37.0–74.0)	65.0 (37.0–71.0)	67.0 (41.0–74.0)
Mean (SD)	63.6 (10.3)	63.0 (10.6)	63.8 (10.9)
Gender, n (%)				0.717
Male	177 (80.8)	94 (81.7)	83 (79.8)
Female	42 (19.2)	21 (18.3)	21 (20.2)
Pathologic T stage at RC, n (%)				0.001
pT2	29 (13.2)	7 (6.1)	22 (21.2)
pT3	146 (66.7)	72 (62.6)	74 (71.1)
pT4	44 (20.1)	36 (31.3)	8 (7.7)
Concomitant CIS at RC, n (%)				0.106
Yes	122 (55.7)	70 (66.7)	52 (50.0)
No	97 (44.3)	45 (33.3)	52 (50.0)
LVI at RC, n (%)				0.467
Yes	142 (64.8)	72 (62.6)	70 (67.3)
No	77 (35.2)	43 (37.4)	34 (32.7)
No. of resected LNs at RC				0.001
Median (range)	20.0 (3.0–52.0)	22.0 (4.0–52.0)	18.0 (3.0–52.0)
Mean (SD)	20.6 (10.4)	23.8 (10.5)	18.8 (11.0)
Pathologic N status at RC, n (%)				0.001
Negative	102 (46.6)	38 (33.0)	64 (61.5)
Positive	117 (53.4)	77 (67.0)	40 (38.5)
Histologic subtype, n (%)				0.293
Pure UC	167 (76.3)	91 (79.1)	76 (73.1)
Mixed UC	52 (23.7)	24 (20.9)	28 (26.9)
Surgical margin status, n (%)				0.727
Negative	179 (81.7)	93 (80.9)	86 (82.7)
Positive	40 (18.3)	22 (19.1)	18 (17.3)
No. of adjuvant chemotherapy, n (%)				0.001
Median (range)	4.0 (3.0–6.0)	4.0 (3.0–6.0)	3.0 (3.0–6.0)
Mean (SD)	4.2 (1.3)	4.6 (1.3)	3.8 (1.2)
Type of urinary diversion, n (%)				0.545
Ileal conduit	24 (11.0)	14 (12.2)	10 (9.6)
Orthotopic neobladder	195 (89.0)	101 (87.8)	94 (90.4)
PD-L1 score on ICs in RC specimens				0.001
IC0 (<1%)	29 (13.2)	8 (7.0)	21 (20.2)
IC1 (≥1% and <5%)	60 (27.4)	26 (22.6)	34 (32.7)
IC2/3 (≥5%)	130 (59.4)	81 (70.4)	49 (47.1)
Follow-up, months				0.531
Median (range)	26.2 (3.1–66.6)	26.2 (3.1–66.6)	26.4 (3.6–60.8)
Mean (SD)	32.5 (24.4)	32.7 (24.8)	32.2 (24.2)

Abbreviations: SD, standard deviation; RC, radical cystectomy; CIS, carcinoma in situ; LVI, lymphovascular invasion; LN, lymph node; UC, urothelial carcinoma; PD-L1, programmed death-ligand 1; IC, immune cell.

Association of Clinicopathologic Characteristics with PD-L1 Expression

The associations between PD-L1 expression and clinicopathologic characteristics are summarized in Table 2. The prevalence of PD-L1 IC0, IC1, and IC2/3 on ICs was 6.0%, 29.1%, and 64.9%, respectively, in patients with positive LNs, and the rates were significantly different from those in patients with negative LNs (P = 0.003). However, there was no association between PD-L1 expression on ICs and any remaining clinicopathologic parameters, including age, gender, tumor stage, concomitant CIS, LVI, surgical margin status, type of urinary diversion, and histologic subtype.

Table 2

Association of Programmed Death-Ligand 1 Expression and Clinicopathologic Characteristics

Parameters	Total	PD-L1 Expression on ICs			P
		IC0	IC1	IC2/3
Age					0.654
<65.0	109	13 (11.9)	28 (25.7)	68 (62.4)
≥65.0	110	16 (14.5)	32 (29.1)	62 (56.4)
Gender					0.569
Male	177	22 (12.4)	47 (26.6)	108 (61.0)
Female	42	7 (16.7)	13 (30.9)	22 (52.4)
Tumor stage					0.640
pT2	29	5 (17.3)	9 (31.0)	15 (51.7)
pT3–4	190	24 (12.6)	51 (26.9)	115 (60.5)
Concomitant CIS					0.324
Yes	122	18 (14.8)	37 (30.3)	67 (54.9)
No	97	11 (11.3)	23 (23.7)	63 (65.0)
LVI					0.154
Yes	142	21 (14.8)	33 (23.2)	88 (62.0)
No	77	8 (10.4)	27 (35.1)	42 (54.5)
Lymph node positivity					0.003
Negative	102	22 (21.6)	26 (25.5)	54 (52.9)
Positive	117	7 (6.0)	34 (29.1)	76 (64.9)
Surgical margin status					0.462
Negative	179	24 (13.4)	52 (29.1)	103 (57.5)
Positive	40	5 (12.5)	8 (20.0)	27 (67.5)
Histologic subtype					0.333
Pure UC	167	19 (11.4)	46 (27.5)	102 (61.1)
Mixed UC	52	10 (19.3)	14 (26.9)	28 (53.8)
Type of urinary diversion					0.786
Ileal conduit	24	3 (12.5)	8 (33.3)	13 (54.2)
Orthotopic neobladder	195	26 (13.3)	52 (26.7)	117 (60.0)

Abbreviations: CIS, carcinoma in situ; LVI, lymphovascular invasion; UC, urothelial carcinoma; PD-L1, programmed death-ligand 1; IC, immune cell.

Association of PD-L1 Expression with RFS

During the mean (SD) follow-up of 32.5 (24.4) months, local recurrence and/or distant metastasis was identified in 115 (52.5%) patients. Figure 3 shows the overall RFS rates estimated using the Kaplan–Meier method. The 2 and 3 year overall RFS rates were 53.8% and 44.5%, respectively. After stratification according to pathologic parameters, extra-vesical tumor stage (≥pT3) and positive LNs were associated with poor RFS (P = 0.040 and P < 0.001, respectively; Figure 4A and B). After stratification according to PD-L1 expression on ICs, RFS was statistically significantly poorer in patients with IC2/3 than in patients with IC0 (P = 0.020) and those with IC1 (P = 0.021; Figure 4C). When PD-L1 expression was dichotomized using a 5% cutoff value, PD-L1 expression on ICs significantly affected RFS (P = 0.003; Figure 4D). The 3 year RFS rate was 54.7% in PD-L1-negative patients and 31.7% in PD-L1-positive patients.

Figure 3

Kaplan–Meier survival curve for overall recurrence-free survival (RFS).

Figure 4

Kaplan–Meier survival curves for recurrence-free survival (RFS) according to (A) pathologic T stage, (B) pathologic N stage, (C) PD-L1 expression score, and (D) PD-L1 expression positivity.

The outcomes of Cox proportional hazard regression analysis of prognostic factors for tumor recurrence after RC are presented in Table 3. Multivariable Cox regression analyses revealed that tumor stage ≥pT3 (hazard ratio [HR] = 1.63; 95% confidence interval [CI]: 1.04–2.55; P = 0.032), positive LNs (HR = 2.27; 95% CI: 1.46–3.52; P = 0.001), and positive PD-L1 expression on ICs (HR = 1.68; 95% CI: 1.17–2.43; P = 0.005) were independently associated with a significantly increased risk of tumor recurrence.

Table 3

Cox Proportional Hazard Regression Analyses to Predict Tumor Recurrence After Cisplatin-Based Combination Adjuvant Chemotherapy Following Radical Cystectomy

Variables	Univariable			Multivariable
	HR	95% CI	P	HR	95% CI	P
Age
<65.0	Ref
≥65.0	1.01	0.99–1.03	0.263
Gender
Male	Ref
Female	1.03	0.64–1.63	0.812
Tumor stage
pT2	Ref			Ref
pT3–4	1.78	1.12–2.78	0.015	1.63	1.04–2.55	0.032
Concomitant CIS
No	Ref
Yes	1.24	0.71–1.97	0.510
LVI
No	Ref			Ref
Yes	1.55	1.16–2.08	0.003	1.31	0.96–1.78	0.092
Lymph node positivity
Negative	Ref			Ref
Positive	2.13	1.42–3.17	0.001	2.27	1.46–3.52	0.001
Histologic subtype
Pure UC	Ref
Mixed UC	1.29	0.74–2.36	0.288
Surgical margin status
Negative	Ref
Positive	1.68	0.83–3.40	0.152
No. of adjuvant chemotherapy
3	Ref
4–6	1.27	0.85–1.90	0.212
Type of urinary diversion
Ileal conduit	Ref
Orthotopic neobladder	0.84	0.56–1.29	0.423
PD-L1 on ICs
Negative	Ref			Ref
Positive	1.84	1.23–2.70	0.004	1.68	1.17–2.43	0.005

Abbreviations: CIS, carcinoma in situ; LVI, lymphovascular invasion; UC, urothelial carcinoma; PD-L1, programmed death-ligand 1; IC, immune cell.

Discussion

In this study, among 219 “high-risk” patients who were treated with cisplatin-based combination AC following RC for BCa, tumor recurrence was identified in 115 (52.5%) patients. However, after stratifying patients according to pathologic parameters, RFS differed significantly according to extra-vesical tumor stage, positive LNs, and positive PD-L1 expression on ICs. In addition to the pathologic T and N stages, positive PD-L1 expression on ICs was a significant prognostic factor for predicting RFS after cisplatin-based combination AC following RC. The present results may help to establish therapeutic strategies for patients with “high-risk” (≥ pT3a and/or pN+) BCa. To the best of our knowledge, this is the first study to evaluate the prognostic value of PD-L1 expression on ICs in this patient population.

Several studies have examined the prognostic value of PD-L1 on ICs as a biomarker in BCa,23–25 and high PD-L1 expression on ICs is associated with both unfavorable23,25 and favorable24 results. These conflicting results may be attributed to the use of different PD-L1 antibodies and inhomogeneous cutoff values to define positive PD-L1 expression.26 In our study, we only used the VENTANA assay with the SP 142 antibody for measuring PD-L1 expression in tumor-infiltrating ICs because, in the past, atezolizumab treatment was only reimbursed by the government for second line treatment for metastatic BCa based on the results of VENTANA test. In addition, we used 5% as the cutoff for positive PD-L1 expression to minimize the impact of heterogeneities between PD-L1 IHC assays. Furthermore, PD-L1 expression was measured only in RC specimens from patients without a history of BCG instillation, chemotherapy, and/or radiotherapy prior to RC. As a result, positive PD-L1 expression on ICs was identified in 59.4% (130/219) of patients, which is similar to the value reported previously.23

We examined the relationship between PD-L1 expression on ICs and clinicopathologic characteristics, and the results indicated that positive PD-L1 expression on ICs was closely associated with LN positivity. This result is consistent with that of a previous study reporting that positive PD-L1 expression on ICs is positively associated with tumor stage, tumor size, histologic grade, and nodal status.23 Taken together, these findings suggest that positive PD-L1 expression on ICs is associated with aggressive pathologic features in BCa.

Pichler et al25 reviewed 83 high-risk (≥pT3a and/or pN+) patients who underwent RC without cisplatin-based AC. In that study, PD-L1 (≥1%) expression was identified in 61.4% (51/83) of patients, and RFS was significantly shorter in patients with positive PD-L1 expression on ICs than in those with negative PD-L1 expression (P = 0.015). The authors hypothesized that high-risk patients with positive PD-L1 expression on ICs might benefit from adjuvant immunotherapy after RC. In our study, we analyzed patients who received cisplatin-based AC following RC, and the results support the need for adjuvant immunotherapy in high-risk patients with positive PD-L1 expression on ICs.

On the other hand, Bellmunt et al24 reviewed 143 urothelial carcinoma samples and detected positive PD-L1 expression (≥5%) on tumor-infiltrating mononuclear cells (TIMCs) in 58 (40.6%) patients. They reported that positive PD-L1 expression in TIMCs was significantly associated with longer survival in patients who developed metastasis and subsequently received platinum-based chemotherapy (P = 0.0007). However, in the entire cohort, 51.9% of patients were T2 or less. In addition, because platinum-based chemotherapy was performed after metastasis was identified, the association between PD-L1 expression and recurrence was not confirmed.

The PD-1/PD-L1 signaling pathway constitutes a mechanism of escape from an antitumor immune response.27 In this study, when patients were stratified by PD-L1 expression on ICs, patients with positive PD-L1 expression on ICs showed a statistically significantly poorer RFS than those with negative PD-L1 on ICs. Although the exact mechanism underlying the regulation of PD-L1 expression in patients with BCa remains to be elucidated, possible mechanisms are as follows: PD-L1 expression in the tumor environment is controlled by the tumor-related stroma in a process called “adaptive immune resistance”28 In this process, PD-L1 is upregulated by interferon-gamma in the tumor niche, and the PD pathway acts to suppress tumor immunity as a negative feedback mechanism.29 However, an exhausted immune state called “immune privilege” is a feature of the tumor microenvironment.30 In this condition, the antitumor function is restricted by several mechanisms including regulation of the spatial distribution of T-cells, promotion of T-cell apoptosis, or impairment of T-cell activation.30,31

Recently, potential role of adjuvant immunotherapy has been examined. In a Phase III IMvigor010 trial, adjuvant atezolizumab in patients with high-risk muscle invasive BCa did not improve DFS (HR = 0.89; P = 0.2446).32 However, in a phase III CheckMate-274 trial, adjuvant nivolumab in patients with high-risk muscle invasive BCa improved DFS in both all randomized patients and in patients whose tumor cells express PD-L1 ≥1%.33 In addition, in a phase III JAVELIN Bladder 100 trial, the addition of maintenance avelumab to best supportive care significantly prolonged OS (HR = 0.56; P < 0.001) in PD-L1 positive patients with unresectable locally advanced or metastatic BCa who had not progressed with first-line chemotherapy.34 Collectively, these trials will hopefully provide guidance for further treatment strategy.

Despite the potential clinical implications of our study, there were several limitations. First, this study had a non-randomized, retrospective design and was conducted at a single, tertiary referral center, which raises concerns for inherent selection bias. Nonetheless, this study used a prospectively maintained database and reflects real-world clinical practice. Second, the mean follow-up period was relatively short, which limited the analysis to one end-point (RFS); other clinically significant oncologic outcomes such as cancer-specific survival and OS were not analyzed. Third, in our study, we only used the VENTANA assay with the SP 142 antibody for measuring PD-L1 expression to avoid heterogeneities between IHC diagnostic assays. However, when interpreting PD-L1 status, discrepancies according to different antibody clones, staining platforms, and scoring algorithms should be considered.35 Finally, data for PD-L1 expression on tumor cells were not available; we could not assess the clinical impact of PD-L1 expression on tumor cells. A large, prospective randomized study is warranted to confirm the results and their clinical implications.

In conclusion, in “high-risk” BCa patients, PD-L1 is widely expressed in ICs from RC specimens. Positive PD-L1 expression on ICs was closely associated with LN positivity and significantly associated with shorter RFS in patients treated with cisplatin-based combination AC following RC for BCa. The present results support the need for adjuvant immunotherapy in “high-risk” patients with positive PD-L1 expression on ICs. Further prospective studies are needed to clarify the role of PD-L1 expression in ICs as a biomarker for BCa.