key: cord-0988596-m34nzgdr
authors: Togashi, Kyo; Hatakeyama, Shingo; Yoneyama, Tohru; Hamaya, Tomoko; Narita, Takuma; Fujita, Naoki; Iwamura, Hiromichi; Okamoto, Teppei; Yamamoto, Hayato; Yoneyama, Takahiro; Hashimoto, Yasuhiro; Ohyama, Chikara
title: Effect of active anticancer therapy on serologic response to SARS‐CoV‐2 BNT162b2 vaccine in patients with urothelial and renal cell carcinoma
date: 2022-03-31
journal: Int J Urol
DOI: 10.1111/iju.14882
sha: 54a364e82493c814c08a426af3725ff598f3d8de
doc_id: 988596
cord_uid: m34nzgdr

OBJECTIVES: To evaluate the serologic response to the BNT162b2 messenger ribonucleic acid vaccine in patients with urothelial carcinoma and renal cell carcinoma. METHODS: Between June 2021 and November 2021, we retrospectively evaluated blood samples from 60 healthy controls (control group), 57 patients with urothelial carcinoma, and 28 patients with renal cell carcinoma who had received two doses of the BNT162b2 vaccine at Hirosaki University Hospital. We determined the immunoglobulin G antibody titers against the severe acute respiratory syndrome coronavirus 2 spike receptor‐binding domain. Seropositivity was defined as ≥15 U/mL. We investigate factors associated with antibody titers and seropositivity in the patients with urothelial carcinoma and renal cell carcinoma. RESULTS: Antibody titers in the control, urothelial carcinoma, and renal cell carcinoma groups were 813, 431, and 500 U/mL, respectively. Seropositivity was 100%, 90%, and 96% in the control, urothelial carcinoma, and renal cell carcinoma groups, respectively. Of the 85 patients, 37 of 57 (65%) and 21 of 28 (75%) were actively undergoing anticancer treatment for urothelial carcinoma and renal cell carcinoma, respectively. Anti‐severe acute respiratory syndrome coronavirus 2 spike immunoglobulin G antibody titers and seropositivity was not significantly different between the patients with urothelial carcinoma and renal cell carcinoma. Anti‐severe acute respiratory syndrome coronavirus 2 spike immunoglobulin G antibody titers were not significantly associated with active anticancer therapy or steroid treatment for immune‐related adverse events. Univariable logistic regression analysis revealed that older age and metastatic disease were significantly and negatively associated with seropositivity. CONCLUSIONS: Patients with urothelial carcinoma or renal cell carcinoma exhibited an adequate antibody response to the BNT162b2 vaccine. Active anticancer therapy was not significantly associated with seropositivity following vaccination with severe acute respiratory syndrome coronavirus 2 BNT162b2 in patients with urothelial carcinoma and renal cell carcinoma.

Patients actively undergoing anticancer therapy are at high risk for impaired serologic response to the SARS-CoV-2 mRNA vaccine. [1] [2] [3] Furthermore, the seropositivity rate in patients with solid tumors was reported as slightly lower (approximately 90%) than in healthy controls. [4] [5] [6] Systemic chemotherapy and ICIs are two immunoregulation agents frequently administered to patients with advanced UC. [7] [8] [9] [10] [11] [12] Treatment with ICIs in combination or ICIs plus TKIs is considered the standard of care for patients with metastatic RCC. [13] [14] [15] [16] [17] [18] Furthermore, immune-related AEs are closely associated with high-dose steroid administration in patients treated with ICIs, and steroid use has been associated with impaired humoral response to SARS-CoV-2 mRNA vaccines in patients with cancer. 5, 19, 20 However, the effect of different types of anticancer therapy and the concomitant use of steroids on antibody responses to SARS-CoV-2 vaccines in patients with UC and RCC remains unknown. Hence, this single-center study evaluated the serologic response to the BNT162b2 mRNA vaccine in patients with UC and RCC treated with anticancer therapy at an academic hospital in Japan.

This retrospective study was approved by the Ethics Committee of Hirosaki University (approval number: 2021-089). Because all participants had previously provided written informed consent for other biomarker studies, the Ethics Committee waived informed consent for our study.

We conducted our study between June 21 and November 1, 2021. The cohort comprised 60 healthy controls (Ctrl group), 57 patients with UC (UC group), and 57 patients with RCC (RCC group) who had received their second dose of the BNT162b2 vaccination at least 7 days before measuring the titer of anti-SARS-CoV-2 antibodies. The Ctrl group included members of the medical staff and medical students at Hirosaki University Hospital. Those with previous SARS-CoV-2 infection or blood samples taken less than 7 days after the second BNT162b2 dose were excluded. Blood samples were collected cross-sectionally and active anticancer treatment was defined at the time of first vaccination. Clinical parameters, such as age, sex, types of anticancer therapy, metastatic disease, and the concomitant use of steroids, were obtained from medical records.

Cross-sectional blood samples collected for regular evaluation were used to measure the titers of IgG antibodies against the SARS-CoV-2 S protein receptor-binding domain using the Elecsys Anti-SARS-CoV-2 S assay (Roche Diagnostics, Meylan, France) on a Cobas 8000/e 801 analytical unit (Roche Diagnostics). According to the manufacturer's data, seropositivity was defined as an anti-SARS-CoV-2 IgG level ≥15 U/ mL, which was shown to be sufficient indication of the presence of neutralizing antibodies.

Active anticancer treatment for UC included systemic chemotherapy using gemcitabine plus cisplatin/carboplatin, pembrolizumab, avelumab, durvalumab, and tremelimumab. Active anticancer treatment for RCC included TKIs alone (axitinib and cabozantinib), ICIs plus TKIs (avelumab plus axitinib or pembrolizumab plus axitinib), and ICI combinations (nivolumab plus ipilimumab). We also included posttreatment patients with localized diseases who were not actively undergoing any treatment (off treatment) in the UC (n = 20, 35%) and RCC (n = 7, 25%) groups.

We evaluated the antibody titers and seropositivity in the Ctrl, UC, and RCC groups as well as in patients with stage M0 and stage M1 disease. We compared the antibody titers and seropositivity between the UC and RCC groups, and patients with stage M0 and stage M1 disease. The effect of different types of anticancer therapies and the concomitant use of steroids on antibody titers and seropositivity rates were compared. We also used univariable logistic regression analysis to investigate the factors associated with seropositivity.

Qualitative and quantitative variables were described as numbers with percentages and medians with IQRs, respectively. Chi-squared, Fisher's exact, Mann-Whitney U, and Student t tests were used for statistical comparison between the Ctrl group and the UC and RCC groups. Univariable logistic regression analysis was performed to identify factors associated with anti-SARS-CoV-2 IgG seropositivity after the second SARS-CoV-2 mRNA vaccination dose, and the OR was calculated with a 95% confidence interval. All statistical analyses were performed using BellCurve for Excel v3.10 (Social Survey Research Information Co. Ltd., Tokyo, Japan) and GraphPad Prism v7.00 (GraphPad Software, San Diego, CA, USA). P value of <0.05 was considered as statistically significant.

The background characteristics of the study cohort are summarized in Table 1 . Briefly, the median ages were 36 (IQR 27-52), 73 (IQR 70-81), and 72 (IQR 68-77) years in the Ctrl, UC, and RCC groups, respectively. No patient had SARS-CoV-2 infection in this cohort. A blood sample was collected from all participants at a median of 2.9 (IQR 1.7-6.2) months after the first vaccine dose. There were 55 patients with stage M1 disease and 40 with ICI therapy. In the UC and RCC groups, 37 of 57 (65%) and 21 of 28 (75%) patients, respectively, were actively undergoing anticancer therapy, and the remainder in both groups were off treatment. Steroids were administrated to nine patients for immune-related AEs and the dose of steroids was 10 mg or less at the time of vaccination.

A cross-sectional representation of anti-SARS-CoV-2 S IgG antibody titers is shown in Figure 1 . After the second BNT162b2 vaccination dose, all participants (100%) in the Ctrl group and 78 of 85 (92%) patients with UC or RCC were seropositive for SARS-CoV-2 S IgG antibodies. The anti-SARS-CoV-2 S IgG antibody titer was not significantly different between the UC (median 431 U/mL) and RCC groups (median 500 U/mL) (P = 0.334, Fig. 2a ). The seropositivity rate in the UC, and RCC groups was 90%, and 96%, respectively (P = 0.417, Fig. 2b ). The anti-SARS-CoV-2 S IgG antibody titer did not significantly differ between patients with nonmetastatic disease (M0; median 458 U/mL) and metastatic disease (M1; median 427 U/mL) (P = 0.319, Fig. 2c ). The seropositivity rate in the patients with stage M0 and M1 disease was 97% and 89%, respectively (P = 0.413, Fig. 2d ).

We observed that 92% (n = 53/58) of patients undergoing active anticancer therapy were seropositive. The seropositivity rate among the patients with active anticancer therapy in the UC and RCC groups was 87% (n = 33/37) and 95% (n = 20/21), respectively. In the UC group, the anti-SARS-CoV-2 S IgG antibody titer did not significantly differ between the off-treatment patients (median 458 U/mL) and those receiving ICI therapy (median 369 U/mL) and between the off-treatment patients and those receiving systemic chemotherapy (median 779 U/mL) (Fig. 3a) . The seropositivity rate in patients with UC in the ICI therapy, chemotherapy, and off-treatment groups was 87%, 86%, and 95%, respectively (Fig. 3b) . In the RCC group, the anti-SARS-CoV-2 S IgG antibody titer did not significantly differ between the offtreatment patients (median 927 U/mL) and those receiving therapy with ICIs AE TKIs (median 369 U/mL) and between the off-treatment patients and those receiving TKIs (median 516 U/mL) (Fig. 3c) . The seropositivity rate in patients with UC in the ICIs AE TKI therapy, TKI therapy, and offtreatment groups was 100%, 91%, and 100%, respectively (Fig. 3d) . The anti-SARS-CoV-2 S antibody titer in patients with concomitant steroid use (median 72 U/mL) was significantly lower than those without concomitant steroid use (median 480 U/mL) (P = 0.014, Fig. 3e ). The seropositivity rate in patients with steroids (À) and steroids (+) was 92% and 89%, respectively (P = 0.557, Fig. 3f ). The seropositivity rate in patients with concomitant steroid use in the UC and RCC groups was 89% and 96%, respectively (Fig. 3f) . We evaluated the effect of prior therapy on anti-SARS-CoV-2 S IgG antibody titer in UC patients who are treated with ICI (n = 30) (Fig. S1a) . The seropositivity in patients with ICI ≤2 lines (n = 28) and ≥3 lines (n = 2) was 89% and 50%, respectively (Fig. S1b) . We observed no significant association between the time anti-SARS-CoV-2 S IgG antibody titer and time from final administration of chemotherapy to initiation of ICIs therapy (Fig. S1) , time from final administration of chemotherapy to vaccination (Fig. S1d) , and time from initiation of ICIs therapy to vaccination (Fig. S1e) .

Univariable logistic regression analysis for seropositivity showed that age (OR 0.92; P = 0.045) and stage M1 disease (OR 0.09; P = 0.029) were significantly and negatively associated with seropositivity ( Table 2) . Summary of the present study was shown in a visual abstract (Fig. S2 ).

The effect of active anticancer treatment on the serologic response to the SARS-CoV-2 mRNA vaccine is a subject of intense interest. Several previous studies showed that patients treated for solid tumors have shown an impaired but sufficiently maintained serologic response (90-95.2%) after receiving the second BNT162b2 dose. 5, 20 Our observation of seropositivity in patients with UC and RCC is consistent with previous studies. [4] [5] [6] However, the response of patients with UC and RCC who were receiving therapy with ICIs and/or TKIs remains unreported. Our study revealed that most of the patients with UC and RCC exhibited an adequate antibody response (90-96%) to the BNT162b2 vaccine, but nonresponders were widely distributed among patients with UC. This observation might be influenced by the older age in the UC group (median 73 years). Although the concomitant use of steroids significantly impacted the titer of antibodies to the SARS-CoV-2 vaccine, it was not associated with seropositivity. This finding might be related to the minimum dose of steroids (prednisone: 5-10 mg) in our cohort.

Although further study is necessary, a minimal dose of steroids may not impair seropositivity to the SARS-CoV-2 mRNA vaccination. Our univariable analysis revealed that older age and M1 disease, not active anticancer therapy, were significantly associated with impaired seropositivity. Older age is a wellknown risk factor for impaired serologic response to vaccinations. Furthermore, impaired serologic response in patients with M1 disease is reasonable in terms of cancer development in the context of an immunosuppressed state. Therefore, it must be recognized that not only active treatment interventions but also older age and metastatic status are key factors involved in impaired serologic response to the BNT162b2 vaccine.

Although we observed that 92% (n = 53/58) of patients undergoing active anticancer therapy were seropositive, the effectiveness of SARS-CoV-2 vaccines cannot be solely measured according to antibody titers. 21 Both antibody and T cell responses are necessary to protect against infection. Although a very low antibody response rate (17.8%) was reported in immunocompromised kidney transplant recipients after the second mRNA vaccination dose, the induction of an anti-S T cell-specific response was observed in 51.1% of these patients after the second mRNA vaccination dose. 22 These observations suggested that the positive response rate for cellular immunity might differ from the antibody titer, meaning that the evaluation of T cell response in individuals with impaired immunogenicity is crucial. Thus, it must be recognized that several issues still remain unknown regarding the level of antibodies necessary to protect against SARS-CoV-2 infection.

The seropositivity rates in patients with UC and RCC in our study are similar to that in previous studies of patients with solid tumors (approximately 90%). [4] [5] [6] However, the definition of anti-SARS-CoV-2 IgG seropositivity varied across these studies because of differences in the study population, sample size, and measurement methods. There are several commercially available kits that measure the titer of anti-SARS-CoV-2 IgG antibodies, and the many antibody testing methods and different cutoff values employed across the studies may affect the results. For example, the LIAISON SARS-CoV-2 TrimetricS IgG assay (Diasorin, Saluggia, Italy) uses a positive cutoff value of 13.0 arbitrary U/mL, 23,24 the Anti-SARS-CoV-2 QuantiVac ELISA (IgG) for S protein (Euroimmun, L€ ubeck, Germany) uses a positive cutoff value of 35.2 binding antibody U/mL, 25 the ARCHITECT SARS-CoV-2 IgG II Quant assay for S protein (Abbott Laboratories, Chicago, IL, USA) uses a positive cutoff value of 50.0 arbitrary U/mL, 26, 27 and the Elecsys Anti-SARS-CoV-2 S assay (Roche Diagnostics) uses a positive cutoff value of ≥15 U/mL for the presence of neutralizing antibodies. Currently, only one study has investigated the agreement of three serologic tests from different suppliers (Abbott, Roche, and Diasorin), 28 and a good agreement (Cohen kappa, 0.71-0.87) was reported. However, the same study also reported the inadequate performance of these tests with samples with low seroprevalence. 28 Thus, these findings highlight the importance of carefully interpreting the results from different tests. Information concerning the activity levels necessary to protect against breakthrough infections is also needed.

The major limitations of our study include the limited sample size in a single-center and retrospective design. We could not compare the antibody titers between the Ctrl and UC/ RCC groups because of the age difference. The duration of long-term immunity remains unclear because we evaluated IgG antibody titers during the early phase of mass immunization in Japan. Because the acquisition of cellular immunity is necessary for infection protection, the measurement of antibody titers alone cannot adequately assess the immune response to vaccination. Furthermore, the efficacy of Pfizer/ BioNTech BNT162b2 for the Omicron variant is limited because it can escape antibody neutralization. 29 The Omicron variant is rapidly becoming the dominant SARS-CoV-2 virus, which limits the usefulness of the present study.

In conclusion, this retrospective study confirmed that undergoing active anticancer therapy did not greatly reduce the rate of anti-SARS-CoV-2 IgG seroconversion after the second BNT162b2 mRNA vaccine in patients with UC or RCC. However, several questions remain unanswered, and further investigation is warranted to determine the duration of immunity under active anticancer therapy, the effect of reduced titers on the protective activity against breakthrough infections, and the efficacy of a third vaccination dose in patients with UC or RCC with an impaired serologic response. between the patients with ICI ≤2 lines (n = 28) and ≥3 lines (n = 2). (c) The association between the anti-SARS-CoV-2 S IgG antibody titer and time from final administration of chemotherapy to initiation of ICIs therapy. (d) The association between the anti-SARS-CoV-2 S IgG antibody titer and time from final administration of chemotherapy to vaccination. (e) The association between the anti-SARS-CoV-2 S IgG antibody titer and time from initiation of ICIs therapy to vaccination. Figure S2 . Visual abstract.

Analyses of risk, racial disparity, and outcomes among US patients with cancer and COVID-19 infection

Seroconversion rates following COVID-19 vaccination among patients with cancer

Adaptive immunity and neutralizing antibodies against SARS-CoV-2 variants of concern following vaccination in patients with cancer: the CAPTURE study

Serologic status and toxic effects of the SARS-CoV-2 BNT162b2 vaccine in patients undergoing treatment for cancer

Evaluation of seropositivity following BNT162b2 messenger RNA vaccination for SARS-CoV-2 in patients undergoing treatment for cancer

Serologic response to COVID-19 infection and/or vaccine in cancer patients on active treatment

Risk stratification for the prognosis of patients with chemoresistant urothelial cancer treated with pembrolizumab

Impact of histological variants on outcomes in patients with urothelial carcinoma treated with pembrolizumab: a propensity score matching analysis

Pembrolizumab for treating advanced urothelial carcinoma in patients with impaired performance status: analysis of a Japanese nationwide cohort

Impact of the objective response to and number of cycles of platinum-based first-line chemotherapy for metastatic urothelial carcinoma on overall survival of patients treated with pembrolizumab

Efficacy and safety of pembrolizumab for older patients with chemoresistant urothelial carcinoma assessed using propensity score matching

Impact of prior intravesical bacillus Calmette-Guerin therapy on the effectiveness of pembrolizumab for patients with metastatic urothelial carcinoma

Avelumab plus Axitinib versus sunitinib for advanced renal-cell carcinoma

Nivolumab plus ipilimumab versus sunitinib in advanced renal-cell carcinoma

Pembrolizumab plus Axitinib versus sunitinib for advanced renal-cell carcinoma

Efficacy and safety of first-line nivolumab plus ipilimumab in patients with metastatic renal cell carcinoma: a multicenter retrospective study

Outcomes of axitinib versus sunitinib as first-line therapy to patients with metastatic renal cell carcinoma in the immune-oncology era

Prognosis of Japanese metastatic renal cell carcinoma patients in the targeted therapy era

Immunogenicity and reactogenicity of SARS-CoV-2 vaccines in patients with cancer: the CANVAX cohort study

Impaired immunogenicity of BNT162b2 anti-SARS-CoV-2 vaccine in patients treated for solid tumors

Neutralizing antibody titres in SARS-CoV-2 infections

Antibody response to COVID-19 vaccination in patients receiving dialysis

Impaired humoral response in renal transplant recipients to SARS-CoV-2 vaccination with BNT162b2 (Pfizer-BioNTech)

Humoral response after SARS-CoV-2 mRNA vaccination in a cohort of hemodialysis patients and kidney transplant recipients

Impaired immune response to SARS-CoV-2 vaccination in dialysis patients and in kidney transplant recipients

Antibody and T cell response to SARS-CoV-2 messenger RNA BNT162b2 vaccine in kidney transplant recipients and hemodialysis patients

Antibody response after a third dose of the mRNA-1273 SARS-CoV-2 vaccine in kidney transplant recipients with minimal serologic response to 2 doses

Side-by-side comparison of three fully automated SARS-CoV-2 antibody assays with a focus on specificity

Omicron neutralising antibodies after third COVID-19 vaccine dose in patients with cancer

This study was funded by the Japan Society for the Promotion of Science (No. 19H05556, 20K09517, 21K09339). The authors would like to thank Yukie Nishizawa, Mitsuharu Miyadate, and Satomi Sakamoto for their invaluable support with data collection.

Kyo Togashi: Data curation; writingreview and editing. Shingo Hatakeyama: Conceptualization; data curation; formal analysis; funding acquisition; investigation; methodology; project administration; resources; software; visualization; writingoriginal draft; writingreview and editing. Tohru Yoneyama: Conceptualization; data curation; formal analysis; funding acquisition; methodology; software; writingreview and editing. Tomoko Hamaya: Data curation; methodology; writingreview and editing. Takuma Narita: Data curation; resources; writingreview and editing. Naoki Fujita: Data curation; methodology; resources; writingreview and

None declared.

Yes (2021-089).

Obtained via an opt-out approach.

N/A.

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