Effectiveness of pembrolizumab in trial-ineligible patients with metastatic urothelial carcinoma

Background The KEYNOTE-045 trial showed that pembrolizumab therapy improved the survival of patients with advanced urothelial carcinoma (UC). However, its effectiveness in trial-ineligible patients remains unclear. Materials and methods We conducted a multicenter retrospective study to evaluate the...

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Veröffentlicht in:Cancer Immunology, Immunotherapy Immunotherapy, 2023-04, Vol.72 (4), p.841-849
Hauptverfasser: Fukuokaya, Wataru, Yanagisawa, Takafumi, Hashimoto, Masaki, Yamamoto, Shutaro, Koike, Yuhei, Imai, Yu, Iwatani, Kosuke, Onuma, Hajime, Ito, Kagenori, Urabe, Fumihiko, Tsuzuki, Shunsuke, Kimura, Shoji, Miki, Jun, Oyama, Yu, Abe, Hirokazu, Kimura, Takahiro
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Sprache:eng
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Zusammenfassung:Background The KEYNOTE-045 trial showed that pembrolizumab therapy improved the survival of patients with advanced urothelial carcinoma (UC). However, its effectiveness in trial-ineligible patients remains unclear. Materials and methods We conducted a multicenter retrospective study to evaluate the effectiveness of pembrolizumab in patients with metastatic UC who were trial-ineligible. The data of 164 consecutive patients with platinum-treated metastatic UC who received pembrolizumab as second-line therapy were analyzed. Trial eligibility was assessed using the KEYNOTE-045 criteria. Inverse probability of treatment weighting (IPTW) was used to balance patient characteristics. Overall survival (OS) and progression-free survival (PFS) were examined using the IPTW-adjusted Kaplan–Meier method. IPTW-adjusted restricted mean survival times (RMSTs) were compared between ineligible and eligible patients. Results Seventy-five patients (45.7%) were classified as ineligible based on the KEYNOTE-045 criteria. Baseline hemoglobin concentration of less than 9.0 g/dL was the most common reason for trial protocol violation ( N  = 23 [14.0%]). An IPTW-adjusted logistic regression model showed that the trial-eligibility was not significantly associated with objective response (OR: 0.65, 95% CI: 0.32 to 1.29, P  = 0.22). Ineligible patients had similar RMST for PFS (difference: 3.8 months, 95% CI: −1.6 to 9.3, P  = 0.17) and RMST for OS (difference: 1.4 months, 95% CI: −5.4 to 8.2, P  = 0.93) compared with eligible patients. Conclusions This study suggests that the effectiveness of pembrolizumab may be retained in ineligible patients with platinum-treated metastatic UC. Expanding trial eligibility criteria for these patients may be beneficial.
ISSN:0340-7004
1432-0851
DOI:10.1007/s00262-022-03291-5