First-Line Enfortumab Vedotin Plus Pembrolizumab in Platinum-Ineligible Urothelial Carcinoma: A Three-Case Series

一线恩福妥单抗联合帕博利珠单抗治疗铂类不适宜化疗的尿路上皮癌:三例病例系列研究

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Abstract

Locally advanced or metastatic urothelial carcinoma (la/mUC) has a poor prognosis. In routine clinical practice, platinum-based chemotherapy has generally been used as first-line treatment. Enfortumab vedotin plus pembrolizumab (EVP) has recently been introduced as another first-line option; however, patients who are platinum-ineligible, such as those with severe renal dysfunction and/or poor performance status, are often underrepresented in clinical studies, and the optimal systemic therapy for this group remains uncertain. Herein, we report three platinum-ineligible patients with la/mUC who received standard-dose EVP as first-line therapy. Platinum ineligibility was defined as creatinine clearance (CrCl) < 30 mL/min and/or Eastern Cooperative Oncology Group performance status (ECOG PS) ≥ 3. In Case 1 (hemodialysis; ECOG PS 1), EVP resulted in improvement of bone metastases and durable disease control, with manageable adverse events (AEs), including grade 2 skin toxicity, dysgeusia, hypothyroidism, and transient peripheral sensory neuropathy that resolved after temporary treatment interruption. In Case 2 (CrCl 23.1 mL/min; ECOG PS 2), EVP induced a partial response in the bladder and nodal lesions; however, treatment was complicated by early-onset grade 4 immune-related nephritis requiring high-dose corticosteroids. Best supportive care was adopted at progression. In Case 3 (ECOG PS 3), rapidly progressive renal pelvic la/mUC showed early disease progression with spinal cord compression despite EVP, leading to the patient being transitioned to best supportive care. Across all three cases, no life-threatening toxicity was clearly attributable to enfortumab vedotin. These observations suggest that standard-dose EVP may be a feasible first-line option for carefully selected platinum-ineligible patients, when administered with close monitoring, flexible dose adjustment, and prompt management of immune-related and other AEs.

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