A multicenter study assessing survival in patients with metastatic renal cell carcinoma receiving immune checkpoint inhibitor therapy with and without cytoreductive nephrectomy

医学 肾细胞癌 内科学 回顾性队列研究 全身疗法 肿瘤科 比例危险模型 队列 癌症 免疫疗法 肾切除术 泌尿科 肾癌 外科 乳腺癌
作者
Evan E. Gross,Mingjia Li,Ming Yin,Delaney Orcutt,Duncan Hussey,Elliot Trott,Sarah K. Holt,Erin R. Dwyer,Joel Kramer,Kaylee Oliva,John L. Gore,George R. Schade,Daniel W. Lin,Scott S. Tykodi,Evan T. Hall,John A. Thompson,Anish Parikh,Yuanquan Yang,Katharine A. Collier,Abdul Miah,Sherry Mori-Vogt,Megan Hinkley,Amir Mortazavi,Paul Monk,Edmund Folefac,Steven K. Clinton,Sarah P. Psutka
出处
期刊:Urologic Oncology-seminars and Original Investigations [Elsevier]
标识
DOI:10.1016/j.urolonc.2022.08.013
摘要

• CN combined with ICI was associated with improved OS compared to ICI alone. • First-line ICI was not linked with change in the association between CN and OS. • Deferment of CN after an initial course of ST was not associated with OS. • Improvement in response to ICI was observed in patients who underwent CN. Cytoreductive nephrectomy (CN) for the treatment of metastatic renal cell carcinoma (mRCC) was called into question following the publication of the CARMENA trial. While previous retrospective studies have supported CN alongside targeted therapies, there is minimal research establishing its role in conjunction with immune checkpoint inhibitor (ICI) therapy. To evaluate the association between CN and oncological outcomes in patients with mRCC treated with immunotherapy. A multicenter retrospective cohort study of patients diagnosed with mRCC between 2000 and 2020 who were treated at the Seattle Cancer Care Alliance and The Ohio State University and who were treated with ICI systemic therapy (ST) at any point in their disease course. Overall survival (OS) was estimated using Kaplan Meier analyses. Multivariable Cox proportional hazards models evaluated associations with mortality. The study cohort consisted of 367 patients (CN+ST n = 232, ST alone n = 135). Among patients undergoing CN, 30 were deferred. Median survivor follow-up was 28.4 months. ICI therapy was first-line in 28.1%, second-line in 17.4%, and third or subsequent line (3L+) in 54.5% of patients. Overall, patients who underwent CN+ST had longer median OS (56.3 months IQR 50.2–79.8) compared to the ST alone group (19.1 months IQR 12.8–23.8). Multivariable analyses demonstrated a 67% reduction in risk of all-cause mortality in patients who received CN+ST vs. ST alone ( P < 0.0001). Similar results were noted when first-line ICI therapy recipients were examined as a subgroup. Upfront and deferred CN did not demonstrate significant differences in OS. CN was independently associated with longer OS in patients with mRCC treated with ICI in any line of therapy. Our data support consideration of CN in well selected patients with mRCC undergoing treatment with ICI.
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