@article{3dcd04c8d752474c9802f048f17556c5,
title = "Phase II Study of Neoadjuvant Nivolumab in Patients with Locally Advanced Clear Cell Renal Cell Carcinoma Undergoing Nephrectomy",
abstract = "Immune checkpoint inhibitor therapy improves survival in patients with metastatic renal cell carcinoma (RCC) but has not been studied well preoperatively in patients with localized disease undergoing nephrectomy. We conducted a single-center study to evaluate the safety and feasibility of neoadjuvant nivolumab in patients undergoing nephrectomy for localized RCC. Eligible patients had a >20% risk of recurrence, as estimated by a preoperative nomogram. Patients received nivolumab every 2 wk for four treatments prior to surgery. The primary endpoints were feasibility, defined as completing at least three treatments without significant surgical delay, and safety, defined as the rate of surgical complications. Treatment effects were assessed by radiomics and immunohistochemistry. A total of 18 patients (11 men; median age 60 yr) with clear cell RCC were enrolled. All received at least one dose of nivolumab and proceeded to nephrectomy without delay; 16/18 patients completed all four doses. Two patients discontinued nivolumab for immune-related adverse events, and four had surgical complications as per the Clavien-Dindo classification. Integrated pathology plus radiomic analysis demonstrated an association between post-treatment immune infiltration and low entropy apparent diffusion coefficient on magnetic resonance imaging. Nivolumab prior to nephrectomy was safe and feasible, without significant surgical delays and with an expected rate of immune-related adverse events. Patient summary: We evaluated the outcomes for patients with localized kidney cancer who received immunotherapy prior to surgery to remove their kidney tumor. In a small group of patients who had cancer confined to the kidney, this approach appeared safe and feasible.",
keywords = "Immune checkpoint inhibitors, Immunotherapy, Neoadjuvant, Nephrectomy, Renal cell carcinoma",
author = "Carlo, {Maria I.} and Kyrollis Attalla and Yousef Mazaheri and Sounak Gupta and Onur Yildirim and Murray, {Samuel J.} and Coskey, {Devyn T.} and Ritesh Kotecha and Lee, {Chung Han} and Feldman, {Darren R.} and Paul Russo and Sujata Patil and Motzer, {Robert J.} and Coleman, {Jonathan A.} and Durack, {Jeremy C.} and Chen, {Ying Bei} and Oguz Akin and {Ari Hakimi}, A. and Voss, {Martin H.}",
note = "Funding Information: Funding/Support and role of the sponsor: This work was sponsored by National Cancer Institute Division of Cancer Treatment and Diagnosis and funded in part by the NIH/NCI Cancer Center Support Grant P30 CA008748. Maria I. Carlo is supported by The Kidney Cancer Association and Harold Amos Medical Faculty Development Award. Ritesh Kotecha is supported (in part) by the Academy of Kidney Cancer Investigators of the CDMRP/DOD (KC200127). Funding Information: Financial disclosures: Martin H. Voss certifies that all conflicts of interest, including specific financial interests and relationships and affiliations relevant to the subject matter or materials discussed in the manuscript (eg, employment/affiliation, grants or funding, consultancies, honoraria, stock ownership or options, expert testimony, royalties, or patents filed, received, or pending), are the following: Ritesh Kotecha reports advisory board consultation for Eisai and reports receiving institutional research funding from Pfizer and Takeda. Chung-Han Lee reports research funding from Eisai, Bristol-Myers Squibb, Exelixis, Pfizer, and Calithera; and consulting or advisory role with Exelixis and Eisai. DF reports research funding from Seattle Genetics and Novartis. Robert J. Motzer reports consulting or advisory role with Pfizer, Novartis, Eisai, Exelixis, Merck, Genentech, Incyte, Lilly, and Roche; institutional research funding from Pfizer, Bristol Myers Squibb, Eisai, Novartis, Genentech, and Roche; and travel/accommodation from Bristol-Myers Squibb. A. Ari Hakimi reports advisory role with Merck. Martin H. Voss reports research grants from Bristol-Myers Squibb and Genentech/Roche; honoraria from Novartis; travel/accommodation from Eisai, Novartis, and Takeda; and consulting or advisory role with Alexion Pharmaceuticals, Bayer, Calithera Biosciences, Corvus Pharmaceuticals, Exelixis, Eisai, GlaxoSmithKline, Natera, Novartis, and Pfizer. The remaining authors declare no competing financial interests. Publisher Copyright: {\textcopyright} 2022 European Association of Urology",
year = "2022",
month = jun,
doi = "10.1016/j.eururo.2022.01.043",
language = "English",
volume = "81",
pages = "570--573",
journal = "European Urology",
issn = "0302-2838",
publisher = "Elsevier",
number = "6",
}