Administration of Nivolumab in Metastatic Renal Cell Cancer Following Treatment With mTOR Inhibitors

BACKGROUND/AIMImmunotherapy with checkpoint inhibitors is currently considered a cornerstone of metastatic renal clear cell cancer (mRCC) therapy. Despite the general improvement in the survival of patients with mRCC, there are some clinical situations that have not been specifically evaluated in cl...

Full description

Saved in:
Bibliographic Details
Published inIn vivo (Athens) Vol. 35; no. 5; pp. 2981 - 2990
Main Authors KOPECKY, JINDRICH, KUBECEK, ONDREJ, BUCHLER, TOMAS, MELICHAR, BOHUSLAV, POPRACH, ALEXANDR, ZEMANOVA, MILADA, KATOLICKA, JANA, KISS, IGOR, HAJEK, JAROSLAV, STUDENTOVA, HANA, SPISAROVA, MARTINA
Format Journal Article
LanguageEnglish
Published International Institute of Anticancer Research 01.09.2021
Online AccessGet full text

Cover

Loading…
More Information
Summary:BACKGROUND/AIMImmunotherapy with checkpoint inhibitors is currently considered a cornerstone of metastatic renal clear cell cancer (mRCC) therapy. Despite the general improvement in the survival of patients with mRCC, there are some clinical situations that have not been specifically evaluated in clinical trials, such as the use of everolimus before nivolumab.PATIENTS AND METHODSWe performed a retrospective analysis evaluating the efficacy of nivolumab in the real-world setting, including a subset of patients with previous mTOR inhibitor therapy.RESULTSFrom a total of 56 patients, 25 were pre-treated with everolimus before receiving nivolumab. The overall progression-free survival (PFS), overall survival (OS), and objective response rate were 10.3, 21.3 months, and 34%, respectively. There were no statistically significant differences in patients who were or were not pre-treated with everolimus.CONCLUSIONmRCC patients should be treated with checkpoint inhibitors and prior use of mTOR inhibitors should not be a definitive exclusion criterium.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0258-851X
1791-7549
DOI:10.21873/invivo.12593