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      Primary Renal Tumour Response in Patients Treated with Nivolumab for Metastatic Renal Cell Carcinoma: Results from the GETUG-AFU 26 NIVOREN Trial.

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          Abstract

          Primary tumour response may impact therapeutic strategies in metastatic renal cell carcinoma (mRCC) but remains unknown in the era of immune checkpoint inhibitors. We aimed to describe the response of the primary tumour in patients who did not undergo upfront cytoreductive nephrectomy (uCN) and were treated with nivolumab in the GETUG-AFU-26 NIVOREN phase 2 trial. Primary tumour response was prospectively assessed, as well as the overall response rate (ORR), progression-free survival (PFS), and overall survival (OS). Among 720 patients, 111 did not undergo uCN, mainly patients with intermediate (45%) and poor (49%) International mRCC Database Consortium (IMDC) risk. In the 111 patients, nivolumab was used in the second line for 63% of patients and the third line or more for 37%, with an ORR of 16% (95% confidence interval [CI] 1025%); with a median follow-up of 24.5 mo (95% CI 21.6-27.1), median PFS was 2.7 mo (95% CI 2.5-4.0) and median OS was 15.9 mo (95% CI 9.5-19.8). A total of 67 patients had an evaluable primary renal lesion, four of whom (6%) experienced shrinkage of more than 30%. Overall, patients who did not undergo uCN had adverse baseline characteristics and nivolumab activity against the primary tumour was limited. PATIENT SUMMARY: In this report, we observed that nivolumab was associated with a limited response of the primary tumour in previously treated patients with metastatic kidney cancer.

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          Author and article information

          Journal
          Eur Urol
          European urology
          Elsevier BV
          1873-7560
          0302-2838
          September 2021
          : 80
          : 3
          Affiliations
          [1 ] Department of Urology, UPEC-Henri Mondor Hospital, Assistance Publique-Hôpitaux de Paris, Créteil, France.
          [2 ] Centre Leon Bérard, Lyon, France.
          [3 ] Centre Eugene Marquis, Rennes, France.
          [4 ] Centre Georges François Leclerc, Dijon, France.
          [5 ] Strasbourg University Hospital, Strasbourg, France.
          [6 ] Hôpital Européen Georges Pompidou, Assistance Publique-Hôpitaux de Paris, Paris, France.
          [7 ] Centre François Baclesse, Caen, France.
          [8 ] Medical Oncology Department, Institut Paoli-Calmettes, Aix-Marseille Université, Marseille, France.
          [9 ] Institut Universitaire du Cancer Toulouse-Oncopole, Toulouse, France.
          [10 ] Institut de Cancérologie de Lorraine, Vandœuvre-lès-Nancy, France.
          [11 ] Limoges University Hospital, Limoges, France.
          [12 ] Centre René Gauducheau, Saint Herblain, France.
          [13 ] Department of Medical Oncology, Montpellier University Hospital, Hôpital Saint Eloi, Montpellier, France.
          [14 ] Hôpital Saint Louis, Assistance Publique-Hôpitaux de Paris, Paris, France.
          [15 ] Centre Jean Perrin, Clermont-Ferrand, France.
          [16 ] GETUG Group, Unicancer, Paris, France.
          [17 ] Gustave Roussy Cancer Campus, Université Paris-Saclay, Villejuif, France.
          [18 ] Gustave Roussy Cancer Campus, Université Paris-Saclay, Villejuif, France. Electronic address: laurence.albiges@gustaveroussy.fr.
          Article
          S0302-2838(21)00389-4
          10.1016/j.eururo.2021.05.020
          34103181
          90b065dd-baf1-4ed5-977c-365ab1f1b8de
          History

          Renal cell carcinoma,Immune checkpoint inhibitors,Nivolumab,Primary renal tumour,Cytoreductive nephrectomy

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