Nivolumab in Combination with Stereotactic Body Radiotherapy in Pretreated Patients with Metastatic Renal Cell Carcinoma. Results of the Phase II NIVES Study.


Journal

European urology
ISSN: 1873-7560
Titre abrégé: Eur Urol
Pays: Switzerland
ID NLM: 7512719

Informations de publication

Date de publication:
Mar 2022
Historique:
received: 01 06 2021
accepted: 15 09 2021
pubmed: 5 10 2021
medline: 19 4 2022
entrez: 4 10 2021
Statut: ppublish

Résumé

Nivolumab showed an overall survival (OS) benefit in pretreated metastatic renal cell carcinoma (mRCC). The role of stereotactic body radiotherapy (SBRT) in mRCC remains to be defined. Our aim was to evaluate the efficacy and safety of SBRT in combination with nivolumab in second- and third-line mRCC patients. The NIVES study was a phase II, single-arm, multicenter trial in patients with mRCC with measurable metastatic sites who progressed after antiangiogenic therapy, of whom at least one was suitable for SBRT. The patients received SBRT to a lesion at a dose of 10 Gy in three fractions for 7 d from the first infusion of nivolumab. Nivolumab was given at an initial dose of 240 mg every 14 d for 6 mo and then 480 mg q4-weekly in responding patients. We hypothesized that nivolumab plus SBRT improves the objective response rate (ORR) compared with nivolumab alone from 25% (derived from historical controls) to 40%. Secondary endpoints were progression-free survival (PFS), OS, disease control rate (DCR) of irradiated and nonirradiated metastases, and safety. Sixty-nine patients were enrolled from July 2017 to March 2019. The ORR was 17% and the DCR was 55%. The median PFS was 5.6 mo (95% confidence interval [CI], 2.9-7.1) and median OS 20 mo (95% CI, 17-not reached). After 1.5 yr of follow-up, 23 patients died. The median time to treatment response was 2.8 mo and median duration of response was 14 mo. No new safety concerns arose. We did not find sufficient evidence to suggest that nivolumab in combination with SBRT provides an added benefit in pretreated mRCC patients; it should however be evaluated in patients with oligometastatic or oligoprogressive disease. Nivolumab in combination with stereotactic body radiotherapy does not provide evidence of increased outcomes in metastatic renal cell carcinoma patients. However this approach was safe and showed a good response of the irradiated lesions.

Sections du résumé

BACKGROUND BACKGROUND
Nivolumab showed an overall survival (OS) benefit in pretreated metastatic renal cell carcinoma (mRCC). The role of stereotactic body radiotherapy (SBRT) in mRCC remains to be defined.
OBJECTIVE OBJECTIVE
Our aim was to evaluate the efficacy and safety of SBRT in combination with nivolumab in second- and third-line mRCC patients.
DESIGN, SETTING, AND PARTICIPANTS METHODS
The NIVES study was a phase II, single-arm, multicenter trial in patients with mRCC with measurable metastatic sites who progressed after antiangiogenic therapy, of whom at least one was suitable for SBRT.
INTERVENTION METHODS
The patients received SBRT to a lesion at a dose of 10 Gy in three fractions for 7 d from the first infusion of nivolumab. Nivolumab was given at an initial dose of 240 mg every 14 d for 6 mo and then 480 mg q4-weekly in responding patients.
OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS METHODS
We hypothesized that nivolumab plus SBRT improves the objective response rate (ORR) compared with nivolumab alone from 25% (derived from historical controls) to 40%. Secondary endpoints were progression-free survival (PFS), OS, disease control rate (DCR) of irradiated and nonirradiated metastases, and safety.
RESULTS AND LIMITATIONS CONCLUSIONS
Sixty-nine patients were enrolled from July 2017 to March 2019. The ORR was 17% and the DCR was 55%. The median PFS was 5.6 mo (95% confidence interval [CI], 2.9-7.1) and median OS 20 mo (95% CI, 17-not reached). After 1.5 yr of follow-up, 23 patients died. The median time to treatment response was 2.8 mo and median duration of response was 14 mo. No new safety concerns arose.
CONCLUSIONS CONCLUSIONS
We did not find sufficient evidence to suggest that nivolumab in combination with SBRT provides an added benefit in pretreated mRCC patients; it should however be evaluated in patients with oligometastatic or oligoprogressive disease.
PATIENT SUMMARY RESULTS
Nivolumab in combination with stereotactic body radiotherapy does not provide evidence of increased outcomes in metastatic renal cell carcinoma patients. However this approach was safe and showed a good response of the irradiated lesions.

Identifiants

pubmed: 34602312
pii: S0302-2838(21)02040-6
doi: 10.1016/j.eururo.2021.09.016
pii:
doi:

Substances chimiques

Nivolumab 31YO63LBSN

Types de publication

Clinical Trial, Phase II Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

274-282

Commentaires et corrections

Type : CommentIn
Type : CommentIn
Type : CommentIn
Type : CommentIn

Informations de copyright

Copyright © 2021 European Association of Urology. Published by Elsevier B.V. All rights reserved.

Auteurs

Cristina Masini (C)

Medical Oncology Unit, Clinical Cancer Centre, AUSL-IRCCS di Reggio Emilia, Reggio Emilia, Italy. Electronic address: masini.cristina@ausl.re.it.

Cinzia Iotti (C)

Radiation Oncology Unit, Clinical Cancer Centre, AUSL-IRCCS di Reggio Emilia, Reggio Emilia, Italy.

Ugo De Giorgi (U)

Department of Medical Oncology, Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST) IRCCS, Meldola, Italy.

Roberto Salvatore Bellia (RS)

Radiotherapy Unit, Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST) IRCCS, Meldola, Italy.

Sebastiano Buti (S)

Medical Oncology Unit, University Hospital of Parma, Parma, Italy.

Francesco Salaroli (F)

Radiotherapy Unit, University Hospital of Parma, Parma, Italy.

Ilaria Zampiva (I)

Medical Oncology Unit, University Hospital, AOUI Verona, Italy.

Renzo Mazzarotto (R)

Radiotherapy Unit, University Hospital, AOUI Verona, Italy.

Claudia Mucciarini (C)

Medical Oncology Unit, Ramazzini Hospital, Carpi, Italy.

Maria Giuseppa Vitale (MG)

Department of Oncology and Hematology, University Hospital of Modena, Modena, Italy.

Alessio Bruni (A)

Radiation Therapy Unit, Department of Oncology and Hematology, University Hospital of Modena, Modena, Italy.

Frank Lohr (F)

Radiation Therapy Unit, Department of Oncology and Hematology, University Hospital of Modena, Modena, Italy.

Giuseppe Procopio (G)

Department of Medical Oncology, Istituto Nazionale dei Tumori IRCCS, Milan, Italy.

Orazio Caffo (O)

Oncology Unit, S. Chiara Hospital, Trento, Italy.

Franco Nole (F)

Medical Oncology Division of Urogenital and Head & Neck Tumors IEO, European Institute of Oncology IRCCS, Milan, Italy.

Franco Morelli (F)

Department of Oncology, IRCCS Ospedale Casa Sollievo della Sofferenza, Opera di Padre Pio, San Giovanni Rotondo, Italy.

Susanne Baier (S)

Oncologia Medica Ospedale Regionale, Bolzano Azienda Sanitaria Alto Adige, Bolzano, Italy.

Consuelo Buttigliero (C)

Department of Oncology, AOU San Luigi Gonzaga, University of Turin, Orbassano (Turin), Italy.

Patrizia Ciammella (P)

Radiation Oncology Unit, Clinical Cancer Centre, AUSL-IRCCS di Reggio Emilia, Reggio Emilia, Italy.

Giorgia Timon (G)

Radiation Oncology Unit, Clinical Cancer Centre, AUSL-IRCCS di Reggio Emilia, Reggio Emilia, Italy.

Emanuela Fantinel (E)

Medical Oncology Unit, Clinical Cancer Centre, AUSL-IRCCS di Reggio Emilia, Reggio Emilia, Italy.

Gabriele Carlinfante (G)

Pathology Unit, Clinical Cancer Centre, AUSL-IRCCS di Reggio Emilia, Reggio Emilia, Italy.

Annalisa Berselli (A)

Medical Oncology Unit, Clinical Cancer Centre, AUSL-IRCCS di Reggio Emilia, Reggio Emilia, Italy.

Carmine Pinto (C)

Medical Oncology Unit, Clinical Cancer Centre, AUSL-IRCCS di Reggio Emilia, Reggio Emilia, Italy.

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