Oncological Outcomes of Delayed Nephrectomy After Optimal Response to Immune Checkpoint Inhibitors for Metastatic Renal Cell Carcinoma.


Journal

European urology oncology
ISSN: 2588-9311
Titre abrégé: Eur Urol Oncol
Pays: Netherlands
ID NLM: 101724904

Informations de publication

Date de publication:
10 2022
Historique:
received: 23 03 2022
revised: 06 06 2022
accepted: 02 07 2022
pubmed: 20 7 2022
medline: 13 10 2022
entrez: 19 7 2022
Statut: ppublish

Résumé

In the current era of immune checkpoint inhibitors (ICIs), the role and optimal timing of a nephrectomy in patients with metastatic renal cell carcinoma (mRCC) remain unknown. To assess the oncological outcomes of patients who responded to ICI-based treatments and were subsequently treated with a delayed nephrectomy. This national retrospective evaluation included 30 patients with mRCC who underwent a nephrectomy after a complete response (CR) or a major partial response (>80%) to ICI treatment at metastatic sites. Partial or radical nephrectomy after a favorable response to ICI treatment. Disease-free survival (DFS), progression-free survival (PFS), overall survival (OS), and potential discontinuation of systemic treatment were assessed. ICI-based treatments included ipilimumab-nivolumab (40%), ICI + tyrosine kinase inhibitor (10%), and nivolumab (50%). A delayed nephrectomy was performed after a median ICI treatment duration of 10 mo. In 19 cases (63.3%), surgeons faced difficulties due to adhesions or inflammatory changes. A complete pathological response was observed in 16.7% of patients. After a median follow-up of 19.5 mo after nephrectomy, 76.7% of patients achieved DFS. At 1 yr, 66.7% of patients were free from systemic treatment. The PFS and OS rates were, respectively, 96.7% and 100% at 1 yr, and 78.3% and 86.1% at 2 yr. Patients with a CR at metastatic sites had a better prognosis than those with a major partial response, in terms of DFS (p = 0.022) and PFS (p = 0.014). Despite potentially challenging surgery, a delayed nephrectomy for patients who responded to ICI treatment provided promising oncological outcomes, and the majority of patients could discontinue systemic treatment. In this study, we evaluated the clinical outcome in patients who responded well to immunotherapy, and subsequently underwent kidney ablation surgery. Three-quarters of patients experienced no recurrence, and in most cases, medical treatment could be discontinued.

Sections du résumé

BACKGROUND
In the current era of immune checkpoint inhibitors (ICIs), the role and optimal timing of a nephrectomy in patients with metastatic renal cell carcinoma (mRCC) remain unknown.
OBJECTIVE
To assess the oncological outcomes of patients who responded to ICI-based treatments and were subsequently treated with a delayed nephrectomy.
DESIGN, SETTING, AND PARTICIPANTS
This national retrospective evaluation included 30 patients with mRCC who underwent a nephrectomy after a complete response (CR) or a major partial response (>80%) to ICI treatment at metastatic sites.
INTERVENTION
Partial or radical nephrectomy after a favorable response to ICI treatment.
OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS
Disease-free survival (DFS), progression-free survival (PFS), overall survival (OS), and potential discontinuation of systemic treatment were assessed.
RESULTS AND LIMITATIONS
ICI-based treatments included ipilimumab-nivolumab (40%), ICI + tyrosine kinase inhibitor (10%), and nivolumab (50%). A delayed nephrectomy was performed after a median ICI treatment duration of 10 mo. In 19 cases (63.3%), surgeons faced difficulties due to adhesions or inflammatory changes. A complete pathological response was observed in 16.7% of patients. After a median follow-up of 19.5 mo after nephrectomy, 76.7% of patients achieved DFS. At 1 yr, 66.7% of patients were free from systemic treatment. The PFS and OS rates were, respectively, 96.7% and 100% at 1 yr, and 78.3% and 86.1% at 2 yr. Patients with a CR at metastatic sites had a better prognosis than those with a major partial response, in terms of DFS (p = 0.022) and PFS (p = 0.014).
CONCLUSIONS
Despite potentially challenging surgery, a delayed nephrectomy for patients who responded to ICI treatment provided promising oncological outcomes, and the majority of patients could discontinue systemic treatment.
PATIENT SUMMARY
In this study, we evaluated the clinical outcome in patients who responded well to immunotherapy, and subsequently underwent kidney ablation surgery. Three-quarters of patients experienced no recurrence, and in most cases, medical treatment could be discontinued.

Identifiants

pubmed: 35853818
pii: S2588-9311(22)00114-6
doi: 10.1016/j.euo.2022.07.002
pii:
doi:

Substances chimiques

Immune Checkpoint Inhibitors 0
Ipilimumab 0
Protein Kinase Inhibitors 0
Nivolumab 31YO63LBSN

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

577-584

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2022 European Association of Urology. Published by Elsevier B.V. All rights reserved.

Auteurs

Géraldine Pignot (G)

Department of Surgical Oncology 2, Institut Paoli-Calmettes, Marseille, France. Electronic address: pignotg@ipc.unicancer.fr.

Antoine Thiery-Vuillemin (A)

Medical Oncology Department, CHRU Besancon - Hopital Jean Minjoz, Besançon, France.

Laurence Albigès (L)

Department of Medical Oncology, Institut Gustave Roussy, Villejuif, France.

Jochen Walz (J)

Department of Surgical Oncology 2, Institut Paoli-Calmettes, Marseille, France.

Hervé Lang (H)

Urology Department, University Hospital of Strasbourg, Strasbourg, France.

Loïc Balssa (L)

Urology Department, CHRU Besancon - Hopital Jean Minjoz, Besançon, France.

Bastien Parier (B)

Urology Department, Bicêtre Hospital, Le Kremlin Bicêtre, France.

Lionnel Geoffrois (L)

Department of Medical Oncology, Institut de Cancérologie de Lorraine, Vandoeuvre lès Nancy, France.

Karim Bensalah (K)

Department of Urology, CHU Rennes - Hopital Pontchaillou, Rennes, France.

Friederike Schlürmann (F)

Department of Medical Oncology, CHRU Brest, Brest, France.

Sylvain Ladoire (S)

Department of Medical Oncology, Centre Georges-François Leclerc, Dijon, France.

Pierre Bigot (P)

Urology Department, CHU d'Angers, Angers, France.

Delphine Borchiellini (D)

Department of Medical Oncology, Centre Antoine Lacassagne, Nice, France.

Ophélie Cassuto (O)

Department of Medical Oncology, Polyclinique St Georges, Nice, France.

Constance Thibault (C)

Department of Medical Oncology, Hôpital Européen Georges Pompidou, Paris, France.

Alexandre Ingels (A)

Urology Department, CHU Henri-Mondor, Créteil, France.

Véronique Saldana (V)

Department of Medical Oncology, CHU Henri-Mondor, Créteil, France.

Guilhem Roubaud (G)

Department of Medical Oncology, Institut Bergonié, Bordeaux, France.

Jean-Christophe Bernhard (JC)

Urology Department, CHU de Bordeaux - Hôpital Pellegrin, Bordeaux, France.

Gwenaelle Gravis (G)

Medical Oncology Department, Institut Paoli-Calmettes, Aix-Marseille Université, Inserm, CNRS, CRCM, Marseille, France.

Philippe Barthélémy (P)

Medical Oncology, Institut de Cancérologie Strasbourg Europe, Strasbourg, France.

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