Evidence map›Paper›PMID 35853818›Full record

ArticleEuropean urology oncology2022

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

Géraldine Pignot, Antoine Thiery-Vuillemin, Laurence Albigès, Jochen Walz, Hervé Lang, Loïc Balssa, Bastien Parier, Lionnel Geoffrois, Karim Bensalah, Friederike Schlürmann and 11 more

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In one paragraph

Article in European urology oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
6.8field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 45 citations in OpenAlex.

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  8. Perioperative therapies for metastatic renal cell carcinoma.Journal of cancer metastasis and treatment · 2025
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  10. 2024 CUA-KCRNC Expert Report: Management of non-clear cell renal cell carcinoma.Canadian Urological Association journal = Journal de l'Association des urologues du Canada · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors at 18 institutions in 1 country.

Géraldine PignotDepartment of Surgical Oncology 2, Institut Paoli-Calmettes, Marseille, France. Electronic address: pignotg@ipc.unicancer.fr.
Antoine Thiery-VuilleminMedical Oncology Department, CHRU Besancon - Hopital Jean Minjoz, Besançon, France.
Laurence AlbigèsDepartment of Medical Oncology, Institut Gustave Roussy, Villejuif, France.
Jochen WalzDepartment of Surgical Oncology 2, Institut Paoli-Calmettes, Marseille, France.
Hervé LangUrology Department, University Hospital of Strasbourg, Strasbourg, France.
Loïc BalssaUrology Department, CHRU Besancon - Hopital Jean Minjoz, Besançon, France.
Bastien ParierUrology Department, Bicêtre Hospital, Le Kremlin Bicêtre, France.
Lionnel GeoffroisDepartment of Medical Oncology, Institut de Cancérologie de Lorraine, Vandoeuvre lès Nancy, France.
Karim BensalahDepartment of Urology, CHU Rennes - Hopital Pontchaillou, Rennes, France.
Friederike SchlürmannDepartment of Medical Oncology, CHRU Brest, Brest, France.
Sylvain LadoireDepartment of Medical Oncology, Centre Georges-François Leclerc, Dijon, France.
Pierre BigotUrology Department, CHU d'Angers, Angers, France.
Delphine BorchielliniDepartment of Medical Oncology, Centre Antoine Lacassagne, Nice, France.
Ophélie CassutoDepartment of Medical Oncology, Polyclinique St Georges, Nice, France.
Constance ThibaultDepartment of Medical Oncology, Hôpital Européen Georges Pompidou, Paris, France.
Alexandre IngelsUrology Department, CHU Henri-Mondor, Créteil, France.
Véronique SaldanaDepartment of Medical Oncology, CHU Henri-Mondor, Créteil, France.
Guilhem RoubaudDepartment of Medical Oncology, Institut Bergonié, Bordeaux, France.
Jean-Christophe BernhardUrology Department, CHU de Bordeaux - Hôpital Pellegrin, Bordeaux, France.
Gwenaelle GravisMedical Oncology Department, Institut Paoli-Calmettes, Aix-Marseille Université, Inserm, CNRS, CRCM, Marseille, France.
Philippe BarthélémyMedical Oncology, Institut de Cancérologie Strasbourg Europe, Strasbourg, France.
Centre Hospitalier Universitaire de Besançon · FRCentre Hospitalier Universitaire Henri-Mondor · FRInstitut Paoli-Calmettes · FRBicêtre Hospital · FRCentre Antoine Lacassagne · FRCentre Georges François Leclerc · FRCentre Hospitalier Régional Universitaire de Brest · FRCentre Hospitalier Universitaire d'Angers · FRCentre National de la Recherche Scientifique · FRHôpital Européen Georges-Pompidou · FRHôpital Pellegrin · FRHôpital Pontchaillou · FRInstitut Bergonié · FRInstitut de Cancérologie de Lorraine · FRInstitut de Cancérologie Strasbourg · FRInstitut Gustave Roussy · FRSaint Laurent Polyclinique · FRUniversité de Strasbourg · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn 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.

objectiveTo assess the oncological outcomes of patients who responded to ICI-based treatments and were subsequently treated with a delayed nephrectomy. DESIGN, SETTING, AND

participantsThis 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.

interventionPartial 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).

conclusionsDespite 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.

Indexed as

Carcinoma, Renal CellKidney NeoplasmsHumansImmune Checkpoint InhibitorsIpilimumabNephrectomyNivolumabProtein Kinase InhibitorsRetrospective StudiesImmune Checkpoint InhibitorsIpilimumabNivolumabProtein Kinase InhibitorsComplete responseMetastatic renal cell carcinomaNephrectomySurgerySurvival

Identifiers

PMID35853818
OpenAlexW4285679063

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.