Evidence map›Paper›PMID 31318983›Full record

Observational studyInternational journal of cancer2020

Long survival of patients with metastatic clear cell renal cell carcinoma. Results of real life study of 344 patients.

Eric Voog, Boris Campillo-Gimenez, Claude Elkouri, Franck Priou, Frederic Rolland, Brigitte Laguerre, Chaza Elhannani, Jacques Merrer, Christian Pfister, Emmanuel Sevin and 27 more

Open access · bronzeAbstract readObservational Study
PubMed Publisher
In one paragraph

Observational study in International journal of cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.5field-weighted citation impact, top 29% 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

7 citing papers in PubMed, 9 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

37 authors at 15 institutions in 1 country.

Eric VoogClinique Victor Hugo, Le Mans, France.ORCID 0000-0001-8366-8003
Boris Campillo-GimenezCentre Eugène Marquis, Rennes, France.
Claude ElkouriHôpital Privé du Confluent, Nantes, France.
Franck PriouCentre Hospitalier de La Roche/Yon, La Roche/Yon, France.
Frederic RollandInstitut de Cancérologie de l'Ouest, Angers, Nantes, France.
Brigitte LaguerreCentre Eugène Marquis, Rennes, France.
Chaza ElhannaniPolyclinique du Parc, Cholet, France.
Jacques MerrerClinique Pasteur, Brest, France.
Christian PfisterCentre Hospitalier Universitaire, Rouen, France.
Emmanuel SevinCentre François Baclesse, Caen, France.
Tifenn L'HaridonCentre Hospitalier de La Roche/Yon, La Roche/Yon, France.
Ali HasbiniClinique Pasteur, Brest, France.
Laura MoiseCentre François Baclesse, Caen, France.
Annick Le RolCentre Hospitalier Intercommunal de Cornouaille, Quimper, France.
Jean Pierre MalhaireCentre Hospitalier Universitaire Brest Morvan, Brest, France.
Remy DelvaInstitut de Cancérologie de l'Ouest, Angers, Nantes, France.
Elodie VauléonCentre Eugène Marquis, Rennes, France.
Oana CojocarasuCentre Hospitalier Le Mans, Le Mans, France.
Philippe DeguiralClinique Mutualiste de l'Estuaire Saint-Nazaire, Saint-Nazaire, France.
Isabelle CuminCentre Hospitalier Bretagne Sud Lorient, Lorient, France.
Caroline CheneauCentre Hospitalier Universitaire Brest Morvan, Brest, France.
Friedrike SchlürmannCentre Hospitalier Intercommunal de Cornouaille, Quimper, France.
Valérie DelecroixClinique Mutualiste de l'Estuaire Saint-Nazaire, Saint-Nazaire, France.
Elouen BoughalemInstitut de Cancérologie de l'Ouest, Angers, Nantes, France.
Delphine MollonCentre Hospitalier Intercommunal de Cornouaille, Quimper, France.
Catherine Ligeza-PoissonClinique Mutualiste de l'Estuaire Saint-Nazaire, Saint-Nazaire, France.
Sophie Abadie-LacourtoisieInstitut de Cancérologie de l'Ouest, Angers, Nantes, France.
Erik MonpetitHôpital Privé Océane, Vannes, France.
Thierry ChatellierClinique Mutualiste de l'Estuaire Saint-Nazaire, Saint-Nazaire, France.
Henry DesclosCentre Hospitalier Saint-Malo, Saint-Malo, France.
Elodie CoquanCentre François Baclesse, Caen, France.
Florence JolyCentre François Baclesse, Caen, France.
Jean Yves TessereauInstitut de Cancérologie de l'Ouest, Angers, Nantes, France.
Sandra DupuyInstitut de Cancérologie de l'Ouest, Angers, Nantes, France.
Delphine Déniel LagadecCentre Hospitalier Universitaire Brest Morvan, Brest, France.
Fanny MarhuendaInstitut de Cancérologie de l'Ouest, Angers, Nantes, France.
Francoise GrudéInstitut de Cancérologie de l'Ouest, Angers, Nantes, France.
Institut de Cancérologie de l'Ouest · FRCentre François Baclesse · FRClinique Mutualiste de l'Estuaire · FRCentre Eugène Marquis · FRCentre Hospitalier de Cornouaille · FRCentre Hospitalier de Bretagne Sud · FRCentre Hospitalier Régional Universitaire de Brest · FRClinique Pasteur · FRRoche (France) · FRCentre Hospitalier de Saint-Malo · FRCentre Hospitalier du Mans · FRCentre Hospitalier Universitaire de Rouen · FRClinique Victor Hugo · FRHôpital privé du Confluent · FRPolyclinique de Bordeaux-Tondu · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The treatment landscape in metastatic renal cell carcinoma has changed fundamentally over the last decade by the development of antiangiogenic agents, mammalian target of rapamycin inhibitors and immunotherapy. Outside of the context of a clinical trial, the treatments are used sequentially. We describe results under real-life conditions of a sequential treatment strategy, before the era of immunotherapy. All patients were treated according to their prognostic score (either Memorial Sloan Kettering Cancer Center or International Metastatic Renal Cell Carcinoma Database Consortium) for advanced renal cell carcinoma. A treatment strategy involving 1 to 4 lines was determined including a rechallenge criterion for the repeat use of a treatment class. Three hundred forty-four patients were included over 3 years. Overall survival was 57 months in patients with good or intermediate prognosis and 19 months in patients with poor prognosis. In the former group, the proportions of patients treated with 2 to 4 treatment lines were 70%, 38% and 16%, respectively. The best objective response rates for lines 1 to 4 were 46%, 36%, 16% and 17%, respectively. Grade III/IV toxicity did not appear to be cumulative. The recommended strategy was followed in 68% of patients. A large proportion of patients with good or intermediate prognosis who progress after two lines of treatment still have a performance status good enough to receive a systemic treatment, which justifies such a strategy. Overall survival of patients with good and intermediate prognosis was long, suggesting a benefit from the applied approach. These results might be used as selection criterion for the treatment of patients in the era of immune checkpoint inhibitors.

Indexed as

AdultAgedAged, 80 and overAngiogenesis InhibitorsAntineoplastic Combined Chemotherapy ProtocolsBevacizumabCarcinoma, Renal CellEverolimusFemaleFranceHumansKidney NeoplasmsMaleMiddle AgedMolecular Targeted TherapyPatient SelectionAngiogenesis InhibitorsBevacizumabEverolimusProtein Kinase Inhibitorsanti-angiogenesis agentsoverall survivalreal life conditionsrenal cell carcinomasequential treatments

Identifiers

PMID31318983
OpenAlexW2962747911

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.