Evidence map›Paper›PMID 37505371›Full record

ArticleClinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico2024

Different outcomes among patients with intermediate-risk metastastic renal cell carcinoma treated with first-line tyrosine-kinase inhibitors.

Álvaro Pinto, Jesús Miranda, Ana Pertejo, Mario Álvarez-Maestro, Pilar González-Peramato, Alfredo Aguilera, Eugenia García, Lucía Trilla, Ángelo Gámez, Enrique Espinosa

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Article in Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.8field-weighted citation impact, top 24% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Álvaro PintoMedical Oncology Department, University Hospital La Paz-IdiPAZ, Paseo Castellana 261, 28046, Madrid, Spain. alvaropintomarin@gmail.com.ORCID http://orcid.org/0000-0002-4719-053X
Jesús MirandaMedical Oncology Department, QuironSalud University Hospital, Madrid, Spain.
Ana PertejoMedical Oncology Department, University Hospital La Paz-IdiPAZ, Paseo Castellana 261, 28046, Madrid, Spain.
Mario Álvarez-MaestroUrology Department, University Hospital La Paz-IdiPAZ, Madrid, Spain.
Pilar González-PeramatoPathology Department, University Hospital La Paz-IdiPAZ, Madrid, Spain.
Alfredo AguileraUrology Department, University Hospital La Paz-IdiPAZ, Madrid, Spain.
Eugenia GarcíaPathology Department, University Hospital La Paz-IdiPAZ, Madrid, Spain.
Lucía TrillaMolecular Oncology and Pathology Lab, University Hospital La Paz-IdiPAZ, Madrid, Spain.
Ángelo GámezMolecular Oncology and Pathology Lab, University Hospital La Paz-IdiPAZ, Madrid, Spain.
Enrique EspinosaMedical Oncology Department, University Hospital La Paz-IdiPAZ, Paseo Castellana 261, 28046, Madrid, Spain.
Hospital Universitario La Paz · ESHospital Universitario Quirónsalud Madrid · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionSystemic therapy of patients with metastatic renal cell carcinoma (mRCC) has improved in the past years, with the advent of new immunotherapy-based combinations as a standard treatment option for first-line therapy. Nevertheless, particularly in good-risk patients by IMDC criteria, tyrosine-kinase inhibitors (TKI) may remain as an option for some patients. We reviewed our experience with TKI as first-line therapy for mRCC patients, trying to identify subgroups of patients that may still benefit from this strategy. MATERIAL AND

methodsAll patients with mRCC treated with first-line TKI, and adequate follow-up, in University Hospital La Paz (Madrid, Spain) between 2007 and 2020 were analyzed. Patients treated inside a clinical trial were excluded from this analysis.

resultsA total of 90 patients treated with first-line TKI were included. Regarding IMDC criteria, 33 patients (36.7%) were good-risk, 41 patients (45.5%) intermediate-risk, and 16 patients (17.8%) poor-risk. With a median follow-up of 49 months, the median overall survival (OS) for good, intermediate, and poor-risk patients was 54, 24, and 16 months (p = 0.004). When intermediate-risk was divided into patients with 1 or 2 risk factors, differences in OS were also statistically significant: patients with 1 risk factor had a median OS of 33 months, while patients with 2 risk factors had a median OS of 16 months, the same as poor-risk patients (p = 0.003). In the multivariate analysis, trying to find out which of the IMDC factors had a more remarkable weight in the prognosis of the patients, both ECOG and hemoglobin levels by themselves were significantly associated with OS.

conclusionIn our group of patients, survival outcomes were different among patients with intermediate-risk with 1 or 2 risk factors by IMDC criteria. These could help select patients that may benefit from first-line treatment with a TKI, particularly in settings with difficult access to novel therapies, such as immunotherapy-based combinations.

Indexed as

Carcinoma, Renal CellKidney NeoplasmsHumansPrognosisProtein Kinase InhibitorsRetrospective StudiesTyrosineProtein Kinase InhibitorsTyrosineImmunotherapyRenal cancerSystemic therapyTyrosine-kinase inhibitors

Identifiers

PMID37505371
OpenAlexW4385329945

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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.