Evidence map›Paper›PMID 41755979›Full record

ArticleCureus2026

Renal Cell Carcinoma: Characteristics of Patients, Treatment, and Disease Progression Based on Real-World Data From a Cancer Center in Medellín, Colombia.

Mauricio Lema, Camila Lema, Diego Morán, Mateo Pineda, Beatriz Preciado, Emilio Pérez

Abstract read
In one paragraph

Article in Cureus, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Mauricio LemaOncology, Clínica de Oncología Astorga, Medellín, COL.
Camila LemaResearch, Clínica de Oncología Astorga, Medellín, COL.
Diego MoránOncology, Clínica de Oncología Astorga, Medellín, COL.
Mateo PinedaResearch, Clínica de Oncología Astorga, Medellín, COL.
Beatriz PreciadoResearch, Clínica de Oncología Astorga, Medellín, COL.
Emilio PérezResearch, Clínica de Oncología Astorga, Medellín, COL.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction Data on demography, stage distribution, treatment, and survival rates of renal cell carcinoma (RCC) in Colombia is not known. This study aims to describe a cohort of patients with RCC treated at the Clínica de Oncología Astorga, in Medellín, Colombia. Methods This retrospective study included all consecutive RCC patients treated at the institution between 2008 and 2023. Clinical, treatment, and survival data were collected from medical records. For metastatic and recurrent patients, risk was dichotomized as low-risk or non-low risk. The latter included those classified as intermediate/high risk in medical records, or cases with de novo metastatic disease or progression within 12 months of initial diagnosis. Event-free survival (EFS), progression-free survival (PFS), and overall survival (OS) were estimated using the Kaplan-Meier method and subgroup analysis was performed using metastatic status. Treatment patterns were compared with the log-rank test. Results Data of 208 patients were analyzed. The median age was 60.4 years (interquartile range (IQR) 51.9-69.8) and 114 subjects (54.8%) were men. Clear-cell histology was available for 167 patients (80.3%). Stages I, II, III, and IV disease was observed in 58 (27.9%), 34 (16.3%), 38 (18.3%), and 48 (23.1%) cases, respectively. Metastatic disease occurred in 107 (51.4%) patients (46 synchronous and 61 metachronous). Low-risk and non-low-risk metastatic disease was detected in 43 (40.2%) and 64 (59.8%) patients, respectively. Among non-metastatic patients, 126 (95.4%) patients underwent nephrectomy. First-line treatment included tyrosine kinase inhibitors (TKI) in 58 (70.7%), immunotherapy (IO) in 12 (14.6%), and other systemic therapies in 12 (14.6%) patients; 34 (31.8%) patients received a second-line regimen, most commonly from TKI to IO. Median OS for the entire cohort was 161.1 months. OS was significantly longer in non-metastatic versus metastatic patients at diagnosis (217.0 vs. 24.9 months; p<0.001). In metastatic disease, median OS differed by risk category (low-risk, 58.4 months vs. non-low-risk, 26.6 months; p=0.01) and by first-line treatment (TKI 42.2 months, IO 18.6 months, surgery 67.3 months; p=0.03). Conclusion In this institution-based real-world of RCC patients from Colombia, more than half presented with or subsequently developed metastatic disease; however, only one-third were able to access second-line therapy, highlighting substantial attrition in treatment sequencing. Non-metastatic status, low-risk metastatic classification, and first-line treatment with TKI were associated with superior survival outcomes.

Indexed as

disease-free survivalimmunotherapykidney neoplasmsneoplasm stagingprogression-free survival

Identifiers

PMID41755979
PMCPMC12933355

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.