Evidence map›Paper›PMID 40322204›Full record

ArticleCancer diagnosis & prognosis

Analysis of Early Progression in Advanced Renal Cell Carcinoma Treated With Nivolumab Plus Ipilimumab.

Naoki Ito, Kosuke Ueda, Satoshi Ohnishi, Hiroki Suekane, Tasuku Hiroshige, Kouta Watanabe, Katsuaki Chikui, Keiichiro Uemura, Kiyoaki Nishihara, Makoto Nakiri and 2 more

Abstract read
In one paragraph

Article in Cancer diagnosis & prognosis. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

12 authors.

Naoki ItoDepartment of Urology, Kurume University School of Medicine, Kurume, Japan.
Kosuke UedaDepartment of Urology, Kurume University School of Medicine, Kurume, Japan.
Satoshi OhnishiDepartment of Urology, Kurume University School of Medicine, Kurume, Japan.
Hiroki SuekaneDepartment of Urology, Kurume University School of Medicine, Kurume, Japan.
Tasuku HiroshigeDepartment of Urology, Kurume University School of Medicine, Kurume, Japan.
Kouta WatanabeDepartment of Urology, Kurume University School of Medicine, Kurume, Japan.
Katsuaki ChikuiDepartment of Urology, Kurume University School of Medicine, Kurume, Japan.
Keiichiro UemuraDepartment of Urology, Kurume University School of Medicine, Kurume, Japan.
Kiyoaki NishiharaDepartment of Urology, Kurume University School of Medicine, Kurume, Japan.
Makoto NakiriDepartment of Urology, Kurume University School of Medicine, Kurume, Japan.
Shigetaka SuekaneDepartment of Urology, Kurume University School of Medicine, Kurume, Japan.
Tsukasa IgawaDepartment of Urology, Kurume University School of Medicine, Kurume, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background/Aim: In the CheckMate 214 trial, approximately 40% of patients with advanced renal cell carcinoma (aRCC) treated with nivolumab plus ipilimumab (NIVO + IPI) achieved long-term survival and a durable response to treatment. However, about 20% of patients experienced early disease progression (EDP). This retrospective study aimed to identify predictive factors for EDP among patients with aRCC treated with NIVO + IPI. Patients and Methods: We retrospectively analyzed clinical information from patients with aRCC, 19 patients in the EDP group and 40 patients in the control disease group, all of whom were treated with NIVO + IPI at Kurume University Hospital between September 2018 and February 2024. Results: The EDP group exhibited significantly worse progression-free survival and overall survival compared to the control disease group. Multivariate analyses revealed that a performance states (PS) ≥2 (p=0.0312) and the presence of bone metastases (p=0.0374) were independent predictors of EDP. Conclusion: Treatment with NIVO + IPI in patients with aRCC who have a poor PS or bone metastases may be linked to a high risk of EDP.

Indexed as

bone metastasisearly disease progressionimmune checkpoint inhibitoripilimumabnivolumabRenal cell carcinoma

Identifiers

PMID40322204
PMCPMC12046654

What OpenQuestion holds

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Registered trials

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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.