Evidence map›Paper›PMID 39614178›Full record

ArticleBMC cancer2024

Prognostic value of B7-H3 expression in metastatic renal cell carcinoma and its impact on immunotherapy response.

Faruk Recep Özalp, Kutsal Yörükoğlu, Eda Çalışkan Yıldırım, Mehmet Uzun, Hüseyin Salih Semiz

Abstract read
In one paragraph

Article in BMC cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
–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

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
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  5. Review
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

5 authors.

Faruk Recep ÖzalpDepartment of Medical Oncology, Dokuz Eylul University Faculty of Medicine, Izmir, Turkey. ozalpfarukrecep@gmail.com.ORCID http://orcid.org/0000-0002-2863-3243
Kutsal YörükoğluDepartment of Pathology, Dokuz Eylul University Faculty of Medicine, Izmir, Turkey.
Eda Çalışkan YıldırımDepartment of Medical Oncology, Dokuz Eylul University Faculty of Medicine, Izmir, Turkey.
Mehmet UzunDepartment of Medical Oncology, Dokuz Eylul University Faculty of Medicine, Izmir, Turkey.
Hüseyin Salih SemizDepartment of Medical Oncology, Dokuz Eylul University Faculty of Medicine, Izmir, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRenal cell carcinoma (RCC) is characterised by its immunogenic and proangiogenic nature and its resistance to conventional therapies. The advent of immune checkpoint inhibitors (ICIs) and tyrosine kinase inhibitors (TKIs) has significantly improved patient survival, but resistance to these treatments remains a challenge. B7-H3, a potential immune checkpoint, has been implicated in modulating the tumour microenvironment and immune escape mechanisms in RCC.

methodsImmunohistochemical analysis of B7-H3 expression was performed in 84 metastatic RCC patients. Tissue microarrays and separate sections of formalin-fixed paraffin-embedded tissue were used for immunohistochemical staining. Membranous staining of the tumor cells was scored and statistical analyses were performed to assess the correlation between B7-H3 expression and treatment outcome.

resultsB7-H3 expression was absent in 31% of patients, while 33.3% had a score of 1+, 31% had 2+, and 4.8% had 3+. High B7-H3 expression correlated with poorer OS (20 months vs. 45 months, p = 0.012). In patients receiving nivolumab, those with high B7-H3 expression had shorter PFS (2 months vs. 8 months, p = 0.037) and OS (17 months vs. 51 months, p = 0.01). B7-H3 expression was the only factor significantly affecting PFS and OS in multivariate analysis.

conclusionHigh B7-H3 expression is associated with poorer survival outcomes and reduced response to nivolumab in metastatic RCC patients. B7-H3 may serve as a predictive biomarker for immunotherapy response. Future studies should explore targeting B7-H3 in combination with existing therapies to enhance treatment efficacy.

Indexed as

B7 AntigensCarcinoma, Renal CellImmunotherapyKidney NeoplasmsAdultAgedAged, 80 and overBiomarkers, TumorFemaleHumansImmune Checkpoint InhibitorsMaleMiddle AgedNivolumabPrognosisRetrospective StudiesB7 AntigensBiomarkers, TumorCD276 protein, humanImmune Checkpoint InhibitorsNivolumabB7-H3ImmunotherapyPredictive markerRCC

Identifiers

PMID39614178
PMCPMC11606205

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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.