Evidence map›Paper›PMID 42736489›Full record

ArticleTargeted oncology2026

One-Week Inflammatory Kinetics After First-Line Nivolumab Plus Ipilimumab in Metastatic Renal Cell Carcinoma: A Multicenter Landmark Analysis.

Toru Inoue, Kazuyuki Numakura, Takahiro Osawa, Sei Naito, Takuma Ishihara, Kojiro Ohba, Kosuke Ueda, Yuya Sekine, Masaharu Oki, Hirohito Naito and 8 more

Abstract readMulticenter Study
In one paragraph

Article in Targeted oncology, 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

18 authors.

Toru InoueDepartment of Urology, Faculty of Medicine, Oita University, 1-1 Idaigaoka, Hasama-machi, Yufu, Oita, 879-5593, Japan. i-toru@oita-u.ac.jp.ORCID http://orcid.org/0000-0002-8290-0322
Kazuyuki NumakuraDepartment of Renal and Urologic Surgery, Asahikawa Medical University, Asahikawa, Japan.
Takahiro OsawaDepartment of Renal and Genitourinary Surgery, Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
Sei NaitoDepartment of Urology, Faculty of Medicine, Yamagata University, Yamagata, Japan.
Takuma IshiharaInnovative and Clinical Research Promotion Center, Gifu University Hospital, Gifu, Japan.
Kojiro OhbaDepartment of Urology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
Kosuke UedaDepartment of Urology, Kurume University School of Medicine, Kurume, Japan.
Yuya SekineDepartment of Urology, Akita University Graduate School of Medicine, Akita, Japan.
Masaharu OkiDepartment of Urology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
Hirohito NaitoDepartment of Urology, Faculty of Medicine, Kagawa University, Miki, Japan.
Haruka MiyataDepartment of Renal and Genitourinary Surgery, Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
Hiroshi KikuchiDepartment of Renal and Genitourinary Surgery, Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
Shin KobayashiDepartment of Renal and Urologic Surgery, Asahikawa Medical University, Asahikawa, Japan.
Shintaro NaritaDepartment of Urology, Akita University Graduate School of Medicine, Akita, Japan.
Norihiko TsuchiyaDepartment of Urology, Faculty of Medicine, Yamagata University, Yamagata, Japan.
Mikio SugimotoDepartment of Urology, Faculty of Medicine, Kagawa University, Miki, Japan.
Tsukasa IgawaDepartment of Urology, Kurume University School of Medicine, Kurume, Japan.
Toshitaka ShinDepartment of Urology, Faculty of Medicine, Oita University, 1-1 Idaigaoka, Hasama-machi, Yufu, Oita, 879-5593, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFirst-line nivolumab plus ipilimumab can produce durable survival in metastatic renal cell carcinoma, yet some patients experience early progression or rapid clinical deterioration before first scheduled imaging. Because radiologic response assessment is typically unavailable until approximately 12 weeks, clinically accessible signals during this pre-imaging interval are needed.

objectiveWe aimed to evaluate whether early changes in blood-based inflammatory biomarkers at predefined post-treatment landmarks were associated with overall survival and to determine which biomarker showed the most consistent early prognostic signal.

methodsIn this multicenter retrospective cohort study across eight Japanese institutions, 219 patients with metastatic renal cell carcinoma treated with first-line nivolumab plus ipilimumab were analyzed. Predefined landmark analyses at 1 week, 1 month, and 3 months compared six blood-based inflammatory biomarkers using restricted cubic splines with multiple imputation. Overall survival was the primary endpoint.

resultsThe 1-week landmark showed the most consistent association with overall survival. Among six biomarkers, change in pan-immune-inflammation value showed the most reproducible pattern. Among 183 patients with paired baseline and 1-week pan-immune-inflammation value data, PIV-BOOST, defined as any pan-immune-inflammation value increase (> 0%) from baseline, was observed in 110 patients (60.1%) and was independently associated with improved overall survival (adjusted hazard ratio 0.60, 95% confidence interval 0.39-0.92; p = 0.018).

conclusionsOne-week inflammatory kinetics provided early prognostic information before first scheduled imaging in first-line nivolumab plus ipilimumab-treated metastatic renal cell carcinoma. A simple direction-of-change rule for pan-immune-inflammation value may complement baseline risk assessment; however, prospective external validation is required before clinical implementation.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsCarcinoma, Renal CellInflammationIpilimumabKidney NeoplasmsNivolumabAgedFemaleHumansKineticsMaleMiddle AgedNeoplasm MetastasisRetrospective StudiesIpilimumabNivolumab

Identifiers

PMID42736489
PMCPMC13631030

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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.