Evidence map›Paper›PMID 41981923›Full record

ArticleInternational journal of urology : official journal of the Japanese Urological Association2026

Real-World Effectiveness and Safety of Pembrolizumab-Lenvatinib Versus Axitinib-Based Regimens in Metastatic Clear Cell Renal Cell Carcinoma: A Multicenter Retrospective Study.

Kohei Kobatake, Keisuke Goto, Akira Fujita, Takashi Babasaki, Takeshi Ueno, Yoshimasa Kurimura, Kenichiro Fukuoka, Fumiaki Kirishima, Kensuke Nishida, Tetsutaro Hayashi and 1 more

Abstract readMulticenter StudyComparative Study
In one paragraph

Article in International journal of urology : official journal of the Japanese Urological Association, 2026. 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
–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

1 citing paper in PubMed.

  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

11 authors.

Kohei KobatakeDepartment of Urology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.ORCID https://orcid.org/0000-0003-2098-3916
Keisuke GotoDepartment of Urology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.
Akira FujitaDepartment of Urology, NHO Fukuyama Medical Center, Fukuyama, Japan.
Takashi BabasakiDepartment of Urology, Hiroshima City Asa Citizens Hospital, Hiroshima, Japan.
Takeshi UenoDepartment of Urology, JA Hiroshima General Hospital, Hatsukaichi, Japan.
Yoshimasa KurimuraDepartment of Urology, Hiroshima Prefectural Hospital, Hiroshima, Japan.
Kenichiro FukuokaDepartment of Urology, NHO Kure Medical Center, Kure, Japan.ORCID https://orcid.org/0000-0002-4849-0614
Fumiaki KirishimaDepartment of Urology, NHO Higashihiroshima Medical Center, Higashihiroshima, Japan.ORCID https://orcid.org/0000-0001-7119-8366
Kensuke NishidaDepartment of Urology, JA Onomichi General Hospital, Onomichi, Japan.
Tetsutaro HayashiDepartment of Urology, Matsuyama Red Cross Hospital, Matsuyama, Ehime, Japan.
Nobuyuki HinataDepartment of Urology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.ORCID https://orcid.org/0000-0001-7014-6812

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo compare the real-world effectiveness and safety of pembrolizumab plus lenvatinib with axitinib-based regimens (avelumab plus axitinib or pembrolizumab plus axitinib) as first-line therapy for metastatic clear cell renal cell carcinoma.

methodsWe retrospectively analyzed 107 patients treated with immuno-oncology plus vascular endothelial growth factor inhibitor combinations between 2017 and 2025. Propensity score matching (1:1, 0.2 caliper) generated 42 matched pairs. Objective response rate, progression-free survival, overall survival, and adverse events were assessed. Multivariable logistic regression and Cox regression analyses were performed in the overall cohort, and conditional logistic regression and stratified Cox regression analyses were applied in the matched cohort.

resultsIn the matched cohort, pembrolizumab plus lenvatinib demonstrated a significantly higher objective response rate than axitinib-based regimens. The incidence of any-grade and grade ≥ 3 adverse events was similar between regimens. However, pembrolizumab plus lenvatinib was associated with higher rates of hypertension (including grade ≥ 3 hypertension), fatigue, appetite loss, and rash in the full-dose subgroup. Progression-free and overall survival did not differ significantly. Multivariate analyses identified pembrolizumab plus lenvatinib treatment as an independent predictor of objective response, whereas survival outcomes were associated with clinical factors rather than the regimen type.

conclusionsPembrolizumab plus lenvatinib achieved a superior tumor response to axitinib-based regimens, whereas survival outcomes were comparable. Treatment selection should balance enhanced antitumor activity with differences in toxicity profiles.

Indexed as

Antibodies, Monoclonal, HumanizedAntineoplastic Combined Chemotherapy ProtocolsAxitinibCarcinoma, Renal CellKidney NeoplasmsPhenylurea CompoundsQuinolinesAgedFemaleHumansMaleMiddle AgedProgression-Free SurvivalRetrospective StudiesTreatment OutcomeAntibodies, Monoclonal, HumanizedAxitiniblenvatinibpembrolizumabPhenylurea CompoundsQuinolinesclear cell renal cell carcinomalenvatinibmetastatic renal cell carcinomapembrolizumabreal‐world evidence

Identifiers

PMID41981923
PMCPMC13080224

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.