Evidence map›Paper›PMID 41387488›Full record

ArticleScientific reports2025

Real-world efficacy and safety of pembrolizumab plus lenvatinib in patients with metastatic renal cell carcinoma: a multi-institutional retrospective study.

Taigo Kato, Yasutomo Nakai, Mototaka Sato, Tetsuya Takao, Toshichika Iwanishi, Shingo Toyoda, Hiroki Osaki, Masao Tsujihata, Koichi Okada, Kenichi Kakimoto and 14 more

Abstract readMulticenter Study
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
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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

24 authors.

Taigo KatoDepartment of Urology, The University of Osaka Graduate School of Medicine, Osaka, Japan. kato@uro.med.osaka-u.ac.jp.
Yasutomo NakaiDepartment of Urology, Osaka International Cancer Institute, Osaka, Japan.
Mototaka SatoDepartment of Urology, Toyonaka Municipal Hospital, Toyonaka, Osaka, Japan.
Tetsuya TakaoDepartment of Urology, Osaka General Medical Center, Osaka, Japan.
Toshichika IwanishiDepartment of Urology, Sakai City Medical Center, Osaka, Japan.
Shingo ToyodaDepartment of Urology, Kindai University, Osaka, Japan.
Hiroki OsakiDepartment of Urology, Osaka Police Hospital, Osaka, Japan.
Masao TsujihataDepartment of Urology, Osaka Rosai Hospital, Osaka, Japan.
Koichi OkadaDepartment of Urology, National Hospital Organization Osaka National Hospital, Osaka, Japan.
Kenichi KakimotoDepartment of Urology, Nippon Life Hospital, Osaka, Japan.
Hiromu HoritaniDepartment of Urology, Higashiosaka City Medical Center, Osaka, Japan.
Yutaka OnoDepartment of Urology, Higashiosaka City Medical Center, Osaka, Japan.
Kensaku NishimuraDepartment of Urology, National Hospital Organization Osaka National Hospital, Osaka, Japan.
Shingo TakadaDepartment of Urology, Osaka Police Hospital, Osaka, Japan.
Kazutoshi FujitaDepartment of Urology, Kindai University, Osaka, Japan.
Hitoshi TakayamaDepartment of Urology, Sakai City Medical Center, Osaka, Japan.
Osamu MiyakeDepartment of Urology, Toyonaka Municipal Hospital, Toyonaka, Osaka, Japan.
Masashi NakayamaDepartment of Urology, Osaka International Cancer Institute, Osaka, Japan.
Yu IshizuyaDepartment of Urology, The University of Osaka Graduate School of Medicine, Osaka, Japan.
Takuji HayashiDepartment of Urology, The University of Osaka Graduate School of Medicine, Osaka, Japan.
Yoshiyuki YamamotoDepartment of Urology, The University of Osaka Graduate School of Medicine, Osaka, Japan.
Koji HatanoDepartment of Urology, The University of Osaka Graduate School of Medicine, Osaka, Japan.
Atsunari KawashimaDepartment of Urology, The University of Osaka Graduate School of Medicine, Osaka, Japan.
Norio NonomuraDepartment of Urology, The University of Osaka Graduate School of Medicine, Osaka, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite the potential of pembrolizumab and lenvatinib combination therapy in treating metastatic renal cell carcinoma (mRCC), real-world evidence on its efficacy and safety remains limited. We retrospectively analyzed data from 118 patients with mRCC who initiated pembrolizumab plus lenvatinib as first-line therapy between August 2022 and March 2024. Patient characteristics, treatment outcomes, and adverse events were evaluated. Oncological outcomes were stratified following the International Metastatic RCC Database Consortium risk classification. The objective response and disease control rates were 69.5% and 98.5%, respectively. Median progression-free survival (PFS) was 26.8 months (95% confidence interval (CI), 23.5-27.8)), whereas the median overall survival (OS) was not reached (95%CI, 20.5- not reached). Grade ≥ 3 treatment-related adverse events occurred in 39.8% of all patients. Clinical outcomes were also compared between patients aged ≥ 75 and < 75 years. Median age was 70 years; 70.3% and 29.7% aged < 75 and ≥ 75 years, respectively. No significant differences were observed in PFS and OS between the two groups (p = 0.14 and p = 0.44, respectively). Pembrolizumab plus lenvatinib demonstrated favorable efficacy and manageable safety in a real-world cohort of patients with mRCC, including older adults.

Indexed as

Antibodies, Monoclonal, HumanizedAntineoplastic Combined Chemotherapy ProtocolsCarcinoma, Renal CellKidney NeoplasmsPhenylurea CompoundsQuinolinesAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedRetrospective StudiesTreatment OutcomeAntibodies, Monoclonal, HumanizedlenvatinibpembrolizumabPhenylurea CompoundsQuinolinesImmune checkpoint inhibitorLenvatinibPembrolizumabRenal cell carcinoma

Identifiers

PMID41387488
PMCPMC12700968

What Socratic 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 Socratic graph.