Evidence map›Paper›PMID 42632880›Full record

ArticleAnnals of surgical oncology2026

Cytoplasmic Morphology Predicts the Tumor Immune Microenvironment and Recurrence in Localized Clear Cell Renal Cell Carcinoma.

Yoshiyuki Furukawa, Kosuke Miyai, Koetsu Hamamoto, Yuichi Arai, Takako Asano, Hiroaki Kobayashi, Masayuki Shinchi, Yujiro Tsujita, Kenji Kuroda, Akio Horiguchi and 3 more

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Article in Annals of surgical oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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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

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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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

13 authors.

Yoshiyuki FurukawaDepartment of Urology, National Defense Medical College, Tokorozawa City, Saitama, Japan.
Kosuke MiyaiDepartment of Basic Pathology, National Defense Medical College, Tokorozawa City, Saitama, Japan.
Koetsu HamamotoDepartment of Urology, National Defense Medical College, Tokorozawa City, Saitama, Japan.
Yuichi AraiDepartment of Urology, National Defense Medical College, Tokorozawa City, Saitama, Japan.
Takako AsanoDepartment of Urology, National Defense Medical College, Tokorozawa City, Saitama, Japan.
Hiroaki KobayashiDepartment of Urology, National Defense Medical College, Tokorozawa City, Saitama, Japan.
Masayuki ShinchiDepartment of Urology, National Defense Medical College, Tokorozawa City, Saitama, Japan.
Yujiro TsujitaDepartment of Urology, National Defense Medical College, Tokorozawa City, Saitama, Japan.
Kenji KurodaDepartment of Urology, National Defense Medical College, Tokorozawa City, Saitama, Japan.
Akio HoriguchiDepartment of Urology, National Defense Medical College, Tokorozawa City, Saitama, Japan.
Kimiya SatoDepartment of Basic Pathology, National Defense Medical College, Tokorozawa City, Saitama, Japan.
Hitoshi TsudaDepartment of Basic Pathology, National Defense Medical College, Tokorozawa City, Saitama, Japan.
Keiichi ItoDepartment of Urology, National Defense Medical College, Tokorozawa City, Saitama, Japan. itok@ndmc.ac.jp.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIt has been suggested that cytoplasmic pattern (CPP) reflects the tumor immune microenvironment in clear cell renal cell carcinoma (ccRCC). This study investigated the associations between CPP and clinicopathological features, including tumor-associated immune cell status (TAICs) and immunosuppressive immune cell infiltration, in localized ccRCC.

methodsThis retrospective analysis included 112 patients with pT1b ccRCC. CPP (clear, mixed, eosinophilic) and TAICs were evaluated on hematoxylin-eosin (HE)-stained sections. Immunohistochemistry for cluster of differentiation 8 (CD8), programmed cell death protein 1 (PD-1), programmed cell death ligand-1 (PD-L1), and FOXP3 was performed. Immune cell infiltration was compared across CPP subtypes. Cox proportional hazards models were used to identify predictors of recurrence and cancer-specific survival.

resultsCPP distribution was clear in 36 patients (32%), mixed in 54 (48%), and eosinophilic in 22 (20%). CPP was significantly associated with nuclear grade, tumor necrosis, and lymphovascular invasion. CPP correlated with TAICs, with eosinophilic tumors showing the highest proportion of the hot phenotype. Infiltration of PD-1-, PD-L1-, CD8-, and FOXP3-positive immune cells increased stepwise from clear to eosinophilic types. Time to recurrence differed significantly among CPP groups (p < 0.0001). The 3-year recurrence-free probability was 63% in the eosinophilic type and 94.8% in the non-eosinophilic type. In multivariate analysis, eosinophilic type was the only independent predictor of recurrence. For cancer-specific survival, eosinophilic type was a significant predictor in univariate analysis.

conclusionsCPP is associated with adverse pathological features and immunosuppressive immune cell infiltration in localized ccRCC. Eosinophilic CPP independently predicted time to recurrence, indicating that CPP may serve as a practical pathological marker for stratifying recurrence risk and guiding postoperative surveillance strategies.

Indexed as

Cytoplasmic patternImmunosuppressive immune cellLocalized clear cell renal cell carcinomaRecurrenceTumor immune microenvironment

Identifiers

PMID42632880

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