Evidence map›Paper›PMID 38701382›Full record

ArticleJournal of clinical oncology : official journal of the American Society of Clinical Oncology2024

Plasma Kidney Injury Molecule-1 for Preoperative Prediction of Renal Cell Carcinoma Versus Benign Renal Masses, and Association With Clinical Outcomes.

Wenxin Xu, Valerie Gaborieau, Samuel M Niman, Anush Mukeria, Xiaowen Liu, Krishna P Maremanda, Ayumi Takakura, David Zaridze, Matthew L Freedman, Wanling Xie and 9 more

Abstract read
In one paragraph

Article in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

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

  1. Pooled it
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  19. Shifting paradigms in the treatment of small renal masses.Translational andrology and urology · 2025
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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

19 authors.

Wenxin XuDana-Farber Cancer Institute, Boston, MA.ORCID 0000-0002-8450-2037
Valerie GaborieauInternational Agency for Research on Cancer, Lyon, France.
Samuel M NimanDana-Farber Cancer Institute, Boston, MA.
Anush MukeriaN.N. Blokhin National Medical Research Centre of Oncology, Moscow, Russia.ORCID 0000-0002-6847-9295
Xiaowen LiuBeth Israel Deaconess Medical Center, Boston, MA.
Krishna P MaremandaBrigham and Women's Hospital, Boston, MA.ORCID 0000-0002-8458-9785
Ayumi TakakuraBrigham and Women's Hospital, Boston, MA.
David ZaridzeN.N. Blokhin National Medical Research Centre of Oncology, Moscow, Russia.ORCID 0000-0002-2824-3704
Matthew L FreedmanDana-Farber Cancer Institute, Boston, MA.ORCID 0000-0002-0151-1238
Wanling XieDana-Farber Cancer Institute, Boston, MA.ORCID 0000-0001-5995-8000
David F McDermottBeth Israel Deaconess Medical Center, Boston, MA.ORCID 0000-0002-2675-5095
Toni K ChoueiriDana-Farber Cancer Institute, Boston, MA.ORCID 0000-0002-9201-3217
Paul J CatalanoDana-Farber Cancer Institute, Boston, MA.ORCID 0000-0002-1105-8852
Venkata SabbisettiBrigham and Women's Hospital, Boston, MA.
Joseph V BonventreBrigham and Women's Hospital, Boston, MA.
Phillip M PierorazioPenn Presbyterian Medical Center, Philadelphia, PA.ORCID 0000-0003-0766-9981
Nirmish SinglaBrady Urological Institute, Johns Hopkins University, Baltimore, MD.ORCID 0000-0001-9495-6983
Paul BrennanInternational Agency for Research on Cancer, Lyon, France.ORCID 0000-0002-0518-8714
Rupal S BhattBeth Israel Deaconess Medical Center, Boston, MA.

Funding

VectorP30CA006516 · NCI · DANA-FARBER CANCER INSTITUTE · PI JENNIFER W MACK · 1985 to 2026
$330.6M
Treating the P13-Kinase/AKTP50CA101942 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI David McDermott · 2003 to 2026
$53.4M
KIDNEY INJURY MOLECULE-1 IN EPITHELIAL REPAIRR01DK072381 · NIDDK · BRIGHAM AND WOMEN'S HOSPITAL · PI BONVENTRE, JOSEPH VINCENT · 2005 to 2025
$8.6M
Mechanisms of Ischemic Kidney Injury and RepairR01DK039773 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI JOSEPH VINCENT BONVENTRE · 1987 to 2026
$6.2M
Mechanisms of Ischemic Kidney Injury and RepairR37DK039773 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI BONVENTRE, JOSEPH VINCENT · 1993 to 2021
$5.2M
Kidney Microphysiological Analysis Platforms (MAP) to Optimize Function and Model DiseaseUH3TR002155 · NCATS · BRIGHAM AND WOMEN'S HOSPITAL · PI BONVENTRE, JOSEPH VINCENT, LEE, LUKE P. · 2019 to 2021
$3.3M
Clinical characterization of Kidney Injury Molecule-1 (KIM-1) as a Biomarker in Renal Cell CarcinomaR01CA258442 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI David McDermott · 2022 to 2026
$2.1M
Combating Resistance to Antiangiogenic Therapy in Renal Cell CarcinomaR01CA196996 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI BHATT, RUPAL S · 2015 to 2019
$2.0M
Spatiotemporal delivery of synergistic drug combinations to kidney cancerR01CA229772 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI SABBISETTI, VENKATA · 2018 to 2022
$1.9M
Congressionally Directed Medical Research Programs W81XWH-22-1-0951Dana-Farber/Harvard Cancer Center Kidney SPORE P50 CA101942-11A1Dana-Farber/Harvard Cancer Center Kidney SPORE P50CA101942-16NCATS NIH HHS UH3 TR002155NCI NIH HHS P30 CA006516NCI NIH HHS P50 CA101942NCI NIH HHS R01 CA196996NCI NIH HHS R01 CA229772NCI NIH HHS R01 CA258442NIDDK NIH HHS R01 DK039773NIDDK NIH HHS R01 DK072381NIDDK NIH HHS R37 DK039773NIH HHS UH3 DK072381World Health Organization 001
6 · The paper itself

Abstract

purposeBoth clear cell and papillary renal cell carcinomas (RCCs) overexpress kidney injury molecule-1 (KIM-1). We investigated whether plasma KIM-1 (pKIM-1) may be a useful risk stratification tool among patients with suspicious renal masses.

methodsPrenephrectomy pKIM-1 was measured in two independent cohorts of patients with renal masses. Cohort 1, from the prospective K2 trial, included 162 patients found to have clear cell RCC (cases) and 162 patients with benign renal masses (controls). Cohort 2 included 247 patients with small (cT1a) renal masses from an academic biorepository, of whom 184 had RCC. We assessed the relationship between pKIM-1, surgical pathology, and clinical outcomes.

resultsIn Cohort 1, pKIM-1 distinguished RCC versus benign masses with area under the receiver operating curve (AUC-ROC, 0.81 [95% CI, 0.76 to 0.86]). In Cohort 2 (cT1a only), pKIM-1 distinguished RCC versus benign masses (AUC-ROC, 0.74 [95% CI, 0.67 to 0.80]) and the addition of pKIM-1 to an established nomogram for predicting malignancy improved the model AUC-ROC (0.65 [95% CI, 0.57 to 0.74]

conclusionAmong patients with renal masses, pKIM-1 is associated with malignant pathology, worse MFS, and risk of death. pKIM-1 may be useful for selecting patients with renal masses for intervention versus surveillance.

Indexed as

Carcinoma, Renal CellHepatitis A Virus Cellular Receptor 1Kidney NeoplasmsAdultAgedBiomarkers, TumorFemaleHumansMaleMiddle AgedNephrectomyPredictive Value of TestsPrognosisProspective StudiesROC CurveBiomarkers, TumorHAVCR1 protein, humanHepatitis A Virus Cellular Receptor 1

Identifiers

PMID38701382
PMCPMC11539753

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Registered trials

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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.