KIM-1 levels in papillary renal cell carcinoma from the CALYPSO trial.

S Sara Coca Membribes F Francesca Jackson-Spence (Barts Cancer Institute, London, United Kingdom) C Cristina Suarez (Department of Medical Oncology Vall d'Hebron Institute of Oncology Hospital Universitari Vall d'Hebron Barcelona Spain) P Poulam M. Patel (Nottingham University Hospitals NHS Trust, Nottingham, United Kingdom) J James M.G. Larkin (The Royal Marsden NHS Foundation Trust, London, United Kingdom) B Begona Perez Valderrama (Hospital Universitario Virgen del Rocio, Sevilla, Spain) A Alejo Rodriguez-Vida (Hospital del Mar, Barcelona, Spain) M Maria Jose Mendez Vidal (Maimonides Institute for Biomedical Research of Cordoba (IMIBIC), Hospital Universitario Reina Sofía, Medical Oncology Department, Córdoba, Spain) B Bernadett Emma Szabados (Barts Cancer Institute, Queen Mary University of London, London, United Kingdom) E Elizabeth Nally (Barts Cancer Institute, London, United Kingdom) C Catherine Graham (Barts Cancer Institute, Queen Mary University of London, London, United Kingdom) G Garima Priyadarshini (Barts Cancer Institure, London, United Kingdom) F Fahmida Jamal (Barts Cancer Institute, London, United Kingdom) C Charlotte Ackerman (Barts Cancer Institute, Queen Mary University of London, London, United Kingdom) T Thomas Powles (Department of Medical Oncology Barts Cancer Institute Queen Mary University of London London UK)

Abstract

557 Background: Kidney Injury Molecule-1 (KIM-1) has emerged as a promising biomarker in clear cell renal cell carcinoma (RCC), but its role in papillary RCC remains unknown. Methods: Serum KIM-1 concentrations were analyzed in patients with papillary RCC (n=32) and clear cell RCC (n=123) enrolled in a prospective randomized phase II trial evaluating durvalumab plus savolitinib (D+S) for papillary RCC. Associations between KIM-1 and clinicopathologic or molecular features were evaluated. Longitudinal changes in KIM-1 with time were correlated with radiologic response, circulating tumor DNA (ctDNA) status and molecular subgroups. Results: The median KIM1 levels for patients (n=32) with papillary RCC who received D+S was 7835 pg/mL. This was significantly higher than the clear cell RCC cohort (n=123) at baseline (5470 pg/mL, p=0.05). Other comparisons between these cohorts are shown in Table 1. In the papillary cohort, higher baseline KIM-1 levels did not correlate with the IMDC score, PD-L1 or TMB, but were lower in MET-driven tumors compared to non-MET driven (4217 vs 19834 pg/mL, p=0.05). Radiological response was associated with lower baseline KIM-1 levels (3368 vs 14154 pg/mL in non-radiological responders, p=0.025). Sequential KIM-1 results (n=19) showed a 54% decrease in radiological responders vs a 7% decrease in non-radiological responders (59% vs 11% in MET vs non-MET driven tumors). ctDNA positivity correlated with higher KIM-1 concentrations (17448 vs 5226 pg/mL in ctDNA-negative), and the combination of ctDNA positivity and elevated KIM-1 identified patients with poorer outcomes. Conclusions: KIM-1 levels are raised in papillary RCC. They correlated with tumor biology, MET status and response to treatment. Clinical trial information: NCT02819596 . Baseline serum KIM-1 levels according to clinical characteristics in papillary and clear cell RCC. Papillary RCC Clear cell RCC Baseline levels (pg/mL) 7835 5470 IMDC poor risk 40127 7998 IMDC intermediate risk 5918 6045 IMDC good risk 9789 4420 No prior nephrectomy 2282 9800 Prior nephrectomy 8705 5000 Presence of liver metastases 21321 6783 Absence of liver metastases 4791 5416

Article Details

Volume / Issue Vol. 44, Issue 7_suppl
Published March 01, 2026
Pages 557-557
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (15)

S

Sara Coca Membribes

F

Francesca Jackson-Spence

Barts Cancer Institute, London, United Kingdom

C

Cristina Suarez

Department of Medical Oncology Vall d'Hebron Institute of Oncology Hospital Universitari Vall d'Hebron Barcelona Spain

P

Poulam M. Patel

Nottingham University Hospitals NHS Trust, Nottingham, United Kingdom

J

James M.G. Larkin

The Royal Marsden NHS Foundation Trust, London, United Kingdom

B

Begona Perez Valderrama

Hospital Universitario Virgen del Rocio, Sevilla, Spain

A

Alejo Rodriguez-Vida

Hospital del Mar, Barcelona, Spain

M

Maria Jose Mendez Vidal

Maimonides Institute for Biomedical Research of Cordoba (IMIBIC), Hospital Universitario Reina Sofía, Medical Oncology Department, Córdoba, Spain

B

Bernadett Emma Szabados

Barts Cancer Institute, Queen Mary University of London, London, United Kingdom

E

Elizabeth Nally

Barts Cancer Institute, London, United Kingdom

C

Catherine Graham

Barts Cancer Institute, Queen Mary University of London, London, United Kingdom

G

Garima Priyadarshini

Barts Cancer Institure, London, United Kingdom

F

Fahmida Jamal

Barts Cancer Institute, London, United Kingdom

C

Charlotte Ackerman

Barts Cancer Institute, Queen Mary University of London, London, United Kingdom

T

Thomas Powles

Department of Medical Oncology Barts Cancer Institute Queen Mary University of London London UK