The CABOLD study: A real life prospective cohort evaluating the combination of cabozantinib and nivolumab among older patients with renal-cell carcinoma.

M Maxime Frelaut (Gustave Roussy, Villejuif, France) N Natacha Naoun (Department of Medical Oncology, Gustave Roussy, Villejuif, France) A Arnaud Pages (4Gustave Roussy Cancer Center, Department of Biostatistics and Epidemiology, villejuif, France) R Ronan Flippot (INSERM U1363, Université Paris Saclay, Villejuif, France) Z Zoé AP Thomas (Gustave Roussy, Villejuif, France) C Capucine Baldini (Gustave Roussy Cancer Campus, Villejuif, France) L Laurence Albiges (Department of Medical Oncology Gustave Roussy Villejuif France)

Abstract

TPS607 Background: In the era of combination therapy, and due to age-related physiological changes, management of older patients with Clear-cell renal cell carcinoma (ccRCC) is a challenge. The combination of cabozantinib and nivolumab is one of the recommended treatments in untreated metastatic or locally advanced ccRCC. However, data regarding the use of this treatment among 70 years old or more (70+) patients are scarce. The CABOLD study seeks to address these gaps by assessing the real-life use of this combination in older patients. Methods: The CABOLD study is a prospective, multicentric, single-arm cohort trial conducted across 10 centers in France. It aims to enroll 50 patients aged 70 years and above with advanced or metastatic ccRCC, who are treatment-naïve in this setting. Eligible participants must have a Performance Status (PS) of 0 to 2. Patients will receive standard-of-care treatment consisting of cabozantinib at 40 mg daily and nivolumab on a 28-day cycle (240 mg on Days 1 and 15 for the first two cycles, followed by 480 mg on Day 1 for subsequent cycles). The starting dose of cabozantinib may be reduced to 20 mg daily at the investigator’s discretion. Patients will benefit of a multi-modal follow-up including medical oncologists, geriatricians and trained nurses to monitor safety closely. Abbreviated geriatric assessment, using G-CODE, will be performed at inclusion, under treatment, and during follow-up, along with quality of life (QoL) evaluation. Optional pharmacological monitoring for cabozantinib will be conducted to assess potential associations with clinical outcomes. Patients will be followed for 12 months in the study, followed by a long-term follow-up after one year. Primary objective is to describe real-life treatment patterns of nivolumab-cabozantinib, including dose modifications and interruptions due to toxicity. Main secondary objectives include efficacy, survival, tolerance, QoL. Enrollment for the study has not yet begun at the time of submission. The CABOLD study is designed to provide insights into the real-world use of cabozantinib and nivolumab in 70+ patients with metastatic ccRCC. By incorporating geriatric assessments and pharmacological monitoring, the trial aims to improve our understanding of treatment tolerability, efficacy, and quality of life in this vulnerable population, potentially guiding tailored therapeutic strategies for older adults with RCC.

Article Details

Volume / Issue Vol. 43, Issue 5_suppl
Published February 10, 2025
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (7)

M

Maxime Frelaut

Gustave Roussy, Villejuif, France

N

Natacha Naoun

Department of Medical Oncology, Gustave Roussy, Villejuif, France

A

Arnaud Pages

4Gustave Roussy Cancer Center, Department of Biostatistics and Epidemiology, villejuif, France

R

Ronan Flippot

INSERM U1363, Université Paris Saclay, Villejuif, France

Z

Zoé AP Thomas

Gustave Roussy, Villejuif, France

C

Capucine Baldini

Gustave Roussy Cancer Campus, Villejuif, France

L

Laurence Albiges

Department of Medical Oncology Gustave Roussy Villejuif France