Phase 2 study of neoadjuvant cabozantinib in patients with locally advanced non-metastatic clear cell renal cell carcinoma.

Authors

Mehmet Asim Bilen

Mehmet Asim Bilen

Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, GA

Mehmet Asim Bilen , Yuan Liu , Bassel Nazha , Jacqueline T Brown , Adeboya O. Osunkoya , Sierra Williams , Wilena Session , Lauren Beth Yantorni , Greta Russler , Sarah Caulfield , Shreyas S. Joshi , Vikram M. Narayan , Christopher Paul Filson , Kenneth Ogan , Omer Kucuk , Bradley Curtis Carthon , Haydn Kissick , Viraj A. Master

Organizations

Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, GA, Departments of Biostatistics and Bioinformatics, Emory University, Atlanta, GA, Emory University Department of Hematology and Medical Oncology, Atlanta, GA, Emory University School of Medicine, Department of Pathology, The Atlanta VA Medical Center, Atlanta, GA, Emory University School of Medicine, Atlanta, GA, Emory University, Atlanta, GA, Winship Cancer Institute of Emory University, Atlanta, GA, Department of Urology, Emory University School of Medicine, Atlanta, GA, Emory University School of Medicine/Atlanta VA Medical Center, Atlanta, GA, Emory University Hospital Midtown, Atlanta, GA

Research Funding

Pharmaceutical/Biotech Company

Background: Cabozantinib is a small molecule inhibitor of the tyrosine kinases c-Met, AXL and VEGFR2 that has been shown to reduce tumor growth, metastasis, and angiogenesis. After the promising results from the METEOR, CABOSUN and Checkmate-9ER trials, cabozantinib was approved for use in patients with advanced renal cell carcinoma (RCC). The increased response rates with cabozantinib in metastatic RCC, along with the other neoadjuvant TKI data, support an expanded role for cabozantinib in the neoadjuvant setting. Methods: Patients with clinical stage ≥ T3Nx or TanyN+ or deemed unresectable by the surgeon with biopsy-proven clear cell RCC were eligible for this study, and received cabozantinib at a starting dose of 60 mg daily for 12 weeks. The primary outcome was objective response rate per RECIST v1.1 (complete and partial responses) at week 12 after the administration of cabozantinib as determined by independent radiologist review. Secondary outcomes included safety, tolerability, clinical outcome (DFS, OS), surgical outcome and quality of life. Results: As of 20 September 2021, 16 biopsy-proven clear cell RCC patients were treated with neoadjuvant cabozantinib. The median age was 56 years (range: 41-84 years) and 81.2% male. All patients completed 12 weeks of treatment, and 15 of them underwent surgery as planned without any delay after completion of 4 weeks wash-out. One patient refused to undergo surgery due to personal reasons and received further systemic treatment. Five patients (31.2%) experienced a partial response, and 11 patients had stable disease. There was no progression of disease while on cabozantinib. Median reduction of primary renal tumor size was 24% (range: 6-45%). The one patient who was deemed to be unresectable became resectable at the end of treatment. Two patients were converted from radical to partial nephrectomy. The most common AEs were diarrhea, nausea, fatigue, hypertension, anorexia, and palmar-plantar erythrodysesthesia syndrome. Intraoperatively, we did not experience any immediate complications. Postoperatively, no surgical complications related to the drug were noted. No treatment related grade 4 or 5 AEs related to cabozantinib or surgery occurred. Two patients had died at the time of analysis (1 due to COVID and 1 unknown cause). Conclusions: Cabozantinib was clinically active and safe in the neoadjuvant setting in patients with locally advanced non-metastatic clear cell RCC. Additional data will be reported including long term outcomes, correlative studies, quality of life, and frailty/sarcopenia indices. Clinical trial information: NCT04022343.

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Abstract Details

Meeting

2022 ASCO Genitourinary Cancers Symposium

Session Type

Poster Session

Session Title

Poster Session C: Renal Cell Cancer; Adrenal, Penile, Urethral, and Testicular Cancers

Track

Renal Cell Cancer,Adrenal Cancer,Penile Cancer,Testicular Cancer,Urethral Cancer

Sub Track

Therapeutics

Clinical Trial Registration Number

NCT04022343

Citation

J Clin Oncol 40, 2022 (suppl 6; abstr 340)

DOI

10.1200/JCO.2022.40.6_suppl.340

Abstract #

340

Poster Bd #

F10

Abstract Disclosures