Cabozantinib in patients (pts) with non-locally pretreated brain metastases (BM) from renal cell carcinoma (RCC): Results of the multicenter CABRAMET phase II trial (NCT03967522).
Abstract
533 Background: Despite dramatic progress in metastatic RCC treatments, pts with BM remain with poor outcome and were mostly excluded from clinical trials. Local treatments on BM are standard today. Methods: Adult pts with histologically proven RCC and BM ≥ 5 mm (or > 8 mm if solitary) including at least one non-locally pretreated, < 3 prior systemic treatments excluding cabozantinib, ECOG PS 0 or 1 and steroids < 40 mg/day were included. Primary endpoint was BM progression free survival rate at 6 months (6m-BM-PFS) according to modified RANO-BM criteria by central review. Secondary endpoints were BM response and response duration, extracranial response, PFS, overall survival and safety. 25 evaluable pts were required to evaluate the main endpoint. Results: 26 pts were included, 25 were evaluable for the primary endpoint and median follow up time was 39.8 months [5.9-49.7]. The 6m-BM-PFS was 56.0% [unilateral 95%CI 37.9-] (14/25 pts). BM response was partial response (PR) for 61.5% (16/26) pts and median duration of response was not reached, 66.7% pts being event-free 24 months after BM response. Extracranial response was PR for 38.5% (10/26). Median PFS was 8.1 months [95%CI 4-11.9], and median BM PFS 8.4 months [95%CI 5.4-NR]. Median overall survival was 15.8 months [95%CI 9.7-35.0]. No new safety signals were observed. Conclusions: This is the first prospective trial assessing cabozantinib in RCC pts with non-locally pretreated BM. These results confirm the efficacy of cabozantinib on BM previously reported in retrospective series. Clinical trial information: NCT03967522 . Pts characteristics. Pts number N = 26 Median age (years) [range] 67 [44-86] Gender: F / M, n 5 / 21 ECOG PS: 0 / 1,n 10 / 16 RCC: non-clear cell / clear cell, n 2 / 24 Prior nephrectomy : n 16 Number of BM: 1 / 2 / >3, n 9 / 7 / 10 Prior BM treatments: Overall/ Surgery/ Radiation, n 10 / 3 / 10 Prior systemic treatment: 0 / 1 / >2, n 7 / 15 / 4 IMDC: Favorable / Intermediate / Poor, n 7 / 10 / 9
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (18)
Sylvie Negrier
Loic Mourey
Institut Claudius Regaud, IUCT-Oncopole, Toulouse, France
Ellen Blanc
Department of Clinical Research and Innovation, Centre Léon Bérard, Lyon, France
Marine Gross-Goupil
University Hospital of Bordeaux, Bordeaux, France
Aude Fléchon
Oncology Department, Centre Léon Bérard, Lyon, France
Ronan Flippot
INSERM U1363, Université Paris Saclay, Villejuif, France
Philippe Barthélémy
Stéphane Oudard
Department of Medical Oncology, Hôpital Européen Georges Pompidou, AP-HP, Paris Cité University, Paris, France
Emeline Colomba
Constance Thibault
Department of Medical Oncology, Hôpital Européen Georges Pompidou, AP-HP, Paris Cité University, Paris, France
Alain Ravaud
Bordeaux University Hospital, Bordeaux University, Bordeaux, France
Christine Chevreau
Institut Claudius Regaud/IUCT-Oncopole, Toulouse, France
Mathilde Donnat
Centre Leon Berard, Lyon, France
Helen Jane Boyle
Centre Leon Bérard, Lyon, France
Cécile Dalban
Centre Léon Bérard, Lyon, France
David Pérol
Centre Léon Bérard, Lyon, France
Bernard Escudier
Gustave Roussy, Villejuif, France
Laurence Albiges
Department of Medical Oncology Gustave Roussy Villejuif France