Abstract 1912TiP
Background
nccRCCs are a heterogenous group of rare histologic subtypes, each with distinct biology and response to treatment. There have been few dedicated randomized phase 3 studies in nccRCC, highlighting an urgent unmet need for effective therapies. Sunitinib is the only TKI to have shown a clinical benefit (vs everolimus) in a broad range of histologic subtypes of metastatic nccRCC (Armstrong et al. Lancet Oncol 2016 ). To date, no single agent or combination has shown a significant overall survival (OS) benefit over sunitinib in any nccRCC subtype. Zanzalintinib (XL092), a novel TKI of VEGFR2, MET, AXL, and MER, has shown antitumor and immunomodulatory activity alone, and synergistic antitumor effect with PD1 inhibition, in animal models (Hsu et al. Mol Cancer Ther 2023 ). In a phase 1 study of metastatic solid tumors including RCC, zanzalintinib showed promising clinical activity and a manageable toxicity profile, alone and with an immune checkpoint inhibitor (ICI) (Sharma et al. ESMO 2022 Abs 481P). STELLAR-304 was designed to assess the efficacy and safety of zanzalintinib + nivolumab versus sunitinib in first-line nccRCC (NCT05678673).
Trial design
STELLAR-304 is a global, randomized, open-label study of adults with unresectable/advanced/metastatic nccRCC that is measurable per RECIST v1.1. The trial includes papillary, unclassified, and translocation-associated histologies (sarcomatoid features are allowed); chromophobe, renal medullary carcinoma, or pure collecting duct histology are excluded. Histologies are confirmed by central pathology review. Prior systemic anticancer therapy for advanced or metastatic nccRCC is not permitted; however, 1 prior systemic adjuvant therapy, including ICI and excluding sunitinib, is allowed for completely resected RCC if recurrence occurred ≥6 months after the last adjuvant therapy dose. Patients (N=291) are randomized 2:1 to zanzalintinib + nivolumab or sunitinib alone. The primary endpoints are PFS and ORR per RECIST v1.1 by blinded independent radiology committee. The secondary endpoint is OS; safety will also be assessed. STELLAR-304 is currently recruiting patients in 29 countries in Europe, North and South America, and the Asia-Pacific region.
Clinical trial identification
NCT05678673.
Editorial acknowledgement
Writing and editorial assistance was provided by Alexus Rivas-John, PharmD (Fishawack Communications Inc., part of Fishawack Health, Conshohocken, PA, USA).
Legal entity responsible for the study
Exelixis, Inc.
Funding
Exelixis, Inc.
Disclosure
S.K. Pal: Financial Interests, Personal, Other, Travel Accommodations/Expenses: Ipsen, CRISPR Therapeutics. T.B. Powles: Financial Interests, Institutional, Research Funding: AstraZeneca, Roche, BMS, Exelixis, Ipsen, MSD, Novartis, Pfizer, Seattle Genetics, Merck Serono, Astellas, Johnson & Johnson, Eisai; Financial Interests, Personal, Advisory Role: AstraZeneca, BMS, Exelixis, Incyte, Ipsen, MSD, Novartis, Pfizer, Seattle Genetics, Merck Serono, Astellas, Johnson & Johnson, Eisai, Roche, Mash Up Ltd; Financial Interests, Personal, Other, Travel Accommodations/Expenses: Roche, Pfizer, MSD, AstraZeneca, Ipsen. R. Kanesvaran: Financial Interests, Personal, Advisory Role: MSD, BMS, Eisai, Astellas, J&J, Pfizer, AstraZeneca, Merck; Financial Interests, Personal, Other, Honoraria; Travel Accommodations/Expenses: MSD, Astellas, AZ; Financial Interests, Personal, Other, Honoraria: BMS, Eisai, J&J, Pfizer, Merck. C. Lee: Financial Interests, Institutional, Research Funding: AstraZeneca, BMS, Calithera, Eisai, Exelixis, Merck; Financial Interests, Personal, Advisory Role: Aveo, BMS, Exelixis, Eisai, Merck, Pfizer, EMD Serono, Cardinal Health; Financial Interests, Personal, Other, Honoraria: AiCME, IDEOlogy Health, Intellisphere, Medscape, Research to Practice. Z. Wang: Financial Interests, Personal, Full or part-time Employment: Exelixis, Inc.; Financial Interests, Personal, Stocks/Shares: Exelixis, Inc.. P. Patel: Financial Interests, Personal, Full or part-time Employment: Exelixis, Inc.. C. Suarez Rodriguez: Financial Interests, Personal, Advisory Role: Astellas Pharma, Bayer, Hoffmann-La Roche LTD, Ipsen, Merck Sharp and Dohme, Pfizer S.L.U, Sanofi- Aventis; Financial Interests, Institutional, Advisory Role: BMS. All other authors have declared no conflicts of interest.
Resources from the same session
1756P - Vizcan: A Swedish population-based study to address cancer outcomes using an interactive platform
Presenter: Anders Berglund
Session: Poster session 23
1757P - A real-world evaluation of the effectiveness of thermogram along with clinical breast examination in community-based breast cancer screening program
Presenter: Rahul Ravind
Session: Poster session 23
1758P - Body composition meets precision medicine: The prognostic value of sarcopenia in patients (pt) treated with Molecularly Targeted Agents (MTA)
Presenter: Cinta Hierro
Session: Poster session 23
1760P - Systematic review of quality of life (QoL) inclusion among endpoints, reporting and impact of QoL results in phase III non-inferiority trials of systemic treatments in oncology
Presenter: Jessica Paparo
Session: Poster session 23
1761P - Incidence of herpes zoster in cancer patients in Europe: A systematic review
Presenter: Inga Posiuniene
Session: Poster session 23
1762P - Are published data up-to-date? Analysis of time to publication in major oncological journals
Presenter: Pawel Sobczuk
Session: Poster session 23
1763P - The challenge for Cancer Trials Ireland (CTI) to sponsor NCI and non-EU sponsored trials in the EU
Presenter: Eibhlin Mulroe
Session: Poster session 23
1886P - Pembrolizumab and denosumab in clear cell renal cell carcinoma (ccRCC): A phase II trial (KeyPAD, ANZUP1601)
Presenter: Craig Gedye
Session: Poster session 23
1887P - Adjuvant everolimus (EVE) in patients (pts) with completely resected very high-risk renal cell cancer (RCC) and clear cell histology: Results from the phase III SWOG S0931 (EVEREST) trial
Presenter: Primo Lara
Session: Poster session 23