| Literature DB >> 31023100 |
Axel Bex1,2,3, Johan V van Thienen4, Mariette Schrier1,4, Niels Graafland1, Teele Kuusk1, Kees Hendricksen1, Brunolf Lagerveld5, Patricia Zondervan6, Jeroen A van Moorselaar6, Christian Blank4, Sofie Wilgenhof4, John Haanen4.
Abstract
Surgery is the standard treatment for nonmetastatic renal cell carcinoma. Despite curative intent, patients with a high risk of relapse have a 5-year metastasis-free survival rate of only 30% and prevention of recurrence is an unmet need. In a Phase III trial (JAVELIN Renal 101), progression-free survival of axitinib + avelumab was superior to sunitinib with a favorable objective response rate and no added toxicity profiles as known for axitinib or avelumab single agent. NEOAVAX is designed as open label, single arm, Phase II trial with a Simon's two-stage design evaluating neoadjuvant axitinib + avelumab followed by complete surgical resection in 40 patients with high-risk nonmetastatic clear-cell renal cell carcinoma. Primary end point is remission of the primary tumor (RECIST 1.1; Response Evaluation Criteria In Solid Tumors) following neoadjuvant therapy. Secondary end points include disease-free survival, overall survival, rate of metastasis and local recurrence, safety, and tolerability. Exploratory end points include investigation of effects on neoangiogenesis, immune infiltrates and myeloid-derived suppressor cell components to support a rationale for the combined use of axitinib and avelumab (NCT03341845).Entities:
Keywords: Phase II; avelumab; axitinib; neoadjuvant; renal cancer
Year: 2019 PMID: 31023100 DOI: 10.2217/fon-2019-0111
Source DB: PubMed Journal: Future Oncol ISSN: 1479-6694 Impact factor: 3.404