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Advaned urothelial Cancer

Novel targeted antibody treatment produced responses in nearly half of patients

<p class="article-intro">In a Phase II single arm trial with an antibody-drug conjugate to target Nectin-4 in advanced urothelial cancers 44 % of patients responded with 12 % having a complete response; median survival time was 11.7 months. Among those patients with cancer that had not previously responded to a checkpoint inhibitor, 41 % responded to EV and 38 % of people with cancer that had metastasized to the liver responded.</p> <hr /> <p class="article-content"><p>A single arm, phase II clinical trial of 125 patients showed treatment with enfortumab vedotin (EV) &ndash; a new agent targeting Nectin-4, a protein found in 97 % of urothelial cancers &ndash; produced responses in 44 % of patients with locally advanced or metastatic forms of urothelial cancer. Patients had previously been treated with platinum chemotherapy and a PD-1 or PD-L1 immune checkpoint inhibitor, but the cancer had progressed despite these treatments. &ldquo;These phase II results replicate the phase I results very closely, which is not often the case in clinical trials,&rdquo; said lead study author Daniel P. Petrylak, MD, a Professor of Medicine (Medical Oncology) and Urology at Yale Cancer Center, New Haven, CT. &ldquo;The fact that we have a therapy that can help people who don&rsquo;t benefit from checkpoint inhibitors is very gratifying.&rdquo;</p> <h2>About the Study</h2> <p>Phase I trial results of EV provided sufficient evidence that it was safe to administer. In March 2018, the U.S. Food and Drug Administration granted it a breakthrough therapy designation for people with locally advanced or metastatic urothelial cancer that has progressed during or following checkpoint inhibitor therapy.<br /> For phase II, investigators enrolled urothelial patients who had been treated with platinum-based chemotherapy and/or checkpoint inhibitors to two groups: group one had been previously treated with both medicines, and group two consisted of people who had not received platinum chemotherapy. Only results from the first group are currently being reported.<br /> In group one, 70 % of enrollees were male and the median age was 69; 35 % of people had cancers in their upper urinary tract, a relatively uncommon site; and enrollees had a median of three prior systemic treatments in the locally advanced or metastatic setting but had not received treatment for at least two weeks prior to enrolling in this trial.</p> <h2>Key Findings</h2> <p>Forty-four percent of people responded to EV resulting in either no growth or shrinkage in their tumors, and 12 % had a complete response with no detectable sign of cancer. The median overall survival time was 11.7 months. Among those patients with cancer that had not responded to a checkpoint inhibitor, 41 % responded to EV, and 38 % of people with cancer that had metastasized to the liver responded to EV. EV was well-tolerated among patients enrolled in the trial. The most common side effects included fatigue (50 % ), alopecia -- or hair loss (49 % ) -- and decreased appetite (44 % ).</p> <h2>Next Steps</h2> <p>A phase III study to confirm these findings is now underway. Group two is still enrolling people in the trial, and there is also a trial in progress to look at the benefits of providing EV for people newly diagnosed with advanced urothelial cancer. The trial is studying EV in combination with pembrolizumab, and EV in combination with a platinum-based chemotherapy.</p></p> <p class="article-footer"> <a class="literatur" data-toggle="collapse" href="#collapseLiteratur" aria-expanded="false" aria-controls="collapseLiteratur" >Literatur</a> <div class="collapse" id="collapseLiteratur"> <p>Petrylak DP et al.: EV-201: Results of enfortumab vedotin monotherapy for locally advanced or metastatic urothelial cancer previously treated with platinum and immune checkpoint inhibitors. ASCO annual Meeting 2019, LBA4505</p> <p><a href="https://ch.universimed.com/fachthemen/1000001333">zur&uuml;ck zum ASCO 2019 Newsroom</a></p> </div> </p>
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