Metastatic Nasopharyngeal Cancer Clinical Trial
Official title:
Phase Ib/II Open-label Study Evaluating the Combination of Bevacizumab Priming With Pembrolizumab in EBER-ISH Positive Nasopharyngeal Carcinoma (NPC)
This is a single center, randomized, phase Ib/II open-label study of pembrolizumab (pembro or MK-3475) with or without bevacizumab in patients with recurrent non-curable or metastatic nasopharyngeal carcinoma (NPC).
The study will consist of 2 treatment arms. In Treatment Arm A, patients will be treated with
intravenous pembrolizumab alone, 21-day cycle. For Treatment Arm B, patients will receive
intravenous pembrolizumab preceded by an infusion of bevacizumab (Day 1 of 21-day cycle).
Each treatment cycle is 3 weeks. Up to 48 patients will be enrolled in this study in 2
stages. The first stage will consist of 30 patients and the remaining 18 patients will be
added if interim data looks promising.
Eligible patients will be randomized 1:1 into either Treatment Arm A or Arm B. Treatment will
continue until tumor progression, intolerance to treatment, or up to 2 years (32 doses of
pembrolizumab/bevacizumab). For patients who have progressed on pembrolizumab alone, cross
over to Arm B is allowed, with repeat biopsy of the lesions before and 1 week after starting
bevacizumab. Patients who discontinue from the trial will not be replaced.
The study will collect serial samples of tumor tissue and blood to determine the PD
biomarkers of immune activation, in the tumor and systemically, following treatment. This is
expected to provide preliminary evidence for immune stimulation using both pembrolizumab and
bevacizumab in NPC. The tumor biopsies will also present an opportunity to determine the
molecular details of tissue and tumor response to anti-angiogenic therapy.
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