Nasopharyngeal Carcinoma Clinical Trial
Official title:
Phase II Open-label Study Evaluating Two Loading Regimens of Sunitinib or Bevacizumab Alternating With Cisplatin and Gemcitabine as Systemic Therapy for Locally Advanced or Metastatic Nasopharyngeal Carcinoma (NPC)
- Hypothesis
We hypothesise that intermittent dosing of the anti-angiogenic RTKI sunitinib or bevacizumab
prior to systemic cisplatin and gemcitabine chemotherapy to transiently "normalise" tumour
vasculature in patients with locally advanced or metastatic NPC will allow greater efficiency
in drug and oxygen delivery, thus potentiating sensitivity to chemotherapy. We hypothesise
that a loading dose of sunitinib for 7 days is required to achieve this sensitization effect
prior to the first cycle of chemotherapy, and that this effect can subsequently be maintained
by a 7 day course of sunitinib prior to each subsequent cycle of chemotherapy. The other
hypothesis tested is that bevacizumab 7 days prior to chemotherapy will achieve normalization
of tumor vasculature as well, and may induce changes in the tumor microenvironment that is
beneficial for antitumour effect.
- Primary objectives
1. To determine the pathological CR* rate of intermittent sunitinib or bevacizumab
administered with combination cisplatin and gemcitabine as systemic therapy for
locally advanced or metastatic NPC.
2. To determine the safety and tolerability of intermittent sunitinib or bevacizumab
administered with combination cisplatin and gemcitabine as systemic therapy for
locally advanced or metastatic NPC.
- Secondary objectives
1. To determine the clinical RR (complete and partial response)+ of intermittent
sunitinib or bevacizumab administered with combination cisplatin and gemcitabine as
systemic therapy for locally advanced or metastatic NPC.
2. To evaluate the pharmacodynamic effects (imaging, circulating and tissue) of
intermittent sunitinib or bevacizumab administered with combination cisplatin and
gemcitabine as systemic therapy for locally advanced or metastatic NPC.
3. To evaluate the early pharmacodynamic effects (imaging, circulating and tissue) of
2 loading doses of sunitinib (ie., 12.5mg or 25mg) and 2 dose level of bevacizumab
(ie. 7.5mg/kg or 2.5mg/kg) given 1 week prior to administration of cisplatin and
gemcitabine chemotherapy.
;
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