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.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT05979961 -
Phase III Trial of Concurrent Chemotherapy Alone in Patients With Low-risk Nasopharyngeal Carcinoma
|
Phase 3 | |
Active, not recruiting |
NCT04242199 -
Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of INCB099280 in Participants With Advanced Solid Tumors
|
Phase 1 | |
Recruiting |
NCT05415098 -
Study of Safety, Pharmacokinetic and Efficacy of APG-5918 in Advanced Solid Tumors or Lymphomas
|
Phase 1 | |
Recruiting |
NCT06055816 -
Gemcitabine Combined With Endostar and Envafolimab in Elderly Patients With Locally Advanced Nasopharyngeal Carcinoma
|
Phase 2 | |
Recruiting |
NCT05547971 -
Development of Intelligent Model for Radioactive Brain Damage of Nasopharyngeal Carcinoma Based on Radio-metabolomics
|
||
Not yet recruiting |
NCT05020925 -
SHR-1701 in Combination With Famitinib in Patients With Recurrent/Metastatic Nasopharyngeal Carcinoma
|
Phase 1/Phase 2 | |
Not yet recruiting |
NCT04548271 -
Camrelizumab Combined With Apatinib in Patients With PD-1 Antagonists Resistant Recurrent/Metastatic Nasopharyngeal Carcinoma
|
Phase 2 | |
Not yet recruiting |
NCT04547088 -
Camrelizumab Combined With Apatinib in Patients With First-line Platinum-resistant Recurrent/Metastatic Nasopharyngeal Carcinoma
|
Phase 2 | |
Recruiting |
NCT02795169 -
Trail Evaluating Carbon Ion Radiotherapy With Concurrent Chemotherapy for Locally Recurrent Nasopharyngeal Carcinoma
|
Phase 1/Phase 2 | |
Terminated |
NCT02801487 -
Trial Evaluating Carbon Ion Radiotherapy With Concurrent Chemotherapy for Locally Recurrent Nasopharyngeal Carcinoma
|
Phase 1/Phase 2 | |
Terminated |
NCT02569788 -
Trail Evaluating Carbon Ion Radiotherapy for Locally Recurrent Nasopharyngeal Carcinoma
|
Phase 1/Phase 2 | |
Completed |
NCT02237924 -
Endostar Combined With Intensity-modulated Radiotherapy Compare With Chemoradiation for Nasopharyngeal Carcinoma
|
Phase 2 | |
Recruiting |
NCT02044562 -
Dietary Nitrate on Plasma Nitrate Levels for Nasopharyngeal Carcinoma Patients
|
N/A | |
Terminated |
NCT01694576 -
NPC Staged N2-3M0:Adjuvant Chemotherapy or Just Observation After Concurrent Chemoradiation
|
Phase 2 | |
Recruiting |
NCT01462903 -
A Study of Adoptive Immunotherapy With Autologous Tumor Infiltrating Lymphocytes in Solid Tumors
|
Phase 1 | |
Completed |
NCT01271439 -
Study of Chemoradiotherapy Combined With Cetuximab in Nasopharyngeal Carcinoma
|
Phase 2 | |
Completed |
NCT00535795 -
Phase III: Assess Conventional RT w/ Conventional Plus Accelerated Boost RT in the Treatment of Nasopharyngeal CA
|
Phase 3 | |
Completed |
NCT00379262 -
Therapeutic Gain by Induction-concurrent Chemoradiotherapy and/or Accelerated Fractionation for Nasopharyngeal Carcinoma
|
Phase 3 | |
Completed |
NCT03398980 -
Late Sequelae of Childhood and Adolescent Nasopharyngeal Carcinoma Survivors After Radiotherapy
|
N/A | |
Not yet recruiting |
NCT05519956 -
Elective Level Ib Irradiation in Nasopharyngeal Carcinoma Patients Based on the International Guidelines
|
Phase 3 |