Clinical Trials Directory

Trials / Unknown

UnknownNCT04398056

Chemotherapy Plus Subsequent Loco-regional Radiotherapy Combined With Toripalimab in the De Novo Metastatic Nasopharyngeal Carcinoma

Chemotherapy Plus Subsequent Loco-regional Radiotherapy Combined With Toripalimab for the de Novo Metastatic Nasopharyngeal Carcinoma: a Single Center, Phase II Clinical Trial.

Status
Unknown
Phase
Phase 2
Study type
Interventional
Enrollment
22 (actual)
Sponsor
Sun Yat-sen University · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to preliminarily evaluate the efficacy and safety of chemotherapy plus subsequent loco-regional radiotherapy combined with toripalimab for the de novo metastatic nasopharyngeal carcinoma.

Detailed description

This is a single center , single arm, phase II study. All eligible patients with the de novo metastatic NPC are treated with chemotherapy plus subsequent loco-regional radiotherapy combined with toripalimab. The primary objective of this study is to assess objective response rate of chemotherapy plus subsequent loco-regional radiotherapy combined with toripalimab in de novo metastatic nasopharyngeal carcinoma . The secondary objective is to assess progression free survival, and Adverse events.

Conditions

Interventions

TypeNameDescription
DRUGChemotherapy plus radiotherapy and Toripalimab1. Chemotherapy: The PF regimen included 5 g/m2 5-fluorouracil via a continuous intravenous infusion over 120 h and an intravenous administration of 100 mg/m2 cisplatin on day 1 for a maximum of six cycles. 2. Radiotherapy, intensity-modulated radiation therapy (IMRT), PTVnx:66-70Gy/30-33F; PTVnd:66~70Gy/30~33F; PTV1:60~64Gy/30~33F; PTV2:50~54Gy/30~33F, 5 fractions per week, for 6 weeks 3. Toripalimab 240mg every three weeks (Q3W) began on the first day of radiotherapy until an intolerable toxicity, or disease progression, or withdrawal of consent, or the investigator determines that he or she has to withdraw from treatment, or has been treated for up to 2 years.

Timeline

Start date
2019-04-01
Primary completion
2022-07-01
Completion
2024-07-01
First posted
2020-05-21
Last updated
2022-07-06

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT04398056. Inclusion in this directory is not an endorsement.