Overview

Triple Antiemetic Regimen for Chemoradiotherapy in Cervical Cancer or Nasopharyngeal Cancer

Status:
Recruiting
Trial end date:
2024-09-30
Target enrollment:
0
Participant gender:
All
Summary
The study is to evaluate the antiemetic effect of adding fosaprepitant to biplet regimen of tropisetron and dexamethasone for patients with cervical cancer or nasopharyngeal cancer treated with radiotherapy and concomitant weekly cisplatin chemotherapy in a south Chinese cohort.
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Shantou University Medical College
Treatments:
Aprepitant
Dexamethasone
Fosaprepitant
Tropisetron
Criteria
Inclusion Criteria:

- histologically confirmed nasopharyngeal carcinoma (AJCC 8th stage II-IVa) or cervical
cancer (adenocarcinoma, squamous cell carcinoma, or adenosquamous carcinoma, clinical
FIGO stage Ib2-IVa;), planning to receive concurrent chemoradiotherapy),18 years or
older, with an Eastern Cooperative Oncology Group (ECOG) performance status of 0-1.

Exclusion Criteria:

- took medications with antiemetic effect within 24 hours before initiation of
concurrent chemoradiotherapy, had severe systemic diseases (such as uncontrolled
diabetes/hypertension) or clinically unstable epileptic seizures require the use of
anticonvulsants; allergic to fosaprepitant, tropisetron or dexamethasone.