Actively Recruiting

Phase 2
Age: 18Years - 65Years
All Genders
NCT05514275

Radiotherapy Combined With Endostatin and Capecitabine for NPC

Led by Zhejiang Cancer Hospital · Updated on 2022-08-24

41

Participants Needed

7

Research Sites

313 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Radiotherapy combined with recombinant human endostatin and capecitabine for patients with nasopharyngeal carcinoma (NPC) resistant to induction chemotherapy.

CONDITIONS

Official Title

Radiotherapy Combined With Endostatin and Capecitabine for NPC

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Newly diagnosed non-keratinizing nasopharyngeal carcinoma confirmed by tissue exam
  • Tumor staged as T3-4N1 or N2-3 without distant metastasis
  • Karnofsky performance score greater than 70
  • Adequate blood counts: leucocytes 800/bcL or more, hemoglobin 90 g/L or more, platelets 100,000/bcL or more
  • Normal liver function with ALT and AST less than 1.5 times upper normal limit, ALP less than 2.5 times upper limit, and normal bilirubin
  • Adequate kidney function with creatinine clearance 60 ml/min or higher
  • Written informed consent given
  • Tumor showed stable or progressive disease after neoadjuvant chemotherapy
Not Eligible

You will not qualify if you...

  • Keratinizing squamous cell carcinoma or basaloid squamous cell carcinoma
  • Treatment intended for palliative care
  • Previous cancers except treated basal or squamous skin cancers or in situ cervical cancer
  • Pregnant or breastfeeding
  • Previous radiotherapy except for small skin cancers outside planned treatment area
  • Previous chemotherapy or surgery to primary tumor or lymph nodes (except diagnostic biopsy)
  • Severe medical conditions such as unstable heart disease, kidney disease, chronic hepatitis, poorly controlled diabetes, or emotional disorders
  • Tumor showed complete or partial response after neoadjuvant chemotherapy

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 7 locations

1

Zhejiang Cancer Hospital

Hangzhou, Zhejiang, China, 310022

Actively Recruiting

2

the First Hospital of Jiaxing

Jiaxing, Zhejiang, China, 314000

Actively Recruiting

3

Jinhua Central Hospital

Jinhua, Zhejiang, China, 321000

Actively Recruiting

4

The Central Hospital of Lishui City

Lishui, Zhejiang, China, 323000

Actively Recruiting

5

Ningbo First Hospital

Ningbo, Zhejiang, China, 315000

Actively Recruiting

6

Ningbo Medical Center Lihuili Eastern Hospital

Ningbo, Zhejiang, China, 315000

Actively Recruiting

7

People's Hospital of Quzhou

Quzhou, Zhejiang, China, 324000

Actively Recruiting

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Research Team

T

Ting Jin, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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