RecruitingPhase 2NCT06055816

Gemcitabine Combined With Endostar and Envafolimab in Elderly Patients With Locally Advanced Nasopharyngeal Carcinoma


Sponsor

Zhejiang Cancer Hospital

Enrollment

40 participants

Start Date

Sep 28, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

Gemcitabine Combined With Endostar and Envafolimab in Elderly Patients With Locally Advanced Nasopharyngeal Carcinoma


Eligibility

Min Age: 65 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a combination of chemotherapy (gemcitabine), an anti-angiogenesis drug (endostar), and an immunotherapy drug (envafolimab) in elderly patients with locally advanced nasopharyngeal carcinoma (cancer of the upper throat/nasal passage area) who cannot tolerate standard intensive treatments. **You may be eligible if...** - You are 65 years or older - You have newly diagnosed nasopharyngeal cancer confirmed by biopsy - Your cancer is at clinical stage III–IVA - Your general health score (Karnofsky) is 60 or above - You have adequate organ function **You may NOT be eligible if...** - You have had a prior cancer diagnosis - You have previously received radiation, chemotherapy, immunotherapy, or targeted therapy - Your life expectancy is less than 6 months Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGEndostar and Envafolimab

Neoadjuvant therapy consisting of gemcitabine (1000mg/m2 d1,8) , endostar (150mg 3-day continuous infusion) and envafolimab (240mg d1) was given every 3 weeks for 3 cycles. Endostar, administered every 3 weeks (150mg 3-day continuous infusion), was given concurrently with intensity-modulated radiotherapy.


Locations(1)

Zhejiang Cancer Hospital

Hangzhou, Zhejiang, China

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NCT06055816


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