RecruitingNCT05950087

Study on the Relationship Between Plasma MRD and cfDNA HPV and the Efficacy and Prognosis of Locally Advanced Cervical Cancer After Concurrent Chemoradiotherapy


Sponsor

Guizhou Provincial People's Hospital

Enrollment

30 participants

Start Date

Nov 1, 2022

Study Type

OBSERVATIONAL

Conditions

Summary

Cervical cancer CC is the most common malignant tumor in the female reproductive system, seriously endangering women's health and life, and is one of the leading causes of death for women worldwide.Globally, HPV causes about 85% of cervical cancers and about 60% of oropharyngeal cancers, causing more than 500,000 cancers each year.ctDNA is a potential biomarker because it contains tumor-specific genetic and epigenetic abnormalities that can be used in cancer diagnosis and prognosis prediction.MRD is considered a promising prognostic marker that can be used to identify individuals at increased risk of recurrence and individuals who may benefit from treatment.The expression level of MRD and plasma HPV before and after radiotherapy and chemotherapy for cervical cancer was analyzed by liquid biopsy ctDNA detection technology, which predicted the efficacy of cervical cancer radiotherapy and chemotherapy, which was helpful for monitoring and estimating the risk of disease recurrence after cervical cancer radiotherapy and chemotherapy, and verified the expression of MRD and plasma HPV as the basis for adjuvant chemotherapy after cervical cancer radiotherapy and the basis for optimal chemotherapy time node selection.


Eligibility

Sex: FEMALEMin Age: 18 YearsMax Age: 75 Years

Plain Language Summary

Simplified for easier understanding

This study is looking at whether certain markers in the blood — specifically circulating tumor DNA and HPV-related genetic material — can predict how well patients with locally advanced cervical cancer respond to combined chemotherapy and radiation (chemoradiotherapy). This may help doctors better personalize treatment. **You may be eligible if...** - You are 18 to 75 years old with a confirmed diagnosis of cervical cancer - Your cancer is locally advanced but you are a candidate for chemoradiotherapy - Your overall health is good (ECOG 0-1) - Your blood counts, liver, and kidney function meet required levels - You are expected to survive at least 6 months **You may NOT be eligible if...** - You are allergic to rubber products - You have a severe active infection, active tuberculosis, active hepatitis B, or AIDS - You have serious pre-existing heart disease - You have cancer that has spread into the fluid around your organs - You have already participated in another clinical trial 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

OTHERConcurrent chemoradiotherapy

Concurrent chemoradiotherapy


Locations(1)

Yong Li

Guiyang, Guizhou, China

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NCT05950087


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