Low-dose Radiotherapy and Neoadjuvant Chemotherapy Sequential Concurrent Chemoradiotherapy for Locally Advanced Nasopharyngeal Carcinoma
NCT ID: NCT05503914
Last Updated: 2022-08-17
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
80 participants
INTERVENTIONAL
2022-08-01
2023-07-01
Brief Summary
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Detailed Description
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Joiner recognized the potential of low-dose fractionated radiotherapy as early as 20 years ago. Namely: high radiosensitivity (HRS), which means that the initial dose can produce radiosensitivity from 0 to 80 cGy. Low-dose fractionated radiation therapy (LDFRT) is a unique radiobiological phenomenon. This phenomenon reports that the effect of induced chemotherapy can be increased by reducing MDR-1 and overcoming the antiapoptotic effect of Bcl-2, resulting in the death of nuclear factors kappa-b29 and p53.This radiation is different from conventional fractionated or large fractionated radiotherapy. Conventional segmentation or high-dose segmentation will not only kill tumor cells, but also make tumor cells resistant to radiation. Studies have shown that low-dose radiotherapy (LDFRT) in the range of 50 - 80 cGy can be used as a chemical sensitizer to enhance the effect of chemotherapy, increase tumor response and improve local control. At present, clinical studies have reported that in locally advanced Squamous cell carcinoma of head and neck#SCCHN#, the clinical experiment of induction chemotherapy (paclitaxel + carboplatin) combined with LDFRT has achieved preliminary success, and showed that the optimal dose is 50-80cGy 4 times / day. Importantly, it did not increase the toxic and side effects of induction chemotherapy. Subsequently, the results of a long-term SCCHN trial reported that the primary endpoint complete response rate (CR), secondary endpoint overall survival (OS), progression free survival (PFS) and toxicity of LDFRT combined with induction chemotherapy had clinical significance. At present, the role of LDFRT in locally advanced nasopharyngeal carcinoma is still unclear. Whether it can improve the efficacy of neoadjuvant chemotherapy is worth exploring.
In conclusion, neoadjuvant chemotherapy combined with LDFRT provides a new idea for tumor treatment. Low dose fractionated radiotherapy is used to enhance the objective remission rate of induction chemotherapy, make high-risk tumor lesions become the target area, and up regulate the apoptotic proteins bax and bcl-x in the microenvironment to achieve the greatest benefit. Therefore, it is of great clinical value to explore the application of neoadjuvant chemotherapy combined with low-dose radiotherapy (LDFRT) sequential concurrent chemoradiotherapy in locally advanced nasopharyngeal carcinoma (NPC).
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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low-dose radiotherapy group
Neoadjuvant chemotherapy combined with low-dose radiotherapy sequential concurrent chemoradiotherapy
low-dose radiotherapy
On the first and second days of induction chemotherapy, local tumor were irradiated with 0.5Gy bid for 4 times.
control group
Neoadjuvant chemotherapy sequential concurrent chemoradiotherapy
No interventions assigned to this group
Interventions
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low-dose radiotherapy
On the first and second days of induction chemotherapy, local tumor were irradiated with 0.5Gy bid for 4 times.
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
2. The primary focus has received immunotherapy
3. Other malignant tumors (except non melanoma skin cancer or cervical carcinoma in situ)
4. Subjects who have received other drug trials in recent 1 month
5. Have a serious history of allergy or special constitution
6. A history of severe lung or heart disease or serious complications, such as uncontrollable hypertension and heart failure.
7. Drug or alcohol addicts
8. Having personality or mental illness, no civil capacity or limited civil capacity
9. Active systemic infection
10. At the same time, they received chronic systemic immunotherapy or hormone therapy other than this study. -
18 Years
70 Years
ALL
No
Sponsors
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Sichuan Cancer Hospital and Research Institute
OTHER
Responsible Party
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Mei Feng
Vice President
Principal Investigators
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feng mei
Role: PRINCIPAL_INVESTIGATOR
Sichuan Cancer Hospital and Research Institute
Locations
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Low-dose Radiotherapy and Neoadjuvant Chemotherapy Sequential Concurrent Chemoradiotherapy for Locally Advanced Nasopharyngeal Carcinoma
Sichuan, Sichuan, China
Countries
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Central Contacts
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Facility Contacts
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feng mei
Role: primary
Other Identifiers
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Ahead-NC-202208
Identifier Type: -
Identifier Source: org_study_id
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