Surgery Plus Reduced Target Chemoradiotherapy Versus Surgery Plus Reduced Dose Chemoradiotherapy for Newly Diagnosed Operable Nasopharyngeal Carcinoma : a Prospective, Multicenter, Radomized Control Trial

Status: Recruiting
Location: See location...
Intervention Type: Radiation
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The goal of this clinical trial is to compare surgery plus reduced target chemoradiotherapy with surgery plus reduced dose chemoradiotherapy in newly diagnosed operable Nasopharyngeal Carcinoma.The main questions it aims to answer are:whether endoscopic surgery combined with reduced dose chemoradiotherapy vs surgery plus target reduction chemoradiotherapy can bring substantial survival benefits, lower toxicity, and shorter treatment cycle for patients with operable nasopharyngeal carcinoma .

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 70
Healthy Volunteers: f
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• Performance Status Score 0-1 points.

• Non-keratinized carcinoma of the nasopharynx (differentiated or undifferentiated, i.e., WHO type II or III) confirmed histologically and/or cytologically.

• Patients with primary nasopharyngeal lesions evaluated as surgically resectable, including T1 (tumor limited to nasopharynx), T2 (tumor limited to the surface of parapharyngeal space) and T3 (tumor limited to the bottom wall of sphenoid sinus) and tumor diameter ≤1.5cm. Resectable retropharyngeal lymph nodes were defined as; The diameter was ≤ 1.5cm, the tissue space was intact, and there was no obvious extranodal invasion; The resectable cervical lymph nodes were defined as ≤ 3cm in diameter, located above the lower edge of the cricoid cartilage, with moderate mobility and no obvious extranodal invasion. Clinical stage: T1-3N1-2M0, T2-3N0M0 (Stage II-III) according to AJCC 8th staging edition.

• Adequate organ function: WBC ≥ 4×10\^9 /L, NEUT ≥ 2×10\^6 /L, HGB ≥ 9 g/dL, PLT count ≥ 100×10\^9/L, TBIL ≤1.5 ULN (TBIL ≤3 ULN for patients with Gilbert Disease), ALT ≤3 ULN, AST ≤3 ULN, ALP ≤3 ULN, ALB ≥ 3 g/dL, INR or APTT≤1.5 ULN, Scr ≤1.5 ULN or Ccr ≥ 60 mL/min.

• Informed Concent signed with willingness to obey the follow-up, treatment, examination and any other programs according to the research protocol.

Locations
Other Locations
China
The Fifth Affiliated Hospital of Sun Yat-sen University
RECRUITING
Zhuhai
Contact Information
Primary
Ming-Yuan Chen, MD,PhD
chmingy@email.sysu.edu.cn
86-13903052650
Backup
You-Ping Liu, PhD
liuyp78@email.sysu.edu.cn
86-137517763276
Time Frame
Start Date: 2022-11-01
Estimated Completion Date: 2032-11-01
Participants
Target number of participants: 384
Treatments
Active_comparator: surgery plus target reduction Chemoradiotherapy
Surgery:~Endoscopic Nasopharyngectomy:Radical Reaction of the Primary Lesion Using Nasal Endoscopy.~Retropharyngeal lymphadenectomy: Radical retropharyngeal LNs reaction using nasal endoscopy.~Neck lymph node dissection Selection of region where the possitive lymph nodes are located.~Intensity modulated radiotherapy with GTV and CTV1 Reduction:~CTV2:50.00Gy/25Fr/2.00Gy. Chemotherapy: cisplatin-based regimens.
Experimental: surgery plus dose reduction Chemoradiotherapy
Surgery:~Endoscopic Nasopharyngectomy: Radical Reaction of the Primary Lesion Using Nasal Endoscopy.~Retropharyngeal lymphadenectomy: Radical retropharyngeal LNs reaction using nasal endoscopy.~Neck lymph node dissection Selection of region where the possitive lymph nodes are located.~Intensity modulated radiotherapy with CTV1 and CTV2 dose Reduction:~CTV1:48.00-50.00Gy/20Fr/2.40-2.50Gy; CTV2:40.00Gy/20Fr/2.00Gy. Chemotherapy: cisplatin-based regimens.
Related Therapeutic Areas
Sponsors
Leads: Ming-Yuan Chen
Collaborators: People's Hospital of Guangxi Zhuang Autonomous Region, Fifth Affiliated Hospital of Guangzhou Medical University, Sun Yat-sen University, The First Affiliated Hospital of University of South China, Fifth Affiliated Hospital, Sun Yat-Sen University, Huazhong University of Science and Technology Union Hospital (Nanshan Hospital), Nanchang City First Hospital

This content was sourced from clinicaltrials.gov

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