Neoadjuvant Tislelizumab Combined With Albumin-paclitaxel, Cisplatin, and Fluorouracil in Patients With Locally Advanced Oral Squamous Cell Carcinoma :A Single-arm, Prospective,Phase II Study

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

TPF is still recommended as the preferred induction chemotherapy regimen for nonsurgical treatment of patients with LA HNSCC. Based on the KEYNOTE-048 study, all major guidelines recommend PD-1 monotherapy or PD-1 combined with chemotherapy as the new first-line standard treatment for patients with advanced HNSCC. The immunotherapy in operable LA HNSCC was also explored as neoadjuvant therapy due to the excellent data in advanced HNSCC. These explorations have also achieved good results. Therefore, this study aims to explore the pathological remission rate, the long-term benefit and safety of Tislelizumab combined with albumin paclitaxel, cisplatin and fluorouracil for locally advanced oral squamous cell carcinoma.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 75
Healthy Volunteers: f
View:

• Signed the informed consent form

• Histopathological diagnosis of oral squamous cell carcinoma

• Age: 18-75 years old , Gender: male and female

• Primary tumor with a clinical stage of III/IVb (T1-2N+M0或T3-4N0-3M0, AJCC2018)

• Eastern Cooperative Oncology Group (ECOG) performance status (PS): 0-1

• No previous systematic therapy for OSCC (including chemotherapy, EGFR inhibitors, VEGFR inhibitors such as bevacizumab, immune checkpoint inhibition such as anti-PD-1 or PD-L1 antibodies, anti-ctLA-4 antibodies, etc.);

• Patients must have at least one measurable lesion according to the Response Evaluation Criteria in Solid Tumors (RECIST v1.1)

• Adequte organ function based on laboratory test values obtained during the screening period:1)Blood routine: white blood cells (WBCs) \>3.0× 109/L, ANC \>1.5× 109/L, platelets \>75× 109/L, hemoglobin \>9 g/L, 2)Liver function: alanine amino transferase/aspartate amino transferase (ALAT/ASAT) \<2.5 times the upper limit of normal and bilirubin \<1.5 times the upper limit of normal,3)Renal function: Serum creatinine \<1.5 times the upper limit of normal,4)Coagulation function: INR, PT, APTT\<1.5 times the upper limit of normal,5)Left ventricular ejection fraction (LVEF) ≥ 50%

• contraception

Locations
Other Locations
China
First affiliated hospital, School of Medicine, Zhejiang University
RECRUITING
Hangzhou
Contact Information
Primary
Lulu Liu, M.D.
liululu2001@zju.edu.cn
0571-87237587
Time Frame
Start Date: 2023-05-08
Estimated Completion Date: 2028-06-30
Participants
Target number of participants: 30
Treatments
Experimental: Treatment
Related Therapeutic Areas
Sponsors
Leads: Weijia Fang, MD

This content was sourced from clinicaltrials.gov

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