Overview

GDF15 Based TPF Induction Chemotherapy for OSCC Patients

Status:
Recruiting
Trial end date:
2024-12-31
Target enrollment:
0
Participant gender:
All
Summary
The purpose of this study is to confirm the predictive value of GDF15 expression for TPF induction in T3/T4cN0M0 patients with OSCC
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Shanghai Jiao Tong University School of Medicine
Criteria
Inclusion Criteria:

- Age: 18 to 75 years old.

- Sex: both males and females.

- Karnofsky performance status (KPS) >60.

- Histological biopsy confirming squamous cell carcinoma of the oral cavity (tongue,
gingiva, buccal mucosa, floor of mouth, palate, and retromolar region).

- GDF1 high expression

- Clinical stage III/IVA (T1-2, N2, M0 or T3-4, N2, M0, UICC[international Union Against
Cancer ] 2002) with resectable lesions.

- Adequate hematologic function: white blood cell >3,000/mm3, hemoglobin>8g/L, platelet
count>80,000/mm3.

- Hepatic function: ALAT(alanine aminotransferase)/ASAT(aspartate transaminase) <2.5
times the upper limit of normal (ULN), bilirubin <1.5 times ULN.

- Renal function: serum creatinine <1.5 times ULN.

- Written informed consent

Exclusion Criteria:

- Evidence of distant metastatic disease and other cancers.

- Surgical procedure of the primary tumors or lymph nodes (except diagnostic biopsy).

- Previous radiotherapy or chemotherapy.

- Other previous malignancies within 5 years.

- Can not tolerate the treatment protocol with systematic diseases such as history of
severe pulmonary or cardiac diseases.

- Legal incapacity or limited legal capacity.

- Creatinine clearance <30ml/min.

- Pregnancy (confirmed by serum or urine β-HCG) or lactation period.