Albumin-bound Paclitaxel Combined With Cisplatin Versus Docetaxel Combined With Cisplatin Induced Chemotherapy in Advanced Head and Neck Squamous Tummor

• Status: Recruiting
• Trial end date: 2021-12-01
• Target enrollment: 0
• Participant gender: All

Summary

Research Topic:

A prospective randomized controlled clinical study of albumin-bound paclitaxel combined with cisplatin (AP regimen) versus docetaxel combined with cisplatin (TP regimen) induced chemotherapy in advanced head and neck squamous cell carcinoma

Expected study duration:

Each subject received a 3-week regimen of AP or TP over 2 cycles.

Research objectives:

To evaluate the efficacy and safety of induction chemotherapy with albumin-bound paclitaxel in patients with advanced head and neck squamous cell carcinoma (HSCC), two induction chemotherapy regimens, AP regimen and TP regimen, were compared.

Trial Design. Single center, open label, controlled clinical study Number of cases: 116 Objective response rate (ORR=CR+PR) was used as the main evaluation index in this study.

• Phase: Phase 4
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Tianjin Medical University Cancer Institute and Hospital
• Treatments: Albumin-Bound Paclitaxel; Docetaxel; Paclitaxel

Criteria

Inclusion Criteria:

• Inclusion criteria:

1. Age ≥18 years old, male or female;

2. Subjects had squamous cell carcinoma of the head and neck confirmed by histrohistology or cytology;

3. CLINICAL STAGE III OR IV WITHOUT DISTANT METASTASES (AJCC 8th)

4. Patients who have not previously received initial treatment with chemotherapy or radiation;

5. KPS acuity 70;

6. Normal bone marrow reserve function and normal liver and kidney function;

7. Expected survival time ≥3 months;

8. Subjects of child-bearing age must agree to use effective contraceptive measures during the study period; The serum or urine pregnancy test must be negative for women of childbearing age 72 hours before the start of chemotherapy;

9. Subjects have good compliance, can carry out treatment and follow-up, and voluntarily abide by the regulations of this study;

10. Subjects voluntarily sign the informed consent.

Exclusion Criteria:

• Exclusion criteria:

1. Patients with distant metastasis;

2. The presence of uncontrolled serious medical diseases, such as combined with serious medical diseases, including serious heart disease, cerebrovascular disease, uncontrolled diabetes, uncontrolled hypertension, uncontrolled infection, active peptic ulcer, etc.;

3. The presence of dementia, altered mental status or any mental illness that would prevent understanding or giving informed consent or filling out questionnaires;

4. Subjects with grade ≥2 peripheral neuropathy according to CTCAE V5.0;

5. A history of allergy or hypersensitivity to any therapeutic ingredient;

6. Suffered from malignant tumors other than squamous cell carcinoma of the head and neck in the past 5 years, except adequately treated basal cell or squamous cell skin cancer, local prostate cancer after radical surgery, and ductal carcinoma in situ after radical surgery;

7. Abnormal results of physical and laboratory tests:

A) Hematologic abnormalities are defined as:

I) Absolute count of neutrophils (ANC) : < 1.5×109 / L; Ii) Platelet (PLT) count:

< 100×109/L; Iii) Hemoglobin (Hb) level < 90g/L;

B) Abnormal liver function is defined as:

I) Total bilirubin (TBIL) level: 1.5 times of the upper limit of normal value of > (ULN); Ii) AST and ALT levels of >ULN were 2.5 times, and BBB>N was 5 times if liver metastasis was present;

C) Definition of abnormal renal function:

1.5 times of serum creatinine > ULN, or the calculated creatinine clearance rate < 50ml/min;

8. Patients who need to be treated with other anti-tumor drugs;

9. Has received any other investigational drug therapy or participated in another interventional clinical trial within 30 days prior to screening;

10. The researcher considers it unsuitable for inclusion;

11. Pregnant or lactating women.