Combination Chemotherapy and Radiation Therapy in Treating Patients With Locally Advanced Head and Neck Cancer

Head and Neck Cancer Clinical Trial

Official title:

Phase II Pilot Study of TPF (Docetaxel, Cisplatin, and 5-FU) Induction Chemotherapy Followed by Concurrent Cisplatin and Reduced Dose Radiation in Locally Advanced Head and Neck Cancer

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT00352118
• Other study ID #: 2005LS012
• Secondary ID: UMN-0502M67486
• Status: Terminated
• Phase: Phase 2
• First received: July 13, 2006
• Last updated: December 3, 2017
• Start date: March 2006
• Est. completion date: April 2008

Study information

• Verified date: December 2017
• Source: Masonic Cancer Center, University of Minnesota
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

RATIONALE: Drugs used in chemotherapy, such as docetaxel, cisplatin, and fluorouracil, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Radiation therapy uses high-energy x-rays to kill tumor cells. Giving combination chemotherapy together with radiation therapy may kill more tumor cells.

PURPOSE: This phase II trial is studying how well giving combination chemotherapy together with radiation therapy works in treating patients with locally advanced head and neck cancer. The doctor also wants to find out if patients who receive this treatment need a feeding tube 1 year after starting treatment.

Description:

OBJECTIVES:

Primary

• Determine feeding tube dependency at 12 months in patients with locally advanced head and neck cancer treated with induction chemotherapy comprising docetaxel, cisplatin, and fluorouracil followed by cisplatin and reduced-dose radiotherapy.

Secondary

• Determine the progression-free, disease-free, and overall survival of patients treated with this regimen.

• Determine the pattern of failure in patients treated with this regimen.

• Evaluate the quality of life of patients treated with this regimen.

• Assess pre- and post-treatment swallowing ability of patients and the impact on their quality of life.

Tertiary

• Quantify salivary flow rates of patients receiving chemotherapy with radiotherapy for head and neck malignancy.

• Evaluate the quality of saliva by examining total protein concentrations.

• Quantify proangiogenic cytokines (interleukin [IL]-1, IL-6, IL-8, and vascular endothelial growth factor) in the saliva of these patients.

• Determine the degree of mucositis and xerostomia of patients receiving chemotherapy with radiotherapy for head and neck malignancy.

• Compare salivary flow rates with the grade of mucositis and xerostomia of patients receiving chemotherapy with radiotherapy for head and neck malignancy.

OUTLINE: This is a pilot study.

• Induction therapy: Patients receive docetaxel IV over 1 hour and cisplatin IV over 1 hour on day 1 followed by fluorouracil IV continuously on days 1- 4. Patients also receive filgrastim (G-CSF) subcutaneously (SC) on days 5-14 or pegfilgrastim SC on day

5. Treatment repeats every 3 weeks for 2 courses in the absence of disease progression or unacceptable toxicity. Patients achieving a partial or clinical complete response proceed to chemoradiotherapy 3 weeks later.

• Chemoradiotherapy: Patients receive cisplatin IV over 1 hour on day 1. Treatment repeats every 3 weeks for 3 courses in the absence of disease progression or unacceptable toxicity. Patients also undergo concurrent reduced-dose radiotherapy 5 days a week for 6 weeks.

• Surgery: Approximately 6 to 8 weeks after completing chemoradiotherapy, patients with residual neck disease or disease initially staged at N2 or greater undergo neck dissection.

Saliva is collected periodically to measure flow rates and quality; quantify proangiogenic cytokines (interleukin [IL]-1, IL-6, IL-8 and vascular endothelial growth factor); and examine the grade of mucositis and xerostomia.

Quality of life is assessed at baseline, before chemoradiotherapy, 1 month after the last radiation treatment, every 3 months for 1 year, and then every 6 months for 1 year.

After completion of study treatment, patients are followed periodically for 5 years and then annually thereafter.

PROJECTED ACCRUAL: A total of 36 patients will be accrued for this study.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 4
• Est. completion date: April 2008
• Est. primary completion date: April 2008
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Histologically confirmed squamous cell carcinoma of the head and neck

• Stage IVA or IVB disease

• Stage III disease allowed provided patient may benefit from organ preservation or patient refused surgery

• Measurable or evaluable disease

• ECOG performance status 0-2

• Absolute neutrophil count = 1,500/mm^3

• Platelet count = 100,000/mm^3

• Creatinine = 1.5 mg/dL OR glomerular filtration rate = 60 mL/min

• Bilirubin normal

• Alkaline phosphatase (AP) and AST or ALT must be within the following ranges:

• AP normal AND AST or ALT = 5 times upper limit of normal (ULN)

• AP = 2.5 times ULN AND AST or ALT = 1.5 times ULN

• AP = 5 times ULN AND AST or ALT normal

Exclusion Criteria:

• Salivary gland, sinus, or nasopharyngeal primary disease

• Evidence of distant metastatic disease

• Pregnant or nursing

• Positive pregnancy test (Fertile patients must use effective contraception during study treatment and for 3 months after completion of study treatment)

• Other malignancy within the past 5 years except for adequately treated basal cell or squamous cell skin cancer, in situ cervical cancer, or other malignancy in which stage and nature of disease is such that it is unlikely to affect survival for the next 3 years

• Peripheral neuropathy = grade 2

• Hearing loss = grade 2

• Severe hypersensitivity reaction to docetaxel or other drugs formulated with polysorbate 80 and/or cisplatin or other platinum analogs

• Poor nutritional status, in the opinion of the investigator

• Active infection

• Active ischemic heart disease

• Myocardial infarction within the past 6 months

• Prior radiotherapy above the clavicles

• Prior chemotherapy

• Prior surgery to the primary tumor except biopsy

• Concurrent amifostine or other investigational agents

Related Conditions & MeSH terms

• Head and Neck Cancer
• Head and Neck Neoplasms

Intervention

Biological:
• filgrastim
subcutaneously on Days 5-14, repeating every 3 weeks for 2 courses.
• pegfilgrastim
If applicable on day 5, repeating every 3 weeks for 2 courses.

Drug:
• cisplatin
Intravenous over 1 hour on day 1, every 3 weeks for 3 courses.
• docetaxel
Intravenous over 1 hour on day 1.
• fluorouracil
Intravenous continuously on days 1-4.

Procedure:
• conventional surgery
As appropriate, neck dissection.

Radiation:
• radiation therapy
60 Gy 5 days/week x 6 weeks with cisplatin

Locations

Country	Name	City	State
United States	Masonic Cancer Center at University of Minnesota	Minneapolis	Minnesota

Sponsors (2)

Lead Sponsor	Collaborator
Masonic Cancer Center, University of Minnesota	National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of Patients With Feeding Tube Dependency	All patients were non-evaluable and study was terminated early. There is no measure of outcome.	at 12 months
Secondary	Number of Days With Progression-free Survival	All patients were non-evaluable and study was terminated early. There is no measure of outcome. Utilizing RECIST criteria.	Between date of registration to date of first treatment failure or death.
Secondary	Number of Days - Overall Survival	All patients were non-evaluable and study was terminated early. There is no measure of outcome. Utilizing RECIST criteria.	Between date of registration to date of death.
Secondary	Number of Days With Disease Free Survival	All patients were non-evaluable and study was terminated early. There is no measure of outcome. RECIST criteria measurement.	From Date of Registration to Date of First Treatment Failure or Death
Secondary	Time to Treatment Failure	All patients were non-evaluable and study was terminated early. There is no measure of outcome. Measure using RECIST criteria.	Number of Days from Complete or Partial Response to First Date of Recurrence or Progression
Secondary	Swallowing Ability - Quality of Life Scores	All patients were non-evaluable and study was terminated early. There is no measure of outcome. Utilizing Swallowing Portion of ASHA Functional Communication Measure for Swallowing (FCM) and Dysphagia Outcome and Severity Scale (DOSS).	Baseline, before chemoradiation, 30 days after last radiation treatment, every 3 months for the first year, then every 6 months for year 2.
Secondary	Quality of Life (QOL) by Functional Assessment of Cancer Therapy-H&N QOL Questionnaire	All patients were non-evaluable and study was terminated early. There is no measure of outcome.	baseline, before chemoradiotherapy, 1 month after the last radiation treatment, every 3 months for 1 year, and then every 6 months for 1 year