Tadalafil in Treating Patients Undergoing Surgery for Cancer of the Oral Cavity or Oropharynx

Donald T. Weed

Status: Completed

Conditions: Head and Neck Cancer

Treatments: Other: Placebo; Drug: Tadalafil

Study type: Interventional

Funder types: Other

Identifiers

NCT00843635

20070918

SCCC-2008006 (Other Identifier)

Details and patient eligibility

About

RATIONALE: Biological therapies, such as tadalafil, may stimulate the immune system in different ways and stop tumor cells from growing.

PURPOSE: This randomized clinical trial is studying how well tadalafil works in treating patients who are undergoing surgery for cancer of the oral cavity or oropharynx.

Full description

OBJECTIVES:

• To analyze the phenotype and the function of the tumor-induced suppressive network associated with squamous cell carcinoma (SCC) of the head and neck in patients with SCC of the oral cavity or oropharynx treated with tadalafil followed by definitive surgical resection.
• To analyze the immune response before and after treatment with tadalafil to determine whether or not tadalafil treatment modulates in these patients.
• To compare two doses of tadalafil to determine whether there are measurable differences in immune response in these patients.
• To analyze treatment-related side effects of tadalafil at each of the two doses tested in these patients.

OUTLINE: Patients are randomized to 1 of 3 treatment arms.

• Arm I: Patients receive oral tadalafil once daily on days 1-20 in the absence of unacceptable toxicity.
• Arm II: Patients receive oral tadalafil (at a higher dose than in arm I) once daily on days 1-20 in the absence of unacceptable toxicity.
• Arm III: Patients receive oral placebo once daily on days 1-20 in the absence of unacceptable toxicity.

All patients undergo scheduled definitive surgical resection on day 23.

Patients undergo blood sample collection at baseline, on day 20, and at 6 weeks after surgical resection for correlative laboratory studies. Patients also undergo tumor tissue sample collection at baseline and at the time of surgical resection. Samples are analyzed for immunological markers by Fluorescence-activated cell sorting (FACS) and Immunohistochemistry (IHC).

After completion of study treatment, patients are followed periodically for at least 3 years.

Enrollment: 35 patients

Sex: All

Ages: 18 to 120 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients with surgically resectable oral cavity SCC, all subsites, T1 - T4, N0 - N3
• Patients with surgically resectable oropharyngeal SCC, all subsites, T1 - T2, N0 - N1
• Patients with surgically resectable T4 oropharyngeal SCC, all subsites, N0 - N3
• Patients must be 18 years old or older

Exclusion criteria

• Patients with previous surgical resection, radiation, or chemotherapy will be excluded to rule out possible effects of local tissue changes secondary to previous treatment

• Patients with surgically unresectable disease at primary site or regional lymph nodes

• Patients with T1 - T2 SCC oropharynx, N2 - N3

• Patients with T3 SCC oropharynx , N0 - N3

• Any patient for whom non-surgical therapy is recommended as treatment of choice after multidisciplinary treatment evaluation

• Patients with an altered mental status or not capacitated for their medical decision making

• Patients with severe or unstable cardiac or cerebrovascular disease are excluded

  • myocardial infarction within the last 90 days
  • unstable angina or angina occurring during sexual intercourse
  • New York Heart Association Class 2 or greater heart failure in the last 6 months
  • uncontrolled arrhythmias
  • hypotension (<90/50 mm Hg), or uncontrolled hypertension (>170/100 mm Hg)
  • stroke within the last 6 months
  • Left ventricle outflow obstruction.

• Pregnant and nursing mothers will not be enrolled given unknown effects to offspring

• Concurrent nitrate, alpha-blocker, or cytochrome P-450 inhibitor use

• Renal Insufficiency defined as creatinine clearance less than 51.

• Creatinine clearance will be determined by the following Cockcroft-Gault Equation: (140-age) * (Wt in kg) * (0.85 if female) / (72 * Cr)

• Patients with hepatic insufficiency.

• Patients currently taking a Phosphodiesterase (PDE) inhibitors for erectile dysfunction

• Patients who are immunocompromised, for reasons not directly related to patients malignancy

• Patients with significant alcohol or drug abuse

• Patients with unilateral blindness, hereditary retinal disorders, or increased risk of blindness

• Patients with unilateral deafness, history of hearing loss, hearing aid dependence, or clinically evident hearing loss

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Triple Blind

---

35 participants in 3 patient groups, including a placebo group

Arm A - Tadalafil 10mg

Experimental group

Description:

Patients will receive 10mg/day Tadalafil orally on days 1 - 20 in the absence of unacceptable toxicity.

Treatment:

Drug: Tadalafil

Arm B - Tadalafil 20mg

Experimental group

Description:

Patients will receive 20mg/day Tadalafil orally on days 1 - 20 in the absence of unacceptable toxicity.

Treatment:

Drug: Tadalafil

Arm C - Placebo

Placebo Comparator group

Description:

Patients receive oral placebo once daily on days 1-20 in the absence of unacceptable toxicity.

Treatment:

Other: Placebo