Photodynamic Therapy Using HPPH in Treating Patients With Recurrent Dysplasia, Carcinoma in Situ, or Stage I Oral Cavity Cancer

OBJECTIVES:

Primary

- To determine the maximum tolerated dose in the oral cavity of photodynamic therapy
(PDT) using HPPH and 665 nm light in patients with recurrent dysplasia, carcinoma in
situ, or stage I squamous cell carcinoma of the oral cavity.

Secondary

- To determine response of dysplasia, carcinoma in situ, and selected patients with T1
squamous cell carcinoma of the oral cavity using PDT with HPPH and 665 nm light.

OUTLINE: This is a dose-escalation study of laser light dose therapy.

Patients receive HPPH IV over 1 hour on day 1. Approximately 24 hours after receiving HPPH,
patients undergo laser light treatment to the tumor bed on day 2. Patients with multicentric
or large area confluent disease receive a second course of treatment at least 8 weeks later
for lesions untreated at the first treatment session.

After completion of study treatment, patients are followed at 1 week, 1 month, 3 months, and
periodically thereafter.

DISEASE CHARACTERISTICS:

- Biopsy-confirmed diagnosis of 1 of the following:

- Mild to severe dysplasia

- Carcinoma in situ (CIS) of the oral cavity

- Carcinoma must be less than 3mm thick

- Stage I (T1) squamous cell carcinoma of the oral cavity

- Recurrent or primary disease

- No T2 or greater squamous cell carcinoma, exophytic CIS, or dysplasia lesions

PATIENT CHARACTERISTICS:

- ECOG performance status 0-2

- Total bilirubin ≤ 2.0 mg/dL

- Creatinine ≤ 2.0 mg/dL

- Alkaline phosphatase ≤ 3 times the upper limit of normal (ULN)

- SGOT ≤ 3 times ULN

- Not pregnant

- Fertile patients must use effective contraception

- No porphyria or hypersensitivity to porphyrin or porphyrin-like compounds

PRIOR CONCURRENT THERAPY:

- Prior therapy of any type allowed

- More than 4 weeks since prior and no concurrent chemotherapy or radiotherapy