Overview

Photodynamic Therapy Plus Brachytherapy in Treating Patients With Lung Cancer

Status:
Completed
Trial end date:
1969-12-31
Target enrollment:
0
Participant gender:
All
Summary
RATIONALE: Photodynamic therapy uses light and drugs that make cnacer cells more sensitive to light to kill tumor cells. Brachytherapy uses radiation to damage tumor cells. Photodynamic therapy combined with brachytherapy may kill more tumor cells. PURPOSE: Phase I trial to study the effectiveness of photodynamic therapy plus brachytherapy in treating patients with recurrent lung cancer that is blocking the lung passages.
Phase:
Phase 1
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Roswell Park Cancer Institute
Treatments:
Hematoporphyrin Derivative
Hematoporphyrins
Criteria
DISEASE CHARACTERISTICS: Histologically confirmed small cell or non-small cell primary lung
cancer with symptomatic endobronchial lesion(s) partially or totally obstructing airway
distal to the carina and accessible by endoscopy Recurrent disease following prior therapy
and/or be ineligible for, or refuse, alternative standard therapy such as: Surgery External
radiation therapy Chemotherapy High grade obstruction necessitating more rapid aeration and
palliation than standard therapy can provide No evidence of encasement or extension of the
tumor to the right or left major pulmonary vessels on CT of the chest No tumor involvement
at trachea or carina

PATIENT CHARACTERISTICS: Age: 18 and over Performance status: ECOG 0-2 Life expectancy: Not
specified Hematopoietic: WBC at least 4,000/mm3 Platelet count at least 100,000/mm3
Hepatic: Bilirubin less than 2 times the upper limit of normal SGOT/SGPT less than 2 times
the upper limit of normal Renal: Creatinine no greater than 2.0 mg/dL Other: Not pregnant
Adequate method of contraception required of all fertile patients Female fertile patients
must have normal serum beta HCG Not eligible for standard therapy and/or other protocol
therapy No hypersensitivity to DHE or other porphyrins Not concurrent photosensitizing
drugs such as: Tetracycline Doxorubicin No contraindications to general anesthesia,
including EKG abnormalities suggestive of acute ischemia

PRIOR CONCURRENT THERAPY: Biologic therapy: Not specified Chemotherapy: No chemotherapy
within 3 weeks prior to study entry No doxorubicin within 8 weeks prior to study entry
Endocrine therapy: Not specified Radiotherapy: Prior radiation therapy dose no higher than
75 Gy to proposed bronchial segment allowed No concurrent external brain radiation therapy
Surgery: Not specified