Overview

Light Dosimetry for Photodynamic Therapy With Porfimer Sodium in Treating Participants With Malignant Mesothelioma or Non-Small Cell Lung Cancer With Pleural Disease Undergoing Surgery

Status:
Recruiting
Trial end date:
2023-09-28
Target enrollment:
0
Participant gender:
All
Summary
This phase I trial studies the side effects and how well light dosimetry system works during photodynamic therapy with porfimer sodium in treating participants with malignant mesothelioma or non-small cell lung cancer with pleural disease undergoing surgery. Light dosimetry measures the amount of laser light given during photodynamic therapy. Photodynamic therapy uses a drug, such as porfimer sodium, that becomes active when it is exposed to light. The activated drug may kill tumor cells. Using light dosimetry for intraoperative photodynamic therapy may help doctors estimate how much light is delivered during photodynamic therapy and decide if the treatment should be stopped or continued.
Phase:
Phase 1
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Roswell Park Cancer Institute
Collaborator:
National Cancer Institute (NCI)
Treatments:
Dihematoporphyrin Ether
Hematoporphyrin Derivative
Trioxsalen
Criteria
Inclusion Criteria:

- Histologically confirmed mesothelioma or non-small cell lung cancer (NSCLC) with
pleural disease without distant disease.

- Subjects must have an Eastern Cooperative Oncology Group (ECOG) scale of 0-2.

- Subjects of child-bearing potential must agree to use adequate contraceptive methods
(e.g., hormonal or barrier method of birth control; abstinence) prior to study entry
and for 6 months after surgery. Should a woman become pregnant or suspect she is
pregnant while she or her partner is participating in this study, she should inform
her treating physician immediately.

- The subject must understand the investigational nature of this study and sign an
Independent Ethics Committee/Institutional Review Board approved written informed
consent prior to receiving any study related procedure.

Exclusion Criteria:

- Patients who have had chemotherapy or radiotherapy within 4 weeks (6 weeks for
nitrosoureas or mitomycin C) prior to entering the study or those who have not
recovered from adverse events due to agents administered more than 4 weeks earlier.

- Patients with known brain metastases should be excluded from this clinical trial
because of their poor prognosis and because they often develop progressive neurologic
dysfunction that would confound the evaluation of neurologic and other adverse events.

- White blood cell (WBC) < 4,000.

- Platelet count < 100,000.

- Total serum bilirubin > 2 mg/dL.

- Serum creatinine > 2 mg/dL.

- Alkaline phosphatase > 3 times the upper normal limit.

- Serum glutamic oxaloacetic transaminase (SGOT) or serum glutamate pyruvate
transaminase (SGPT) > 3 times the upper normal limit.

- Uncontrolled intercurrent illness including, but not limited to, ongoing or active
infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac
arrhythmia, or psychiatric illness/social situations that would limit compliance with
study requirements.

- Pregnant or nursing female subjects.

- Unwilling or unable to follow protocol requirements.

- Any condition which in the investigator?s opinion deems the subject an unsuitable
candidate to receive porfimer sodium.

- Received an investigational agent within 30 days prior to enrollment.