Light therapy shows promise against tough lung cancer
NCT ID NCT02153229
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether adding a light-activated drug (photodynamic therapy) during surgery can help people with a rare lung cancer called epithelioid malignant pleural mesothelioma live longer. About 52 adults with cancer limited to one side of the chest will receive either standard surgery plus chemotherapy, or the same with an extra light treatment during surgery. The goal is to see if the combination improves survival.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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52 people
The number who actually took part.
- Started
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Jun 2014
- Expected to finish
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Dec 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patients with a histologic diagnosis of MPM, epithelioid subtype, who in the opinion of the attending thoracic surgeon can receive a macroscopically complete resection of tumor. * Patients must have disease limited to the hemithorax. * Patients who have received prior surgery, gene therapy, or combination chemotherapy will be permitted if it has been at least 30 days since the last treatment. * Subjects treated with pemetrexed previously will be eligible only if 30 days have elapsed between the last dose of pemetrexed and the date of surgery. * ECOG performance status of 0-1. * Medical suitability for resection, including documented medical and cardiac clearance. * 18 years of age or older. * Patients must sign a document that indicates that they are aware of the investigative nature of the treatment of this protocol, and the potential benefits and risks. Patients unwilling or unable due to cognitive impairment to sign informed consent are excluded from the study. EXCLUSION CRITERIA * Patients with active invasive cancers, other than MPM, that require additional treatment, except non-melanomatous skin cancer, superficial bladder or cervical cancer, and early-stage prostate cancer * Pregnant or lactating patients. * Patients who have a history of HIV disease. * Patients who have a white count less than 2,500 per cubic mm or platelets less than 100,000/cubic mm. * Serum creatinine equal or greater than 2.5 mg/deciliter. * Patients who have severe liver disease including cirrhosis, Grade III-IV elevations in liver function studies, or bilirubin in excess of 1.5 mg/deciliter. * Patients with porphyria or hypersensitivity to porphyrin or porphyrin-like compounds. * Patients who have been treated with pemetrexed if the last dose of pemetrexed is \< 30 days to the date of surgery. * Patients that have been treated with prior Mantle field radiation. * Patients with distant metastatic disease or otherwise not confined to the ipsilateral hemithorax. * Subjects who have received more than 2 doses of neo-adjuvant chemotherapy
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Roswell Park Cancer Institute
Buffalo, New York, 14263, United States
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University of Pennsylvania
Philadelphia, Pennsylvania, 19104, United States