TerminatedPhase 2NCT00601848

Photodynamic Therapy in Treating Patients With Resectable Non-Small Cell Lung Cancer That Has Spread to the Pleura

RATIONALE: Photodynamic therapy uses a drug, such as porfimer sodium, that is absorbed by tumor cells. The drug becomes active when it is exposed to light. When the drug is active, tumor cells are killed. Giving photodynamic therapy during surgery may kill any tumor cells that remain after surgery. PURPOSE: This phase II trial is studying the side effects and how well photodynamic therapy given during surgery works in treating patients with resectable non-small cell lung cancer that has spread to the pleura.

Checked against the public recordLast updated Nov 24, 2020 · Source: ClinicalTrials.gov

StatusTerminated
PhasePhase 2
U.S. locations1
SponsorAbramson Cancer Center at Penn Medicine
01
Study overview

What this study is about

Purpose
Treatment
Study type
Interventional
Phase
Phase 2
Sponsor
Abramson Cancer Center at Penn Medicine
Interventions being studied
Drug: chemotherapy; Drug: porfimer sodium; Other: immunohistochemistry staining method; Other: laboratory biomarker analysis; Procedure: spectroscopy; Procedure: therapeutic conventional surgery
02
Explore related studies

How this study is categorized

These labels come from structured fields and exact terms in the public record.

03
Public criteria

Who may be able to participate

DISEASE CHARACTERISTICS: * Histologically confirmed non-small cell lung cancer (NSCLC) * Must have clinical and/or pathological evidence of pleural spread * Primary tumor must be resectable as assessed by the attending thoracic surgeon * Patients who have received or are currently receiving two-to-four courses of standard front-line chemotherapy are eligible PATIENT CHARACTERISTICS: * Must be medically fit to tolerate surgery * No CTCAE v3.0 grade III-IV elevations in liver transaminases * Bilirubin ≤ 1.5 mg/dL * No known HIV infection * Not pregnant or nursing PRIOR CONCURRENT THERAPY: * See Disease Characteristics * No prior treatment for NSCLC except pleurodesis or standard front-line chemotherapy * No prior pemetrexed disodium chemotherapy * No prior mantle radiotherapy * No concurrent chemotherapy or radiotherapy during the active study treatment period * Post-operative radiotherapy will be administered as clinically indicated

Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.

04
Study sites

U.S. locations

  • Abramson Cancer Center of the University of PennsylvaniaPhiladelphia, Pennsylvania

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Nov 24, 2020. Always confirm current availability with the study team.

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