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Interstitial Photodynamic Therapy following Palliative Radiotherapy in Treating Patients with Inoperable Malignant Central Airway Obstruction
Trial Status: active
This phase I/II trial studies the side effects of interstitial photodynamic therapy following palliative radiotherapy and how well it works in treating patients with inoperable malignant central airway obstruction. Patients who have advanced stage cancer tumors in the lung can often have the breathing passages to the lung partially or completely blocked. These tumors could be due to lung cancer or other cancers (e.g., renal, breast, kidney, etc.) that spread to the lung. This blockage puts the patient at a higher risk for respiratory failure, post-obstructive pneumonia, and prolonged hospitalizations. Treatment for these patients may include bronchoscopic intervention (such as mechanical removal, stenting, laser cauterization, or ballooning), radiation therapy with and without chemotherapy. While palliative x-ray radiotherapy may help in shrinking the tumor, high dose curative radiotherapy that can ablate (a localized, nonsurgical destruction) the tumor also has high risk to cause significant toxicity, including bleeding, abnormal connections or passageways between organs or vessels and abnormal scar tissue that can also produce airway obstruction. Photodynamic therapy (PDT) is another possible treatment that can provide local control of the tumor. PDT consists of injecting a light sensitive drug (photosensitizer, PS) into the vein, waiting for the PS to accumulate in the tumor, and then activating it with a red laser light. Radiation therapy uses high energy x-rays, particles, or radioactive seeds to kill cancer cells and shrink tumors. Giving interstitial photodynamic therapy following palliative radiotherapy may improve tumor response and survival without the serious side effects that are associated with the typical high dose curative x-ray radiotherapy alone in patients with malignant central airway obstruction.
Inclusion Criteria
Age >= 18 years of age
Eligibility checklist before registration requires review of case by the interventional pulmonologist/s and radiation oncologist/s to approve anatomic feasibility of an airway intervention and palliative radiotherapy
Patients with pathologic diagnosis of inoperable solid malignancy involving extrabronchial tumor growth that causes airway obstruction and not amenable to curative radiotherapy. All patients will have tumors requiring bronchoscopic intervention with endobronchial ultrasound (EBUS) at the time of I-PDT
Participants have at least one measurable lesion which is also the target lesion for Response Evaluation Criteria in Solid Tumors (RECIST) measurement
Patients amenable to receive standard of care palliative radiotherapy to the target tumor, as determined by the radiation oncologist/s
Amenable to high resolution chest CT (with or without contrast due to contraindication) with 0.625-1.25 mm slice thickness and slice interval 0.5-1 mm
Tumor is accessible and amenable to I-PDT, as determined by the interventional pulmonologist/s
Have an Eastern Cooperative Oncology Group (ECOG) performance status of ≤ 3
Platelets ≥ 100,000 cells/mm^3 (International System of Units [SI] units 100 x 10^9/L)
International normalized ratio (INR) < 1.5 and activated partial thromboplastin time (aPTT) < 1.5 x ULN. PTT or aPTT per institutional standards for participating external sites
Participants 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 3 months after receiving the study drug. 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
Participant or legal representative must understand the investigational nature of this study and sign an Independent Ethics Committee/Institutional Review Board approved written informed consent form prior to receiving any study related procedure
Exclusion Criteria
Pregnant or nursing female participants
Co-existing ophthalmic disease likely to require slit-lamp examination within the next 30 days following I-PDT treatment
Any condition which in the investigator’s opinion deems the participant an unsuitable candidate to receive the I-PDT
CT imaging suggestive of target tumor invasion into a major blood vessel (typically proximal to segmental vessels)
Known hypersensitivity/allergy to porphyrin
Patients who are not cleared by the anesthesiologist to undergo an advanced bronchoscopy procedure under general anesthesia
Patients diagnosed with porphyria
Patients with known allergy to eggs
Patients unwilling or unable to follow protocol requirements
Additional locations may be listed on ClinicalTrials.gov for NCT06306638.
I. To test the safety of our image-based treatment planning for image-guided interstitial photodynamic therapy (I PDT) with endobronchial ultrasound (EBUS) following standard of care palliative radiotherapy (p-XRT). (Phase I)
II. To assess the efficacy of our image-based treatment planning for image-guided I-PDT following standard of care p-XRT. (Phase II)
SECONDARY OBJECTIVES:
I. To assess objective tumor response. (Phase I)
II. To evaluate changes in quality of life. (Phase I and II)
III. To measure changes in functional lung capacity. (Phase I and II)
IV. To measure the relationship between the measured objective tumor response (at 12 +/- 2 weeks post I-PDT) and changes in therapeutic laser light transmission within the target tumor, as a future dosimetric marker for response. (Phase I and II)
V. To assess treatment effects on the immune contexture. (Phase I and II)
VII. To monitor progression free survival. (Phase I and II)
EXPLORATORY OBJECTIVE:
I. Assess the relationship between drug levels in the plasma to tumor response.
OUTLINE: This is a phase I study, followed by a phase II.
PHASE I: Patients are assigned to 1 of 2 cohorts.
COHORT 1: Patients receive verteporfin (Visudyne) intravenously (IV) over 10 minutes and then undergo I-PDT with EBUS 60-120 minutes after Visudyne for 1 treatment session. 33 to 44 days later, patients undergo standard of care (SOC) p-XRT over a single fraction. Patients receive Visudyne IV over 10 minutes and then undergo I-PDT with EBUS 60-120 minutes after Visudyne for 1 treatment session. Patients undergo blood and tissue sample collection on study. Patients also undergo computed tomography (CT) throughout the trial.
COHORT 2: Patients undergo SOC p-XRT over a single fraction. Patients receive Visudyne IV over 10 minutes and then undergo I-PDT with EBUS 60-120 minutes after Visudyne for up to 2 treatment sessions at least 12 weeks apart. Patients undergo blood and tissue sample collection on study. Patients also undergo CT throughout the trial.
PHASE II: Patients undergo SOC p-XRT over a single fraction. Patients receive Visudyne IV over 10 minutes and then undergo I-PDT with EBUS 60-120 minutes after Visudyne for up to 2 treatment sessions at least 12 weeks apart. Patients undergo blood and tissue sample collection on study. Patients also undergo CT throughout the trial.
After completion of study treatment, patients are followed up at 30 days and 8, 12, and 24 weeks.
