A Novel Method for Treating Lung Met w/Combo of Electric Fields & Rad Therapy: A Single-Arm

Metastatic Cancer Clinical Trial

Official title:

A Novel Method for Treating Lung Metastases With the Combination of Electrical Fields and Radiation Therapy: A Single-Arm Pilot Study

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT05555342
• Other study ID #: UCI 21-222 [HS# 1723]
• Secondary ID: 1723
• Status: Active, not recruiting
• Phase: Early Phase 1
• Start date: January 3, 2023
• Est. completion date: December 2028

Study information

• Verified date: October 2023
• Source: University of California, Irvine
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a phase 0, pilot prospective study to determine the feasibility of combined irreversible electroporation (IRE) and radiation therapy in subjects with lung tumors with metastatic cancer of any histology. These are subjects who have advanced disease (stage IV) or previously treated disease that has become progressive, recurrent, or metastatic.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 6
• Est. completion date: December 2028
• Est. primary completion date: September 29, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Patients must have histologically or cytologically confirmed metastatic cancer of any histology. There must be a lung tumor present, although the lung tumor does not specifically need to have been biopsied.

• Patients must have advanced disease (stage IV) or previously treated disease that has become progressive, recurrent, or metastatic.

• Patients may have received any number of prior systemic or local therapies. There will be no prespecified washout period prior to IRE. However, systemic therapy will be halted while receiving IRE and radiation, and can be restarted following completion of radiation therapy.

• Up to 3 lesions may be included for treatment. The selected lesion(s) should be amenable to ablation and irradiation and patients will be eligible for ablation and irradiation in the judgment of the treating radiologist and radiation oncologist. If more than one lesion is selected, they should be separated by at least 5 cm to minimize lung irradiation. The target lesion for treatment by IRE and radiation will be a tumor not previously treated by radiation. This target lesion must be measurable, defined as the ability to be accurately measured in at least one dimension (longest diameter to be recorded for non-nodal lesions and short axis for nodal lesions) as >10 mm with spiral CT scan. The upper limit to the target lesion is 6 cm maximal diameter, but it also must be planned to be encompassed entirely by an IRE ablative zone. Any number of IRE probes will be allowed such that the entire tumor can be ablated.

• Must be age = 18 years. Children are excluded from this study but will be eligible for future pediatric trials, if applicable.

1. Both men and women and members of all races and ethnic groups are eligible for this trial. Non-English speaking, deaf, hard of hearing and illiterate individuals are eligible for this trial.

• Performance status: ECOG performance status =2 (Karnofsky =50%).

• Life expectancy of =3 months.

• Adequate organ and marrow function as defined below. Labs should be performed within 14 days of treatment.

1. Platelets =50,000/mcL

2. Hemoglobin =8 g/dL

3. Absolute neutrophil count =1,000/mcL

4. INR <1.5

• Female patients of childbearing potential must have a negative urine or serum pregnancy during screening. If the urine test is positive or cannot be confirmed as negative, a serum pregnancy test will be required.

• The effects of ionizing radiation (i.e. radiation therapy) on the developing human fetus are known to have the potential for congenital abnormalities and fetal harm. Women of child-bearing potential must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry and until completion of radiation therapy. Should a woman become pregnant or suspect she is pregnant during this period, she should inform her treating physician immediately.

1. A female of child-bearing potential is any woman (regardless of sexual orientation, having undergone a tubal ligation, or remaining celibate by choice) who meets the following criteria:

1. Has not undergone a hysterectomy or bilateral oophorectomy; or

2. Has not been naturally postmenopausal for at least 12 consecutive months (i.e., has had menses at any time in the preceding 12 consecutive months).

• Patients must not have a history of (non-infectious) pneumonitis that required steroids or have current pneumonitis.

• Ability to understand and willingness to sign a written informed consent document

Exclusion Criteria:

• Patient's whose target lesion has been previously treated with radiation therapy.

• Patients who have not recovered from adverse events due to prior anti-cancer therapy administered.

• Patients may not be receiving any other investigational agents 2 weeks prior to enrollment and until end of all therapeutic interventions.

• Patients with cardiac arrhythmias, pacemakers, or implanted defibrillator.

• Patients with epilepsy.

• Patients with 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.

• Patients must not be pregnant due to the potential for congenital abnormalities and fetal harm caused by ionizing radiation.

• Patients with disease amenable to curative intent therapy.

• Patient has a known additional malignancy that is progressing or requires active treatment; exceptions include basal cell carcinoma of the skin, squamous cell carcinoma of the skin.

Related Conditions & MeSH terms

• Lung Neoplasms
• Lung Tumor
• Metastatic Cancer
• Neoplasm Metastasis

Intervention

Procedure:
• Irreversible electroporation (IRE) ablation
IRE will be performed using the NanoKnife or Aliya System. CT or cone-beam CT will be used to direct electrode placement.

Radiation:
• Radiation Therapy
Moderate-dose radiation therapy to the target tumor(s) in 1 fraction.

Locations

Country	Name	City	State
United States	Chao Family Comprehensive Cancer Center University of California, Irvine	Orange	California

Sponsors (1)

Lead Sponsor	Collaborator
University of California, Irvine

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Feasibility, measured as the number of patients completing both IRE and the single fraction of radiation	Number of patients completing treatment of both IRE and the single fraction of radiation. Up to 6 replacements are allowed (total subjects 6-12)	Up to 3 years
Secondary	Number of grade 3-5 adverse events	Severe toxicity will be measured by cumulative CTCAE v5.0 grade 3-5 events. Evaluation of Grade 3-5 toxicity will be made at 30 days	Up to 3 years
Secondary	Local failure at the treated site	Local failure rate at the treated site will be determined using cumulative incidence rates with death as a competing event at 12 months after initiation of treatment	Up to 3 years
Secondary	Duration of response	The duration of response is measured from the time of treatment initiation until local failure is objectively documented	Up to 3 years
Secondary	Progression-free survival	Progression-free survival (PFS) is defined as the duration of time from start of treatment to time of progression or death, whichever occurs first. Estimates at 6 and 12 months will be made.	Up to 3 years
Secondary	Overall survival	The duration of time from start of treatment to time of progression or death, whichever occurs first. Estimates at 6 and 12 months will be made.	Up to 3 years
Secondary	Number of grade 1-5 adverse events	Toxicity will be measured by cumulative CTCAE v5.0 grade 1-5 events. Evaluation of Grade 1-5 toxicity will be made at 30 days	Up to 3 years
Secondary	Patient reported quality of life	Mean summary score of the Functional Assessment of Cancer Therapy-Lung (FACT-L). Functional Assessment of Cancer Therapy-Lung (FACT-L) Scale is a 36-item self-reported instrument that measures multidimensional quality of life for lung cancer patients. Questions are scored on a 5-point Likert Scale. The FACT-L includes the FACT-G (general) assessment which is comprised of four subscales including Physical Well-Being (score = 0-28), Social/Family Well-Being (score= 0-28), Emotional Well Being (score = 0-24), and Functional Well-Being (score = 0-28), for a total score min/max = 0-108, plus, the Lung Cancer Subscale (nine lung cancer related items, score = 0-45). Total scores range from 0-136, with higher scores indicating better quality of life.	Up to 3 years
Secondary	Forced vital capacity	Pulmonary function is assessed by the volume change (mL) in the value of forced vital capacity (FVC)	Up to 3 years
Secondary	Forced expiratory volume at 1 second (FEV1)	Pulmonary function is assessed by volume change (mL) in the value of forced expiratory volume at 1 second (FEV1)	Up to 3 years
Secondary	Diffusing capacity for carbon monoxide (DLCO)	Pulmonary function is assessed by change in the value of diffusing capacity for carbon monoxide (DLCO) measured in mL/min/kPa	Up to 3 years