Transarterial Chemoembolization for the Treatment of Lung Cancer and Lung Metastases

Description

This phase II trial evaluates how well transarterial chemoembolization (TACE) works for treating patients with non-small cell lung cancer or lung metastases. TACE is a minimally invasive procedure that involves injecting chemotherapy directly into an artery that supplies blood to tumors, and then blocking off the blood supply to the tumors. Mitomycin (chemotherapy), Lipiodol (drug carrier), and Embospheres (small plastic beads that block off the artery) are injected into the tumor-feeding artery. This traps the chemotherapy inside the tumor and also cuts off the tumor\'s blood supply. As a result, the tumor is exposed to a high dose of chemotherapy, and is also deprived of nutrients and oxygen. TACE can be effective at controlling or stopping the growth of lung tumors.

Conditions

Lung Non-Small Cell Carcinoma, Mediastinal Neoplasm, Pleural Neoplasm, Lung Metastases From Any Primary, Endobronchial Metastases, Colon Cancer, Sarcoma

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Study Overview

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Study Details

Study overview

This phase II trial evaluates how well transarterial chemoembolization (TACE) works for treating patients with non-small cell lung cancer or lung metastases. TACE is a minimally invasive procedure that involves injecting chemotherapy directly into an artery that supplies blood to tumors, and then blocking off the blood supply to the tumors. Mitomycin (chemotherapy), Lipiodol (drug carrier), and Embospheres (small plastic beads that block off the artery) are injected into the tumor-feeding artery. This traps the chemotherapy inside the tumor and also cuts off the tumor\'s blood supply. As a result, the tumor is exposed to a high dose of chemotherapy, and is also deprived of nutrients and oxygen. TACE can be effective at controlling or stopping the growth of lung tumors.

Transarterial Chemoembolization for the Treatment of Lung Cancer and Lung Metastases

Transarterial Chemoembolization for the Treatment of Lung Cancer and Lung Metastases

Condition
Lung Non-Small Cell Carcinoma
Intervention / Treatment

-

Contacts and Locations

Duarte

City of Hope Medical Center, Duarte, California, United States, 91010

New York

Memorial Sloan Kettering Cancer Center, New York, New York, United States, 10065

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Lung cancer or lung metastases, with lung, endobronchial, pleural, or mediastinal tumors that are progressing on systemic therapy (or the patient cannot tolerate systemic therapy), and that are not amenable to resection, thermal ablation, or ablative radiation therapy
  • * Lung-dominant disease (majority of active tumor volume is in the chest)
  • * At least 18 years old
  • * Eastern Cooperative Oncology Group (ECOG) performance status \> 2
  • * Oxygen saturation \< 92% on room air
  • * Forced expiratory volume in 1 second (FEV1) \< 60%
  • * No measurable treatable disease, per Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1 (for example, unable to measure tumor size on CT, or lung nodules are all \< 1 cm)
  • * Life expectancy \< 6 months
  • * Pulmonary hypertension (diagnosed or suspected on echocardiography, CT, magnetic resonance imaging \[MRI\], or direct pressure measurement)
  • * Recent pulmonary embolism (within 3 months)
  • * Pulmonary arteriovenous malformation
  • * Active lung infection (pneumonia, empyema, or lung abscess requiring therapy within 1 month)
  • * Symptomatic heart failure (American College of Cardiology \[ACC\]/American Heart Association \[AHA\] stage C or D)
  • * Left bundle branch block (contraindication to pulmonary angiography)
  • * Renal failure (estimated glomerular filtration rate \[eGFR\] \< 30 mL/min/1.73 m\^2)
  • * Pregnancy or intent to become pregnant
  • * Breast feeding
  • * Altered mental status that would interfere with consent or follow-up
  • * Platelets \< 50,000 (after transfusion, if needed)
  • * International normalized ratio (INR) \> 2 (after transfusion, if needed)
  • * Hemoglobin \< 7 (after transfusion, if needed)
  • * Hyperthyroidism or history of hyperthyroidism, including subclinical hyperthyroidism (contraindication to lipiodol)
  • * Planned radioactive iodine imaging or therapy (contraindication to lipiodol)
  • * Allergy to lipiodol or mitomycin
  • * Allergy to iodinated contrast that cannot be treated with steroid / diphenhydramine premedication
  • * Any condition that, in the opinion of the investigator, would interfere with evaluation of the investigational product, or that would affect subject safety

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

City of Hope Medical Center,

Franz E Boas, MD, PRINCIPAL_INVESTIGATOR, City of Hope Medical Center

Study Record Dates

2026-10-28