CompletedPhase 1NCT04200417

Chemoembolization for Lung Tumors

This study is being done to determine if it is safe to perform lung chemoembolization and if the lung chemoembolization procedure can successfully deliver chemotherapy to lung tumors.

Checked against the public recordLast updated May 16, 2025 · Source: ClinicalTrials.gov

StatusCompleted
PhasePhase 1
U.S. locations4
SponsorMemorial Sloan Kettering Cancer Center
01
Study overview

What this study is about

Purpose
Treatment
Study type
Interventional
Phase
Phase 1
Sponsor
Memorial Sloan Kettering Cancer Center
Interventions being studied
Procedure: Chemoembolization; Drug: Mitomycin C; Drug: Lipiodol; Drug: Embospheres
02
Explore related studies

How this study is categorized

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

Treatment approach
03
Public criteria

Who may be able to participate

Inclusion Criteria: * Lung, endobronchial, pleural, or mediastinal metastases that are not responding to systemic chemotherapy, and that are not amenable to ablation, resection, or SBRT. * At least 18 years old. * ECOG performance status 0 or 1 Exclusion Criteria: * Primary lung cancer * \>50% of a lung is replaced with tumor * Oxygen saturation \<92% on room air * FEV1 \<60% * Pulmonary hypertension (diagnosed or suspected on echocardiography, CT, 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 (dyspnea, volume overload) * Left bundle branch block (contraindication to pulmonary angiography) * Renal failure (eGFR \<30 mL/min/1.73m\^2) * Pregnancy * Breastfeeding * Altered mental status that would interfere with consent or follow-up * Platelets \< 100,000 (after transfusion, if needed) * INR\>2 (after transfusion, if needed) * Hemoglobin \<7 (after transfusion, if needed) * Hyperthyroidism (contraindication to lipiodol) * Planned radioactive iodine imaging or therapy (contraindication to lipiodol) * Allergy to lipiodol or mitomycin * Allergy to iodinated contrast that can not be treated with steroid / diphenhydramine premedication * Any condition that, in the opinion of the investigator, would interfere with evaluation of the investigational product or interpretation of subject safety or study results

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

  • Memoral Sloan Kettering Monmouth (Consent only)Middletown, New Jersey
  • Memorial Sloan Kettering Cancer Center @ Commack (Consent Only)Commack, New York
  • Memoral Sloan Kettering Westchester (Consent only)Harrison, New York
  • Memorial Sloan Kettering Cancer CenterNew York, New York

Source and freshness
Processed from ClinicalTrials.gov. Last public update: May 16, 2025. Always confirm current availability with the study team.

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