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Embolisation of metastatic lung lesions using radiopharmaceutical Yttrium -90 in patients with various malignancies to decrease metastatic disease burden

Role of Transarterial Radioembolisation in Metastatic Lung Lesions - NIL

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/06/068822
Enrollment
9
Registered
2024-06-12
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: C800- Disseminated malignant neoplasm, unspecified Health Condition 2: C349- Malignant neoplasm of unspecifiedpart of bronchus or lung

Interventions

Intervention1: Y-90 microsphere radioembolisation: transarterial radioembolisation with the above mentioned agent to be done via the predominant tumor feeding pulmonary or bronchial artery Control Int

Sponsors

Bela Jain senior resident
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: measureable metastatic lung lesions (Biopsy proven or positive on FDG PET CT), ECOG less than or equal to 2, Karnofsky score more than 60, Hemoglobin more than 9 g/dl, WBC more than 1500/microlitre, platelets more than 50000/microlitre, PT less than 1.3 and INR less than 1.5, FEV1more than 60%, serum creatinine less than 1.3

Exclusion criteria

Exclusion criteria: previous history of interstitial lung disease, COPD, active lung infection, pulmonary hypertension, pulmonary AV malformation, Symptomatic heart failure, LBBB, Predictive dose to lung parenchyma exceeding 30 Grey in dose planning, allergy to contrast/plastic, renal failure, coagulative disorder, survival expectancy of less than 3 months.

Design outcomes

Primary

MeasureTime frame
size of lung lesion to be measured on FDG PET CT to see for any reduction in size/resolutionTimepoint: 6 weeks, 3 months

Secondary

MeasureTime frame
To establish the dose response relationship of transarterial radioembolization in metastatic lung lesions using volumetric methods. Response to be assessed using FDG PET CTTimepoint: 6 weeks, 3 months

Countries

India

Contacts

Public ContactDr Bela Jain

AIIMS, New Delhi

bela1102@yahoo.in9458289669

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026