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Lung Cancer Radiotherapy Using Realtime Dynamic Multileaf Collimator (MLC) Adaptation And Radiofrequency Tracking

Phase I Feasibility Study of Lung Cancer Radiotherapy Using Realtime Dynamic Multileaf Collimator (MLC) Adaptation and Radiofrequency Tracking

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02514512
Acronym
LIGHTSABR
Enrollment
20
Registered
2015-08-03
Start date
2015-09-01
Completion date
2026-12-01
Last updated
2026-02-06

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

Conditions

Lung Neoplasms, Neoplasms

Keywords

Lung Cancer, Stereotactic Ablative Radiotherapy (SABR), MLC Tracking, Radiotherapy

Brief summary

A research study into a new technology for adjustment of the radiotherapy beam to account for movement of lung tumours as the patient breathes during radiotherapy.

Detailed description

Twenty patients 18 years of age or more and undergoing Stereotactic Body Radiotherapy (SBRT) at Northern Sydney Cancer Centre for lung cancer will receive the new treatment. Participants will be physically able to undergo all aspects of treatment and intellectually able to provide written informed consent and complete questionnaires. Beacons will be implanted in the patients' lung to allow the Multi Leaf Collimator (MLC) tracking equipment to follow precisely the movement of the lung. The difference in ability to track tumour movement between MLC and the current standard method will be compared to identify changes in study outcomes. Audiovisual (AV) Biofeedback will also be used to regulate patients' breathing during radiotherapy.

Interventions

DEVICEMLC Tracking

Treat patient with Non FDA approved MLC Tracking

Sponsors

Royal North Shore Hospital
Lead SponsorOTHER
University of Sydney
CollaboratorOTHER
Varian Medical Systems
CollaboratorINDUSTRY

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Aged 18 or older * Has provided written Informed Consent for participation in this trial and is willing to comply with the study * Patients undergoing external beam radiotherapy at Northern Sydney Cancer Centre * Histologically proven Stage I Non Small Cell Lung Cancer (NSCLC) oligometastatic lung metastases (3 or less). Histological diagnosis will be obtained if clinically indicated. * MRI/4D-CT prior to insertion of Calypso beacons * Patient must be able to have Varian Calypso beacons placed in the lung (if on anticoagulants, must be cleared by Local Medical Officer (LMO) or cardiologist). * Eastern Cooperative Oncology Group (ECOG) performance status 0-2 * Body habitus enabling Calypso tracking (as per Calypso Determining a Patient's Localisation Designation \& Orientation before implantation) * A maximum of three metastases to the lung from any non-haematological malignancy. Multiple metastases will be treated separately. * Tumour diameter ≤ = 5cm

Exclusion criteria

* Previous high-dose thoracic radiotherapy. * Less than two Calypso beacons implanted in the lung. * Calypso beacons are spaced by greater than 9cm or less than 1cm. * Calypso beacons are less than 19cm from outer chest wall * Cytotoxic chemotherapy within 3 weeks of commencement of treatment, or concurrently with treatment. Hormonal manipulation agents are allowable (e.g. aromatase inhibitors, selective oestrogen receptor modulators, and gonadotropin releasing hormone receptor modulators) * Targeted agents (such as sunitinib, bevacizumab and tarceva) within 7 days of commencement of treatment, or concurrently with treatment * Women who are pregnant or lactating. * Unwilling or unable to give informed consent * Unwilling or unable to complete quality of life questionnaires

Design outcomes

Primary

MeasureTime frameDescription
To demonstrate feasibility of MLC tracking for lung cancerAssessed at 2 yearsPercentage of fractions delivered without software or mechanical failure

Secondary

MeasureTime frameDescription
Audio Visual (AV) BiofeedbackAssessed at 2 yearsFraction of patients for whom AV biofeedback improves breathing regularity
Coefficient of variation in breathing patternsAssessed at 2 yearsBreathing variations over imaging and treatment sessions with and without AV biofeedback using a statistical process for coefficient of variation
Target volumesAssessed at 2 yearsTarget volumes between the 4 Dimensional (4D) planning MLC tracking and Internal Target Volume (ITV) (standard) planning
Lung doseAssessed at 2 yearsDifference in dose to healthy lung in treatment plans between 4D planning and ITV planning
Treated dose - MLC trackingAssessed at 2 yearsDifference between the treated dose and planned dose for MLC tracking
Treated dose - standardAssessed at 2 yearsDifference between the estimated treated dose and planned dose for ITV treatments
4D Cone Beam CT (CBCT) image qualityAssessed at 2 yearsImage quality and target position differences between the Calypso-based 4D CBCT image reconstruction and Revs Per Minute (RPM)-based 4D CBCT image reconstruction using Feldkamp filtered backprojection (FDK and iterative reconstruction algorithms.
Breathing variations with and without continuous positive air pressure (CPAP)At time of treatmentTo quantify the breathing variations over treatment sessions with and without application of continuous positive air pressure (CPAP)

Countries

Australia

Contacts

PRINCIPAL_INVESTIGATORThomas Eade, MD

RNSH

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 7, 2026