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

Not Applicable
Active, not recruiting
Conditions
Neoplasms
Lung Neoplasms
Interventions
Device: MLC Tracking
Registration Number
NCT02514512
Lead Sponsor
Royal North Shore Hospital
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.

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
20
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

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
MLC Tracking SABRMLC TrackingPatients are treated with MLC tracking
Primary Outcome Measures
NameTimeMethod
To demonstrate feasibility of MLC tracking for lung cancerAssessed at 2 years

Percentage of fractions delivered without software or mechanical failure

Secondary Outcome Measures
NameTimeMethod
Lung doseAssessed at 2 years

Difference in dose to healthy lung in treatment plans between 4D planning and ITV planning

Treated dose - MLC trackingAssessed at 2 years

Difference between the treated dose and planned dose for MLC tracking

Treated dose - standardAssessed at 2 years

Difference between the estimated treated dose and planned dose for ITV treatments

Audio Visual (AV) BiofeedbackAssessed at 2 years

Fraction of patients for whom AV biofeedback improves breathing regularity

Coefficient of variation in breathing patternsAssessed at 2 years

Breathing variations over imaging and treatment sessions with and without AV biofeedback using a statistical process for coefficient of variation

Target volumesAssessed at 2 years

Target volumes between the 4 Dimensional (4D) planning MLC tracking and Internal Target Volume (ITV) (standard) planning

4D Cone Beam CT (CBCT) image qualityAssessed at 2 years

Image 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 treatment

To quantify the breathing variations over treatment sessions with and without application of continuous positive air pressure (CPAP)

Trial Locations

Locations (1)

Royal North Shore Hospital

🇦🇺

St Leonards, New South Wales, Australia

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