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Lung NeoplasmsPhase 1/2NCT04369872

Microwave Ablation of Primary and Secondary Lung Malignancies

A Phase 1/2 study testing Microwave ablation in people with Lung Neoplasms and Neoplasm Metastasis, run by University of Calgary at 1 site in Canada.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Surgery is the first choice of treatment for early-stage primary pulmonary malignancies, but up to 15% of all patients, and 33% of patients greater than 75 years of age, are not surgical candidate's due to locally advanced disease, poor cardiopulmonary reserve and significant medical co-morbidities. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Lung Neoplasms, Neoplasm Metastasis
What is being tested?
Microwave ablation
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
35 participants
Where
1 siteCanada
Study dates
1 May 2020to 31 Dec 2022
Phase
Phase 1/2
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Non-Small Cell Lung Carcinoma and metastatic lesions from lung, colorectal, breast, sarcoma, melanoma
  • Patient median estimate survival of > 1 year, as determined by the treating physician
  • ECOG 0-1
  • <5 lesions in either lung
  • Limited and/or controlled extra-pulmonary disease - to be determined by multidisciplinary consensus
  • Not amenable to surgery, SBRT or chemotherapy (or patient refusal)
  • Patient will have documentation by surgeon and/or radiation oncologist that the patient is unamenable to surgery and SBRT

Who cannot join

  • Lesions >3cm in size
  • Lesions within 1 cm of any critical mediastinal structure (e.g. aorta, main pulmonary arteries, esophagus, phrenic nerve), diaphragm or pleura
  • FEV1≤35% predicted
  • Clinically significant emphysema (to be determined by the treating physician)
  • Previous pneumonectomy
  • Inability to tolerate pneumothorax as judged by referring clinician's clinical assessment
Show all 11Show fewer
  • Inability to tolerate general anaesthetic
  • Inability to provide informed consent
  • INR > 1.5
  • Platelets < 100
  • PTT > 40

Trial locations and contacts

1 site in 1 country.

Canada1 site, 1 recruiting
  • Foothills Medical Centre

    Calgary, Alberya, T2N2T9

    Stefan J Przybojewski, 403-944-4634, stefan.przybojewski@albertahealthservices.ca

    Recruiting

Other trials in Canada

About this study

Official title: Microwave Ablation of Primary and Secondary Lung Malignancies: A Phase I-II Single Centre Prospective Safety and Efficacy Trial

Surgery is the first choice of treatment for early-stage primary pulmonary malignancies, but up to 15% of all patients, and 33% of patients greater than 75 years of age, are not surgical candidate's due to locally advanced disease, poor cardiopulmonary reserve and significant medical co-morbidities. Some patients are also unwilling to undergo surgery. This has prompted the development of alternatives to surgery so that local control of unresectable tumors can be achieved.

Stereotactic body radiation therapy (SBRT) is currently an alternative therapy for these patients with 3-year survival rates of between 42 and 60%. SBRT has excellent local control rates and a favorable toxicity profile relative to other surgical and non-surgical therapies. Radiation pneumonitis (RP), amongst others, is one of the major toxicities which can limit the maximal radiation dose that can be safely delivered to thoracic tumors. Reported rates of SBRT induced RP requiring clinical intervention range from 0% to 29% and life-threatening toxicities have been reported in up to 12% of cases in various studies. The potential for toxicities from SBRT could limit the number of times a patient could be treated with SBRT for residual, recurrent or new pulmonary lesions over time.

Read more

Following the first report of thermal ablation for lung malignancies in 2000, this modality has been used to treat primary and secondary malignancies and has emerged as an effective, low-cost, safe and repeatable alternative to SBRT for local tumour control. The most widely practised technique is radiofrequency ablation (RFA). Microwave ablation (MWA) is a relatively new therapy and offers all the advantages of RFA, but with significant additional advantages 3. These include reduced procedure times, lower complication rates, increased ablative temperatures, improved propagation of thermal energy particularly in the lung, improved efficacy in lesions that are in close proximity to blood vessels due to reduced heat-sink effect, and less procedure associated pain 2,3. Using high energy MWA to treat 87 pulmonary tumors, Egashira et al achieved a primary technical success rate of 94% and technique effectiveness of 98% at a median of 15 months.

MWA is performed by Interventional Radiologists using CT guidance. The treatment is performed under general anaesthesia and is repeatable. Multiple lesions can be ablated in one treatment session. Patients can potentially be discharged the same day of treatment, if there are no adverse events.

MWA is a relatively new treatment option that could be considered in situations where the patient is not a candidate for further treatment with surgery, SBRT or chemotherapy, or the patient declines the recommended standard available treatments.

Objectives for Phase I:

The primary objective for Phase I of this study will be to demonstrate the Safety of MWA performed for treatment of lung malignancy in patients not suitable for surgery, chemotherapy or SBRT.

Primary objective (Safety): to determine the proportion of patients experiencing local adverse events at one week definitively related to the mwa procedure.

Secondary objective (Feasibility): To determine the proportion of patients in whom technical success of MWA was achieved by assessing completion of ablation on CT at the time of the procedure, indicated by replacement of tumor by ground glass change (including a 5mm ablation zone in normal surrounding lung parenchyma).

Objectives for Phase II Primary objective (Efficacy): To demonstrate efficacy by measuring the proportion of patients demonstrating absence of residual tumor on follow up CT at 1 month after MWA.

Secondary objective: To determine the proportion of patients needing re-treatment for recurrent tumor at 1 month post MWA.

Being tested
Microwave ablation
Keywords
Lung Cancer, Lung Metastases
Medical subject headings
Lung Neoplasms, Neoplasm Metastasis

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Microwave ablationProcedure or surgery

    Microwave ablation of lung lesion using Solero Microwave Tissue Ablation system.

Study groups in NCT04369872
Study groupRoleWhat they receive
Microwave AblationExperimentalStudy participants will receive percutaneous microwave ablation of their malignant lung neoplasm.
Receives: Procedure: Microwave ablation

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Rate of adverse outcomes following microwave ablation

    Proportion of patients experiencing local adverse events at one week definitively related to the mwa procedure.

    Measured: 1 week post treatment

  2. Efficacy of microwave ablation of lung lesions

    To demonstrate efficacy by measuring the proportion of patients demonstrating absence of residual tumor on follow up CT at 1 month after MWA.

    Measured: 1 month post treatment

  3. Rate of technical success

    Proportion of patients in whom technical success of MWA was achieved by assessing completion of ablation on CT at the time of the procedure, indicated by replacement of tumor by ground glass change (including a 5mm ablation zone in normal surrounding lung parenchyma).

    Measured: 1 month post treatment

Secondary outcomes (1)
  1. Re-treatment rate.

    To determine the proportion of patients needing re-treatment for recurrent tumor at 1 month post MWA.

    Measured: 1 month post treatment

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted30 Apr 2020
  2. Study start1 May 2020
  3. Primary completion31 Dec 2022 (estimated)
  4. Study completion31 Dec 2022 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 1/2
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
35 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04369872
Sponsor's protocol ID
HREBA.CC-19-0304
Status last verified
Apr 2020
First submitted
28 Apr 2020
Last updated
9 Nov 2020
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
Yes
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A Phase 1/2 study testing Microwave ablation in people with Lung Neoplasms and Neoplasm Metastasis, run by University of Calgary at 1 site in Canada.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 11 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 9 Nov 2020. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Canada. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this combined phase mean?

Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Stefan J Przybojewski, MB ChB (403-944-4634, Stefan.Przybojewski@albertahealthservices.ca), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Rate of adverse outcomes following microwave ablation (time frame: 1 week post treatment). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 9 Nov 2020.

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