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Trial Title:
Non Surgical Treatment (Microwave Ablation) of Breast Cancer
NCT ID:
NCT05887154
Condition:
Breast Cancer Stage I
Conditions: Official terms:
Breast Neoplasms
Conditions: Keywords:
breast cancer
microwave ablation
MRI
Study type:
Interventional
Study phase:
N/A
Overall status:
Not yet recruiting
Study design:
Allocation:
N/A
Intervention model:
Single Group Assignment
Primary purpose:
Treatment
Masking:
None (Open Label)
Intervention:
Intervention type:
Device
Intervention name:
Microwave ablation
Description:
microwave ablation
Arm group label:
Microwave ablation
Summary:
In the Netherlands approximately one out of seven women will develop breast cancer during
her life. Most of these breast cancers are early stage, 40% of the women have stage 1.
Stage 1 breast cancer means that the cancer is small (size <2cm) and only in the breast
tissue or it might be found in lymph nodes close to the breast. The standard treatment
for stage 1 breast cancer is breast conserving surgery (BCS), sentinel lymph node
procedure (SLNP) and additional radiotherapy. This standard treatment protocol results in
a10 years survival rate of 95% for stage 1 disease. However, nowadays there is a
discussion whether these early stage breast cancer could be treated less invasively. To
reduce the invasiveness of breast cancer treatment, without compromising breast cancer
specific survival, minimally invasive ablation procedure of the breast tumor can be an
option for small breast lesions.
Patients with a tumor size<2 cm will undergo ultra guided microwave ablation (MWA) with
local anesthesia. After a small incision 2-3 millimeters, an MWA electrode is placed at
the end of the tumor with ultrasound guidance. The microwaves in MWA create heat around
the needle and destroy the cancer cells. There are several advantages of ablation
procedures: it is a minimal invasive technique, with a small or absent cutaneous scar and
thereby potentially improving patient quality of life. Furthermore, ablative treatment
can be done under local anesthesia and/or conscious sedation instead of general
anesthesia and in daycare setting, which can reduce treatment cost. A post procedural MRI
(after ablation) can determine whether the ablation procedure of the tumor volume is
complete. The purpose of this study is to assess whether minimally invasive microwave
ablation (MWA) followed by postprocedural MRI scan can be an alternative treatment for
breast surgery in early stage breast cancer. Is the quality of life, the cosmetic
outcome, fear of breast cancer recurrence, and costs in patient treated with MWA
comparable or better compared to patients treated with breast surgery?
Criteria for eligibility:
Criteria:
Inclusion Criteria:
- age should be 18 years and older
- a solid non-lobular invasive breast tumor with a size <2cm based upon ultrasound and
MRI measurements
- without mammographic or MRI evidence of extensive disease
- no involved lymph nodes on ultrasound and MRI scan.
Exclusion Criteria:
- more than one breast tumor,
- (lymph node) metastases
- breast implants
- indication for neoadjuvant chemotherapy.
- pacemaker,
- pregnant
- breastfeeding
Gender:
Female
Minimum age:
18 Years
Maximum age:
N/A
Healthy volunteers:
No
Start date:
July 1, 2023
Completion date:
June 1, 2024
Lead sponsor:
Agency:
University Medical Center Groningen
Agency class:
Other
Source:
University Medical Center Groningen
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT05887154