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Premarking of Axillary Nodes Before Start of Neoadjuvant Chemotherapy Using Magnetic Approach

Axillary Lymph Node Identification Before Neoadjuvant Chemotherapy Using MagTrace (Superparamagnetic Iron Oxide Nanoparticles, SPIO) and Magseed, in Clinically Node Negative and Node Positive Patients: a Feasibility Study.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05625698
Acronym
SENTINEO
Enrollment
80
Registered
2022-11-23
Start date
2021-10-01
Completion date
2023-11-28
Last updated
2024-01-26

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

Conditions

Breast Cancer

Keywords

neoadjuvant chemotherapy, sentinel node, axillary clearance

Brief summary

Breast cancer is one of the commonest types of cancers in females. Treatments include surgery followed by anti-estrogen therapy, radiotherapy and chemotherapy. During breast surgery, the surgeon removes the cancer from the breast and lymph nodes (glands) from the armpit. Historically, all armpit lymph nodes were surgically removed but this approach is associated long term problems of arm swelling. In more recent times, an increasingly more selective approach is used to treat the armpit nodes. In the presence of cancer spreads in the nodes, an axillary clearance surgery is done otherwise, only the first node(s) also called sentinel node(s) that drain fluids from the cancer, is surgically removed. The identification of nodes using the latter approach is helped by injecting a tracer in the breast and via the lymphatic channels, the tracer is then concentrated in the sentinel nodes. Over recent years, neoadjuvant (preoperative) chemotherapy is being increasingly used to treat breast cancers. This treatment approach can lead up to a large of number of complete cancer response. This in turn can cause difficulties in locating the breast cancer / armpit nodes during surgery after the chemotherapy. New developments like superparamagnetic iron oxide nanoparticles (SPIO or MagTrace®) has been used as an alternate liquid tracer to mark sentinel nodes to facilitate armpit surgery. In addition, small magnetic clip called Magseed® has also been developed which can be inserted into the relevant lymph nodes thereby marking their anatomical position to facilitate surgery. Both MagTrace and Magseed can be used to pre-mark the cancer and armpit nodes before the start of neoadjuvant chemotherapy. In theory, premarking armpit nodes using a magnetic approach is associated with better surgical accuracy in the armpit but there is limited supporting data. Therefore, this study aims to investigate the feasibility of premarking armpit nodes, with or without cancer spread, using magtrace and magseed respectively before patients undergo neoadjuvant chemotherapy.

Detailed description

Breast cancer is one of the commonest types of cancers in females. Treatments include surgery followed by anti-estrogen therapy (tablet form), radiotherapy (radiation) and chemotherapy (intravenous / tablet form). During breast surgery, the surgeon removes the cancer from the breast and lymph nodes (glands) from the armpit. Historically, all armpit lymph nodes (clearance) were removed irrespective of the stage of armpit disease which can lead to over-treatment and unnecessary long term arm lymphoedema (swelling). However, the modern approach has become more selective. If there are cancer spread in the nodes at diagnosis, a clearance operation is carried out otherwise only the first node(s) that the cancer spreads to, is removed. The latter procedure is called sentinel node biopsy and it is usually done by injecting a radioactive liquid tracer near the breast cancer. The tracer is then drained via the breast lymphatic channels and concentrated in the relevant armpit nodes where it can be detected by using a detector probe during surgery. In recent years, there are increasing uses of preoperative (neoadjuvant, NACT) chemotherapy in certain breast cancer subtypes with good cancer response. In up to 70% of cases, the treated cancer had disappeared both, in the breast and armpit, after NACT. Consequently, it can be difficult to locate and surgically remove these nodes in the armpits even with the usual injection of tracer after NACT. These difficulties are due to the damage of lymphatic channels in the breast by NACT and become fibrotic. Therefore, the tracer injected after NACT will no longer be drained correctly to mark the correct nodes in the armpit as the lymphatic channels are altered. In turn, this can lead to wrong sentinel nodes being removed from the armpit, which then can cause inaccurate planning for further treatments. Over recent times, superparamagnetic iron oxide nanoparticles (SPIO or MagTrace®) has been used as an alternate liquid tracer to mark sentinel nodes to facilitate armpit surgery. In addition, small magnetic clip called Magseed® has also been developed. Magseed® can be directly inserted into the relevant lymph nodes thereby marking their anatomical position to facilitate surgery. Both MagTrace and Magseed are longer lasting materials in the body than the radioactive technetium. Therefore, these new techniques give rise to an opportunity to premark the armpit nodes before the damage to lymphatic channels (with MagTrace) and before the cancer in the nodes disappear (with magseed), after NACT. In theory, premarking armpit nodes using a magnetic approach is associated with better surgical accuracy in the armpit but there is limited supporting data. Therefore, this study aims to investigate the feasibility of injecting MagTrace before NACT and then identify the sentinel node at surgery, three to six months later. The aim is also to investigate if a metastatic lymph node can be marked with Magseed® before NACT and together with MagTrace identify the metastatic node, as well as additional sentinel nodes at surgery, three to six months later. The overall aim is to facilitate logistics at surgery, finding the right SN and minimize axillary surgery. OBJECTIVES: Primary objectives: 1. Cohort 1, Node Negative Patients before NACT: To evaluate the SN detection rate with Magtrace® injected before NACT 2. Cohort 2, Node Positive Patients before NACT: To evaluate per-operative identification and removal rate of a Magseed clipped metastatic index lymph node Secondary objectives: 1. Node Negative Patients before NACT: To evaluate the concordance of SN detection by Magtrace® injected before NACT and Technetium (Tc99) +/- blue dye (BD) injected after NACT, respectively 2. Node Positive Patients before NACT: To evaluate: * the SN detection rate with Magtrace® injected before NACT * the concordance of SNs detected by Magtrace® injected before NACT and Tc99 + BD injected after NACT, during targeted axillary dissection (TAD) * the number of metastatic SNs and metastatic additional lymph nodes from the axillary dissection ENDPOINTS: Primary endpoints: * Cohort 1, SN detection rate * Cohort 2, Identification rate and removal rate of clipped index metastatic lymph node Secondary endpoints: * Cohort 1, Concordance of SNs identified with Magtrace and Tc99 after NACT * Cohort 2, a) SN detection rate. b) Concordance of SNs identified with MagTrace and Tc99 after NACT. c) Number of metastatic lymph nodes among SNs and additional lymph nodes * Cohort 1+2, Incidence of serious adverse events (SAEs).

Interventions

DRUGMagTrace only

see information in arm descriptions

COMBINATION_PRODUCTMagTrace and Magseed

see information in arm descriptions

Sponsors

Uppsala University Hospital
CollaboratorOTHER
Vastra Gotaland Region
Lead SponsorOTHER_GOV

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Intervention model description

This is a feasibility study

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* A patient meeting the following criteria is eligible for participation in the study: * Patients 18 years of age or older * Patients with breast cancer planned to undergo preoperative chemotherapy (NACT) with a) planned sentinel lymph node biopsy (SNB) or b) axillary lymph node dissection, in conjunction with the beast surgery after NACT

Exclusion criteria

* Intolerance / hypersensitivity to iron or dextran compounds or SPIO. * Patients who are required to undergo MR to evaluate tumour response * Pregnancy or breast feeding * Patients with an iron overload disease. * Patient deprived of liberty or under guardianship. * Inability to understand given information, give informed consent, undergo study procedures * MRI (subgroup of patients): Conditions contraindicating MRI including, but not limited to, BMI \> 40 kg/m2, claustrophobia, metallic implants or internal electrical devices (e.g. Pacemaker).

Design outcomes

Primary

MeasureTime frameDescription
Detection rate of axillary sentinel node after neoadjuvant chemotherapyTime between injection of magnetic tracer and technetium-99 is between 3-4 months-Cohort 1: Patients with clinically node negative axillary nodes who undergo neoadjuatnt chemotherapy- Injected with Magtrace (magnetic non particles) near the breast cancer. Detection rate of SN using magtrace to be compared with there rate using the standard comparator Technetium-99
Detection rate of pre-marked metastatic axillary node(s) with magseed after neoadjuvant chemotherapyTime between magseed insertion of magnetic tracer and surgery will be 3-4 monthsCohort 2: Patients with clinically node positive axillary nodes who undergo neoadjuatnt chemotherapy- Injected with Magtrace (magnetic non particles) near the breast cancer. Detection rate of SN using magtrace to be compared with there rate using the standard comparator Technetium-99

Secondary

MeasureTime frameDescription
Concordance rate of axillary Sentinel Node (SN) identified with BOTH MagTrace and Technetium-99 after neoadjuvant chemotherapyTime between injection of magnetic tracer and technetium-99 is between 3-4 months-Cohort 1: Lymph nodes removed that contain BOTH Magtrace and Technetium-99
Concordance rate of Sentinel Node and non-Sentinel Nodes identified with BOTH magtrace and technetium-99Time between injection of magnetic tracer and technetium-99 is between 3-4 months-Cohort 2: Patients with clinically node positive axillary nodes who undergo neoadjuvant chemotherapy. Targeted axillary dissection followed by axillary clearance to be carried out for comparison of concordance rates
Incidence of serious adverse events (SAEs)Through study completion, an average of 1 yearFor both cohort 1 and 2: clinically node negative and positive patients respectively

Countries

Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026