search
Back to results

Axillary Staging in Node Positive Breast Cancer Patients Receiving PST. SNB vs PET/MRI

Primary Purpose

Breast Cancer Female, Node-positive Breast Cancer, Sentinel Lymph Node

Status
Recruiting
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
PET/MRI
Sponsored by
Oreste Davide Gentilini
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Breast Cancer Female focused on measuring primary systemic therapy, node positive breast cancer, surgery after primary systemic therapy, PET/MRI

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Signed informed consent;
  • Age > 18 years;
  • Proven diagnosis of early BC of any size;
  • Patients candidate to primary systemic therapy (PST);
  • Positive axillary nodes at diagnosis, confirmed by either citology or histology confirmation. Patients with clear overt clinical and radiological nodal involvement might be enrolled as well without FNA or microhystology

Exclusion Criteria:

  • inflammatory BC;
  • pregnancy;
  • contraindication to PET;
  • distant metastases;
  • no surgery after PST;
  • contraindication to MRI;
  • claustrophobia;
  • allergy to the MR contrast agent;
  • severe renal insufficiency.

Sites / Locations

  • Ospedale San RaffaeleRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Node positive BC patients undergoing PST

Arm Description

Patients with breast cancer of any size with positive axillary nodes and candidates to PST will undergo PET/MRI both prior to PST and after PST before surgery

Outcomes

Primary Outcome Measures

Axillary surgery vs PET/MRI.
Results from SNB (Sentinel Node Biopsy), AD (Axillary Dissection) or any axillary surgery will be compared to results from preoperative PET/MRI.

Secondary Outcome Measures

Staging power of PET/MRI will be compared to preoperative A-US (Axillary ultrasound)
Results on the status of axillary nodes from preoperative A-US will be compared to results of preoperative PET/MRI.
Correlation between PET/MRI parameters and prognosis
Quantitative analysis of PET/MRI exams will allow to extract standard imaging biomarkers to be correlated with tumour clinical and pathological data. Image analysis will be carried out both at staging and at the end of PST. Functional parameters from PET image analysis include Standardized Uptake Value and Metabolic Tumor Volume. From breast MR images, the quantitative and semiquantitative data are related to DWI and DCE MR sequences. Specifically, from the so-called Time Intensity Curve (TIC) obtained from the dynamic DCE some parameters can be extracted, for example Time To Peak, Peak Enhancement Percentage, Signal Enhancement Ratio and Initial Enhancement Percentage. From DWI MR sequence Apparent Diffusion Coefficient map can be calculated.

Full Information

First Posted
May 25, 2020
Last Updated
September 27, 2023
Sponsor
Oreste Davide Gentilini
Collaborators
IBFM- Consiglio Nazionale delle Ricerche
search

1. Study Identification

Unique Protocol Identification Number
NCT04826211
Brief Title
Axillary Staging in Node Positive Breast Cancer Patients Receiving PST. SNB vs PET/MRI
Official Title
Targeting the Future of Axillary Staging in Node Positive Breast Cancer Patients Receiving Primary Systemic Therapy. A Comparative Study Between Sentinel Node Biopsy vs PET/MRI.
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Recruiting
Study Start Date
November 4, 2019 (Actual)
Primary Completion Date
April 1, 2024 (Anticipated)
Study Completion Date
April 1, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Oreste Davide Gentilini
Collaborators
IBFM- Consiglio Nazionale delle Ricerche

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The management of axillary nodes in breast cancer patients is a highly debated and evolving field. To date, an increasing number of patients with positive lymph nodes receives primary systemic therapy (PST) prior to surgery leading to down-staging axillary nodes in about 40% of women. However, the available diagnostic methods have several limitations in properly evaluating the response after treatment both in the breast and in the nodes and might lead to either under or over-treatment in these patients. Fully integrated scanners capable of simultaneous acquisition of PET and MRI have now been developed, with the potential to combine the specificity obtained by the functional imaging of PET, with the superior sensitivity of MRI, to provide higher diagnostic accuracy. It is expected that PET/MRI could better determine the response after PST to distinguish patients with negative versus patients with positive axillary nodes after medical treatment. As the excision of axillary nodes has mainly a staging purpose, the reliable identification of node negative patients might eventually spare women from unnecessary surgery. An accurate over-time and final imaging work-up might help choose the appropriate type of surgery according to the extent of nodal involvement: either SNB or complete axillary clearance.
Detailed Description
HYPOTHESIS: Hybrid PET/MRI might be a non-invasive, one-stage, operator-independent imaging modality to accurately define nodal status after PST, properly select type of surgical approach and might eventually lead to the omission of axillar surgery in some breast cancer patients showing complete imaging response. AIMS: The primary endpoint is to compare the staging power between SNB (or lymphoadenectomy) vs PET/MRI in detecting axillary lymph node macro-metastases (>2 mm).Additionally the PET/MRI and A-US results will be confronted and ultimately related to pathology result, calculating the concordance rate in terms of positive vs negative nodes and number of positive nodes detected by each method. The staging power of both preoperative exams will be evaluated by considering how many times the results from PET/MRI or A-US could have indicated the most appropriate axillary treatment according to pathological findings. EXPERIMENTAL DESIGN: Patients with breast cancer of any size with positive axillary nodes and candidates to PST will undergo PET/MRI prior to PST. The study population will then be split into two groups: women with positive axillary lymph nodes after PST (Group 1, 60% of the total) women with negative axillary lymph nodes after PST (Group 2, 40% of the total). A total of 110 women will guarantee two well-powered independent analysis. one for Group 1 (n=66; power>90%; Type I error rate of 0.05) and one for Group 2 (n=44; power>80%; Type I error rate of 0.05).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer Female, Node-positive Breast Cancer, Sentinel Lymph Node
Keywords
primary systemic therapy, node positive breast cancer, surgery after primary systemic therapy, PET/MRI

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
110 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Node positive BC patients undergoing PST
Arm Type
Experimental
Arm Description
Patients with breast cancer of any size with positive axillary nodes and candidates to PST will undergo PET/MRI both prior to PST and after PST before surgery
Intervention Type
Diagnostic Test
Intervention Name(s)
PET/MRI
Intervention Description
All included patients will undergo PET/MRI both prior to PST and prior to surgery. In order to analyze results the population will be divided into two groups: women with positive axillary lymph nodes after PST (Group 1) and women with negative axillary lymph nodes after PST (Group 2).
Primary Outcome Measure Information:
Title
Axillary surgery vs PET/MRI.
Description
Results from SNB (Sentinel Node Biopsy), AD (Axillary Dissection) or any axillary surgery will be compared to results from preoperative PET/MRI.
Time Frame
Within 1 month after surgery results from axillary surgery will be available and compared to preoperative PET/MRI
Secondary Outcome Measure Information:
Title
Staging power of PET/MRI will be compared to preoperative A-US (Axillary ultrasound)
Description
Results on the status of axillary nodes from preoperative A-US will be compared to results of preoperative PET/MRI.
Time Frame
At 12 months
Title
Correlation between PET/MRI parameters and prognosis
Description
Quantitative analysis of PET/MRI exams will allow to extract standard imaging biomarkers to be correlated with tumour clinical and pathological data. Image analysis will be carried out both at staging and at the end of PST. Functional parameters from PET image analysis include Standardized Uptake Value and Metabolic Tumor Volume. From breast MR images, the quantitative and semiquantitative data are related to DWI and DCE MR sequences. Specifically, from the so-called Time Intensity Curve (TIC) obtained from the dynamic DCE some parameters can be extracted, for example Time To Peak, Peak Enhancement Percentage, Signal Enhancement Ratio and Initial Enhancement Percentage. From DWI MR sequence Apparent Diffusion Coefficient map can be calculated.
Time Frame
At baseline and at 5 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Signed informed consent; Age > 18 years; Proven diagnosis of early BC of any size; Patients candidate to primary systemic therapy (PST); Positive axillary nodes at diagnosis, confirmed by either citology or histology confirmation. Patients with clear overt clinical and radiological nodal involvement might be enrolled as well without FNA or microhystology Exclusion Criteria: inflammatory BC; pregnancy; contraindication to PET; distant metastases; no surgery after PST; contraindication to MRI; claustrophobia; allergy to the MR contrast agent; severe renal insufficiency.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
ORESTE DAVIDE GENTILINI, PI
Phone
02-26433939
Email
gentilini.oreste@hsr.it
First Name & Middle Initial & Last Name or Official Title & Degree
ROSA DI MICCO, SI
Email
dimicco.rosa@hsr.it
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
GENTILINI
Organizational Affiliation
IRCCS San Raffaele
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ospedale San Raffaele
City
Milano
State/Province
MI
ZIP/Postal Code
20132
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
ORESTE DAVIDE GENTILINI
Email
gentilini.oreste@hsr.it
First Name & Middle Initial & Last Name & Degree
ROSA DI MICCO
First Name & Middle Initial & Last Name & Degree
LUIGI GIANOLLI
First Name & Middle Initial & Last Name & Degree
CARLA CANEVARI
First Name & Middle Initial & Last Name & Degree
PIETRO PANIZZA
First Name & Middle Initial & Last Name & Degree
CLAUDIO LOSIO
First Name & Middle Initial & Last Name & Degree
ELENA VENTURINI
First Name & Middle Initial & Last Name & Degree
ZUBER VERONICA
First Name & Middle Initial & Last Name & Degree
ANNARITA SAVI

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
25282709
Citation
Taneja S, Jena A, Goel R, Sarin R, Kaul S. Simultaneous whole-body (1)(8)F-FDG PET-MRI in primary staging of breast cancer: a pilot study. Eur J Radiol. 2014 Dec;83(12):2231-2239. doi: 10.1016/j.ejrad.2014.09.008. Epub 2014 Sep 28.
Results Reference
background
PubMed Identifier
27023002
Citation
Melsaether AN, Raad RA, Pujara AC, Ponzo FD, Pysarenko KM, Jhaveri K, Babb JS, Sigmund EE, Kim SG, Moy LA. Comparison of Whole-Body (18)F FDG PET/MR Imaging and Whole-Body (18)F FDG PET/CT in Terms of Lesion Detection and Radiation Dose in Patients with Breast Cancer. Radiology. 2016 Oct;281(1):193-202. doi: 10.1148/radiol.2016151155. Epub 2016 Mar 29.
Results Reference
background
PubMed Identifier
17164229
Citation
Veronesi U, De Cicco C, Galimberti VE, Fernandez JR, Rotmensz N, Viale G, Spano G, Luini A, Intra M, Veronesi P, Berrettini A, Paganelli G. A comparative study on the value of FDG-PET and sentinel node biopsy to identify occult axillary metastases. Ann Oncol. 2007 Mar;18(3):473-8. doi: 10.1093/annonc/mdl425. Epub 2006 Dec 12.
Results Reference
background
PubMed Identifier
26291922
Citation
Gentilini O, Veronesi U. Staging the Axilla in Early Breast Cancer: Will Imaging Replace Surgery? JAMA Oncol. 2015 Nov;1(8):1031-2. doi: 10.1001/jamaoncol.2015.2337. No abstract available.
Results Reference
background
PubMed Identifier
28905091
Citation
van Nijnatten TJA, Goorts B, Voo S, de Boer M, Kooreman LFS, Heuts EM, Wildberger JE, Mottaghy FM, Lobbes MBI, Smidt ML. Added value of dedicated axillary hybrid 18F-FDG PET/MRI for improved axillary nodal staging in clinically node-positive breast cancer patients: a feasibility study. Eur J Nucl Med Mol Imaging. 2018 Feb;45(2):179-186. doi: 10.1007/s00259-017-3823-0. Epub 2017 Sep 14.
Results Reference
background
PubMed Identifier
25112399
Citation
Heusch P, Nensa F, Schaarschmidt B, Sivanesapillai R, Beiderwellen K, Gomez B, Kohler J, Reis H, Ruhlmann V, Buchbender C. Diagnostic accuracy of whole-body PET/MRI and whole-body PET/CT for TNM staging in oncology. Eur J Nucl Med Mol Imaging. 2015 Jan;42(1):42-8. doi: 10.1007/s00259-014-2885-5. Epub 2014 Aug 12.
Results Reference
background
PubMed Identifier
16670863
Citation
Stadnik TW, Everaert H, Makkat S, Sacre R, Lamote J, Bourgain C. Breast imaging. Preoperative breast cancer staging: comparison of USPIO-enhanced MR imaging and 18F-fluorodeoxyglucose (FDC) positron emission tomography (PET) imaging for axillary lymph node staging--initial findings. Eur Radiol. 2006 Oct;16(10):2153-60. doi: 10.1007/s00330-006-0276-4. Epub 2006 May 3.
Results Reference
background

Learn more about this trial

Axillary Staging in Node Positive Breast Cancer Patients Receiving PST. SNB vs PET/MRI

We'll reach out to this number within 24 hrs