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Breast Cancer: Axillary Conservation After Neoadjuvant Chemotherapy in Micro Metastatic Sentinel Lymph Nodes. (NEONOD2)

Primary Purpose

Breast Cancer

Status
Recruiting
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Omission of Axillary dissection
Sponsored by
Istituto Clinico Humanitas
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Breast Cancer

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  1. Age: 18 ≤75 years
  2. Breast carcinoma with infiltrating histotype
  3. Tumor size: cT1 - cT2 - cT3
  4. Positive axillary lymph nodes (cN +) at the initial diagnosis by clinical, ultrasound and cyto-microhistology evaluation
  5. Neoadjuvant chemotherapy performed
  6. Negative axillary lymph nodes (cN-) from the NAC by clinical and ultrasound assessment
  7. Absence of distant metastases (M0)
  8. Negative medical history for previous infiltrating breast cancer

Exclusion Criteria:

  1. Current pregnancy or lactation status
  2. Inflammatory breast cancer
  3. In situ breast cancer
  4. Synchronous contralateral breast cancer
  5. Co-morbidity and/or medical disorder precluding any adjuvant therapy
  6. Co-morbidity and/or medical/mental disorder making impossible making a regular follow-up
  7. Other cancers in the previous 3 years (except forcarcinoma in situ of the uterine cervix, basalioma, squamous cell carcinoma or non-melanoma skin cancer)

Sites / Locations

  • Istituto Clinico HumanitasRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Group 1: experimental

Group 2: standard

Arm Description

patients with micro metastatic sentinel lymph node and/or parasentinella lymph node (ypN1mi). Axillary dissection is not performed.

patients with negative sentinel lymph node (ypN0) or with ITC finding (ypN0 / YpN0 (i +)). Axillary dissection is not performed as standard treatment.

Outcomes

Primary Outcome Measures

Disease-free or death-free survival for any reason (DFS)
Evaluating whether in patients operated for breast cancer (cT1-T2-T3) with sentinel node micrometastases (SLNypN1mi) after neoadjuvant chemotherapy (NAC), the preservation of axillary lymph nodes is not associated with a clinically relevant prognostic deterioration using Kaplan-Meier Product Limit Estimator and the log-rank test

Secondary Outcome Measures

Global Survival (OS)
Kaplan-Meier Product Limit Estimator and the log-rank test
Regional Disease Free Survival (RDFS)
Kaplan-Meier Product Limit Estimator and the log-rank test
Disease-free distance survival (DDFS)
Kaplan-Meier Product Limit Estimator and the log-rank test

Full Information

First Posted
July 10, 2019
Last Updated
April 15, 2021
Sponsor
Istituto Clinico Humanitas
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1. Study Identification

Unique Protocol Identification Number
NCT04019678
Brief Title
Breast Cancer: Axillary Conservation After Neoadjuvant Chemotherapy in Micro Metastatic Sentinel Lymph Nodes.
Acronym
NEONOD2
Official Title
Breast Carcinoma T1-T2-T3 / cN +: Axillary Conservation of Lymph Nodes in the Presence of Micro Metastases in Sentinel Lymph Node, in cN- After Neoadjuvant Chemotherapy - Studio NEONOD 2
Study Type
Interventional

2. Study Status

Record Verification Date
November 2020
Overall Recruitment Status
Recruiting
Study Start Date
June 21, 2019 (Actual)
Primary Completion Date
June 21, 2027 (Anticipated)
Study Completion Date
June 21, 2027 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Istituto Clinico Humanitas

4. Oversight

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

5. Study Description

Brief Summary
Italian multicentric non inferiority clinical study to verify whether the omission of axillary lymph node intervention in patients with SLN (Sentinel Lymph Nodes) ypN1mi after NAC (Neo Adiuvant Chemotherapy) does not lead to a significant deterioration in survival or in the risk of regional or distant recurrence, compared to patients with negative SLN (SLN ypN0) after NAC ,where the omission of axillary treatment is currently the standard treatment.
Detailed Description
The study includes patients with cN+ positive axillary lymph nodes at initial diagnosis and who also have negative clinical and instrumental evaluation after NAC. Based on the sentinel lymph nodes definitive histological evaluation patients are allocated in one of the 2 comparison groups (Group 1 experimental or Group 2 standard) or in Group 3 internal control group. Group 3 is not used in statistical comparison with the other two groups but it's aim is to evaluate the appropriateness of the cases. Referring to bio-pathologic characteristics after surgery patients will receive: no further treatment complementary radiotherapy adjuvant medical therapy (hormonal therapy and/or biological therapy) Irradiation: Group 1 (experimental) and Group 2 (standard): irradiation won't be performed neither in the axillary region nor in the other lymph node stations Group 3 (internal control): after conservative or radical surgery, patients will be subjected to loco-regional irradiation according to Guidelines. Duration: Patients enrollment in the study protocol will last for 3 years. Patients will have to be followed for the subsequent 5 years during which they will have to undergo to periodic visits and follow-up checks provided for by the current standard guidelines: clinical examination every six months for the first 5 years mammography and breast ultrasound yearly axillary ultrasound yearly

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
850 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Group 1: experimental
Arm Type
Experimental
Arm Description
patients with micro metastatic sentinel lymph node and/or parasentinella lymph node (ypN1mi). Axillary dissection is not performed.
Arm Title
Group 2: standard
Arm Type
Active Comparator
Arm Description
patients with negative sentinel lymph node (ypN0) or with ITC finding (ypN0 / YpN0 (i +)). Axillary dissection is not performed as standard treatment.
Intervention Type
Procedure
Intervention Name(s)
Omission of Axillary dissection
Intervention Description
In Group 1 and 2: Axillary dissection won't be performed
Primary Outcome Measure Information:
Title
Disease-free or death-free survival for any reason (DFS)
Description
Evaluating whether in patients operated for breast cancer (cT1-T2-T3) with sentinel node micrometastases (SLNypN1mi) after neoadjuvant chemotherapy (NAC), the preservation of axillary lymph nodes is not associated with a clinically relevant prognostic deterioration using Kaplan-Meier Product Limit Estimator and the log-rank test
Time Frame
5 years of follow up after surgery
Secondary Outcome Measure Information:
Title
Global Survival (OS)
Description
Kaplan-Meier Product Limit Estimator and the log-rank test
Time Frame
5 years of follow up after surgery
Title
Regional Disease Free Survival (RDFS)
Description
Kaplan-Meier Product Limit Estimator and the log-rank test
Time Frame
5 years of follow up after surgery
Title
Disease-free distance survival (DDFS)
Description
Kaplan-Meier Product Limit Estimator and the log-rank test
Time Frame
5 years of follow up after surgery

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age: 18 ≤75 years Breast carcinoma with infiltrating histotype Tumor size: cT1 - cT2 - cT3 Positive axillary lymph nodes (cN +) at the initial diagnosis by clinical, ultrasound and cyto-microhistology evaluation Neoadjuvant chemotherapy performed Negative axillary lymph nodes (cN-) from the NAC by clinical and ultrasound assessment Absence of distant metastases (M0) Negative medical history for previous infiltrating breast cancer Exclusion Criteria: Current pregnancy or lactation status Inflammatory breast cancer In situ breast cancer Synchronous contralateral breast cancer Co-morbidity and/or medical disorder precluding any adjuvant therapy Co-morbidity and/or medical/mental disorder making impossible making a regular follow-up Other cancers in the previous 3 years (except forcarcinoma in situ of the uterine cervix, basalioma, squamous cell carcinoma or non-melanoma skin cancer)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Corrado Tinterri, MD
Phone
+390282244012
Email
corrado.tinterri@cancercenter.humanitas.it
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Corrado Tinterri, MD
Organizational Affiliation
Istituto Clinico Humanitas
Official's Role
Principal Investigator
Facility Information:
Facility Name
Istituto Clinico Humanitas
City
Rozzano
State/Province
MI
ZIP/Postal Code
20089
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Corrado Tinterri, MD
Phone
+390282244012
Email
corrado.tinterri@cancercenter.humanitas.it

12. IPD Sharing Statement

Learn more about this trial

Breast Cancer: Axillary Conservation After Neoadjuvant Chemotherapy in Micro Metastatic Sentinel Lymph Nodes.

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