Omission of Breast Surgery for Breast Cancer Patients With pCR on MRI and Vacuum-assisted Biopsy After NAC (OPTIMIST) (OPTIMIST)
Primary Purpose
Breast Cancer Invasive
Status
Recruiting
Phase
Not Applicable
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Breast surgery omission
Sponsored by
About this trial
This is an interventional treatment trial for Breast Cancer Invasive focused on measuring neoadjuvant chemotherapy, pathological complete response, vacuum-assisted bIopsy, omission of breast surgery
Eligibility Criteria
Inclusion Criteria:
- Sex: female
- Age: 20 years and older
- Patients with no clinical/radiologic distant metastasis
- Tumor type: Invasive ductal carcinoma
- Tumor subtype: HER2 positive(including luminal B type, triple negative
- Extent of disease: initial tumor size ≤ 5cm, cN0-2
- Patients with measurable tumor size
- Patients who are expected to achieve pCR after neoadjuvant chemotherapy (MRI size ≤ 1.0 cm AND L-to-B SER ≤ 1.6)
- Patients with clip inserted to the primary tumor site before or during neoadjuvant chemotherapy
- Patients with informed consent who are competent to make a voluntary decision
Exclusion Criteria:
- Multifocal lesion (≥2)
- Extent of residual microcalcification after neoadjuvant chemotherapy > 2cm
- Bilateral breast cancer or inflammatory breast cancer
- Contraindication to radiotherapy
- History of previous contralateral breast cancer
- Breast cancer patients with distant metastasis
- Allergic history to MRI contrast
- Male breast cancer
- Patients incapable of giving informed consent owing to poor general conditions
- Patients with BRCA mutation
- Patients willing to receive breast surgery
- Patients with a history of cancer diagnosis within 5 years (However, skin cancer other than melanoma and breast carcinoma in situ other than ductal carcinoma in situ can be registered even if 5 years have not passed since the diagnosis)
Sites / Locations
- Seoul National University HospitalRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Patients with pCR predicted by MRI and vacuum-assisted biopsy (VAB) after neoadjuvant chemotherapy
Arm Description
When there is no residual tumor cells on the vacuum-assisted biopsy specimen, breast surgery will be omitted. In the case of clinical N0 AND MRI size ≤ 0.5cm AND lesion-to-background signal enhancement ratio ≤1.6, sentinel lymph node biopsy will be omitted. Otherwise, sentinel lymph node biopsy will be performed. If necessary, axillary lymph node dissection will be performed.
Outcomes
Primary Outcome Measures
Disease-Free Survival
Proportion of patients with no disease recurrence (including loco-regional recurrence, distant metastasis, and contralateral breast cancer) or death.
Secondary Outcome Measures
Ipsilateral Breast Tumor Recurrence-Free Survival Ipsilateral Breast Tumor Recurrence-Free Survival
Proportion of patients with no disease recurrence in the ipsilateral breast or death
Overall Survival
Proportion of patients with no death.
Invasive Disease-Free Survival Invasive Disease-Free Survival
Proportion of patients with no invasive disease recurrence (including loco-regional recurrence, distant metastasis, and contralateral breast cancer) or death.
QoL, symptoms, and medical cost
Analysis of QoL survey (BREAST-Q), procedure-related symptoms, and medical cost
Rate of residual axillary lymph node metastasis on axillary surgery
Proportion of patients with metastatic lymph nodes among those with pCR on VAB
Full Information
NCT ID
NCT05505357
First Posted
August 16, 2022
Last Updated
October 30, 2022
Sponsor
Seoul National University Hospital
Collaborators
Ministry of Health & Welfare, Korea
1. Study Identification
Unique Protocol Identification Number
NCT05505357
Brief Title
Omission of Breast Surgery for Breast Cancer Patients With pCR on MRI and Vacuum-assisted Biopsy After NAC (OPTIMIST)
Acronym
OPTIMIST
Official Title
Omission of Breast Surgery for Predicted Pathologic Complete Response Patients With MRI and Vacuum-assisted bIopsy in Breast Cancer After Neoadjuvant Chemotherapy a Multicenter, Single-arm, Non-inferiority Trial
Study Type
Interventional
2. Study Status
Record Verification Date
October 2022
Overall Recruitment Status
Recruiting
Study Start Date
September 22, 2022 (Actual)
Primary Completion Date
March 2026 (Anticipated)
Study Completion Date
March 2031 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Seoul National University Hospital
Collaborators
Ministry of Health & Welfare, Korea
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
A prospective, multicenter, single-arm non-inferiority trial to demonstrate that breast cancer patients who are predicted to have a pathologic complete response on MRI and vacuum-assisted biopsy after neoadjuvant chemotherapy, and are omitted breast surgery have a non-inferior 5-year disease-free survival compared to those who had received breast surgery.
Detailed Description
[Background & Rationale for Study]
Optimization (rather than de-escalation) of surgery for breast cancer is essential for our patients, and thus it is an important topic discussed actively in all major conferences regarding breast cancer and oncology.
A previous study showed that lesion-to-background parenchymal signal enhancement ratio (L-to-B SER) ≤1.6 and/or size ≤ 0.2cm on breast MRI can distinguish pathological complete response (pCR) from minimal residual cancer following neoadjuvant chemotherapy (NAT). In a separate prospective study, 40 patients with near pCR (either tumor size ≤ 0.5 cm or L-to-B SER ≤ 1.6 on MRI) were enrolled and evaluated for the accuracy of US-guided biopsy aided by MRI in predicting pCR in the breast after NAC. US-guided multiple core needle biopsy (CNB) or VAB of the tumor bed, followed by standard surgical excision, was performed. Matched biopsy and surgical specimens were compared to assess pCR. In result, obtaining at least 5 biopsy cores based on tumor size ≤ 0.5 cm and an L-to-B SER of ≤ 1.6 on MRI resulted in 100% NPV and accuracy. No differences in accuracy were noted between CNB and VAB (90% vs. 90%). It was demonstrated that patients who meet these stringent criteria on MRI may forego surgery for breast cancer.
Also, a pooled analysis of data from The Royal Marsden, MD Anderson Cancer Center, and Seoul National University Hospital showed that a VAB obtaining at least 6 cores for a lesion ≤2cm on imaging after neoadjuvant chemotherapy can accurately predict pCR at a FNR of 3.2%.
For patients who would not benefit from surgery, it is unnecessary in terms of both personal and national medical expenses. Therefore, in order to establish the rationale for whether surgery could be omitted for patients with predicted pCR, it is necessary to demonstrate that the survival rate of patients who skipped breast surgery after confirming no residual cancer on VAB is non-inferior than that of patients who underwent breast surgery.
[Study Objectives]
To show non-inferiority in terms of disease-free survival (DFS) of omission of breast surgery for breast cancer patients who show no residual tumor on VAB after neoadjuvant chemotherapy.
[Study design]
Prospective, multicenter, single-arm, non-inferiority trial
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer Invasive
Keywords
neoadjuvant chemotherapy, pathological complete response, vacuum-assisted bIopsy, omission of breast surgery
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
533 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Patients with pCR predicted by MRI and vacuum-assisted biopsy (VAB) after neoadjuvant chemotherapy
Arm Type
Experimental
Arm Description
When there is no residual tumor cells on the vacuum-assisted biopsy specimen, breast surgery will be omitted. In the case of clinical N0 AND MRI size ≤ 0.5cm AND lesion-to-background signal enhancement ratio ≤1.6, sentinel lymph node biopsy will be omitted. Otherwise, sentinel lymph node biopsy will be performed. If necessary, axillary lymph node dissection will be performed.
Intervention Type
Procedure
Intervention Name(s)
Breast surgery omission
Intervention Description
For patients who are expected to achieve pathologic complete response after neoadjuvant chemotherapy based on MRI findings, vacuum-assisted biopsy will be performed on the main primary lesion marked with a clip. In case of pCR on vacuum-assisted biopsy specimen, breast surgery will be omitted.
Primary Outcome Measure Information:
Title
Disease-Free Survival
Description
Proportion of patients with no disease recurrence (including loco-regional recurrence, distant metastasis, and contralateral breast cancer) or death.
Time Frame
5 years after axillary surgery or VAB (in case of axillary surgery omission)
Secondary Outcome Measure Information:
Title
Ipsilateral Breast Tumor Recurrence-Free Survival Ipsilateral Breast Tumor Recurrence-Free Survival
Description
Proportion of patients with no disease recurrence in the ipsilateral breast or death
Time Frame
5 years after axillary surgery or VAB (in case of axillary surgery omission)
Title
Overall Survival
Description
Proportion of patients with no death.
Time Frame
5 years after axillary surgery or VAB (in case of axillary surgery omission)
Title
Invasive Disease-Free Survival Invasive Disease-Free Survival
Description
Proportion of patients with no invasive disease recurrence (including loco-regional recurrence, distant metastasis, and contralateral breast cancer) or death.
Time Frame
5 years after axillary surgery or VAB (in case of axillary surgery omission)
Title
QoL, symptoms, and medical cost
Description
Analysis of QoL survey (BREAST-Q), procedure-related symptoms, and medical cost
Time Frame
1 year after axillary surgery or VAB (in case of axillary surgery omission)
Title
Rate of residual axillary lymph node metastasis on axillary surgery
Description
Proportion of patients with metastatic lymph nodes among those with pCR on VAB
Time Frame
Upon axillary surgery
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Sex: female
Age: 20 years and older
Patients with no clinical/radiologic distant metastasis
Tumor type: Invasive ductal carcinoma
Tumor subtype: HER2 positive(including luminal B type, triple negative
Extent of disease: initial tumor size ≤ 5cm, cN0-2
Patients with measurable tumor size
Patients who are expected to achieve pCR after neoadjuvant chemotherapy (MRI size ≤ 1.0 cm AND L-to-B SER ≤ 1.6)
Patients with clip inserted to the primary tumor site before or during neoadjuvant chemotherapy
Patients with informed consent who are competent to make a voluntary decision
Exclusion Criteria:
Multifocal lesion (≥2)
Extent of residual microcalcification after neoadjuvant chemotherapy > 2cm
Bilateral breast cancer or inflammatory breast cancer
Contraindication to radiotherapy
History of previous contralateral breast cancer
Breast cancer patients with distant metastasis
Allergic history to MRI contrast
Male breast cancer
Patients incapable of giving informed consent owing to poor general conditions
Patients with BRCA mutation
Patients willing to receive breast surgery
Patients with a history of cancer diagnosis within 5 years (However, skin cancer other than melanoma and breast carcinoma in situ other than ductal carcinoma in situ can be registered even if 5 years have not passed since the diagnosis)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Han-Byoel Lee
Phone
+82-2-2072-3447
Email
hblee80@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Hong-Kyu Kim
Phone
+82-2-2072-2980
Email
hkkim4592@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Han-Byoel Lee
Organizational Affiliation
Seoul National University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Seoul National University Hospital
City
Seoul
Country
Korea, Republic of
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Han-Byoel Lee
Email
hblee80@gmail.com
First Name & Middle Initial & Last Name & Degree
Hong-Kyu Kim
Email
hkkim4592@gmail.com
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
Available on Request (hblee80@gmail.com; hblee.md@snu.ac.kr)
IPD Sharing Time Frame
March 2032
IPD Sharing Access Criteria
Upon request
Citations:
PubMed Identifier
29380033
Citation
Kim SY, Cho N, Shin SU, Lee HB, Han W, Park IA, Kwon BR, Kim SY, Lee SH, Chang JM, Moon WK. Contrast-enhanced MRI after neoadjuvant chemotherapy of breast cancer: lesion-to-background parenchymal signal enhancement ratio for discriminating pathological complete response from minimal residual tumour. Eur Radiol. 2018 Jul;28(7):2986-2995. doi: 10.1007/s00330-017-5251-8. Epub 2018 Jan 29.
Results Reference
background
PubMed Identifier
32418044
Citation
Lee HB, Han W, Kim SY, Cho N, Kim KE, Park JH, Ju YW, Lee ES, Lim SJ, Kim JH, Ryu HS, Lee DW, Kim M, Kim TY, Lee KH, Shin SU, Lee SH, Chang JM, Moon HG, Im SA, Moon WK, Park IA, Noh DY. Prediction of pathologic complete response using image-guided biopsy after neoadjuvant chemotherapy in breast cancer patients selected based on MRI findings: a prospective feasibility trial. Breast Cancer Res Treat. 2020 Jul;182(1):97-105. doi: 10.1007/s10549-020-05678-3. Epub 2020 May 16.
Results Reference
background
PubMed Identifier
33026457
Citation
Tasoulis MK, Lee HB, Yang W, Pope R, Krishnamurthy S, Kim SY, Cho N, Teoh V, Rauch GM, Smith BD, Valero V, Mohammed K, Han W, MacNeill F, Kuerer HM. Accuracy of Post-Neoadjuvant Chemotherapy Image-Guided Breast Biopsy to Predict Residual Cancer. JAMA Surg. 2020 Dec 1;155(12):e204103. doi: 10.1001/jamasurg.2020.4103. Epub 2020 Dec 16.
Results Reference
background
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Omission of Breast Surgery for Breast Cancer Patients With pCR on MRI and Vacuum-assisted Biopsy After NAC (OPTIMIST)
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