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Basket Study for Oligo-metastatic Breast Cancer (ANISE)

Primary Purpose

HER2-positive Breast Cancer

Status
Not yet recruiting
Phase
Phase 2
Locations
Netherlands
Study Type
Interventional
Intervention
Trastuzumab deruxtecan
Sponsored by
The Netherlands Cancer Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for HER2-positive Breast Cancer focused on measuring Oligometastatic disease (max 3 lesions)

Eligibility Criteria

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

Inclusion Criteria: Histologic proof of infiltrating HER2-positive breast cancer (as determined by IHC 3+ and/or amplification by ISH)[8] Histologic or cytologic proof of breast cancer metastases (at least one lesion) Histologic determination of level of ER-expression Oligo-metastatic disease as determined by standard of care diagnostics. The number of total individual distant metastases is limited to three, either in one organ or in 2-3 organ systems. Clustered lymph nodes that can be irradiated with curative intent in a single field are defined as single lesion. Pleuritis carcinomatosa, miliary spread of metastases (even within one organ), or peritoneal spread of metastases rules out oligo-metastatic disease and is not allowed. Initial staging by PET-CT (whole body) and MRI of breast and brain are mandatory, as is MRI liver or spine and pelvis in case of liver or bone metastases respectively. In case of recurrent disease, a disease-free interval of 24 months. Measurable disease according to RECIST1.1 Patients must be at least 18 years of age and be able to give written informed consent and comply with study procedures. World Health Organization (WHO) performance status 0 or 1 Exclusion Criteria: prior line of therapy for metastatic disease. Exceptions are endocrine therapy or radiation considered to be part of the curative treatment, within 3 months before enrolment leptomeningeal disease or central nervous metastases clinically relevant obstruction or compression of spinal cord, central nervous, gastro-intestinal or cardiovascular system, that cannot be alleviated before start of treatment. other malignancy, unless treated with curative intention and a long-term survival probability of >95%, including in-situ or pre-malignant lesions.

Sites / Locations

  • Antoni van Leeuwenhoek

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Trastuzumab-deruxtecan

Arm Description

5.4mg/kg on a three weekly (21 day) basis, with the goal of 16 cycles leading to a treatment period of year, including local treatment. The first 8 cycles of T-DXd are administered neo-adjuvant, and 8 cycles adjuvant, after completion of local treatment.

Outcomes

Primary Outcome Measures

Complete radiologic response
Number of patients to achieve radiologic response as defined by RECIST 11 with clearnace of ctDNA

Secondary Outcome Measures

Number of patients free of progression
as defined by RECIST
Overall Survival
time from start treatment to death from any cause
Number of patients with pathological complete response
after resection of primary tumor and/or metastatic lesions after neo-adjuvant treatment
Number of patients with metabolic response
as measured with PDG-PET
Number of patients with metabolic response
as measured by clearance of ctDNA
Incidence of Treatment-Emergent Adverse Events (Safety and Tolerability)
determined accoriding to CTCAE v5.0 or Clavien-Dindo (in case of surgical resection)

Full Information

First Posted
July 25, 2023
Last Updated
August 7, 2023
Sponsor
The Netherlands Cancer Institute
Collaborators
Daiichi Sankyo, Inc., AstraZeneca
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1. Study Identification

Unique Protocol Identification Number
NCT05982678
Brief Title
Basket Study for Oligo-metastatic Breast Cancer
Acronym
ANISE
Official Title
Basket Study for Oligo-metastatic Breast Cancer Part 1: Trastuzumab-deruxtecan for HER2-positive Oligo-metastatic Breast Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
October 1, 2023 (Anticipated)
Primary Completion Date
October 1, 2027 (Anticipated)
Study Completion Date
October 1, 2034 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
The Netherlands Cancer Institute
Collaborators
Daiichi Sankyo, Inc., AstraZeneca

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 study will include patients with HER2-positive breast cancer and 1- 3 distant metastatic lesions, all amenable for curative intervention. Patients will be stratified by prior therapy and ER expression. In the initial baskets patients with be treated with trastuzumab-deruxtecan. Patients are treated with T-DXd 5.4mg/kg on a three weekly (21 day) basis, with the goal of 16 cycles leading to a treatment period of year, including local treatment. The first 8 cycles of T-DXd are administered neo-adjuvant, and 8 cycles adjuvant, after completion of local treatment. The proposed M22BOL trial is based on an important knowledge gap for regarding breast cancer patients with 'oligo-metastatic' disease who are usually not included in clinical trials for patients with metastatic disease since loco-regional treatments (radiation, surgery) with curative intent is not allowed in clinical trials for metastatic breast cancer. Moreover, neo-adjuvant trial protocols for early breast cancer exclude patients with distant metastases that can be treated with curative intent. This basket trial evaluates T-DXd for oligo-metastatic breast cancer with the goal to induce deep responses and subsequently long-lasting disease remissions and potentially cure.
Detailed Description
The study will include patients with HER2-positive breast cancer and 1- 3 distant metastatic lesions, all amenable for curative intervention. Patients will be stratified by prior therapy and ER expression. Given the basket-design of this trial other baskets for oligo-metastatic breast cancer can be added, such as but not limited to other breast cancer subtypes or with other promising drugs. Baskets for de novo oligo-metastatic disease I. ER+/HER2+ II. ER-/HER2+ Baskets for oligo-metastatic disease after prior chemo/anti-HER2 therapy for primary disease III. ER+/HER2+ IV. ER-/HER2+

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HER2-positive Breast Cancer
Keywords
Oligometastatic disease (max 3 lesions)

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
72 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Trastuzumab-deruxtecan
Arm Type
Experimental
Arm Description
5.4mg/kg on a three weekly (21 day) basis, with the goal of 16 cycles leading to a treatment period of year, including local treatment. The first 8 cycles of T-DXd are administered neo-adjuvant, and 8 cycles adjuvant, after completion of local treatment.
Intervention Type
Drug
Intervention Name(s)
Trastuzumab deruxtecan
Intervention Description
T-DXd 5.4mg/kg on a three weekly (21 day) basis, with the goal of 16 cycles leading to a treatment period of year, including local treatment. The first 8 cycles of T-DXd are administered neo-adjuvant, and 8 cycles adjuvant, after completion of local treatment.
Primary Outcome Measure Information:
Title
Complete radiologic response
Description
Number of patients to achieve radiologic response as defined by RECIST 11 with clearnace of ctDNA
Time Frame
up to one year after start treatment
Secondary Outcome Measure Information:
Title
Number of patients free of progression
Description
as defined by RECIST
Time Frame
assessed up to 10 years
Title
Overall Survival
Description
time from start treatment to death from any cause
Time Frame
assessed up to 10 years
Title
Number of patients with pathological complete response
Description
after resection of primary tumor and/or metastatic lesions after neo-adjuvant treatment
Time Frame
assessed immediately after surgery
Title
Number of patients with metabolic response
Description
as measured with PDG-PET
Time Frame
assessed up to 12 months
Title
Number of patients with metabolic response
Description
as measured by clearance of ctDNA
Time Frame
assessed up to 10 years
Title
Incidence of Treatment-Emergent Adverse Events (Safety and Tolerability)
Description
determined accoriding to CTCAE v5.0 or Clavien-Dindo (in case of surgical resection)
Time Frame
assessed up to 30 days after last treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Histologic proof of infiltrating HER2-positive breast cancer (as determined by IHC 3+ and/or amplification by ISH)[8] Histologic or cytologic proof of breast cancer metastases (at least one lesion) Histologic determination of level of ER-expression Oligo-metastatic disease as determined by standard of care diagnostics. The number of total individual distant metastases is limited to three, either in one organ or in 2-3 organ systems. Clustered lymph nodes that can be irradiated with curative intent in a single field are defined as single lesion. Pleuritis carcinomatosa, miliary spread of metastases (even within one organ), or peritoneal spread of metastases rules out oligo-metastatic disease and is not allowed. Initial staging by PET-CT (whole body) and MRI of breast and brain are mandatory, as is MRI liver or spine and pelvis in case of liver or bone metastases respectively. In case of recurrent disease, a disease-free interval of 24 months. Measurable disease according to RECIST1.1 Patients must be at least 18 years of age and be able to give written informed consent and comply with study procedures. World Health Organization (WHO) performance status 0 or 1 Exclusion Criteria: prior line of therapy for metastatic disease. Exceptions are endocrine therapy or radiation considered to be part of the curative treatment, within 3 months before enrolment leptomeningeal disease or central nervous metastases clinically relevant obstruction or compression of spinal cord, central nervous, gastro-intestinal or cardiovascular system, that cannot be alleviated before start of treatment. other malignancy, unless treated with curative intention and a long-term survival probability of >95%, including in-situ or pre-malignant lesions.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Marleen Kok, MD
Phone
+31205129111
Ext
9111
Email
m.kok@nki.nl
First Name & Middle Initial & Last Name or Official Title & Degree
Robbert-Jan Gielen, MD
Phone
+3120512
Ext
9111
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marleen Kok, MD
Organizational Affiliation
Antoni van Leeuwenhoek
Official's Role
Principal Investigator
Facility Information:
Facility Name
Antoni van Leeuwenhoek
City
Amsterdam
Country
Netherlands
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Robbert-Jan Gielen, MD
First Name & Middle Initial & Last Name & Degree
Ingrid Mandjes, MSc
First Name & Middle Initial & Last Name & Degree
Marleen Kok, MD

12. IPD Sharing Statement

Plan to Share IPD
Undecided
IPD Sharing Plan Description
to de decided

Learn more about this trial

Basket Study for Oligo-metastatic Breast Cancer

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