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Classified Treatment Strategy for De-novo Metastatic Breast Cancer After Systemic Adjuvant Therapy (CS)

Primary Purpose

Breast Neoplasms, Treatment, Metastatic Breast Cancer

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
surgical treatment 1
surgical treatment 2
Systemic therapy
Sponsored by
Changhai Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Breast Neoplasms focused on measuring Breast Neoplasms, de-novo metastatic breast cancer, surgical treatment

Eligibility Criteria

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

Study Population Operable stage IV breast cancer patients, whose primary lesion is invasive breast cancer confirmed by pathology, and metastases can be confirmed by pathology or imaginology examination

Inclusion Criteria:

  • Operable stage IV breast cancer patients,whose primary lesion is invasive breast cancer confirmed by pathology, and metastases can be confirmed by pathology or imageology examination.
  • ECOG-PS 0-2.
  • Bone marrow, liver and kidney should be fully functional.
  • Patients didn't received the locoregional surgery of the primary tumor in de novo.
  • For the patient who accepted systematic treatment before operation, the systematic treatment must be administered within a year since diagnosed.

Exclusion Criteria:

  • Accompanied with other primary malignant tumors.
  • More than two visceral organ involvement.
  • Patients who can't plan for follow-up effectively and regularly.
  • Multiple liver metastases with deranged liver function tests (SGOT/SGPT more than four times the upper normal limit).

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm 4

    Arm Type

    Experimental

    Experimental

    Experimental

    Experimental

    Arm Label

    1 Primary and metastatic lesions PCR

    2 Primary lesions NPCR and metastatic lesions PCR

    3 Primary lesions PCR and metastatic lesions NPCR

    4 Primary lesions NPCR and metastatic lesions NPCR

    Arm Description

    surgery 1 Mastectomy OR Breast conserving surgery

    surgery 1 Mastectomy OR Breast conserving surgery

    surgery 2 Resection of metastasis

    Systemic therapy Endocrine therapy or chemotherapy or targeted therapy

    Outcomes

    Primary Outcome Measures

    Overall survival
    Overall survival (OS), which defined as the time from the beginning of diagnosis of breast cancer to the death with any causes.

    Secondary Outcome Measures

    Distant progression free survival
    Distant disease free survival (D-DFS), which defined as the time from the diagnosis of de novo stage IV breast cancer to the confirmed time of distant progression, or death due to any other cause.
    Locoregional progression free survival
    Defined as time between the time of diagnosis and the time of locoregional recurrence, or death occurred.

    Full Information

    First Posted
    March 9, 2022
    Last Updated
    July 17, 2022
    Sponsor
    Changhai Hospital
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05285332
    Brief Title
    Classified Treatment Strategy for De-novo Metastatic Breast Cancer After Systemic Adjuvant Therapy
    Acronym
    CS
    Official Title
    Classified Treatment Strategy for De-novo Metastatic Breast Cancer After Systemic Adjuvant Therapywhich Patients Will Benefit From Surgery
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    July 2022
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    August 1, 2022 (Anticipated)
    Primary Completion Date
    December 31, 2030 (Anticipated)
    Study Completion Date
    May 1, 2031 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Changhai Hospital

    4. Oversight

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

    5. Study Description

    Brief Summary
    For patients with de novo stage IV breast cancer, the current debate is whether local surgery can improve the survival of patients. There is no clinical study on the classification after systemic treatment of de novo stage IV breast cancer patients. In fact, the clinical stage of tumor can change with the change of treatment. For example, the stage Ⅲ of locally advanced breast cancer can down-staging to the stage Ⅱ after systemic treatment. Similarly, patients with stage Ⅳ can down-staging to stage Ⅱ or stage Ⅲ after systemic treatment. At this time, the patient can receive surgical treatment. Therefore, this study is to first treat de novo stage IV breast cancer patients with systemic treatment, according to the response after systemic treatment to give different treatment measures(surgery or continued systemic treatment). The investigators hope that this study will provide new ideas for the treatment of de novo stage IV breast cancer and other de novo stage IV cancers.
    Detailed Description
    This study analysed and summarized the outcomes of the primary and metastatic lesions after first-line systemic therapy in patients with newly diagnosed breast cancer and then inferred the timing of surgical treatment. According to the tumour heterogeneity characteristics between the primary and metastatic tumours, the investigators investigated the following A, B and C scenarios. After systemic therapy in patients with de novo metastatic breast cancer, the outcomes of primary and metastatic lesions were mainly divided into four categories (Fig. 1a, b, c, d). It is worth noting that after treatment, the four conditions of a, b, c, and d may alternate with the progression of the tumour or modification of the treatment plan. Therefore, only a proactive evaluation and timely treatment can identify the time window for tumour treatment. The time window for surgical treatment is important because, once missed, the tumour may progress with new metastatic lesions. Figure 1-a: Imaging study indicates complete remission of primary and metastatic tumours. Diagnostic surgical treatment can be performed to determine whether a pathologic complete response (PCR) is achieved and to develop a subsequent treatment plan. Figure 1-b: Imaging study indicates complete remission of the metastatic tumour with residual primary tumour. The state of the patient in this scenario could be equivalent to that of patients with early resectable breast cancer. Surgical treatment of the primary tumour should be promptly performed. Figure 1-c: Complete remission of the primary and residual metastatic tumour. Surgical treatment can be selected for isolated and resectable metastatic tumour. Figure 1-d: No remission or even progression of the primary and metastatic tumours. The systemic treatment plan should be replaced, and the surgical treatment should not be considered.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Breast Neoplasms, Treatment, Metastatic Breast Cancer, Survival
    Keywords
    Breast Neoplasms, de-novo metastatic breast cancer, surgical treatment

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Sequential Assignment
    Masking
    None (Open Label)
    Allocation
    Non-Randomized
    Enrollment
    362 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    1 Primary and metastatic lesions PCR
    Arm Type
    Experimental
    Arm Description
    surgery 1 Mastectomy OR Breast conserving surgery
    Arm Title
    2 Primary lesions NPCR and metastatic lesions PCR
    Arm Type
    Experimental
    Arm Description
    surgery 1 Mastectomy OR Breast conserving surgery
    Arm Title
    3 Primary lesions PCR and metastatic lesions NPCR
    Arm Type
    Experimental
    Arm Description
    surgery 2 Resection of metastasis
    Arm Title
    4 Primary lesions NPCR and metastatic lesions NPCR
    Arm Type
    Experimental
    Arm Description
    Systemic therapy Endocrine therapy or chemotherapy or targeted therapy
    Intervention Type
    Procedure
    Intervention Name(s)
    surgical treatment 1
    Other Intervention Name(s)
    surgery 1
    Intervention Description
    Mastectomy OR Breast conserving surgery
    Intervention Type
    Procedure
    Intervention Name(s)
    surgical treatment 2
    Other Intervention Name(s)
    surgery 2
    Intervention Description
    Resection of metastasis
    Intervention Type
    Drug
    Intervention Name(s)
    Systemic therapy
    Intervention Description
    Endocrine therapy or chemotherapy or targeted therapy
    Primary Outcome Measure Information:
    Title
    Overall survival
    Description
    Overall survival (OS), which defined as the time from the beginning of diagnosis of breast cancer to the death with any causes.
    Time Frame
    5 years
    Secondary Outcome Measure Information:
    Title
    Distant progression free survival
    Description
    Distant disease free survival (D-DFS), which defined as the time from the diagnosis of de novo stage IV breast cancer to the confirmed time of distant progression, or death due to any other cause.
    Time Frame
    5 years
    Title
    Locoregional progression free survival
    Description
    Defined as time between the time of diagnosis and the time of locoregional recurrence, or death occurred.
    Time Frame
    5 years

    10. Eligibility

    Sex
    Female
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    75 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Study Population Operable stage IV breast cancer patients, whose primary lesion is invasive breast cancer confirmed by pathology, and metastases can be confirmed by pathology or imaginology examination Inclusion Criteria: Operable stage IV breast cancer patients,whose primary lesion is invasive breast cancer confirmed by pathology, and metastases can be confirmed by pathology or imageology examination. ECOG-PS 0-2. Bone marrow, liver and kidney should be fully functional. Patients didn't received the locoregional surgery of the primary tumor in de novo. For the patient who accepted systematic treatment before operation, the systematic treatment must be administered within a year since diagnosed. Exclusion Criteria: Accompanied with other primary malignant tumors. More than two visceral organ involvement. Patients who can't plan for follow-up effectively and regularly. Multiple liver metastases with deranged liver function tests (SGOT/SGPT more than four times the upper normal limit).
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    YU YUE, doctor
    Phone
    +86 13564261349
    Email
    dr-array@hotmail.com
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    YU YUE, doctor
    Organizational Affiliation
    Department of thyroid and breast surgery, Changhai Hospital
    Official's Role
    Study Chair

    12. IPD Sharing Statement

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    Classified Treatment Strategy for De-novo Metastatic Breast Cancer After Systemic Adjuvant Therapy

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