Overview
This is a randomized clinical trial (OMIT study) evaluating the efficacy of metastasectomy in patients with oligo-metastatic breast cancer.
Eligibility
Inclusion Criteria:
- women aged 18-70 years old;
- ECOG score: 0-2 points;
- the expected life period is more than 3 months;
- Histologically confirmed metastatic breast cancer: locations include central lung lesions, peripheral lung lesions or liver metastases;
- PET-CT or other imaging showed patients with ≤3 metastastatic sites, involving 1-2 organs mentioned above, single lesion ≤5cm;
- according to the RECIST 1.1 edition, there is at least one measurable lesion;
- the main organs are functioning normally, meeting the following criteria: Blood
routine: Hb > 90g/L (no blood transfusion within 14 days); ANC > 1.5 x 109/L; PLT > 75
- 109/L;Liver function: total bilirubin TBIL is less than 1.5 x ULN (upper limit of normal value); ALT and AST are less than 3 x ULN; if there is liver metastasis, ALT and AST are less than 5 x ULN;Renal function: serum creatinine < 1 x ULN;
- participants voluntarily joined the study, signed informed consent, and followed up.
Exclusion Criteria:
- the number of metastastatic sites ≥ 3, or the surgeon determines that the R0 resection cannot be achieved;
- with metastatic lesions other than liver or lung
- patients with local recurrence
- palliative radiation therapy or interventional therapy have been performed previously for metastatic lesions
- has received systemic treatment for metastatic disease, such as chemotherapy, targeted therapy, endocrine therapy, immunotherapy, etc.
- pregnant or lactating women, women of childbearing age who cannot practice effective contraceptives;
- involvement in clinical trials of unlisted drugs within 4 weeks before the start of this study;
- severe cardiopulmonary insufficiency, severe liver and kidney insufficiency;