Metastasis-directed Therapy for Oligometastases of Breast Cancer

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18-80
SponsorTokyo Medical and Dental University

About this trial

OLIGAMI trial is a multi-institutional, two-arm, open-label, randomized controlled phase III trial being conducted with the participation of 50 hospitals belonging to Japan Clinical Oncology Group. After the first registration, all patients will be performed in a 12-week, subtype-specific, systemic therapy consisting of CDK4/6 inhibitors with hormonal therapy for luminal BC, docetaxel with trastuzumab and pertuzumab for HER2-positive BC, chemotherapy with immune checkpoint inhibitors for triple-negativeBC expressing PD-L1, and olaparib for cases harboring BRCA mutations. For other triple-negative BC, chemotherapy will be administered. If this 12-week systemic therapy does not cause any progression or complete response, patients proceed to second registration for randomization; arm A continues same systemic therapy alone, and arm B performs MDT followed by same systemic therapy. The MDT will involve either RT or surgery, and RT will involve mainly SBRT and partly conventional RT.

Eligibility criteria

Qualifiers

Histologically diagnosed as invasive breast cancer. Biopsy from oligometastasis is desirable but not required.

Histologically proven positive/negative for ER, PgR, and HER2, and classified as luminal, HER2-positive, or TN breast cancer.

One of the following <1> to <4>; <1>In case of no history of breast cancer in the past, either (i) or (ii) below.

Diagnosed with advanced breast cancer with oligometastasis by neck to pelvis enhanced CT, FDG-PET (PET/CT), and brain enhanced MRI.

Disqualifiers

Active malignancies curatively treated with no evidence of disease for >= 5 years prior to randomization.

Infection with care.

Fever up 38 degrees Celsius.

Childbearing potential, delivery after 28 days, breastfeeding

Trial design

Treatments tested in this trial

  • Systemic therapy for 12 weeks after primary registration
  • Radiation therapy (SBRT/conventional RT)
  • Surgery
  • Same systemic therapy after secondary registration

Treatment groups

340 Participants
are divided into 2 treatment groups