Breast CancerPhase 3OLIGAMINCT06135714
Metastasis-directed Therapy for Oligometastases of Breast Cancer
A Phase 3 study testing Systemic therapy for 12 weeks after primary registration, Radiation therapy (SBRT/conventional RT) and Surgery in people with Breast Cancer and Oligometastasis, run by Tokyo Medical and Dental University at 1 site in Japan.
Trial summary
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. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Breast Cancer, Oligometastasis, Metastatic Breast Cancer
- What is being tested?
- Systemic therapy for 12 weeks after primary registration, Radiation therapy (SBRT/conventional RT) and Surgery
- Type of treatment
- Injection or infusion, Surgery or procedure
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 146 participants
- Where
- 1 siteJapan
- Study dates
- 8 Nov 2023to 31 Oct 2035
- Phase
- Phase 3
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
None listed.
Who cannot join
- 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
- Mental disorders.
- Continuously take steroids or immunosuppressive drugs.
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- Unstable angina or history of cardiac infarction within 6months.
- Uncontrolled Hypertension.
- Uncontrolled Diabetes mellitus.
- Congestive heart failure deserved class II of New York Heart Association (NYHA), uncontrolled Dilated or Hypertrophic cardiomyopathy.
- Severe arrhythmia need to cure (except Atrial fibrillation, Paroxysmal supraventricular tachycardia)
- Interstitial pneumonia, pulmonary fibrosis, severe emphysema diagnosed chest CT scan.
- HBs Ag+
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Ikuno Nishibuchi, M.D.Ph.D. contact
Japan1 site, 1 recruiting
- Recruiting
Institute of Science Tokyo
Bunkyō-Ku, Tokyo, 113-8510
Toshiyuki Ishiba, +81-3-5803-2101, ishsrg2@tmd.ac.jp
About this study
Official title: a Randomized Trial for OLIGo Metastases Breast cAncer With or Without Metastasis-dIrected Therapy
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.
Read the detailed description
A brief background discussion: Oligometastases were initially described as a concept bridging localized disease with widespread distant metastases, but a consensus on its definition has yet to be reached. Recently, the term "metastasis-directed therapy" (MDT) was coined to encompass local therapy for distant metastases, including surgery and radiation therapy (RT), especially stereotactic body radiation therapy (SBRT). Though OLIGO-BC1 and SABR-COMET have indicated the potential benefits of MDT for oligometastases , NRG-BR002 revealed no significant difference in progression-free survival (PFS). As a definitive conclusion to this clinical question has not been reached, there is an increasing demand for phase III trials focusing on breast cancer (BC). We planned the JCOG2110, also called as OLIGAMI trial. Trial design: 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: OLIGAMI trial will encompass all subtypes of advanced BC. The key criteria of the first registration are as follows: 1) Histologically diagnosed as invasive BC. Biopsy from oligometastases is desirable but not required. 2) Diagnosed with advanced BC with oligometastases by neck to pelvis enhanced CT, FDG-PET,and brain enhanced MRI. 3) Oligometastases defined as: (i) Maximum diameter of each tumor is 3 cm or less. (ii) Total number of 3 or less. (iii) In case of brain metastasis, maximum diameter is 2 cm or less and asymptomatic. 4) The patient with local recurrence is included. 5) De novo stage IV BC is included. The criteria of secondary registration are as follows: 1) The planned number of courses of systemic therapy has been performed. 2) No progression or new distant metastasis by response evaluation. 3) At least one oligometastasis remains. Specific Aims: OLIGAMI trial aims to confirm the superiority of MDT to systemic therapy for oligometastases of BC. The primary endpoint is overall survival (OS) after randomization, while the secondary endpoints include OS after first registration, PFS, progression site (oligometastases vs. non-oligometastases), PFS specifically related to MDT (restricted arm B), proportion of adverse events and serious adverse events, and the non-progression proportion of health-related quality of life. Statistical methods: The sample size was calculated as 268 to detect 12% of 5-year OS difference with a one-sided alpha of 0.05, power of 70%, 3 years of accrual, and 5 years of follow up. Therefore, we assumed the planned sample size for second registration for randomization as 270. We set the number of first registration as 340, assuming that there may be some patients with progression or complete response after the systemic therapy for 12 weeks. Present accrual and target accrual: The patient accrual will start in November 2023. Enrolment of 340 patients for first registration is planned over a 3-year accrual period.
- Conditions
- Breast Cancer, Oligometastasis, Metastatic Breast Cancer
- Being tested
- Systemic therapy for 12 weeks after primary registration, Radiation therapy (SBRT/conventional RT), Surgery, Same systemic therapy after secondary registration
- Keywords
- SBRT, Surgery, Stereotactic Body Radiation Therapy, Metastasis-directed Therapy
- Medical subject headings
- Breast Neoplasms
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Systemic therapy for 12 weeks after primary registrationDrug
- Luminal BC
- Denovo stage IV Premenopausal(PRE): Aromatase inhibitor(AI) + CDK4/6 inhibitor(CDK) +LHRH agonist, or Fulvestrant(FUL) + CDK4/6 inhibitor +LHRH agonist Postmenopausal(POST): AI + CDK
- Recurrence after completion of postoperative endocrine therapy PRE: AI + CDK +LHRH agonist, or FUL + CDK +LHRH agonist POST: AI + CDK, or FUL + CDK
- Recurrence during postoperative endocrine therapy PRE: FUL + CDK +LHRH agonist, or AI + CDK +LHRH agonist POST: FUL + CDK
- HER2-positive BC
Pertuzumab + Trastuzumab + Taxane (docetaxel or paclitaxel)
・Triple negative BC.
- PD-L1 negative - following a) or b)
- Taxane (naive for taxane)
- S-1 or Capecitabine or Eriblin (previously treated with taxane)
- PD-L1 positive - following a) or b)
- Pembrolizumab + Gemcitabine + Carboplatin
- Atezolizumab + Nab-paclitaxel
- BRCA-mutation positive Olaparib
Radiation therapy (SBRT/conventional RT)Procedure or surgery
Brain: 18-24Gy/1Fr. or 27Gy/3Fr. or 30Gy/5Fr. Lung: 42Gy/4Fr.(peripheral) or 50Gy/8Fr.(central) or 60Gy/25Fr.(ultra central) Liver/Adrenal: 40Gy/5Fr. Bone: 35Gy/5Fr. Distant lymph node: 45/10Fr. or 60Gy/25Fr.
SurgeryProcedure or surgery
Surgery for the oligometastases
Same systemic therapy after secondary registrationDrug
- Luminal BC
- Denovo stage IV Premenopausal(PRE): Aromatase inhibitor(AI) + CDK4/6 inhibitor(CDK) +LHRH agonist, or Fulvestrant(FUL) + CDK4/6 inhibitor +LHRH agonist Postmenopausal(POST): AI + CDK
- Recurrence after completion of postoperative endocrine therapy PRE: AI + CDK +LHRH agonist, or FUL + CDK +LHRH agonist POST: AI + CDK, or FUL + CDK
- Recurrence during postoperative endocrine therapy PRE: FUL + CDK +LHRH agonist, or AI + CDK +LHRH agonist POST: FUL + CDK
- HER2-positive BC
Pertuzumab + Trastuzumab + Taxane (docetaxel or paclitaxel)
・Triple negative BC.
- PD-L1 negative - following a) or b)
- Taxane (naive for taxane)
- S-1 or Capecitabine or Eriblin (previously treated with taxane)
- PD-L1 positive - following a) or b)
- Pembrolizumab + Gemcitabine + Carboplatin
- Atezolizumab + Nab-paclitaxel
- BRCA-mutation positive Olaparib
| Study group | Role | What they receive |
|---|---|---|
| Arm A: Standard of care | Placebo comparator | Continuation of systemic drug therapy. Receives: Drug: Systemic therapy for 12 weeks after primary registration; Drug: Same systemic therapy after secondary registration |
| Arm B: Metastasis-directed therapy followed by Standard of care | Experimental | Metastasis-directed therapy (radiation or surgery for oligometastasis) + systemic drug therapy. Receives: Drug: Systemic therapy for 12 weeks after primary registration; Procedure: Radiation therapy (SBRT/conventional RT); Procedure: Surgery; Drug: Same systemic therapy after secondary registration |
What is being measured
The primary outcome is the main question the study is designed to answer.
Overall survival after second registration
Measured: 5 years
Secondary outcomes (7)
Overall survival after primary registration
Measured: 5 years
Progression-free survival
Measured: 5 years
Progression site (oligometastasis, lesion other than oligometastasis)
Measured: 5 years
Oligometastatic progression-free survival for each definitive local therapy (group B only)
Measured: 5 years
Adverse event rate
Measured: 5 years
Serious adverse event rate
Measured: 5 years
HR-QOL non-worsening rate
Measured: 5 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted18 Nov 2023
- Study start8 Nov 2023
- Primary completion8 Nov 2029 (estimated)
- Study completion31 Oct 2035 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Breast CancerStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 3
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- 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.
- Masking
- None (open label)
- Enrolment
- 146 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Tokyo Medical and Dental University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Toshiyuki Ishiba, M.D.Ph.D., Institute of Science Tokyo Hospital
- Investigators
- Toshiyuki Ishiba, M.D.Ph.D., Principal investigator, Institute of Science TokyoTadahiko Shien, M.D.Ph.D., Study chair, Okayama UniversityIkuno Nishibuchi, M.D.Ph.D., Principal investigator, Hiroshima UniversityFumitaka Hara, M.D.Ph.D., Principal investigator, The Cancer Institute Hospital of Japanese Foundation for Cancer ResearchNaoto Shikama, M.D.Ph.D., Study chair, Juntendo University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06135714
- Sponsor's protocol ID
- JCOG2110
- Acronym
- OLIGAMI
- Status last verified
- Oct 2026
- First submitted
- 13 Nov 2023
- Last updated
- 7 Oct 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes
Publications
Sasaki K, Ishiba T, Nishibuchi I, Hara F, Sekino Y, Machida R, Shibata T, Kawahara D, Sagara Y, Naito Y, Terata K, Ozaki Y, Shimomura A, Sakai T, Shigematsu H, Sudo K, Nozawa K, Yoshimura M, Shikama N, Mizowaki T, Shien T. A randomized controlled trial of metastasis-directed therapy for oligometastases in breast cancer: OLIGAMI trial (JCOG2110). Jpn J Clin Oncol. 2026 May 7;56(5):659-665. doi: 10.1093/jjco/hyag019.
PubMed 41615067