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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.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record

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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
What is being tested?
Systemic therapy for 12 weeks after primary registration, Radiation therapy (SBRT/conventional RT) and Surgery
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.
Show all 13Show fewer
  • 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.

Toshiyuki Ishiba, M.D.Ph.D. contact

+81-3-5803-2101

ishsrg2@tmd.ac.jp

Ikuno Nishibuchi, M.D.Ph.D. contact

Japan1 site, 1 recruiting
  • Institute of Science Tokyo

    Bunkyō-Ku, Tokyo, 113-8510

    Toshiyuki Ishiba, +81-3-5803-2101, ishsrg2@tmd.ac.jp

    Recruiting

Other trials in Japan

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.

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
    1. 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
    2. Recurrence after completion of postoperative endocrine therapy PRE: AI + CDK +LHRH agonist, or FUL + CDK +LHRH agonist POST: AI + CDK, or FUL + CDK
    3. 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.

    1. PD-L1 negative - following a) or b)
    2. Taxane (naive for taxane)
    3. S-1 or Capecitabine or Eriblin (previously treated with taxane)
    4. PD-L1 positive - following a) or b)
    5. Pembrolizumab + Gemcitabine + Carboplatin
    6. Atezolizumab + Nab-paclitaxel
    7. 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
    1. 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
    2. Recurrence after completion of postoperative endocrine therapy PRE: AI + CDK +LHRH agonist, or FUL + CDK +LHRH agonist POST: AI + CDK, or FUL + CDK
    3. 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.

    1. PD-L1 negative - following a) or b)
    2. Taxane (naive for taxane)
    3. S-1 or Capecitabine or Eriblin (previously treated with taxane)
    4. PD-L1 positive - following a) or b)
    5. Pembrolizumab + Gemcitabine + Carboplatin
    6. Atezolizumab + Nab-paclitaxel
    7. BRCA-mutation positive Olaparib
Study groups in NCT06135714
Study groupRoleWhat they receive
Arm A: Standard of carePlacebo comparatorContinuation 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 careExperimentalMetastasis-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.

  1. Overall survival after second registration

    Measured: 5 years

Secondary outcomes (7)
  1. Overall survival after primary registration

    Measured: 5 years

  2. Progression-free survival

    Measured: 5 years

  3. Progression site (oligometastasis, lesion other than oligometastasis)

    Measured: 5 years

  4. Oligometastatic progression-free survival for each definitive local therapy (group B only)

    Measured: 5 years

  5. Adverse event rate

    Measured: 5 years

  6. Serious adverse event rate

    Measured: 5 years

  7. 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.

  1. First posted18 Nov 2023
  2. Study start8 Nov 2023
  3. Primary completion8 Nov 2029 (estimated)
  4. Study completion31 Oct 2035 (estimated)

Resources

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)
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

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