ClinicalTrials.gg
CompletedNCT03430479Updated Jan 19, 2023

Anti PD-1 Antibody With Radiation Therapy in Patients With HER2-negative Metastatic Breast Cancer

A Phase 1/2 interventional study of Cohort A in Breast Cancer, sponsored by Kyoto Breast Cancer Research Network. Completed at 1 site in Japan. Open to female participants aged 20 Years and older. Per ClinicalTrials.gov, last updated 2023-01-19.

Sponsored by Kyoto Breast Cancer Research Network · Phase 1/2, Interventional, and Treatment

From the registry’s dates

  • Registered 7 months after the study started (first participant enrolled Jun 2017, registered Feb 2018).

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Phase
Phase 1/2
Study type
Interventional
Enrollment
32
Allocation
Non-randomized
Ages
20 Years and older
Sex
Female
01

Where this study stands

Counted across the records on this site · 2026-11-14

Among 266 studies in Breast Neoplasms with a site in Japan — 51 open to participants now, 113 under way, 56 of them phase 3. Breast Neoplasms · Japan.

Enrollment
211th of 248
32 · median 281
Started
2017
with 13 others
Phase 1/2
25 of 266
12 open now
Registered
132nd of 266
by date

Among the 266 studies in Breast Neoplasms with a site in Japan, this one is the 211th largest by enrollment of the 248 interventional ones that give a count, is one of 14 that started in 2017, is one of 25 in phase 1/2, and was the 132nd registered.

Breast Neoplasms

14,829 studies on the registry are indexed under Breast Neoplasms; 3,320 are open to participants now.

Browse Breast Neoplasms studies →

Open to participants now

51 of the 266 studies in Breast Neoplasms with a site in Japan are open now. Recruiting first, the newest first:

46 more — sign in →

All 51 open studies →

A study can be open while its sites in Japan have not opened yet or have stopped. Only those recruiting at a site in Japan →

Who these studies take

Of the 2,399 Breast Neoplasms studies recruiting now, 1,570 (65%) set no upper age limit and 592 (25%) stop at 75 or younger; 103 take children under 18; 215 take healthy volunteers.

This study: 20 Years and older · female · no healthy volunteers.

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02

Study summary

The aim of this study is to evaluate the safety and efficacy of anti PD-1 antibody with radiation therapy in patients with HER2-negative metastatic breast cancer.

03

Conditions studied

  • Breast Cancer

Browse trials for

04

Who can participate

Ages eligible
20 Years and older
Sexes eligible
Female
Accepts healthy volunteers
No

Eligibility criteria

Inclusion Criteria:

  • Cohort A
  1. Documentation of ER-positive and/or PR-positive tumor (>=1% positive stained cells) .
  2. Patients must satisfy the following criteria for prior therapy:

    • Progressed during treatment or within 12 months of completion of hormone therapy.

    or Progressed while prior hormone therapy for advanced/ breast cancer. Two previous line of hormone therapy for advanced/metastatic disease is allowed.

  3. Patients who have hormone therapy that can be expected for advanced /metastatic disease.

    Cohort B

  4. Patients who have come to be non-responsive more than two
  5. Prior chemotherapy with anthracycline and taxane agent

    Cohort A and B

  6. Female patients who are or cytologically confirmed to have breast cancer
  7. Patients who have distant metastatic lesion as follow

    • More than one bone lesion for radiation therapy
  8. Patients with cancer confirmed to be -negative.(
  9. Patients with a based on 1.1.
  10. Patients aged >= 20 years at
  11. Patients with PS of 0 to 1.
  12. Patients without any severe disorder in the major organs.
  13. Patients expected to survive for ≥ 90 days.
  14. Patients of must be using an acceptable method of to avoid pregnancy and must not be breastfeeding for 18 weeks after the last dose of product
  15. Patients who have provided written informed consent themselves.

Exclusion Criteria:

-

Exclusion Criteria:

  1. Patients who have neuropathy (more than Grade 2)
  2. Patients with any active disease or a history of known autoimmune disease.
  3. Patients who has a history of pneumonitis or interstitial lung disease.
  4. Active, untreated central nervous system metastasis.
  5. Patients with pericardial effusion, pleural effusion or ascites requiring treatment
  6. Patients with uncontrolled diabetes mellitus
  7. Patients with a condition requiring systemic treatment with either or other medications within 28 days of the enrollment.
  8. Patients who has received radiotherapy within 28 days of study registration, or radiotherapy for thorax within 56 days of the enrollment.
  9. Pregnant or breast-feeding women.
  10. Prior therapy with Nivolumab, anti antibody therapies, any other antibody or drug specifically targeting T-cell co-stimulation or checkpoint pathways
  11. Patients considered ineligible for participation in this study by their attending physicians
Terms in these criteria, in plain language(16)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Adjuvant and neoadjuvant

Neoadjuvant treatment is given before the main treatment (usually surgery), often to shrink a tumour. Adjuvant treatment is given after it, to lower the chance of the cancer coming back.

Metastases

Cancer that has spread from where it began to other parts of the body. “Metastatic” cancer is cancer that has spread this way.

Line of therapy

A line of therapy is one course of treatment, which may combine several drugs. First-line is the first course given; second-line follows when that stops working or is not tolerated.

“Two prior lines” means two courses that count separately under the study’s rules — not simply two drugs. Ask the study team if you are unsure how yours are counted.

Histologically or cytologically confirmed

The diagnosis was confirmed by looking at a sample under a microscope: tissue from a biopsy or surgery (histology), or cells from a fluid or needle sample (cytology).

Your pathology report is the document that shows this.

HER2

HER2 is a protein, made from the ERBB2 gene, that drives the growth of some cancers. A study may look for a level of the protein, extra copies of the gene, or a particular change in it.

In breast cancer, protein tests are read as HER2-positive, HER2-low or HER2-negative; other cancers use their own rules. Check which test result the study requires.

Measurable disease

The amount of disease can be tracked with a defined measurement, so the study can see whether it shrinks or grows. It might be a tumour measured on a scan or, in some blood cancers such as myeloma, a marker measured in blood or urine.

The criteria or the study team say which measurement counts — having no tumour visible on a scan does not by itself rule you out.

RECIST

The standard rules for measuring tumours on CT or MRI scans, to tell whether a cancer is shrinking, stable or growing during treatment.

“Measurable disease per RECIST 1.1” usually means at least one tumour 10 mm or more at its longest on a CT scan, or a lymph node 15 mm or more across its short axis.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

ECOG performance status

A scale of how much an illness limits everyday activity. For people being assessed to join a study, scores run from 0 (fully active) to 4; lower is more active.

0
Fully active, no restrictions.
1
Limited in strenuous activity, but walking and able to do light work, such as housework or office work.
2
Walking and able to look after yourself, but unable to work; up and about more than half of waking hours.
3
Able to look after yourself only in part; in bed or a chair more than half of waking hours.
4
Unable to look after yourself at all; in bed or a chair all day.

Studies most often ask for 0–1 or 0–2. Your doctor gives the score; the WHO scale uses the same steps. The full scale also has 5, which records death.

Childbearing potential

Able to become pregnant: from the first period until menopause, unless permanently unable to through surgery (removal of the womb, or of both ovaries or both fallopian tubes).

Criteria for people of childbearing potential usually ask for a negative pregnancy test and for contraception during the study and for a time after it.

Contraception

Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.

Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.

Investigational drug or device

A drug or device being studied in a clinical trial.

It may be new, or already approved and being studied for another use, dose or form. Criteria often leave out people who took part in another study of one within a recent period, commonly 30 days or five half-lives.

Autoimmune disease

A condition in which the immune system attacks the body’s own tissues, such as rheumatoid arthritis, lupus, psoriasis, type 1 diabetes or inflammatory bowel disease.

Immunotherapy studies often leave out active autoimmune disease, and some name exceptions, such as thyroid disease on replacement hormone. Check the exceptions this study lists.

Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.

Immunosuppression

A weakened immune system. It can come from an illness, such as HIV or some blood cancers, or from medicines that turn the immune system down, for example after an organ transplant or for an autoimmune disease; steroids at higher doses count.

Read whether the line is about a condition or about medicines, and which medicines and doses it means.

PD-1, PD-L1 and checkpoint inhibitors

PD-1, PD-L1 and CTLA-4 are proteins that act as brakes on the immune system. Checkpoint inhibitors, such as pembrolizumab or nivolumab, block them so the immune system can attack a cancer.

PD-L1 can also be measured in a tumour sample. Some scores count stained tumour cells only (TPS); others also count certain immune cells (CPS). The study names the score and the minimum it uses.

05

Study design

Phase
Phase 1 / Phase 2
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Single group
Masking
Double (Participant, Care provider)
Enrollment
32 participants (actual)

Study arms

  • Experimental
    Cohort A

    Drug: Cohort A

  • Experimental
    Cohort B

    Drug: Cohort A

Interventions

  • DrugCohort A

    Radiation + Nivolumab + hormone therapy

This study also gives Nivolumab. No intervention listed here names it: that was found by reading the record.

06

What researchers measure

Primary outcomes

  1. Phase Ib : dose-limiting toxicity rate

    Time frame: 2 years

07

Study locations

1 site
  • Kyoto University Hospital
    Kyoto, 606-8507, Japan
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Jun 2017 to primary completion in Nov 2018, 17 months.

Of 166 non-industry phase 1/2 interventional studies under Breast Neoplasms, half reached primary completion within 67 months of starting (the median), counting those still running; a quarter within 45 and three quarters within 95. This study's 17 months is below that.

Counting every sponsor, half of 327 studies reached it within 61 months; a quarter within 45 and three quarters within 88.

How these figures are worked out, and which studies are left out of them.

Registered
Feb 6, 2018
First posted
Feb 13, 2018
StartActual
Jun 22, 2017
Primary completionActual
Nov 30, 2018
CompletionActual
Apr 1, 2021
Last update
Jan 19, 2023
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jan 19, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT03430479
Lead sponsor
Kyoto Breast Cancer Research Network
Responsible party
Sponsor
First posted
Feb 13, 2018
Start date
Jun 22, 2017
Primary completion
Nov 30, 2018
Completion
Apr 1, 2021
Last update
Jan 19, 2023

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2023. You cannot join it, but the record below documents what was studied.

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Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

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Studies of the drug tested here: Nivolumab

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