This trial is testing pembrolizumab (pembro) + chemotherapy (chemo) in people with certain types of breast cancer called hormone receptor positive/ human epidermal growth factor receptor 2-negative (HR+/HER2-) locally advanced inoperable or metastatic breast cancer (MBC).

Phase 1

• Conditions: Treatment of patients with HR+/HER2- locally recurrent inoperable or MBC whose tumors express PD-L1; MedDRA version: 20.0Level: LLTClassification code 10027475Term: Metastatic breast cancerSystem Organ Class: 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps); MedDRA version: 21.1Level: LLTClassification code 10072740Term: Locally advanced breast cancerSystem Organ Class: 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps); MedDRA version: 23.0Level: PTClassification code 10083232Term: HER2 negative breast cancerSystem Organ Class: 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps); Therapeutic area: Diseases [C] - Cancer [C04]

• Registration Number: EUCTR2020-005407-38-PL
• Lead Sponsor: Merck Sharp & Dohme LLC

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2021-04-14
• Last Update Posted: 26 February 2024

Recruitment & Eligibility

• Status: ot Recruiting
• Sex: All
• Target Recruitment: 800

Inclusion Criteria

1. Has locally recurrent inoperable or metastatic HR+/HER2- breast
cancer, which has not been previously treated with cytotoxic
chemotherapy in the noncurative setting.
2. Has progressed on prior endocrine therapy and is now a
chemotherapy candidate, meeting the characteristics in regard to
previous treatments of one of the following 4 groups:
GROUP 1: Has progressed on 2 or more lines of endocrine therapy for
advanced/metastatic HR+/HER2-disease, with at least 1 given in
combination with a CDK4/6 inhibitor. Prior treatment with mTOR and/or
PI3-K inhibitors is allowed.
OR
GROUP 2a: Has progressed on 1 line of previous endocrine therapy for
advanced/metastatic disease AND had a disease recurrence within 24
months of definitive surgery for the primary tumor and while on
adjuvant endocrine therapy. Prior use of CDK4/6 inhibitors is required,
either in the adjuvant and/or metastatic setting. Prior treatment with
mTOR and/or PI3-K inhibitors is allowed.
OR
GROUP 2b: Has progressed within 12 months of starting 1 line of
endocrine therapy with a CDK4/6 inhibitor for advanced/metastatic
HR+/HER2- disease.
OR
GROUP 3: If no prior treatment with a CDK4/6 inhibitor for
advanced/metastatic disease and/or early stage disease (adjuvant),
participants must have progressed within 6 months of starting 1 line of
endocrine therapy with or without an mTOR or PI3-K inhibitor for
metastatic disease AND had a relapse within 24 months of definitive
surgery for primary tumor and while receiving adjuvant endocrine
therapy.
3. Has presented a documented radiographic disease progression as
assessed by the investigator and/or histology [biopsy or cytology] for
participants presenting with new metastatic lesions) during or after the
last administered endocrine therapy prior to entering the study.
o There is evidence of radiographic disease progression based on
investigator review of at least 2 scans following initiation of the last
endocrine therapy (or combination) for metastatic disease.
o A laboratory report indicating tumor marker elevation cannot be used
as documentation of local or distant disease recurrence.
4. Is a chemotherapy candidate that meets the following criteria:
o Participants who received taxane and/or anthracyclines (or
capecitabine) in the neoadjuvant/adjuvant setting can be treated with
same class of chemotherapy (taxane or anthracycline or capecitabine) if
=12 months have elapsed between the completion of treatment with
curative intent and first documented local or distant disease recurrence.
o Participants who will be selected to receive liposomal doxorubicin
must have a LVEF of at least 50% or above the institution limit of
normal, as assessed by ECHO or MUGA scan performed prior to the first
dose administration.
5. Provides a new or the last obtained core biopsy, preferably consisting
of multiple cores, taken from a locally recurrent or a distant (metastatic)
lesion not previously irradiated for central determination of hormone
receptor status (ER and PgR), HER2, and PD-L1 status.
6. Has centrally confirmed PD-L1 CPS =1 and HR+ (ER and/or PgR)
/HER2– breast cancer as defined by the most recent ASCO/CAP
guidelines on most recent tumor biopsy.
7. Has an ECOG Performance Status of 0 or 1, as assessed within 7 days
prior to the first dose of study treatment.
8. Demonstrates adequate organ function, within 10 days prior to the
start of study treatment.
9. Participants are at least 18 years of age.
10. Male participants are eligible to participa

Exclusion Criteria

1. Has breast cancer amenable to treatment with curative intent.
2. Has a history or current evidence of any condition, therapy, or
laboratory abnormality that is specifically contraindicated per the
current locally-approved labeling, that might confound the results of the study, interfere with the participant's involvement for the full duration of the study, or is not in the best interest of the participant to be involved, in the opinion of the treating investigator.
3. Has significant cardiac disease.
4. Has advanced/metastatic, symptomatic visceral spread at risk of
rapidly evolving into life-threatening complications, such as
lymphangitic lung metastases, bone marrow replacement,
carcinomatous meningitis, significant symptomatic liver metastases,
shortness of breath requiring supplemental oxygen, symptomatic pleural effusion requiring supplemental oxygen, symptomatic pericardial effusion, symptomatic peritoneal carcinomatosis, or the need to achieve rapid symptom control.
5. Has skin only disease. Participants who have metastatic disease
fulfilling the previous criteria in addition to skin disease can be enrolled.
6. Has a known germline BRCA mutation and has not received previous
treatment with PARP inhibition either in the adjuvant or metastatic
setting (where available and not medically contraindicated). Singleagent PARP inhibitor therapy does not count as a line of endocrine therapy.
7. Has received prior chemotherapy for locally recurrent inoperable or
metastatic breast cancer.
8. Has received prior therapy with an anti-PD-1, anti-PD-L1, or anti-PDL2 agent or with an agent directed to another stimulatory or coinhibitory T-cell receptor.
9. Has received prior systemic anticancer therapy with other
investigational agents within 4 weeks prior to randomization.
10. Has received prior radiotherapy within 2 weeks of start of study
intervention or radiation-related toxicities requiring corticosteroids.
11. Has received a live or live attenuated vaccine within 30 days prior to
the first dose of study intervention.
12. Has received an investigational agent or has used an investigational
device within 4 weeks prior to study intervention administration.
13. Has a diagnosis of immunodeficiency or is receiving chronic systemic steroid therapy or any other form of immunosuppressive therapy within 7 days prior the first dose of study intervention.
14. Has a known additional malignancy that is progressing or has
required active treatment within the past 3 years.
15. Has known active CNS metastases. Participants with known brain
metastases may participate provided that the brain metastases have
been previously treated (except with chemotherapy) and are
radiographically stable per local radiology/investigator review. To
demonstrate radiographic stability of previously treated brain
metastases, a minimum of 2 posttreatment brain scan assessments are
required:
1) The first brain scan must be acquired after treatment of brain
metastases has been completed;
2) The second brain scan must be obtained during screening and =4
weeks after the previous posttreatment brain scan.
16. Has diagnosed carcinomatous meningitis.
17. Has severe hypersensitivity (=Grade 3) to pembrolizumab and/or
any of its excipients. Or has any hypersensitivity to the planned
chemotherapy agent and/or any of their excipients.
18. Has an active autoimmune disease that has required systemic
treatment in past 2 years except replacement therapy.
19. Has a history of pneumonitis/inte

Study & Design

• Study Type: Interventional clinical trial of medicinal product
• Study Design: Not specified