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NCT Number: NCT05205200

Immune Therapy in HR-positive/HER2-negative Metastatic Breast Cancer(ENIGMA)-BCTOP-L-M02

This study is a prospective, open-label, phase II clinical study for patients with HR+/HER2- advanced breast cancer.

Recruiting

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Key information

Age range

18 year–75 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 2

Primary location

Fudan University Shanghai cancer center

Shanghai, 200032, China

Location status: Recruiting

Location contact

Min U He, M.D.

CONTACT

[email protected]

021-64175590 ext. 88603

About this study

Patients with SNF2 subtype of HR+/HER2- advanced breast cancer confirmed by the Department of Pathology and Key Laboratory of Breast Cancer of Fudan University Affiliated Cancer Hospital are planned to be enrolled. Five treatment arms were set up based on the whether they have exposed to CDK4/6 inhibitors before. The main purpose is to evaluate immune therapy in SNF2 subtype of HR+/HER2- advanced breast cancer and prepare for subsequent randomized controlled phase III clinical studies with larger sample size.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Females ≥18 years and ≤ 75 years old;
  • Histologically confirmed HR + / HER2- invasive breast cancer (specific definition: immunohistochemical detection of ER> 10% tumor cell positive is defined as ER positive, PR> 10% tumor cell positive is defined as PR positive, ER and / or PR Positive is defined as HR positive; HER2 0-1 + or HER2 is ++ but negative followed by FISH detection, no amplification, defined as HER2 negative);
  • Subtype of similarity network fusion-2 (SNF-2) confirmed by the Department of Pathology and Key Laboratory of Breast Cancer of Fudan University Affiliated Cancer Hospital
  • Locally advanced breast cancer (incapable of radical local treatment) or recurrent metastatic breast cancer;
  • Measurable disease according to Response Evaluation Criteria in Solid Tumors v1.1 (RECIST v1.1); or unmeasurable lytic or mixed (osteolytic + osteoblastic) bone lesions in the absence of measurable lesions;
  • Has adequate bone marrow function: absolute neutrophil count > 1.5x10ˆ9 /L; platelet count > 75x10ˆ9 /L, hemoglobin > 9g/dL;
  • Patients had received no previous chemotherapy or targeted therapy for metastatic disease
  • Has adequate liver function and kidney function: serum creatinine
  • ECOG score ≤ 2 and life expectancy ≥ 3 months;
  • Participants voluntarily joined the study, has signed informed consent before any trial related activities are conducted, has good compliance and has agreed to follow-up.

Exclusion criteria

  • Treatment with chemotherapy, radiotherapy, immunotherapy or surgery (outpatient clinic surgery excluded) for metastatic disease
  • Symptomatic, untreated, or actively progressing CNS metastases(glucocorticoids or mannitol needed to control symptoms);
  • Significant cardiovascular disease(including congestive heart failure, angina pectoris, myocardial infarction or ventricular arrhythmia in the last 6 months);
  • is pregnant or breast feeding;
  • Malignant tumors in the past five years (except cured skin basal cell carcinoma and cervical carcinoma in situ).
  • History of autoimmune disease
  • Positive test for human immunodeficiency virus
  • Active hepatitis B or hepatitis C
  • Uncontrolled pleural effusion and ascites
  • Thyroid dysfunction.

Treatment and study plan

SHR-1316

Drug

PD-L1 antibody

SHR6390

Drug

CDK4/6 inhibitor

Nab paclitaxel

Drug

Albumin bound paclitaxel

SERD

Drug

Fulvestrant

AI

Drug

aromatase inhibitor

Primary outcomes

  1. PFS

    Time frame: Randomization until the first occurrence of disease progression or death from any cause, which ever occurs first, through the end of study (approximately 5 years)

    time to progressive disease (according to RECIST1.1)

Secondary outcomes

  1. ORR

    Time frame: Randomization until the first occurrence of disease progression or death from any cause, which ever occurs first, through the end of study (approximately 5 years)

    The proportion of participants whose best outcome is complete remission or partial remission (according to RECIST1.1)

  2. CBR

    Time frame: Randomization until the first occurrence of disease progression or death from any cause, which ever occurs first, through the end of study (approximately 5 years)

    the percentage of subjects with CR+PR+SD and last more than 24 weeks in all of the

  3. OS

    Time frame: Randomization to death from any cause, through the end of study (approximately 5 years)

    time to death due to any cause

Study contacts

Contact information is provided by the study sponsor or research team.

Zhi-Ming Shao

CONTACT

[email protected]

86-021-64175590 ext. 8888

Zhong-Hua Wang

CONTACT

Sponsors and collaborators

Lead sponsor

Fudan University

Other

Collaborators

  • Affiliated Hospital of Nantong University
  • Chongqing University Cancer Hospital
  • First Affiliated Hospital Xi'an Jiaotong University
  • First Hospital of China Medical University
  • Fujian Medical University Union Hospital
  • Liaoning Cancer Hospital & Institute
  • Ningbo Medical Center Lihuili Hospital
  • Northern Jiangsu People's Hospital
  • Peking University Cancer Hospital & Institute
  • Shanghai 6th People's Hospital
  • Shanghai First Maternity and Infant Hospital
  • Sun Yat-sen University

Registry information

Official study title

Immune Therapy in HR-positive/HER2-negative Metastatic Breast Cancer

Important dates

Study start
2022
Primary completion
2025
Study completion
2026
First posted
Jan 25, 2022
Registry last updated
Feb 8, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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