Study of Camrelizumab Plus Chemotherapy as Neoadjuvant Therapy in Participants With Triple Negative Breast Cancer (TNBC)

• Status: Not yet recruiting
• Trial end date: 2025-06-30
• Target enrollment: 0
• Participant gender: Female

Summary

The purpose of this study is to evaluate the efficacy and safety of Camrelizumab in Combination With Nab-Paclitaxel and carboplatin as Neoadjuvant Therapy in Participants With Triple Negative Breast Cancer (TNBC).

• Phase: Phase 2/Phase 3
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Tianjin Medical University Cancer Institute and Hospital
• Collaborator: Jiangsu HengRui Medicine Co., Ltd.
• Treatments: Carboplatin; Paclitaxel

Criteria

Inclusion Criteria:

• Newly diagnosed breast cancer;

• 18-75 Years, female;

• ECOG Performance Status of 0-1;

• Life expectancy is not less than 3 months;

• Histologically documented TNBC (negative human epidermal growth factor receptor 2 [HER2], estrogen receptor [ER], and progesterone receptor [PgR] status);

• Tumor stage: II-III;

• At least one measurable lesion according to RECIST 1.1;

• Adequate hematologic and organ function.;

• Must be willing to use an adequate method of contraception for the course of the study.

Exclusion Criteria:

• Stage Ⅳ (metastatic) breast cancer or bilateral breast cancer;

• Inflammatory breast cancer;

• Has received prior any anti-tumor therapy within the past 12 months prior to signing informed consent, including chemotherapy, targeted therapy, radiation therapy, immunotherapy, biotherapy and TACE;

• Has received prior therapy with an anti-programmed cell death protein 1 (anti-PD-1), anti-programmed death - ligand 1 (anti-PD-L1), or anti-PD-L2 agent or with an agent directed to another co-inhibitory T-cell receptor (e.g., cytotoxic T-lymphocyte-associated antigen-4 [CTLA-4];

• Has a history of invasive malignancy ≤5 years prior to signing informed consent except for adequately treated basal cell or squamous cell skin cancer or in situ cervical cancer;

• Major surgical procedure within 4 weeks prior to initiation of study treatment;

• Active or history of autoimmune disease or immune deficiency diseases except history of autoimmune-related hypothyroidism, controlled Type 1 diabetes mellitus;

• Has a history of (non-infectious) pneumonitis, interstitial lung disease or uncontrollable systematicness diseases;

• Administration of a live attenuated vaccine within 28 days prior to initiation of study treatment or anticipation of need for such a vaccine during the study;

• Has a known history of Human Immunodeficiency Virus (HIV);

• Has known active Hepatitis B, Hepatitis C or Autoimmune hepatitis;

• Severe infections within 4 weeks prior to initiation of study treatment, including but not limited to hospitalization for complications of infection, bacteremia, or severe pneumonia;

• Has active infection (CTCAE≥2) needed the treatment of antibiotic within 2 weeks prior to initiation of study treatment;

• Has evidence of active tuberculosis within 1year prior to initiation of study treatment;

• Prior allogeneic stem cell or solid organ transplantation;

• Pre-existing motor or sensory neuropathy of a severity≥grade 2;

• Has significant cardiovascular disease;

• Has a known hypersensitivity to the components of the study treatment or other hypersensitivity reactions to chimeric or humanized antibodies or fusion proteins;

• Female patients during pregnancy and lactation, fertile women with positive baseline pregnancy tests or women of childbearing age who are unwilling to take effective contraceptive measures throughout the trial;

• History of neurological or psychiatric disorders, including epilepsy or dementia;

• Any other situation evaluated by researchers.