Clinical trial · Interventional
Nab-P+Cb+PD1 Inhibitors as Neoadjuvant Therapy for Early TNBC
Nab-P+Cb+PD1 Inhibitor Neoadjuvant Therapy for Early TNBC: a Single Center, Non Blinded, Randomized Phase II Clinical Trial
NCT06817525CI-TRIAL-00098551recruitingPhase 2ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
We plan to explore the efficacy and safety of albumin-bound paclitaxel+carboplatin+Camrelizumab in neoadjuvant therapy for early TNBC patients, optimize the administration method and drug combination therapy.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Triple-negative Breast Cancer | Triple-Negative Breast Carcinoma | ALIAS | 0.90 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| 6*Nab-P (d 1)+6*Cb ( d 1)+6*PD1 (d 1) | Drug | — | UNRESOLVED |
| 6*Nab-P (d 1,8,15)+6*Cb ( d 1)+6*PD1 (d 1) | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- ACTIVE_COMPARATOR
- label
- 6*Chemotherapy drugs(Nab-P, d1, Cb, d1)+6*Immunosuppressants(d1)
- description
- Group A: 6\*Albumin-bound paclitaxe (260 mg/m²,d 1)+6\*Carboplatin (AUC=5, d 1)+6\*Camrelizumab (200 mg, d 1);
- interventionNames
- Drug: 6*Nab-P (d 1)+6*Cb ( d 1)+6*PD1 (d 1)
- type
- ACTIVE_COMPARATOR
- label
- 6*Chemotherapy drugs(Nab-P, d1,8,15, Cb, d1)+6*immunosuppressants(d1, )
- description
- Group B: 6\*Albumin-bound paclitaxe (125 mg/m²,d 1,8,15)+6\*Carboplatin (AUC=5, d 1 )+6\*Camrelizumab (200 mg, d 1);
- interventionNames
- Drug: 6*Nab-P (d 1,8,15)+6*Cb ( d 1)+6*PD1 (d 1)
Primary outcomes (1)
- measure
- Pathological Complete Response rate(pCR)
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
- Maximum age
- 65 Years
Show eligibility criteria text
Inclusion Criteria: 1. Age: 18-65 years old; 2. Clinically and pathologically confirmed cT2- cT4d, or cT1c with axillary lymph node metastasis; 3. Three negative type and invasive breast cancer confirmed by histopathology; Three negative breast cancer is defined as: * ER and PR negative (IHC nuclear staining\<10%) * Her-2 negative (IHC 0, 1+without FISH, or IHC 2+without FISH amplification) 4. Clinically measurable lesions: Measurable lesions displayed by ultrasound, mammography, or MR (optional) within one month prior to screening; 5. Organ and bone marrow function tests within 2 weeks before chemotherapy indicate no contraindications for chemotherapy: * Absolute value of neutrophil count ≥ 2.0 × 109/L * Hemoglobin ≥ 100g/L * Platelet count ≥ 100 × 109/L * Total bilirubin\<1.5 ULN (upper limit of normal) * Creatinine\<1.5 × ULN * AST/ALT \< 1.5×ULN; * Thyroid stimulating hormone (TSH) ≤ upper limit of normal (ULN); If there are abnormalities, T3 and T4 levels should be examined. If T3 and T4 levels are normal, they can be selected * Prothrombin time (PT) and activated partial thromboplastin time (APTT) ≤ 1.5 ULN, while meeting international standards Normalization ratio (INR) ≤ 1.5 ULN (not receiving anticoagulant therapy); 6. Cardiac ultrasound EF value ≥ 55%; 7. Women of childbearing age who tested negative for serum pregnancy test 14 days before randomization; 8. ECOG score ≤ 1 point; 9. Voluntary signing of informed consent Exclusion Criteria: 1. There is evidence of metastatic breast cancer (in order to exclude metastatic breast cancer, chest and abdomen CT and bone scanning should be performed at any time point before diagnosis and randomization; PET/CT scanning can be used as an alternative imaging inspection method); 2. Have Received chemotherapy, endocrine therapy, targeted therapy, radiation therapy, etc. for this disease; 3. The patient has a second primary malignant tumor, in addition to: fully treated skin cancer; 4. Received treatment with anti-PD-1, anti-PDL1, anti-PD-L2 drugs, or other immunotherapy; 5. Diagnosed with immunodeficiency or autoimmune diseases; 6. Severe lung or heart disease; 7. Hepatitis B and C are in active phase; 8. History of organ transplantation or bone marrow transplantation; 9. Pregnant or lactating women; 10. Due to serious and uncontrollable medical conditions, researchers believe there are contraindications to chemotherapy; 11. Screening for clinically significant bleeding symptoms or significant bleeding tendencies within the previous month; 12. Screening for arteriovenous thrombosis events such as deep vein thrombosis and pulmonary embolism that occurred within the previous 3 months.
References
Publications (0)
Data not yet available
No reference posted for this study.