Overview

Exploratory Study of Advanced Breast Cancer in HER2 Positive Patients With Failure of Multi-line Therapy Treated by Combination of Inetetamab (Cipterbin) + PD-1 Inhibitor Combined With Utidelone.

Status:
Recruiting
Trial end date:
2022-10-30
Target enrollment:
0
Participant gender:
Female
Summary
This study plans to explore the efficacy and safety of chemotherapy combined with inetetamab and PD-1 inhibitors in HER2 positive advanced breast cancer who failed to receive trastuzumab and TKIs, and explore the dominant population of dual antibody combination to further guide the precise and individualized treatment of advanced HER2 positive breast cancer.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Henan Cancer Hospital
Treatments:
Immune Checkpoint Inhibitors
Criteria
Inclusion Criteria:

1. Age: 18-75 years old female patients;

2. The results showed that HER-2 was positive at least once in patients with recurrent
and metastatic breast cancer confirmed by pathology: HER-2 (+ + +) was confirmed by
immunohistochemistry; if HER-2 (+ +), fish / CISH was required to confirm HER-2
amplification;

3. Previous treatment (including neoadjuvant, adjuvant and rescue therapy) received at
least trastuzumab and TKIs;

4. It is allowed that the previous rescue chemotherapy does not exceed 3 lines, and must
be disease progression before being included in the study; it is allowed to receive
rescue endocrine therapy; chemotherapy allows to receive one of the chemotherapy of
albumin binding paclitaxel, vinorelbine, gemcitabine, capecitabine and aribrin;

5. At least one target lesion can be defined according to RECIST 1.1, and the target
lesion has not received radiotherapy (or other local treatment), unless it progresses
after the treatment;

6. Before the study, chemotherapy and targeted therapy must be completed for at least 2
weeks, and endocrine therapy and antiangiogenic drug treatment for 1 week;

7. ECoG PS: 0-1 points;

8. The expected survival time was more than 3 months;

9. The function of the main organs is normal, that is to say, it meets the following
standards:

1)Blood routine examination standard should meet (no blood transfusion and blood products
within 14 days, not used G-CSF and other hematopoietic stimulating factors were corrected)

- Hb≥90g/L;

②ANC≥1.5×109/L;

③PLT≥75×109/L; 2)Biochemical examination should meet the following standards:

- TBIL<1.5×ULN;

- Alt, AST < 2.5 × ULN, liver metastasis < 5 × ULN;

- Bun and Cr ≤ 1 × ULN or creatinine clearance rate ≥ 50ml / min (Cockcroft
Gault formula).

10.Women of childbearing age must have a pregnancy test (serum) within 7
days before enrollment, and the results are negative, and they are willing
to use appropriate contraceptive methods during the trial and within 8 weeks
after the last administration of the trial drug; 11.The subjects volunteered
to join the study, signed the informed consent form, had good compliance and
cooperated with the follow-up.

Exclusion Criteria:

1. Symptomatic, uncontrolled brain metastases or leptomeningeal metastases.However,
patients with stable condition after local treatment for 4 weeks could be enrolled;

2. There was effusion in the third space which could not be controlled by drainage or air
pressure;

3. Interstitial lung disease, non-infectious pneumonia, memory pneumonia, pulmonary
fibrosis and other diseases;

4. Those who have a history of live attenuated vaccine vaccination in the 28 days before
the first study medication or are expected to receive live attenuated vaccine in the
study;

5. Other malignant tumors in the past 3 years, excluding cervical carcinoma in situ,
basal cell carcinoma of skin or squamous cell carcinoma of skin;

6. Patients with hypertension who could not be reduced to normal range after
antihypertensive drug treatment (systolic blood pressure > 140 mmHg, diastolic blood
pressure > 90 mmHg);

7. Suffering from serious or uncontrollable diseases, including but not limited to:

1) Active viral infection, such as HIV, HBV active phase (HBsAg positive and HBV-DNA ≥ 103,
hepatitis C antibody positive); 2) Previous severe cardiovascular diseases: uncontrollable
hypertension; myocardial infarction, unstable arrhythmia, congestive heart failure,
pericarditis, myocarditis, etc. in the first six and six patients; according to NYHA
standard, grade III ~ IV cardiac insufficiency, or left ventricular ejection fraction
(LVEF) < 50% according to NYHA standard; 8.Patients with a history of psychotropic
substance abuse and unable to quit or with mental disorders; 9.According to the judgment of
the researchers, there are other patients with accompanying diseases that seriously
endanger the safety of patients or affect patients to complete the study; 10.Pregnant or
lactating women; 11.The researchers think it is not suitable for the participants.