Clinical Study of Xinmailong Injection on Reducing Cardiovascular Toxicity in Adjuvant Chemotherapy in Breast Cancer

Peking Union Medical College60 enrolled

Overview

Totally 60 subjects will be included in the study. The present study was aimed to observe and evaluate the effect of Xinmailong injection on reducing cardiovascular toxicity associated with adjuvant chemotherapy after breast cancer surgery. The primary endpoint was 6 months of cardiac safety. Secondary endpoints included 3 months of cardiac safety, adverse events (AE), severe adverse events (SAE), and DFS.

After signing the informed consent, the patients in the control group will receive Epirubicin 45mg/m2 d1, 2 + cyclophosphamide 600mg/ m2 d1, repeated every 14 or 21 days for 4 cycles, followed by paclitaxel 175 mg/m2 (or docetaxel 75 mg/m2) on day 1, repeated every 21 days for 4 cycles. Patients in the Xinmailong group were given 5 mg/kg of Xinmailong injection every cycle on d0, d1, d2, d3, d4 on the same chemotherapy regimen as those in the control group. The patients-general condition, vital signs, blood routine, liver and kidney function, electrocardiogram, myocardial enzymes, troponin, BNP and echocardiography should be examined every week. Breast ultrasound were performed every week. Chest CT were evaluated after 8 cycles of chemotherapy. After adjuvant chemotherapy, adjuvant radiotherapy and endocrine therapy were given according to the situation, and long-term survival was observed. The patients will be followed up for 5 years, once every 6 months with in 1-3 years, once every 12 months within 4-5 years.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Breast Neoplasms Cardiac Event Chemotherapeutic Toxicity

Interventions

Xinmailong InjectionDRUG

Xinmailong injection is extracted, separated, purified and refined from Periplaneta americana. It is the second class of new drugs and the only small molecular bioactive peptide preparation approved by the State Pharmaceutical Administration (P.R.China) for the prevention and treatment of heart failure. Its main constituents include complex nucleoside bases and binding amino acids.

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: 1. age ≥18 years, female; 2. after radical mastectomy, EC - T adjuvant chemotherapy is planned. 3. No relevant treatment (such as antineoplastic therapy, immunotherapy, etc.) that may affect the outcome of treatment was received before admission. 4. ECOG PS score: 0-2 points; 5. Laboratory criteria: * white blood cells were more than 4 x 109 /L, and neutrophil count (ANC) was more than 1.5 x 109 /L. * platelet (\>100 \*109/L); hemoglobin (\>10g/dL); serum creatinine (\<1.5 \*normal value) upper limit (ULN); aspartate aminotransferase (AST) (\<2.5 \*ULN); alanine aminotransferase (ALT) (\<2.5 \*ULN); total bilirubin (\<1.5 \*ULN); serum creatinine (\<1.5 \*ULN); the volunteers voluntarily joined the study, signed informed consent, and had good compliance and follow-up. Exclusion Criteria: 1. cockroach or xinmailong allergy (including xinmailong test positive). 2. Pregnant or lactation woman 3. severe bleeding tendency; 4. With mental disease 5. With severe infection or active gastrointestinal ulcers 6. allergic to chemotherapeutic agents; 7. Disease-free period of other malignant tumor is less than 5 years(except cured basal cell skin cancer and cervical carcinoma in situ). 8. With severe liver disease (such as cirrhosis), kidney disease, respiratory disease or diabetes 9. taking part or participating in other clinical trials within one month. 10. previous history of severe cardiovascular disease or cardiovascular disease risk factors were ≥ 4.

Locations (1)

National Cancer Center

Beijing, China

RECRUITING

Outcomes

Primary Outcomes

The rate of no cardiac events during chemotherapy

Adverse events (AEs) and laboratory tests graded according to the NCI CTCAE (version 4.0) .No cardiac events were defined until all relevant indicators (Electrocardiograph, Echcardiography and myocardial enzyme) were normal during chemotherapy.

Time frame: up to 12 months

Secondary Outcomes

Disease-free survival (DFS)

The time between the start of a randomized clinical trial and the onset of disease recurrence or death from any cause

Time frame: 5 years

Data from ClinicalTrials.gov

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