A Study of Mitoxantrone Hydrochloride Liposome Injection in Patients With Advanced HER2 Negative Breast Cancer

NCT ID: NCT04927481

Last Updated: 2024-02-23

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE2
• Total Enrollment: 28 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-06-11
• Study Completion Date: 2023-01-17

Brief Summary

This is a multicenter, open-label, single-arm, phase II study to evaluate the safety and efficacy of Mitoxantrone Hydrochloride Liposome in patients with advanced HER2 negative breast cancer.

Detailed Description

This is a multicenter, open-label, single-arm, phase II study to evaluate the safety and efficacy of Mitoxantrone Hydrochloride Liposome in patients with advanced HER2 negative breast cancer. Eligible patients will receive Mitoxantrone Hydrochloride Liposome 20 mg/m2 by an intravenous infusion (IV), every 21 days (q3w, 1 cycle) until disease progression, intolerable toxicity, death, or investigator or patient decision.

Conditions

Breast Cancer

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Mitoxantrone Hydrochloride Liposome Injection

Patients with advanced HER2 negative breast cancer will receive 20 mg/m2 Mitoxantrone Hydrochloride Liposome injection every 21 days (a cycle) for about 6 cycles.

Group Type: EXPERIMENTAL

Mitoxantrone Hydrochloride Liposome Injection

Intervention Type: DRUG

Mitoxantrone Hydrochloride Liposome 20 mg/m2, IV, on day 1 of each 21-day cycle (q3w).

Interventions

Mitoxantrone Hydrochloride Liposome Injection

Mitoxantrone Hydrochloride Liposome 20 mg/m2, IV, on day 1 of each 21-day cycle (q3w).

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Voluntarily participate in this study and sign informed consent form;

2. Male or female patients aged 18 to 75 years (inclusive);

3. Histologically confirmed diagnosis of HER-2 negative breast cancer (Including immunohistochemistry HER2 0 or 1+, immunohistochemistry HER2 2+ must be confirmed as negative by in situ hybridization);

4. Patients with unresectable locally advanced or recurrent breast cancer with disease progression after first-line or higher chemotherapy；

5. Hormone receptor (HR) negative breast cancer or HR-positive breast cancer that is not suitable for endocrine treatment or is resistant to endocrine treatment.

6. Prior treatment with both an anthracycline (i.e., doxorubicin or epirubicin) and a taxane (i.e., paclitaxel or docetaxel) at least (acceptable for patients not previously treated with anthracyclines due to high risk factors for cardiotoxicity), and four prior chemotherapy regimens at most；

7. At least one measurable lesion according to RECIST v1.1;

8. Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 2;

9. Patients must meet the following criteria prior to treatment (not receiving blood transfusion or growth factors therapy within 14 days before the first administration):

• Absolute neutrophil count (ANC) ≥ 1.5 × 109/L;
• Hemoglobin ≥ 90g / L;
• Platelet count ≥ 90 × 109/L;
• Creatinine ≤1.5 × upper limit of normal (ULN);
• Total bilirubin ≤ 1.5×ULN;
• Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 3 ×ULN (≤ 5 ×ULN for liver metastasis);

10. For women of childbearing potential: the serum pregnancy test must be negative, and patients are willing to take adequate contraceptive measures during the treatment period and for at least 6 months after the last dose of the study drug;

11. Good compliance and willingness to cooperate with follow-up visits.

Exclusion Criteria

1. Patients who have severe allergic reactions to mitoxantrone hydrochloride or liposome preparation ingredients;

2. History of other malignancy within 3 years, except for radical cure of carcinoma in situ of the cervix, basal cell carcinoma or squamous cell carcinoma of the skin;

3. Brain metastases and meningeal metastasis;

4. Patients with active hepatitis B (HBsAg positive with hepatitis B virus DNA ≥ 2000 IU/mL), active hepatitis C (hepatitis C virus antibody positive with hepatitis C virus RNA above the lower limit of detection of the study center), or human immunodeficiency virus (HIV) antibody positive;

5. Life expectancy < 3 months;

6. Previous treatment with the anthracyclines, with the total cumulative dose (doxorubicin equivalent) >350 mg/m2;

7. Adverse events from the previous treatment have not resolved to ≤ Grade 1 based on CTCAE (except for the toxicity without safety risk judged by the investigator, such as alopecia, hyperpigmentation);

8. Impaired cardiac function or serious cardiac disease:

• Long corrected QT interval syndrome or corrected QT interval > 480 ms;
• Complete left bundle branch block, II-III degree atrioventricular block;
• Severe, uncontrolled arrhythmias requiring pharmacological treatment;
• History of chronic congestive heart failure, New York Heart Association ≥ grade 3;
• Cardiac ejection fraction < 50% within 6 months prior to screening;
• Heart valve disease with CTCAE ≥ grade 3;
• ECG evidence of myocardial infarction, unstable angina, severe ventricular arrhythmias, history of severe pericardial disease, and acute ischemic or active conduction system abnormalities within 6 months prior to screening;

9. Uncontrollable hypertension (defined as a measured systolic blood pressure ≥ 160 mmHg or diastolic blood pressure ≥ 100 mmHg under pharmacological control);

10. Active bacterial, fungal or viral infections that require intravenous infusion treatment within 1 week prior to the first dose;

11. Any anticancer treatment (including chemotherapy, radiotherapy, molecular targeted therapy, immunotherapy, endocrine therapy) within 4 weeks prior to the first dose, immunomodulators as adjuvant therapy for malignancy within 2 weeks prior to the first dose, any anti-tumor proprietary Chinese medicine (except for those in the category of supporting and relieving symptoms) within 2 weeks prior to the first dose;

12. Patients who enrolled in any other clinical trials within 4 weeks prior to the first dose;

13. Patients who undergone major surgery within 12 weeks before the first dose, or have a surgical schedule during the study period;

14. Patients with thrombosis or thromboembolism within 6 months prior to screening;

15. Lactating female;

16. Serious and/or uncontrolled medical condition that, in the judgment of the investigator, may affect the patient's participation in this study (including, but not limited to: diabetes not effectively controlled, kidney disease requiring dialysis, severe liver disease, life-threatening autoimmune and bleeding disorders, substance abuse, neurological disorders, etc.);

17. Not suitable for this study as decided by the investigator due to other reasons.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

CSPC ZhongQi Pharmaceutical Technology Co., Ltd.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

qingyuan zhang, PhD

Role: PRINCIPAL_INVESTIGATOR

The Second Affiliated Hospital of Harbin Medical University

Locations

Anhui Provincial Hospical

Hefei, Anhui, China

Cancer Center Sun Yat-sen University

Guozhou, Guodong, China

Affiliated Hospital of Hebei University

Baoding, Hebei, China

The Fourth Hospital of Hebei Medical University

Shijiazhuang, Hebei, China

Tangshan People's Hospital

Tangshan, Hebei, China

Xingtai People's Hospital

Xingtai, Hebei, China

Harbin Medical University Cancer Hospital

Harbin, Heilongjiang, China

Daqing People's Hospital

Daqing, Helongjiang, China

Cancer Hospital of Jiamusi City

Jiamusi, Helongjiang, China

The First Affiliated Hospital of Xinxiang Medical University

Xinxiang, Henan, China

Cancer Hospital of Henan Province

Zhengzhou, Henan, China

The First Affiliated Hospital of Zhengzhou University

Zhengzhou, Henan, China

Henan Provincial People's Hospital

Zhenzhou, Henan, China

Union Hospital affiliated to Tongji Medical College of Huazhong University of Science and Technology

Wuhan, Hubei, China

Zhongnan Hospital of Wuhan University

Wuhan, Hubei, China

Hubei Cancer Hospital

Wuhan, Hubei, China

Changsha Kexin Cancer Hospital

Changsha, Hunan, China

Yiyang Central Hospital

Yiyang, Hunan, China

The third Hospital of Nanchang

Nanchang, Jiangxi, China

The second hospital of Jinlin University

Changchun, Jinlin, China

The second hospital of Dalian Medical University

Dalian, Liaoning, China

The First Affiliated Hospital of Jinzhou Medical University

Jinzhou, Liaoning, China

The First hospital of China Medical University

Shenyang, Liaoning, China

Shanxi Provincial Cancer Hospital

Taiyuan, Shanxi, China

Yuncheng Central Hospital

Yuncheng, Shanxi, China

Sichuan Cancer Hospital & Institute

Chengdu, Sichuan, China

The second people's hospital of neijiang

Neijiang, Sichuan, China

Affiliated tumor Hospital of Xinjiang Medical University

Ürümqi, Xinjiang, China

The First Affiliated Hospital of Xinjiang Medical University

Ürümqi, Xinjiang, China

Countries

China

Other Identifiers

HE071-CSP-021

Identifier Type: -

Identifier Source: org_study_id