Inetetamab Plus Cyclophosphamide Metronomic Chemotherapy Plus Aromatase Inhibitor in Metastatic HER2+/HR+ Breast Cancer

Breast Cancer Clinical Trial

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Official title:

A Phase II Single-arm Clinical Trial of the Efficacy and Tolerability of Inetetamab Combined With Cyclophosphamide Metronomic Chemotherapy and Aromatase Inhibitor in Metastatic HER2+/HR+ Breast Cancer

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04941885
• Other study ID #: SYSU-2021
• Status: Recruiting
• Phase: Phase 2
• Start date: June 25, 2021
• Est. completion date: July 1, 2025

Study information

• Verified date: July 2021
• Source: Sun Yat-sen University
• Contact: Shusen Wang, MD
• Phone: +86-13926168469
• Email: wangshs[@]sysucc.org.cn
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Antibody-dependent cell-mediated cytotoxicity (ADCC) is one of the important mechanisms for suppressing tumors of Trastuzumab. Pre-clinical data suggest that the ADCC effect of Inetetamab, an anti-HER2 monoclonal antibody with a modified Fc segment, is 1.11 times that of trastuzumab. Previous studies indicated that enhanced ADCC effects can be transformed into clinical benefits. Immune induction through cyclophosphamide metronomic chemotherapy may further enhance the ADCC effect of anti-HER2 monoclonal antibodies. Therefore, we conducted this study to explore the efficacy and the safety of Inetetamab combined with cyclophosphamide metronomic chemotherapy and aromatase inhibitors(AI) in the treatment of metastatic HER2-positive and HR-positive breast cancer patients and to explore the possible mechanisms.

Description:

Trastuzumab is a humanized monoclonal antibody, and antibody-dependent cell-mediated cytotoxicity (ADCC) is one of its important mechanisms for suppressing tumors. Pre-clinical data suggest that the ADCC effect of Inetetamab, an anti-HER2 monoclonal antibody with a modified Fc segment, is 1.11 times that of trastuzumab. Previous studies indicated that enhanced ADCC effects can be transformed into clinical benefits, but the absolute benefits are still unsatisfactory. Further improvement of ADCC effects and monoclonal antibody-induced immune responses may improve the clinical benefits. Immune induction through cyclophosphamide metronomic chemotherapy may further enhance the ADCC effect of anti-HER2 monoclonal antibodies. According to previous clinical studies, for HR-positive and HER2-positive metastatic breast cancer patients, metronomic chemotherapy combined with endocrine therapy and anti-HER2 targeted therapy may be one of the treatment options. Therefore, we conducted this study to explore the efficacy and the safety of Inetetamab combined with cyclophosphamide metronomic chemotherapy and aromatase inhibitors(AI) in the treatment of metastatic HER2-positive and HR-positive breast cancer patients, and we further exploring the possible mechanisms.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 78
• Est. completion date: July 1, 2025
• Est. primary completion date: July 1, 2023
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

1. Voluntarily sign the informed consent form;

2. 18-75 years old;

3. The expected survival period is =12 weeks;

4. Eastern Cooperative Oncology Group (ECOG) score [0-2] points;

5. The diagnosis of invasive carcinoma by histology or cytology; Estrogen receptor (ER) positive (defined as >1% nuclear ER staining); HER2 negative (defined as IHC 0 or 1+, or HER2(2+) with HER2 FISH detection no amplification);

6. Inoperable or recurrent/metastatic breast cancer patients with aromatase inhibitor treatment failure;

7. In the state of disease progression before enrollment;

8. Measurable disease according to RECIST version 1.1 or only bone metastasis;

9. Adequate hematological, hepatic and renal function;

10. NYHA class I or II and Left ventricular ejection fraction (LVEF) =50%.

11. The diagnosis of invasive carcinoma by histology or cytology: Hormone receptor (HR) positive (defined as >1% nuclear estrogen receptor staining); HER2 positive (defined as IHC 3+, or HER2 FISH detection amplification);

12. In the state of disease progression before enrollment;

13. Have lesions able to and agree to perform tissue biopsy at the time requested in the study;

14. Treatment =1 line after recurrence/metastasis, or relapse within 12 months after completing trastuzumab-based adjuvant therapy or during trastuzumab adjuvant therapy;

15. Previously received trastuzumab for anti-HER2 therapy;

16. Measurable disease according to RECIST version 1.1.

Exclusion Criteria:

1. Allergic to the ingredients of Inetetamab, cyclophosphamide or similar drugs;

2. Concomitant diseases/conditions that is not controllable, and any other major illness that, in the investigator's judgment, will substantially increase the risk associated with the patient's participation in this study;

3. Patients who cannot accept drugs orally;

4. Women who are pregnant or breastfeeding or planning to give birth;

5. Patients with currently symptomatic brain or meningeal metastasis;

6. History of other primary malignancy;

7. Resistant to steroidal or nonsteroidal aromatase Inhibitor;

8. Have used Inetetamab;

9. Patients with life-threatening, symptomatic, metastatic visceral disease.

Related Conditions & MeSH terms

• Breast Cancer
• Breast Neoplasms

Intervention

Drug:
• Inetetamab Plus Cyclophosphamide Metronomic Chemotherapy Plus AI
Each participant receives Inetetamab plus cyclophosphamide metronomic chemotherapy plus AI.

Locations

Country	Name	City	State
China	Shusen Wang	Guangzhou	Guangdong

Sponsors (1)

Lead Sponsor	Collaborator
Sun Yat-sen University

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Objective response rate (ORR)	The proportion of best overall response of either complete or partial response.	1 year
Secondary	Clinical benefit rate (CBR)	Response and progression will be evaluated using RECIST 1.1. Evaluation will occur every 3 months till progression or termination of the study. CBR is defined as ratio of participants who have stable disease for over 24 weeks.	1 year
Secondary	Progression free survival (PFS)	Time from the date of treatment to the date of tumor progression.	1 year
Secondary	Duration of response (DOR)	Time from the first assessment of the tumor as complete or partial response to the first assessment as PD (Progressive Disease) or death from any cause.	1 year
Secondary	Overall survival (OS)	Time from the date of treatment to the date of death.	3 years
Secondary	Number of Participants with Adverse Events	Number of participants with adverse events related to the treatment.	1 year
Secondary	The quality of life	Using Functional Assessment of Cancer therapy -Breast (FACT-B) scale. The minimum and maximum values are 0 and 144, respectively. Higher scores mean better outcome.	1 year