TKIs vs. Pertuzumab in HER2+ Breast Cancer Patients With Active Brain Metastases (HER2BRAIN)

Brain Metastases Clinical Trial

Official title:

Anti-HER2 TKI Versus Pertuzumab in Combination With Dose-dense Trastuzumab and Taxane as First Line in HER2-positive Breast Cancer Patients With Active Brain Metastases: A Phase II, Multicenter, Double-blind, Randomized Clinical Trial

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT04760431
• Other study ID #: HER2BRAIN
• Status: Not yet recruiting
• Phase: Phase 2
• Start date: October 1, 2021
• Est. completion date: September 30, 2025

Study information

• Verified date: January 2021
• Source: Second Affiliated Hospital, School of Medicine, Zhejiang University
• Contact: Xuexin He, MD
• Phone: 18329139569
• Email: xuexinhe[@]zju.edu.cn
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a prospective, randomized, 2-arm, Phrase 2, superiority and multicenter study to compare the efficiency of Anti-HER2 TKI versus Pertuzumab in Combination With Dose-dense Trastuzumab and Taxane in HER2-positive breast cancer patients with active refractory brain metastases.

Description:

This is a prospective, randomized, 2-arm, Phrase 2, superiority and multicenter study. HER2-positive breast cancer patients with active refractory brain metastases are included. There will be two group: Group A (Trastuzumab, Taxanes and Pertuzumab) and Group B (Trastuzumab, Taxanes and TKIs). The primary outcome is objective response rate (ORR).

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 120
• Est. completion date: September 30, 2025
• Est. primary completion date: September 30, 2024
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

1. Patients provided written informed consent

2. Women aged 18-75 years

3. Histologically or cytologically confirmed HER2-positive (IHC 3+ or ISH+) breast cancer

4. Patients of HER2 positive breast cancer with a documented central nervous system (CNS) recurrence/progression (by imaging) during or after Trastuzumab based therapy

5. At least one measurable and progressive lesion in the CNS (=10 mm on T1-weighted, gadolinium-enhanced MRI)

6. Previous treatment with HER2 inhibitors to be discontinued prior to first study treatment administration (at least 14 days for trastuzumab and other antibodies, at least 7 days for lapatinib)

7. Previous chemotherapy and hormonal therapy (adjuvant and metastatic regimens) allowed, but chemotherapy must have been discontinued at least 14 days and hormonal therapy at least 7 days prior to first study treatment administration

8. Prior surgery, whole brain radiotherapy or stereotactic radiosurgery allowed provided that there is unequivocal evidence of one or more new and/or progressive brain metastases after completion of whole brain radiotherapy or stereotactic radiosurgery

9. Previous radiotherapy allowed, but radiotherapy must have been discontinued at least 14 days prior to first study treatment administration

10. Normal cardiac function

11. Patients must have recovered to baseline condition or to Common Terminology Criteria for Adverse Events (CTCAE) version 5.0 grade = 1 from any acute CTCAE v. 5.0 grade =2 side effects of previous treatments

12. Without infection of human immunodeficiency virus (HIV) on central laboratory assay results prior to randomization

13. Alanine aminotransferase (ALT) </= 2.5 × the upper limit of normal (ULN), Aspartate aminotransferase (AST) </= 2.5 × ULN prior to randomization

14. Total bilirubin (TBIL) </= 1.25 × ULN

15. Alkaline phosphatase (ALK) </= 2.5 × ULN

16. Gamma glutamyl transpeptidase (GGT) </= 2.5 × ULN

17. Albumin >/= 30g/L

18. Eastern Cooperative Oncology Group (ECOG) performance score of 0 to 1

19. A life expectancy of at least 1 month

20. Women of child-bearing age should take effective contraceptive measures

21. Serum total bilirubin (TBil) </= 1.5 × ULN

22. Serum creatinine (Scr) </= 1.5 × ULN

23. WBC >/= 3×109/L, Blood neutrophil count >/= 1×109/L, Platelet count >/= 100×109/L, HB >/= 9 g/dL

Exclusion Criteria:

1. Lack of histological or cytological confirmation of HER2-positive (IHC 3+ or ISH-positive) breast cancer

2. Cerebral hernia

3. Need radiotherapy or surgery immediately

4. Active cerebral infarction or hemorrhage

5. Only meningeal metastasis

6. Earlier exposure to doxorubicin or pirarubicin at a dosage of more than 360 mg/m2

7. Earlier exposure to epirubicin at a dosage of more than 900 mg/m2

8. Prior treatment with HER2-tyrosine kinase inhibitors

9. Treatment with trastuzumab emtansine within 6 months

10. Any other current malignancy or malignancy diagnosed within the past five years (other than carcinoma in situ or stage Ia carcinoma of the cervix, skin basal cell carcinoma and papillary thyroid carcinoma at early stage)

11. Active infection with human immunodeficiency virus (HIV) prior to first study treatment administration.

12. History of participating any other clinical trials within 30 days prior to randomization

13. Known hypersensitivity (Grade 3 or 4) to any of the trial drugs

14. Pregnancy or lactation

15. Current severe systemic disease (for example, clinically significant cardiovascular, pulmonary, or renal disease)

16. Legal incompetence or limitation.

17. Considered unable to complete the study or sign the informed consent due to a medical or mental disorder by the investigator.

Related Conditions & MeSH terms

• Brain Metastases
• Brain Neoplasms
• Breast Neoplasms
• HER2-positive Breast Cancer
• Neoplasm Metastasis
• Neoplasms, Second Primary

Intervention

Drug:
• Trastuzumab
8 mg/kg loading dose for Cycle 1, followed by 6 mg/kg for subsequent cycles, administered by IV infusion every week until disease progression, unacceptable toxicity, withdrawal of consent, or study termination.
• Taxanes
Docetaxel: 75 mg/m2, administered by IV infusion every 3 weeks Paclitaxel: 175 mg/m2, administered by IV infusion every 3 weeks Paclitaxel (Albumin bound): 260 mg/m2, administered by IV infusion every 3 weeks Paclitaxel Liposome: 135-175 mg/m2, administered by IV infusion every 3 weeks
• Pertuzumab
840 milligrams (mg) loading dose of pertuzumab, followed every 3 weeks thereafter by a dose of 420 mg via intravenous (IV) infusion until disease progression, unacceptable toxicity, withdrawal of consent, or study termination.
• Tyrosine kinase inhibitor
Pyrotinib: 400mg po within 30 minutes after a meal, QD, every 3 weeks Neratinib: 240mg po QD, every 3 weeks Tucatinib: 300mg po Q12H

Locations

Country	Name	City	State
China	Peking University International Hospital	Beijing	Beijing
China	Sun Yat-sen University Cancer Center	Guangzhou	Guangdong
China	First Affiliated Hospital, Zhejiang University, School of Medicine	Hangzhou	Zhejiang

Sponsors (4)

Lead Sponsor	Collaborator
Second Affiliated Hospital, School of Medicine, Zhejiang University	Peking University International Hospital, Sun Yat-sen University, Zhejiang University

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Objective Response Rate (ORR)	The sum of complete response (CR) rate and partial response (PR) rate by measurement of target lesions (intracranial lesions)	up to 3 years
Secondary	Objective Response Rate 2 (ORR2)	The sum of complete response (CR) rate and partial response (PR) rate by measurement of extracranial lesions	up to 3 years
Secondary	Progression-free Survival (PFS)	PFS is defined as time from randomization to disease progression or death, whichever occurs first.; Progression of disease was determined if at least 1 of the following criteria applied: At least a 20% increase in the sum of the diameters (SoD) of target lesions taking as reference the smallest SoD recorded since the treatment started, together with an absolute increase in the SoD of at least 5 mm; Appearance of 1 or more new lesions; Unequivocal progression of existing non-target lesions	up to 3 years
Secondary	Overall Survival (OS)	OS is defined as time from randomization to death for any cause. If there is no death reported for a subject before the date cutoff for OS analysis, OS will be censored at the last contact date at which the subject is known to be alive.; For patients who had not died up to the cut-off date, the date they were last known to be alive was derived from the patient status records, the trial completion record, radiological imaging assessments, the study treatment termination record, and the randomization date.	up to 3 years
Secondary	Clinical benefit rate (CBR)	CBR is defined as the sum of CR rate, PR rate, and more than 6 months' SD (stable disease) rate	up to 3 years
Secondary	Disease control rate (DCR)	DCR is defined that the sum of CR rate, PR rate, and SD rate.	up to 3 years
Secondary	Peripheral neurotoxicity	Peripheral neurotoxicities are defined as the number of patients who suffer from neurotoxicities (NCI CTCAE v5.0)	30 days after last treatment