Eribulin Plus Cisplatin Versus Gemcitabine Plus Cisplatin in Triple Negative Breast Cancer (TNBC)

NCT04517292 | Unknown Phase 2

• 1 other identifier: GEP
• Study Type: interventional
• Target: 160
• Locations: 1 country
• Sites: 1

Brief Summary

Eribulin Plus Cisplatin Versus Gemcitabine Plus Cisplatin in Triple Negative Breast Cancer (TNBC)

Conditions

Breast Cancer

Keywords

triple negative breast cancer; first line chemotherapy; Eribulin; Cisplatin

Outcome Measures

Primary Outcomes (1)

• PFS

  Progression Free Survival

  approximately 6 weeks

Secondary Outcomes (3)

• ORR

  approximately 6 weeks

• Number of Participants with Adverse Events as a Measure of Safety and Tolerability

  approximately 18 weeks

• OS

  From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 100 months

Study Arms (2)

Eribulin,cisplatin

EXPERIMENTAL

EP (Eribulin and cisplatin combination)

Drug: Eribulin,cisplatin

Gemcitabine,cisplatin

ACTIVE COMPARATOR

GP (gemcitabine and cisplatin combination)

Drug: Gemcitabine,cisplatin

Interventions

Eribulin,cisplatin DRUG

Eribulin 1.4mg/m2, IV , D1, D8；Cisplatin 75 mg/m2, IV，D1

Eribulin,cisplatin

Gemcitabine,cisplatin DRUG

Gemcitabine 1250 mg/m2, IV , D1, D8； Cisplatin 75 mg/m2, IV, D1

Gemcitabine,cisplatin

Eligibility Criteria

• Age: 18 Years - 70 Years
• Sex: female
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Females with age between 18 and 70 years old
• Histological proven unresectable recurrent or advanced breast cancer, including de novo stage IV disease.
• Triple-negative for estrogen receptor (ER), progestogen receptor (PR), and human epithelial receptor-2 (HER2) by immunohistochemistry (ER \<1%, PR \<1% and Her2 negative). A negative Her2 gene amplification should be verified by FISH test for those patients with Her2 (2+). For those with Her2 (1+), FISH test might be considered by the investigator.
• No prior chemotherapy for metastatic breast cancer is permitted. Prior administration of chemotherapy in the adjuvant/neoadjuvant setting is acceptable if completed 6 months before the enrollment.
• At least one measurable disease according to the response evaluation criteria in solid tumor (RECIST 1.1)
• Performance status no more than 1
• All patients enrolled are required to have adequate hematologic, hepatic, and renal function
• Life expectancy longer than 12 weeks
• No serious medical history of heart, lung, liver and kidney
• Be able to understand the study procedures and sign informed consent.
• Patients with good compliance.

You may not qualify if:

• Pregnant or lactating women (female patients of child-bearing potential must have a negative serum pregnancy test within 14 days before the first day of drug dosing, or, if positive, a pregnancy should be ruled out by ultrasound)
• Women of child-bearing potential, unwilling to use adequate contraceptive protection during the process of the study
• Treatment with radiotherapy at the axial skeleton within 4 weeks before the first treatment or has not recovered from all toxicities of previous radiotherapy
• Treatment with an investigational product within 4 weeks before the first treatment
• Patients with symptomatic central nervous system metastases are not permitted, except for those with stable and asymptomatic brain metastases who have completed cranial irradiation, and have at least one measurable lesion outside the brain. Radiotherapy should be completed within 4 weeks prior to the registration
• Other active malignancies (including other hematologic malignancies) or other malignancies within the last 5 years, except for cured nonmelanoma skin cancer or cervical intraepithelial neoplasia.
• Patients having a history of clinically significant cardiovascular, hepatic, respiratory or renal diseases, clinically significant hematological and endocrinal abnormalities, clinically significant neurological or psychiatric conditions
• Uncontrolled serious infection

Sponsors & Collaborators

• Fudan University: lead

Study Sites (1)

Fudan University Shanghai Cancer center

Shanghai, 200032, China

Location

MeSH Terms

Conditions

Breast Neoplasms; Triple Negative Breast Neoplasms

Interventions

eribulin; Cisplatin; Gemcitabine

Condition Hierarchy (Ancestors)

Neoplasms by Site; Neoplasms; Breast Diseases; Skin Diseases; Skin and Connective Tissue Diseases

Intervention Hierarchy (Ancestors)

Chlorine Compounds; Inorganic Chemicals; Nitrogen Compounds; Platinum Compounds; Heterocyclic Compounds; Deoxycytidine; Cytidine; Pyrimidine Nucleosides; Pyrimidines; Heterocyclic Compounds, 1-Ring

Study Officials

• Jian Zhang, MD,PhD

  Fudan University

  PRINCIPAL INVESTIGATOR

Central Study Contacts

Jian Zhang, MD,PhD

CONTACT

8664175590; syner2000@163.com

Yiqun Du, MD,PhD

CONTACT

8664175590; dyqlh2010@163.com

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Associate chief physician

Study Record Dates

• First Submitted: August 16, 2020
• First Posted: August 18, 2020
• Study Start: October 8, 2020
• Primary Completion: July 30, 2022
• Study Completion: October 31, 2022
• Last Updated: August 18, 2020

Record last verified: 2020-08

Locations

CN (1)