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Clinical Trials/NCT02615457
NCT02615457RecruitingPhase 4

Huaier Granule in Treating Women With Triple Negative Breast Cancer

Shandong University1 site in 1 country300 target enrollmentStarted: October 2015Last updated:
Conditions
Interventions
Drugs

Trial Snapshot

Phase
Phase 4
Status
Recruiting
Sponsor
Enrollment
300
Locations
1
Primary Endpoint
Disease free survival (DFS)

Study Overview

Brief Summary

RATIONALE:

Huaier (Trametes robiniophila Murr) is a traditional Chinese medicine, which has been widely used in China for many years. The investigators previous study has reported that Huaier could exert great inhibitory effects on breast cancer cells both in vitro and in vivo.

PURPOSE:

To evaluate the efficacy and safety of Huaier Granule in treating women who have triple negative breast cancer that has been surgically removed.

Detailed Description

OBJECTIVES:

Compare the disease-free survival (DFS) and overall survival (OS) of patients with triple negative breast cancer who are randomized to adjuvant Huaier Granule group vs. those randomized to Blank-control group.

OUTLINE:

Patients are randomized to the following one of two treatment groups and are followed annually.

Arm I: Patients taking Huaier Granule for adjuvant treatment after the triple negative breast cancer has been surgically removed.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 75 Years (Adult, Older Adult)
Sex
Female
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Age: ≥ 18 and ≤ 75 years, female;
  • Triple negative breast cancer has been surgically removed;
  • The triple negative breast cancer has been confirmed by pathological examination and Immunohistochemistry (IHC);
  • Not receiving any preoperative anticancer drugs;
  • The liver and kidney function satisfies the following conditions within 3 days after surgery (excluding day 3): aspartate aminotransferase (AST), glutamic-oxalacetic transaminase (ALT) < 2 upper limit of normal (ULN), total bilirubin ≤ 1.5 ULN, serum creatinine < 1.5 ULN;
  • Other laboratory tests meet the following requirements within 3 days after surgery (excluding day 3): Hb ≥ 90g/l, platelet count ≥ 100×109/L, absolute neutrophil count > 1.5×109/L;
  • The expected survival time ≥ 6 months;
  • The subjects volunteer to sign the informed consent.

Exclusion Criteria

  • Patients with stage IV breast cancer;
  • Triple negative breast cancer was not surgically removed;
  • Non-triple negative breast cancer patients confirmed by pathological examination and Immunohistochemistry (IHC);
  • Pregnant or lactating women;
  • Those with active bleeding due to various reasons;
  • Those with HIV infection or AIDS-associated diseases;
  • Those with severe acute and chronic diseases;
  • Those with severe diabetes;
  • Those with serious infectious diseases;
  • Those who can not take drugs by oral route;
  • Drug abusers or those with psychological or mental diseases that may interfere with study compliance;
  • Conditions that are considered not suitable for this study investigators

Arms & Interventions

Arm I

Experimental

Patients taking Huaier Granule for adjuvant treatment after the triple negative breast cancer has been surgically removed. The Huaier Granule (Qidong Gaitianli Medicines Co., Ltd.) should be given orally from the 3rd day after surgery up to 5 years after surgery or until study termination.

Intervention: Huaier Granule (Drug)

Outcomes

Primary Outcomes

Disease free survival (DFS)

Time Frame: Up to 10 years

Time from randomization to recurrence, metastasis, appearance of a second primary tumor, or death from any cause, whichever occurs first, assessed up to 10 years.

Secondary Outcomes

  • Overall survival (OS)(Up to 10 years)

Investigators

Sponsor
Shandong University
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Qifeng Yang

Professor

Shandong University

Study Sites (1)

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