TCM as an Adjuvant Treatment in Breast Cancer Patients

December 30, 2024 updated by: Yang Mooi Lim, Universiti Tunku Abdul Rahman

A Systemic Approach to Study the Traditional Chinese Medicine as an Adjuvant Treatment in Breast Cancer Patients

Chinese herbs can alleviates the side effects caused by conventional treatment in breast cancer patients and affects the syndrome element differentiation by altering the specific set of proteomes at specific time point of treatment.

Study Overview

Status

Recruiting

Intervention / Treatment

Detailed Description

The previous studies have reported that adjuvant Chinese herbs therapy can improve the survival of breast cancer patients by alleviating the side effects of conventional treatments. Protein expression determines the phenotype of a patient that contributes to the onset of side effects in breast cancer patients caused by conventional treatment. Chinese herbs treatment will alleviate the treatment-related side effects by altering the protein expression in the patients. Associating changes in protein levels with the onset of side effects caused by conventional treatments could be used to identify clinically relevant diagnostic biomarkers. In addition, a set of proteome that is being expressed at diseased state will exhibit the phenotype that is also correlated to the TCM syndrome differentiation. Hence, this study aims to determine the proteome profile for the syndrome differentiation of breast cancer patients treated with adjuvant Chinese herbs for musculoskeletal pain. A quasi-experimental study with purposive sampling will be conducted on 30 breast cancer patients recruited from Tung Shin hospital. All participants will be invited to complete a structured questionnaire to collect their demographic information, pain score, syndrome element differentiation, quality of life, stress, body constitution and other relevant information, including cancer type, cancer stage, and cancer treatment. The questionnaires will be self-administered either at the outpatient waiting room or in the ward of the study hospital. Blood of the patients will be collected for determination of protein expression, biochemical markers and cytokines. The study is an in-point analysis where 2 time-points of data collection and analysis will be carried out at baseline, and immediate post Chinese herbs treatment. Informed consent will be obtained before participant enrolment according to a clinical trial protocol. Statistical differences for protein expression, biochemical markers, cytokines and mean pain score before and after Chinese herbs treatment will be compared using the paired-sample t test.

Study Type

Interventional

Enrollment (Estimated)

30

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • Kuala Lumpur
      • Bukit Bintang, Kuala Lumpur, Malaysia, 55100
        • Recruiting
        • Tung Shin Hospital
        • Contact:
        • Principal Investigator:
          • Yang Mooi Lim

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Postmenopausal women as determined by cessation of menses for at least 1 year or FSH>20 mIU/mL
  • Histology confirmed stage 2 to 3 hormone-receptor positive breast cancer patient
  • Currently taking letrozole for at least 1 month
  • Reported ongoing musculoskeletal pain or stiffness, which started or worsened after initiation of letrozole
  • Had a baseline average pain score over the past week on the Brief Pain Inventory Short Form (BPI-SF) of ≥4 points on a scale of 0 to 10.
  • Completed all indicated surgery, chemotherapy and radiation therapy
  • Agreed to take prescribed Chinese herbs
  • No evidence of distant metastasis
  • Follow-up for the duration of the study
  • No acute disease in the past month
  • Able to communicate to practitioner and interviewer
  • Willing to give informed consent

Exclusion Criteria:

  • Pregnant or nursing woman or woman of childbearing potential without effective method of birth control.
  • Patients who default subsequent follow-up/ has irregular follow-up.
  • Patients who directly involved in other study at the same time.
  • History of non-compliance to medical regime and patients who are unwilling or unable to comply with the protocol.
  • Bedridden and/ or cancer metastasis to bone/ lung.
  • Concurrent infection requiring intravenous antibiotics
  • History of allergy to Chinese herbs
  • Had previously received Chinese herbs for their AI-induced musculoskeletal symptoms
  • Had received Chinese herbs within one month prior to study entry
  • Current use of steroids or narcotics for pain relief within the past 2 weeks
  • Subjects with acute onset of a chronic illness or with acute disease in the past month or had pre-existing chronic diseases
  • Patients with concomitant severe illness or metastatic disease (poorly controlled hypertension, hypothyroidism, diabetes mellitus, liver diseases, osteoarthritis, rheumatoid arthritis, gout or neuropathic arthropathy, autoimmune or inflammatory joint disease, bone fracture, stroke)

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Chinese Herbs
Participants received standardized Chinese Herbs treatment orally twice daily for 1 week.
Chinese Herbs

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Feasibility of the study (Adherence)
Time Frame: Immediate post 1 week of Chinese Herbs intervention
The feasibility of the adherence will be determined by the number of sachets of Chinese herbs taken.
Immediate post 1 week of Chinese Herbs intervention

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Feasibility of the study (Dropout rate)
Time Frame: Immediate post 1 week of Chinese Herbs intervention
The feasibility will be assessed by dropout rate of the patients.
Immediate post 1 week of Chinese Herbs intervention
Change in the pain score
Time Frame: Baseline and immediate post 1 week of Chinese Herbs intervention
The pain score of breast cancer patients will be assessed by Brief Pain Inventory-Short Form (BPI-SF). BPI-SF is a validated and reliable tool used to assess the severity or intensity of pain on scale ranging from 0 (no pain) to 10 (worst pain imaginable). Higher scores mean a worse outcome.
Baseline and immediate post 1 week of Chinese Herbs intervention
Change in Syndrome element differentiation
Time Frame: Baseline and immediate post 1 week of Chinese Herbs intervention
Syndrome Element Differentiation rating scale will be used to determine the syndrome element differentiation of the patients. Syndrome Element Differentiation rating scale can quantify the syndrome elements of this patient based on the clinical manifestations. The quantitative output weight values of syndrome elements are acquired from clinical input data based on the severity and frequency of each sign and symptom. Based on the quantitative output value, the syndrome elements can then be categorized into four levels of health state or severity: normal (<70), mild (≥ 70 to <100), moderate (≥100 to <150), and severe (≥ 150).
Baseline and immediate post 1 week of Chinese Herbs intervention
Change in quality of life as assessed by WHO-BREF (World Health Organization Quality of Life)
Time Frame: Baseline and immediate post 1 week of Chinese Herbs intervention

The quality of life will be assessed by the WHO-BREF questionnaire in this study. The WHOQOL-BREF instrument comprises 26 items, measuring the following broad domains: physical health, psychological health, social relationships, and environment, with scores ranging from 0 to 100. The four domain scores denote an individual's perception of the quality of life in each domain. Domain scores are scaled in a positive direction in which higher scores denote a higher quality of life.

  • the minimum and maximum values: 0, 100
  • higher scores mean a better outcome.
Baseline and immediate post 1 week of Chinese Herbs intervention
Change in stress
Time Frame: Baseline and immediate post 1 week of Chinese Herbs intervention
The Depression Anxiety Stress Scales (DASS) is a self-report instrument designed to measure the negative emotional states of depression, anxiety and stress. A short version, the DASS 21 scale consists of a list of 21 symptoms with 7 item per scale, each of which is to be rated on a four-point scale of how much you had that symptom in the last week from 'never' to 'most of the time'. In this study, stress will be determined by stress domain of DASS-21 which consists of 7 items.
Baseline and immediate post 1 week of Chinese Herbs intervention
Change in body constitution assessed by Constitution in Chinese Medicine Questionnaire (CCMQ)
Time Frame: Baseline and immediate post 1 week of Chinese Herbs intervention

The body constitution will be determined by Constitution in Chinese Medicine Questionnaire (CCMQ). It has 60 items measuring the 9 body constitution types: gentleness, Qi-deficiency, Yang-deficiency, Yin-deficiency, phlegm-wetness, wetness-heat, blood-stasis, Qi-depression, and special diathesis.

  • the minimum and maximum values: 0, 100
  • higher scores mean a worse outcome.
Baseline and immediate post 1 week of Chinese Herbs intervention
Change in protein expression
Time Frame: Baseline and immediate post 1 week of Chinese Herbs intervention
The serum proteome will be analyzed by liquid chromatography coupled with tandem mass spectrometry (LC-MS/MS).
Baseline and immediate post 1 week of Chinese Herbs intervention
Change in Liver Function Test
Time Frame: Baseline and immediate post 1 week of Chinese Herbs intervention
The liver function of the patients will be determined by measuring the alanine aminotransferase (ALT), aspartate aminotransferase (AST), and alkaline phosphatase.
Baseline and immediate post 1 week of Chinese Herbs intervention
Change in CEA (Carcino-Embryonic Antigen)
Time Frame: Baseline and immediate post 1 week of Chinese Herbs intervention
Change in CEA (Carcino-Embryonic Antigen) will be determined by laboratory examination.
Baseline and immediate post 1 week of Chinese Herbs intervention
Change in CRP (C-Reactive Protein)
Time Frame: Baseline and immediate post 1 week of Chinese Herbs intervention
Change in CRP (C-Reactive Protein) will be determined by laboratory examination.
Baseline and immediate post 1 week of Chinese Herbs intervention
Change in Progesterone
Time Frame: Baseline and immediate post 1 week of Chinese Herbs intervention
Change in Progesterone will be determined by laboratory examination.
Baseline and immediate post 1 week of Chinese Herbs intervention
Change in Estradiol
Time Frame: Baseline and immediate post 1 week of Chinese Herbs intervention
Change in Estradiol will be determined by laboratory examination.
Baseline and immediate post 1 week of Chinese Herbs intervention
Change in Cytokine levels of serum
Time Frame: Baseline and immediate post 1 week of Chinese Herbs intervention
The cytokines in serum samples of breast cancer patients will be detected by the Quantibody array, multiplexed sandwich enzyme-linked immunosorbent assay (ELISA) based quantitative array platform (Genomax technology) for quantitative measurement of cytokines in human serum. The unit of measurement for the cytokines is the same.
Baseline and immediate post 1 week of Chinese Herbs intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Yang Mooi Lim, Universiti Tunku Abdul Rahman (UTAR)

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

April 22, 2022

Primary Completion (Estimated)

December 1, 2024

Study Completion (Estimated)

December 1, 2024

Study Registration Dates

First Submitted

March 19, 2021

First Submitted That Met QC Criteria

April 9, 2021

First Posted (Actual)

April 14, 2021

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

December 30, 2024

Last Verified

December 1, 2024

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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