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NCT Number: NCT04843865

TCM 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.

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Tung Shin Hospital

Bukit Bintang, Kuala Lumpur, 55100, Malaysia

Location status: Recruiting

Location contact

King Keong Chung

CONTACT

[email protected]

0122027322

Yang Mooi Lim

PRINCIPAL_INVESTIGATOR

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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)

Treatment and study plan

Chinese Herbs

Dietary Supplement

Chinese Herbs

Primary outcomes

  1. 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.

Secondary outcomes

  1. 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.

  2. 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.

  3. 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).

  4. 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.
  5. 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.

  6. 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.
  7. 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).

  8. 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.

  9. 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.

  10. 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.

  11. Change in Progesterone

    Time frame: Baseline and immediate post 1 week of Chinese Herbs intervention

    Change in Progesterone will be determined by laboratory examination.

  12. Change in Estradiol

    Time frame: Baseline and immediate post 1 week of Chinese Herbs intervention

    Change in Estradiol will be determined by laboratory examination.

  13. 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.

Study contacts

Contact information is provided by the study sponsor or research team.

Chin Long Poo

CONTACT

[email protected]

0178853596

Sponsors and collaborators

Lead sponsor

Universiti Tunku Abdul Rahman

Other

Registry information

Official study title

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

Important dates

Study start
2022
Primary completion
2024
Study completion
2024
First posted
Apr 14, 2021
Registry last updated
Dec 31, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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