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TCM in the Treatment of Lung Adenocarcinoma

Primary Purpose

Lung Adenocarcinoma

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Jing-yan-kang Granule
PC chemotherapy and symptomatic treatment
Sponsored by
Henan University of Traditional Chinese Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Lung Adenocarcinoma

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • A confirmed diagnosis of LADC.
  • Age ranges from17years to75years.
  • A KPS score ≥40.
  • Without radiotherapy, immunotherapy and targeted therapy.
  • Without participanting in any other trial.
  • With signed informed consent.

Exclusion Criteria:

  • Pregnant, nursing or may become pregnant women.
  • The patient has a history of allergy to any of the components of the intervention drug;
  • Patients with severe liver and kidney dysfunction, cardiovascular and cerebrovascular diseases.
  • Unconscious or unable to communicate normally.
  • Patients with poor compliance.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Other

    Arm Label

    Experimental Group

    Control Group

    Arm Description

    On the basis of PC chemotherapy and symptomatic treatment, the patients in the experimental group will receive jing-yuan-kang granule with one dose daily.

    All the patients in control group will receive PC chemotherapy and symptomatic treatment without other treatment.

    Outcomes

    Primary Outcome Measures

    The quality of life will be evaluated by The European Organization for Research and Treatment of Cancer Quality of life Questinnaire Core-30(EORTC QLQ-C30) scale
    A score of 1-4 will be administrated for each item in EORTC QLQ-C30 . The higher scores will indicate the worse outcomes.
    Quality of life will be evaluated by Quality of life Questinnaire Lung Cancer-13(QLQ-LC13)
    A score of 1-4 will be administrated for each item in QLQ-LC13. The higher scores will indicate the worse outcomes.

    Secondary Outcome Measures

    Karnofsky(KPS) scores
    Physical conditions will be evaluated by KPS scores with a score of 0-100. A higher score will indicate a better physical conditon.
    TCM syndrome index
    TCM symptom index will be recorded and calculated referring to the Guiding Principles of Clinical Research of New Chinese Medicine Treating Primary Bronchial Lung Cancer (2002 Edition) published by National Medical Products Administration of China. A total of scores of all the related symptoms will be calculated with a 0-4 for each symptom at baseline and after treatment. A higher value will indicate a worse symptom. The difference of TCM symptoms between baseline and posttreatment will be calculated first. Then, we will obtain the TCM syndrome index by the ratio between the above difference and the scores at baseline.
    Change of tumor volume
    Change of tumor volume will be assessed by the length of longest diameter. The longger diameter will indicate worse disease.
    Adverse events will be evaluated and recorded at any time.
    Safety

    Full Information

    First Posted
    July 3, 2020
    Last Updated
    July 18, 2020
    Sponsor
    Henan University of Traditional Chinese Medicine
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04482829
    Brief Title
    TCM in the Treatment of Lung Adenocarcinoma
    Official Title
    Efficacy and Safety of Jing-yuan-kang Granule in the Treatment of Lung Adenocarcinoma
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    July 2020
    Overall Recruitment Status
    Unknown status
    Study Start Date
    September 15, 2020 (Anticipated)
    Primary Completion Date
    December 30, 2020 (Anticipated)
    Study Completion Date
    June 30, 2022 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Henan University of Traditional Chinese Medicine

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    This study is to evaluate the efficacy and safety of Jin-yuan-kang granule in the treatment of lung adenocarcinoma (LUAD) preliminarily, and provide reference for further study.
    Detailed Description
    Lung adenocarcinoma (LUAD) is a type of non-small cell lung cancer (NSCLC) with a rapid disease progression and poor treatment effect. The LUAD patients have a short median survival time with 8-11 months. Up to now, chemotherapy is still the first-line treatment for LUAD. PC protocol (pemetrexed + cisplatin) is most commonly used, which is also recommended by NCCN guidelines. However, critical side effects have limited the application and efficacy. Patients will undergo poor quality of life, and the disease will progress rapidly. We still face the stern situation for the treatment of LUAD. It is urgent to develop new treatment and management strategies. Our previous study showed that jing-yuan-kang granule has certain curative effect on LUAD. This is a multi-certers, randomized, controlled clinical trial to assess the efficacy and safety of Jing-yuan-kang granule in improving quality of life for LUAD patients. After a 2-week wash-out period, a total of 144 LUAD patients will be randomly assigned into experimental or control group with a ratio of 1:1. On the basis of that all the participants will receive PC chemotherapy and symptomatic treatment, the patients in the experimental group will receive jing-yuan-kang granule with no other treatments for control group. The primary outcome is quality of life. The secondary outcomes include Karnofsky (KPS) scores, clinical symptoms, and change of tumor volume. Safety and adverse events will also be assessed.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Lung Adenocarcinoma

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    144 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Experimental Group
    Arm Type
    Experimental
    Arm Description
    On the basis of PC chemotherapy and symptomatic treatment, the patients in the experimental group will receive jing-yuan-kang granule with one dose daily.
    Arm Title
    Control Group
    Arm Type
    Other
    Arm Description
    All the patients in control group will receive PC chemotherapy and symptomatic treatment without other treatment.
    Intervention Type
    Drug
    Intervention Name(s)
    Jing-yan-kang Granule
    Intervention Description
    Jing-yuan-kang granule will be administered 6 days on and 1 days off for 12weeks.
    Intervention Type
    Drug
    Intervention Name(s)
    PC chemotherapy and symptomatic treatment
    Intervention Description
    Drugs used in PC chemotherapy includes Pemetrexed and Cisplatin. Pemetrexed disodium for injection 500 mg per square meter, intravenous drip on day 1 in each treatment cycle. Cisplatin injection 75 mg per square meter, intravenous drip from day 1 to day 3 in each treatment cycle. One treatment cycle will be continued for 21 days and 4 cycles will be performed. If necessary, symptomatic treatment will also be used.
    Primary Outcome Measure Information:
    Title
    The quality of life will be evaluated by The European Organization for Research and Treatment of Cancer Quality of life Questinnaire Core-30(EORTC QLQ-C30) scale
    Description
    A score of 1-4 will be administrated for each item in EORTC QLQ-C30 . The higher scores will indicate the worse outcomes.
    Time Frame
    Change at 3 weeks, 6 weeks, 9 weeks, and 12 weeks after treatment compared to baseline.
    Title
    Quality of life will be evaluated by Quality of life Questinnaire Lung Cancer-13(QLQ-LC13)
    Description
    A score of 1-4 will be administrated for each item in QLQ-LC13. The higher scores will indicate the worse outcomes.
    Time Frame
    Change at 3 weeks, 6 weeks, 9 weeks, and 12 weeks after treatment compared to baseline.
    Secondary Outcome Measure Information:
    Title
    Karnofsky(KPS) scores
    Description
    Physical conditions will be evaluated by KPS scores with a score of 0-100. A higher score will indicate a better physical conditon.
    Time Frame
    Change at 3 weeks, 6 weeks, 9 weeks, and 12 weeks after treatment compared to baseline.
    Title
    TCM syndrome index
    Description
    TCM symptom index will be recorded and calculated referring to the Guiding Principles of Clinical Research of New Chinese Medicine Treating Primary Bronchial Lung Cancer (2002 Edition) published by National Medical Products Administration of China. A total of scores of all the related symptoms will be calculated with a 0-4 for each symptom at baseline and after treatment. A higher value will indicate a worse symptom. The difference of TCM symptoms between baseline and posttreatment will be calculated first. Then, we will obtain the TCM syndrome index by the ratio between the above difference and the scores at baseline.
    Time Frame
    Change at 3 weeks, 6 weeks, 9 weeks, and 12 weeks after treatment compared to baseline.
    Title
    Change of tumor volume
    Description
    Change of tumor volume will be assessed by the length of longest diameter. The longger diameter will indicate worse disease.
    Time Frame
    Change at 12 weeks after treatment compared to baseline.
    Title
    Adverse events will be evaluated and recorded at any time.
    Description
    Safety
    Time Frame
    at baseline, up to 6 weeks and 12 weeks after treatment.

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    75 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: A confirmed diagnosis of LADC. Age ranges from17years to75years. A KPS score ≥40. Without radiotherapy, immunotherapy and targeted therapy. Without participanting in any other trial. With signed informed consent. Exclusion Criteria: Pregnant, nursing or may become pregnant women. The patient has a history of allergy to any of the components of the intervention drug; Patients with severe liver and kidney dysfunction, cardiovascular and cerebrovascular diseases. Unconscious or unable to communicate normally. Patients with poor compliance.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Dan-dan Wei
    Phone
    +8613849186250
    Email
    1617924593@qq.com
    First Name & Middle Initial & Last Name or Official Title & Degree
    Shi-qing Jiang
    Phone
    +8613607640006
    Email
    jiangshiqing66@126.com

    12. IPD Sharing Statement

    Learn more about this trial

    TCM in the Treatment of Lung Adenocarcinoma

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