Herbal Treatment to Improve Chemotherapy Delivery (HATCHED)
Colon Cancer
About this trial
This is an interventional treatment trial for Colon Cancer focused on measuring Colon Cancer, Traditional Chinese Medicine, Adverse Effect of Chemotherapy, Chemotherapy
Eligibility Criteria
Inclusion Criteria:
- Patient with pathological diagnosis of colon cancer; no residual tumor at the resection margin.
tumor-node-metastasis(TNM)Stage II (high-risk)or III colon cancer according to 8th edition of American Joint Committee on Cancer(AJCC)Staging Manual. High-risk stage II disease is characterized by at least one of the following:
- T4 tumor,
- inadequately sampled nodes (<12 lymph nodes),
- clinical presentation with bowel obstruction or perforation,
- poorly differentiated histology ,exclusive of those cancers that are High degree of microsatellite instability(MSI-H),
- lymphovascular invasion,perineural invasion(PNI).
- Underwent radical surgery no more than six weeks ago and plan to start chemotherapy.
- Have not been enrolled in other therapeutic clinical trials within the near 30 days.
- Age between 18 to 75 years; All genders; Eastern Cooperative Oncology Group - performance status(ECOG-PS)from 0 to 2; Women who are pregnant, lactating or of reproductive age are not eligible, while those of reproductive age using secure contraceptives are eligible.
- No history of previous malignancy other than adequately treated in situ carcinoma of the uterine cervix or basal or squamous cell carcinoma of the skin, unless there has been a disease-free interval of at least 5 years.
- Laboratory testing: blood routine examination: WBC≥3.5×109/L,NEUT≥1.5×109/L,PLT≥100×109/L,HGB≥90g/L;biochemical tests:TBIL≤1.5×ULN,AST(SGOT),ALT(SGPT)≤2.5×ULN,Scr≤1.5×ULN;CEA after surgery was normal.
- Consented.
- Agree not to be enrolled in other interventional studies during the research.
Exclusion Criteria:
- Patients not suitable for chemotherapy of CapeOX ,which will be determined by the investigator or the attending physician.
- Clinically relevant cardiovascular and/or cerebrovascular disease,active hepatitis,severe abnormalities in liver/ renal function tests.
- Known allergy to any of the components of study drug.
- Those who cannot take the study drug orally because of bowel obstruction and/or require for peripheral vein nutrition.
- Malabsorption or diseases that affect the absorption.
- Unstable situations or situations that may endanger the safety of patients and their compliance, such as severe mental illness,schizophrenia.
- Colostomy
Sites / Locations
- Beijing Chao Yang HospitalRecruiting
- Civil Aviation General HospitalRecruiting
- Oncology Department of Xiyuan Hospital of China Academy of Chinese Medical SciencesRecruiting
- Beijing Cancer HospitalRecruiting
- Chongqing University Cancer HospitalRecruiting
- Guangdong Provincial Hospital of Traditional Chinese MedicineRecruiting
- The Third People's Hospital of ZhengzhouRecruiting
- Henan Provincial People's HospitalRecruiting
- Zhengzhou Hospital of Traditional Chinese MedicineRecruiting
- Jiangsu Province Hospital of Traditional Chinese MedicineRecruiting
- Shanghai Zhongshan HospitalRecruiting
- Tianjin Union Medical CenterRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
Placebo Comparator
TCM group
Placebo group
Tonifying Spleen and Kidney Sequential Regimen(TSKSR) will be prescribed to the participants in each course of chemotherapy.
Placebo of Tonifying Spleen and Kidney Sequential Regimen(TSKSR)similar in color,smell and texture with TSKSR will be prescribed to participants in each course of chemotherapy.