This study will compare the experiment group with the control group. Patients meeting the inclusion criteria will be allocated to the experimental group or control group at a ratio of 1:1. Patients in the experimental group will receive the SHP application on CV8. Patients in the control group will receive the placebo plaster application on CV8. All patients of two groups will be treated with acupoint application once per day from the day before chemotherapy and will last 3 days. All plasters will be taken back by the experimenter to the research center after application.

The standard treatment procedures are as follows: Ensure the CV8, disinfect the application site with iodophor, allow to dry then stick the SHP or placebo plaster on the CV8 at about 8am. Each application lasts 10 hours. If patients have obviously burning sensation and severe itching, or skin redness, swelling, blisters and other discomfort, the plaster would be immediately removed the plaster and deal with corresponding treatment.

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