Prophylactic TCM for Mitigation of EGFR-TKI Related Dermatological Adverse Effect
Advanced Lung Adenocarcinoma
About this trial
This is an interventional prevention trial for Advanced Lung Adenocarcinoma focused on measuring advanced lung adenocarcinoma, EGFR-TKI, traditional Chinese medicine, skin toxicity, quality of life, prophylaxis
Eligibility Criteria
Inclusion Criteria:
- Patients with histologically confirmed diagnosis of locally advanced or metastatic lung adenocarcinoma with EGFR mutations,
- Patients with an Eastern Cooperative Oncology Group performance status score of 0-2,
- Patients receiving afatinib as first-line treatment to ensure a shorter time to observe skin adverse effects of any grade,
- Patients with measurable disease evaluated by the Response Evaluation Criteria in Solid Tumors (version 1.1),
- Patients with brain metastases were included after adequate treatment.
Exclusion Criteria: -
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Experimental
Placebo Comparator
Study arm
Control arm
Patients receive afatinib and TCM. TCM recipe was chosen from three essential TCM formulas, including Bai He Gu Jin Tang (yin nourishing), Wen Dan Tang (phlegm reducing), and Qing Shang Fang Fen Tang (heat clearing). The packages contained 1.6 g TCM preparations, which were manufactured in powder form by Sun Ten Pharmaceutical (Taichung, Taiwan) according to the good manufacturing practice requirements. Patients were instructed to intake three packages of TCM preparations with each meal three times a day, for a total of nine packages per day. Administration of TCM was initiated at the same time as afatinib and continued for a total of three months.
Patients receive afatinib and placebo. Placebo without the medical ingredients was prepared to be similar to the weight, color, smell, taste, and packaging of the TCM formulas. The packages contained 1.6 g placebo preparations, which were manufactured in powder form by Sun Ten Pharmaceutical (Taichung, Taiwan) according to the good manufacturing practice requirements. Patients were instructed to intake three packages of placebo preparations with each meal three times a day, for a total of nine packages per day. Administration of placebo was initiated at the same time as afatinib and continued for a total of three months.