Observation on the Therapeutic Effect of Huaier Granules in the Adjuvant Treatment of Non-small Cell Lung Cancer After Radical Surgery

Non-small Cell Lung Cancer Clinical Trial

Official title:

Observational Study on the Efficacy and Safety of Huaier Granules Compared With Platinum Containing Dual Drug Combination Chemotherapy in Adjuvant Therapy for Resectable Stage II-IIIA Non-small Cell Lung Cancer After Radical Surgery

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT06109454
• Other study ID #: HE-202306
• Status: Recruiting
• Start date: March 21, 2024
• Est. completion date: October 2028

Study information

• Verified date: May 2024
• Source: Liaoning Tumor Hospital & Institute
• Contact: Hongxu Liu, PhD
• Phone: +8618040097698
• Email: hxliu[@]cmu.edu.cn
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

This study is a multicenter, prospective, and observational clinical study aimed at exploring whether the 3-year DFS in the Huaier group is not inferior to the control group receiving standard platinum dual-drug chemotherapy.

Description:

This study is a small sample observational study, mainly exploring whether the 3-year DFS of the Huaier group is not inferior to the control group receiving standard platinum dual drug chemotherapy. Therefore, this study will conduct a small sample exploratory analysis. It is expected to include 240 non-small cell lung cancer patients who have been diagnosed with stage Ⅱ-ⅢA and are eligible for surgery at selected research centers from April 2023 to July 2025. Among them, 120 patients in the Huaier Granule group refused to undergo adjuvant chemotherapy due to reasons such as intolerance or disagreement, and agreed to receive Huaier Granule monotherapy as an adjuvant treatment; There are 120 patients in the control group, all of whom plan to receive standard chemotherapy as an adjuvant treatment plan (including platinum based dual-drug combination chemotherapy).

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 240
• Est. completion date: October 2028
• Est. primary completion date: September 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• 18 years old = age = 75, regardless of gender.

• Confirmed as non-small cell lung cancer by histopathology, with pathological staging of stage ?-?A.

• Received radical R0 resection of lung cancer within 2 months before enrollment, and did not receive any postoperative adjuvant therapy or preoperative neoadjuvant therapy.

• ECOG(Eastern Cooperative Oncology Group)score:0-2.

• The patient voluntarily participated in the study, agreed to cooperate with the researcher for data collection, and signed an informed consent form.

Exclusion Criteria:

• Known to be allergic to the components of Huaier granules or avoid or use Huaier granules with caution (Huaier group).

• Those who have difficulty swallowing, complete or incomplete gastrointestinal obstruction, active gastrointestinal bleeding, perforation, and other causes of difficulty in taking oral medication.

• Non-small cell lung cancer patients who plan to receive targeted therapy, immunotherapy, chemotherapy combined with immunotherapy, radiotherapy, synchronous radiotherapy and chemotherapy during the study period.

• The patient has a history of other new malignant tumors within 5 years.

• The expected survival time of the patient is less than half a year.

• Surgical complications that have not recovered or are accompanied by severe infections after radical resection of lung cancer.

• Pregnant or lactating women or planned pregnancy preparation.

• The patient has received other traditional Chinese patent medicines and simple preparations with anti-tumor effect in the past one month (including but not limited to compound cantharidin capsule, cinobufagin capsule, Kangai injection, Brucea javanica injection, etc., the specific instructions shall prevail).

• The patient suffers from severe mental illness or other reasons that the researcher deems unsuitable to participate in this study.

Related Conditions & MeSH terms

• Carcinoma, Non-Small-Cell Lung
• Lung Neoplasms
• Non-small Cell Lung Cancer

Intervention

Drug:
• Huaier granule
The subjects voluntarily gave up postoperative adjuvant therapy, including chemotherapy, targeted therapy, immunotherapy, and radiation therapy, and agreed to take Huaier granules.The subjects took Huaier granules orally, one bag (10g) per time, three times a day. Until the end of the study, intolerable toxicity, withdrawal from the study for any reason or death, or when the researcher determines that there is no further benefit, whichever occurs first. Please refer to the drug manual for specific usage. It is recommended that patients start taking Huaier granules 1-2 weeks after surgery.

Other:
• Control
The subjects received standard platinum dual drug chemotherapy.The subjects were treated with carboplatin injection (300mg/m2, intravenous injection, first day) combined with pemetrexed disodium (pathological type: adenocarcinoma, intravenous injection, 500mg/m2) or albumin bound paclitaxel (pathological type: squamous cell carcinoma, 260mg/m2, intravenous injection, first day) every three weeks, with a maximum of four cycles.

Locations

Country	Name	City	State
China	Liaoning Cancer Hospital & Institute	Shenyang	Liaoning

Sponsors (3)

Lead Sponsor	Collaborator
Liaoning Tumor Hospital & Institute	Huazhong University of Science and Technology, LinkDoc Technology (Beijing) Co. Ltd.

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Changes in peripheral blood lymphocyte subpopulations	Observe and describe the changes in peripheral blood lymphocyte subpopulations from baseline, peripheral blood lymphocyte subpopulations include but are not limited to CD3+T, CD4+T, and CD8+T.	start of treatment until 3-year follow-up
Primary	3-year disease-free survival (DFS) rate	The proportion of participants who did not experience disease recurrence or death within 3 years after undergoing lung cancer radical surgery.	start of treatment until 3-year follow-up
Secondary	1-year or 2-year DFS rate	The proportion of participants who did not experience disease recurrence or death within 1 or 2 years after undergoing lung cancer radical surgery	start of treatment until 1-year or 2-year follow-up
Secondary	1-year, 2-year or 3-year overall survival (OS) rate	The proportion of subjects who survived within 1 year, 2 years or 3 years after undergoing radical lung cancer surgery among all subjects.	start of treatment until 1-year, 2-year or 3-year follow-up
Secondary	1-year, 2-year or 3-year local recurrence free survival (LRFS) rates	The proportion of subjects who did not experience local recurrence of lung cancer within 1 year, 2 years or 3 years after undergoing radical lung cancer surgery.	start of treatment until 1-year, 2-year or 3-year follow-up
Secondary	1-year, 2-year or 3-year distant metastasis free survival (DMFS) rates	The proportion of subjects who did not experience distant metastasis within 1 year, 2 years, or 3 years after undergoing lung cancer radical surgery	start of treatment until 1-year, 2-year or 3-year follow-up
Secondary	Quality of Life Score (SF-36 Scale)	The Health Survey Short Form[(SF-36 Scale (Chinese Version) ]developed by the US Medical Bureau research team was used for evaluation. The scale has 36 items and aims to evaluate the health and functional status of multiple age groups, different diseases, and control populations.Note that all items are scored so that a high score defines a more favorable health state. In addition, each item is scored on a 0 to 100 range so that the lowest and highest possible scores are 0 and 100, respectively.	start of treatment until 3-year follow-up
Secondary	The incidence and severity of adverse events (AE) and severe adverse events (SAE)	The definitions and severity grading of AE and SAE can refer to the corresponding descriptions in the definition and evaluation section of AE. The incidence rate is defined as the proportion of subjects who have experienced AE and SAE to the corresponding total population.	start of treatment until 3-year follow-up