Assessment of the Efficacy of Immunomodulatory Therapy With Thymosin Alpha 1 (Tα1) Following Surgical Resection in Patients With Stage I Non-Small Cell Lung Cancer

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

To explore the effect of thymosin alpha 1 (Tα1) on postoperative peripheral blood circulating tumor cells and immunosenescence in patients with early-stage non-small cell lung cancer (NSCLC).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 75
Healthy Volunteers: f
View:

• Pathologically confirmed stage I (per AJCC 8th edition) invasive NSCLC

• Resectable tumor

• undergoing lobectomy and systemic lymph node dessection

• Without a previous history of malignant tumors or other concurrent malignancies

• Naïve to any anticancer therapies or other immunostimulatory agents

• Eastern Cooperative Oncology Group (ECOG) performance status (PS) score 0-1, with cardiac, pulmonary, hepatic, cerebral, and renal functions capable of withstanding surgery

• Aged ≥18 years and ≤75 years

• Having signed written informed consent and capable of adhering to the visit schedule and related procedures outlined in the study protocol

Locations
Other Locations
China
National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College
RECRUITING
Beijing
Contact Information
Primary
Yousheng Mao
youshengmao@gmail.com
8610-67781331
Backup
Li Fu
fulipumc@163.com
Time Frame
Start Date: 2024-06-30
Estimated Completion Date: 2025-12-30
Participants
Target number of participants: 40
Treatments
No_intervention: Control group
only observation after surgery
Experimental: Tα1 group
Tα1 treatment for 3 months after surgery
Sponsors
Leads: Yousheng Mao

This content was sourced from clinicaltrials.gov