Efficacy and Safety of Modified Si Jun Zi Tang in Perioperative NSCLC Treatment

Non Small Cell Lung Cancer Clinical Trial

— MSJZT-NSCLC  

Official title:

A Multi-center, Prospective, Exploratory Study Evaluating the Efficacy and Safety of a Modified Si Jun Zi Tang Formula in the Perioperative Treatment of Non-small Cell Lung Cancer

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT06445881
• Other study ID #: IIT20240018C-R1
• Status: Recruiting
• Phase: Phase 2
• Start date: June 1, 2024
• Est. completion date: December 31, 2026

Study information

• Verified date: June 2024
• Source: First Affiliated Hospital of Zhejiang University
• Contact: Jianzhen Shan, MD
• Phone: +86-571-87235409
• Email: jianzhenshan[@]163.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Chemotherapy combined with immunotherapy is the current standard perioperative treatment for non-small cell lung cancer (NSCLC). However, this regimen has multiple side effects and shows variable efficacy among individuals. In China, adjunctive traditional Chinese medicine is widely accepted by lung cancer patients. Modified Si Jun Zi Tang, a classic formula in traditional Chinese medicine, is known for its benefits in unifying and strengthening the spleen. This study aims to evaluate whether the addition of Modified Si Jun Zi Tang to chemotherapy and immunotherapy during the neoadjuvant phase can improve the R0 resection rate, objective response rate (ORR), and safety in patients with resectable and potentially resectable NSCLC. Secondary objectives include assessing whether this combination can improve 1-year and 2-year disease-free survival (DFS) post-surgery. Additionally, we will collect relevant biological samples to identify tumor markers associated with efficacy, prognosis, and side effects, providing a theoretical basis for modernizing and standardizing traditional Chinese medicine.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 60
• Est. completion date: December 31, 2026
• Est. primary completion date: December 31, 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

1. Age = 18 and = 75 years.

2. Pathologically confirmed non-small cell lung cancer (NSCLC) with no prior treatment for this tumor.

3. Clinical stage II-IIIB (N2) tumors assessed as resectable or potentially resectable by a multidisciplinary team (MDT).

4. Eastern Cooperative Oncology Group (ECOG) performance status (PS) score of 0 - 1.

5. Adequate organ function, including:

Bone marrow: Absolute neutrophil count (ANC) = 1.5 x 10^9/L, platelets = 80 x 10^9/L, hemoglobin = 90 g/L. Liver: Total bilirubin = 1.5 times the upper limit of normal (ULN), aspartate aminotransferase (AST or SGOT) and alanine aminotransferase (ALT or SGPT) = 3 times ULN. Kidneys: Creatinine clearance rate = 45 mL/min (using the standard Cockcroft-Gault formula) or = 1.5 times ULN.

6. At least one measurable lesion according to RECIST v1.1 criteria.

7. For women: Must be surgically sterilized, postmenopausal, or use highly effective contraception during and for 3 months after treatment; must not be pregnant or breastfeeding during the treatment period.

8. Patients must have compliance and geographic proximity to ensure adequate follow-up.

Exclusion Criteria:

1. Patients with a history of autoimmune diseases, active tuberculosis, active hepatitis (HBV DNA <2000 IU), or HIV infection.

2. Patients expected to be unable to tolerate surgery, such as those with severe cardiopulmonary insufficiency or coagulation disorders (APTT <1.5 times ULN, INR >2.0, PT >16 seconds).

3. History of other malignancies within the past 2 years, except for cured cervical carcinoma in situ, basal cell carcinoma of the skin, superficial bladder cancer [Ta, Tis & T1], or papillary thyroid carcinoma.

4. Any unstable systemic disease (including active systemic infections requiring systemic treatment, liver disease, kidney disease, or metabolic disorders, acute cerebral infarction or cerebral hemorrhage, etc.).

5. Significant cardiovascular events: congestive heart failure > NYHA Class 2; unstable angina, active coronary artery disease (CAD) (myocardial infarction over 1 year before study entry is allowed); severe arrhythmias requiring treatment (use of beta-blockers or digoxin is allowed) or uncontrolled hypertension.

6. Significant neurological or psychiatric disorders, including epilepsy, dementia, etc.

7. Patients with interstitial lung disease or a history of interstitial pneumonia.

8. Participation in other anti-tumor drug clinical trials within 4 weeks prior to enrollment.

9. Previous use of PD-1/PD-L1 inhibitors or other anti-tumor immunotherapy drugs.

10. Known history of allogeneic organ transplantation or allogeneic hematopoietic stem cell transplantation or planned transplantation.

11. Known allergy to the drugs or drug excipients used in the study or severe allergic reactions to other monoclonal antibodies.

12. Presence of other severe physical or laboratory abnormalities that may increase the risk of participating in the study, interfere with study results, or any other condition that, in the investigator's judgment, may affect the conduct or results of the clinical study.

Related Conditions & MeSH terms

• Carcinoma, Non-Small-Cell Lung
• Lung Neoplasms
• Non Small Cell Lung Cancer
• Perioperative Complication

Intervention

Drug:
• Modified Si Jun Zi Tang
Modified Si Jun Zi Tang is a classic formula in traditional Chinese medicine, known for its benefits in unifying and strengthening the spleen.

Locations

Country	Name	City	State
China	the First Affilated Hospital of Zhejiang University	Hangzhou	Zhejiang

Sponsors (1)

Lead Sponsor	Collaborator
First Affiliated Hospital of Zhejiang University

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	R0 Resection Rate	The proportion of patients achieving complete surgical resection with negative margins (R0 resection) after neoadjuvant therapy.	Assessed at the time of surgery, approximately 2-4 months after starting treatment.
Primary	Objective Response Rate (ORR)	The proportion of patients achieving partial or complete response as defined by RECIST v1.1 criteria.	Assessed after 2 cycles of treatment (approximately 6 weeks) and before surgery, if applicable.
Primary	Incidence of Adverse Reactions	The proportion of patients experiencing treatment-related adverse reactions, graded according to the Common Terminology Criteria for Adverse Events (CTCAE) v5.0.	Assessed throughout the treatment period, from the start of treatment up to one year post-surgery.
Secondary	1-Year Disease-Free Survival (DFS)	The proportion of patients who remain free of disease recurrence or progression one year after surgery.	Assessed one year post-surgery.
Secondary	2-Year Disease-Free Survival (DFS)	The proportion of patients who remain free of disease recurrence or progression two years after surgery.	Assessed two years post-surgery.