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

Phase 2

Recruiting

• Conditions: Non Small Cell Lung Cancer; Perioperative Complication
• Interventions: Drug: Modified Si Jun Zi Tang

• Registration Number: NCT06445881
• Lead Sponsor: First Affiliated Hospital of Zhejiang University

Brief 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.

Detailed Description

Not available

Study Timeline

• Status Verified: 2024-06
• Study Start: 2024-06-01
• Study First Submitted: 2024-06-02
• Study First Submitted QC: 2024-06-02
• Last Update Submitted: 2024-06-02
• Study First Posted: 2024-06-06
• Last Update Posted: 2024-06-06
• Primary Completion: 2025-12-31
• Study Completion: 2026-12-31

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 60

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.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Modified Si Jun Zi Tang Combined with Chemotherapy and Immunotherapy	Modified Si Jun Zi Tang	Participants will receive Modified Si Jun Zi Tang combined with chemotherapy (albumin-bound paclitaxel or pemetrexed + carboplatin) and PD1 monoclonal antibody, followed by surgery if feasible. Postoperatively, they will continue with Modified Si Jun Zi Tang and PD1 monoclonal antibody for up to one year.

Primary Outcome Measures

Name	Time	Method
R0 Resection Rate	Assessed at the time of surgery, approximately 2-4 months after starting treatment.	The proportion of patients achieving complete surgical resection with negative margins (R0 resection) after neoadjuvant therapy.
Objective Response Rate (ORR)	Assessed after 2 cycles of treatment (approximately 6 weeks) and before surgery, if applicable.	The proportion of patients achieving partial or complete response as defined by RECIST v1.1 criteria.
Incidence of Adverse Reactions	Assessed throughout the treatment period, from the start of treatment up to one year post-surgery.	The proportion of patients experiencing treatment-related adverse reactions, graded according to the Common Terminology Criteria for Adverse Events (CTCAE) v5.0.

Secondary Outcome Measures

Name	Time	Method
1-Year Disease-Free Survival (DFS)	Assessed one year post-surgery.	The proportion of patients who remain free of disease recurrence or progression one year after surgery.
2-Year Disease-Free Survival (DFS)	Assessed two years post-surgery.	The proportion of patients who remain free of disease recurrence or progression two years after surgery.

Trial Locations

Locations (1)

the First Affilated Hospital of Zhejiang University; 🇨🇳 Hangzhou, Zhejiang, China