Evaluating the Safety and Efficacy of Pembrolizumab Combined With MWA for Advanced NSCLC

Non Small Cell Lung Cancer Clinical Trial

Official title:

A Prospective，Single Center, Randomized Control，Phase III Clinical Study for Evaluating the Safety and Efficacy of Pembrolizumab Combined With MWA for Patients With Stage ⅢB-Ⅳ NSCLC Who Failed With First-line Therapy

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03769129
• Other study ID #: ZZWMAICI-005
• Status: Recruiting
• Phase: N/A
• Start date: November 1, 2018
• Est. completion date: November 1, 2029

Study information

• Verified date: February 2023
• Source: Second Affiliated Hospital of Guangzhou Medical University
• Contact: zhang zhenfeng, MD,PHD
• Phone: 02034153532
• Email: zhangzhf[@]gzhmu.edu.cn
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a prospective, randomized, single clinical study designed to evaluate its safety and efficacy by using Microwave Ablation combine with Pembrolizumab in patients with Stage ⅢB-Ⅳ Non-small Cell Lung.Cancer (NSCLC) who failed with first-line therapy.

Description:

Lung cancer is one of the most common malignant tumors in the world and has become the No. 1 cause of death from malignant tumors in China. Non-small cell lung cancer (NSCLC) includes squamous cell carcinomas, adenocarcinomas, and large cell carcinomas and accounts for about 80-85% of all lung cancers. NSCLC cancer cells divide slowly in a diffusive manner and metastasize at a relatively late stage compared to small cell carcinomas. A majority of patients with NSCLC are already in advanced stages and have a low 5-year survival rate.

Treatments for advanced NSCLC include chemotherapy ,targeted therapies and immunotherapy. The microwave ablation is the good choice for patients who cannot tolerate surgical resection. A large number of studies have shown that local minimally invasive ablation therapy within a certain temperature range can stimulate the body to produce an immune response to varying degrees. The study found that for a variety of malignant tumor models, thermal ablation local treatment of in situ tumors, while the disappearance of other metastatic lesions, and treated mice are resistant to secondary vaccination of the same tumor, proving that thermal ablation therapy stimulates long-lasting Anti-tumor immunity. Pembrolizumab are representative drugs for immunosuppressive agents, and its indications have been approved in various types of tumors, including advanced melanoma, advanced squamous non-small cell lung cancer, advanced renal cell carcinoma, and classical Hodgkin's lymphoma and late recurrent head and neck squamous cell carcinoma patients. Whether the combination of the two can cause a stronger anti-tumor immune response in the body. However, the flexibility, safety and efficacy of using Microwave Ablation combine with Pembrolizumab in NSCLC patients are still unclear.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 100
• Est. completion date: November 1, 2029
• Est. primary completion date: November 1, 2026
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Pathologically diagnosed IIIB or IV non-small cell lung cancer.

2. Previously accepted first-line standard treatment failure or recurrence

3. At least one measurable lesion.

4. The patient has not received any other anti-cancer treatment within four weeks.

5. Any gender, age =18 years

6. ECOG PS : 0-2 points

7. Expected survival = 6 months

8. The level of organ function meets the following criteria.

(1) subject to the standard blood test: ANC = 1.5×109 / L, PLT = 50×109 / L, Hb = 90g/L.

(2) biochemical tests must meet the following criteria: TBIL<1.5×ULN, ALT, AST <2.5×ULN ( if liver metastasis ALT, AST can be <5×ULN), BUN, and Cr = 1×ULN).

9. Female patients in child bearing period must have evidence of negative pregnancy test, and agree to take effective contraceptive measures until 6months after therapy.

10. Subjects volunteered to join the study, signed informed consent, good compliance, with follow-up.

Exclusion Criteria:

1. Patients with two or more kinds of tumors.

2. Patients with active viral or bacterial infection, and have failed to be controlled by anti-infective treatment.

3. Patients with seropositive response of Human immunodeficiency virus (HIV) and syphilis, or fail to control the hepatitis B virus or hepatitis C virus infection.

4. Patients with active rheumatic diseases, organ transplantation and other diseases affecting the immune system seriously.

5. Patients with severe heart and lung dysfunction.

6. Patients with severe chronic diseases of kidney, liver and other important organs.

7. Patients with any other serious illness that the investigators consider it will may affect the patient's treatments, follow-up or assessment, including any uncontrolled clinically significant neurological or psychiatric disorders, immunoregulatory diseases, metabolic diseases, infectious diseases and so on.

8. Patients who take part in clinical trials of other drugs or biological therapy at present or within 30 days before enrollment.

9. Patients who need long-term use of immunosuppressive drugs or patients who are undergoing treatment of autoimmune diseases.

10. Patients who need long-term use of glucocorticoid.

11. Women patients in gestation period or suckling period.

Related Conditions & MeSH terms

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

Intervention

Drug:
• Pembrolizumab
Pembrolizumab

Procedure:
• microwave ablation
microwave ablation

Locations

Country	Name	City	State
China	zhang Zhenfeng	Guangzhou	Guangdong

Sponsors (1)

Lead Sponsor	Collaborator
Second Affiliated Hospital of Guangzhou Medical University

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Overall survival	Overall survival (OS) will be defined as the elapsed time from the enrollment to death from any cause. For surviving patients, follow-up will be censored at the date of last contact (or last date known to be alive). Follow-up for OS will occur every 12 weeks (±1 month) until death or withdrawal of consent from the study.	2 years
Secondary	Incidence of Treatment-Emergent Adverse Events(Safety)	All the local reactions, systemic reactions, all the adverse events and serious adverse events obtained during the study of all the patients included in the first stage and the second stage of this study	2 years
Secondary	Progression-Free Survival	From enrollment to progression of disease.	2 years