Local Therapy in Advanced NSCLC With Non-progressive Disease (PD) After First Line Therapy

Lung Neoplasms Clinical Trial

— LOCAL  

Official title:

Local Consolidative Therapy (LCT) in Patients With Advanced Stage Non-small Cell Lung Cancer Who do Not Progress After Front Line Systemic Therapy

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03046316
• Other study ID #: CTONG1602
• Status: Recruiting
• Phase: N/A
• Start date: June 1, 2020
• Est. completion date: July 1, 2026

Study information

• Verified date: July 2020
• Source: Guangdong Association of Clinical Trials
• Contact: ZHEN WANG, PhD,MD
• Phone: +8683827812
• Email: hunterol[@]163.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a prospective single arme real-world study clinical study, which aims to investigate the overall benefit and safety of consolidative therapy in advanced NSCLC (stage III/IV) patients , who do not progress after front line systemic therapy (chemotherapy, target therapy or immunological checkpoint inhibitors).

Description:

It is required that pathological diagnosis and genetic profile including epidermal growth factor receptor (EGFR), anaplastic lymphoma kinase (ALK) and ROS proto-oncogene 1 (ROS1) be established prior to enrollment. Standard front line systemic should be given according to clinical practice. Molecular targeting drugs for patients with driving mutations should be acquired legally. Patients without driving mutations should undergo standard first line chemotherapy and or immunological checkpoint inhibitors. One cycle is three weeks and response evaluation is done every two cycles. CR, PR and SD should be confirmed after four cycles of therapy.

Patients, who achieve non-PD after four cycles of treatment, with distant metastasis involving no more than five total metastatic lesions, will be screened and enrolled.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 60
• Est. completion date: July 1, 2026
• Est. primary completion date: July 1, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Male or female, age >= 18 years, with life expectancy of at least 12 weeks.

• Patients with histologically documented metastatic (stage IV) non-small cell lung cancer.

• Subjected to driving genes examination including EGFR, ALK and ROS1.

• Achieve complete response (CR)/partial response (PR)/stable disease (SD) after front line systemic treatment (chemotherapy, targeted therapy or immunological checkpoint inhibitors).

• Total metastatic lesions is limited to five.

• Eastern Cooperative Oncology Group (ECOG) performance status (PS) of <= 2.

• Patients must have measurable disease according to the RECIST (version 1.1) criteria.

• Adequate organ function as defined by the following criteria:

• Liver function: aspartate aminotransferase (AST) and alanine aminotransferase (ALT) <= 2.5 upper limit of normal (ULN) in the absence of liver metastases or up to 5 ULN in case of liver metastases. Total bilirubin <= 1.5 ULN.

• Bone marrow function: Granulocyte count >= 1,500/mm3 and platelet count =100,000/mm3 and hemoglobin >= 80g/dl.

• Renal function: serum creatinine <= 1.5 ULN or creatinine clearance >= 60 ml/min. (based on modified Cockcroft-Gault formula).

• Adequate coagulating function.

• For all females of childbearing potential a negative serum/urine pregnancy test must be obtained within 48 hours before enrollment. Postmenopausal women must have been amenorrhoeic for at least 12 months to be considered of non-childbearing potential. Males must agree to use effective contraception during the study period and for at least 12 weeks after completion of the study treatment.

• Written (signed) informed Consent to participate in the study.

• Willingness and ability to comply with scheduled visits, treatment plans, laboratory tests, and other study procedures.

Exclusion Criteria:

• Stage I-III a NSCLC completing radical treatment , then undergoing systemic anti-cancer treatment after recurrence.

• Patients with PFS no more than 3 months. to first line theray.

• Patients with history of any other malignancies within 5 years (except for adequately treated carcinoma in situ of the cervix or basal or squamous cell skin cancer).

• Prior palliative surgery or other local therapy specifically directed against advanced lung cancer.

• Contraindication for localized treatment including surgery, radiotherapy or interventional therapy judged by physicians.

• Patients with any unstable systemic disease (including active infections, significant cardiovascular disease, any significant hepatic, renal or metabolic disease).

• Patients who are at risk (in the investigator's opinion) of transmitting human immunodeficiency virus (HIV) through blood or other body fluids.

• Nursing or lactating women.

• Sexually active males and females (of childbearing potential) unwilling to practice contraception during the study.

• Patients who has mental disorder or other disease that contribute to no compliance.

• Unwilling to write informed consent to participate in the study.

• Patients who is unwilling to accept the follow-up.

Related Conditions & MeSH terms

• Lung Neoplasms

Intervention

Other:
• local consolidative treatment
local consolidative treatment to primary or metastases, which includes surgery, radiotherapy or interventional therapy

Locations

Country	Name	City	State
China	Guangdong General Hospital	Guangzhou	Guagndong

Sponsors (1)

Lead Sponsor	Collaborator
Guangdong Association of Clinical Trials

Country where clinical trial is conducted

China, 

References & Publications (16)

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Rusthoven KE, Kavanagh BD, Cardenes H, Stieber VW, Burri SH, Feigenberg SJ, Chidel MA, Pugh TJ, Franklin W, Kane M, Gaspar LE, Schefter TE. Multi-institutional phase I/II trial of stereotactic body radiation therapy for liver metastases. J Clin Oncol. 2009 Apr 1;27(10):1572-8. doi: 10.1200/JCO.2008.19.6329. Epub 2009 Mar 2. — View Citation

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* Note: There are 16 references in all — Click here to view all references

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Progression free survival	month	8 months
Secondary	Response rate	percentage(%)	6 months
Secondary	Lung Cancer Symptom Scale	quality of life	12 months
Secondary	overall survival	month	2 years