Non-Small Cell Lung Cancer (NSCLC) Clinical Trials

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Application of the RecistTM Criteria in Evaluating the Efficacy of Targeted Therapy for Advanced Non-small Cell Lung Cancer With Positive Driving Genes

Status: Recruiting
Location: See location...
Intervention Type: Diagnostic test
Study Type: Observational
SUMMARY

Investigators established the efficacy evaluation criteria for tumor markers (RecistTM) in the preliminary research. Among patients with advanced non-small cell lung cancer, patients with positive driving genes are more likely to exhibit abnormalities in tumor markers, which suggests that this criteria may be more suitable for evaluating the efficacy of targeted therapy in driving gene positive patients. Moreover, The judgment rules of the prelimary criteria still need further improvement. Therefore, in order to broaden the application scope of the RecistTM criteria, further improve the evaluation rules of RecistTM criteria, and multi-dimensionally confirm the reliability of RecistTM criteria on efficacy evaluation, investigators plan to conduct research on the application of RecistTM criteria in evaluating the efficacy of targeted therapy for advanced non-small cell lung cancer with positive driving genes.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
View:

• NSCLC patients with stage IIIB-IV

• Driver gene positive (EGFR,ALK,C-MET, ROS,RET, HER2);

• First line targeted therapy.

• Performance status of 0-2 on the ECOG criteria.

• Any one of the tumor markers is more than three times higher than the normal level, and the tumor markers include: CEA\>15ng/ml,CA-199\>105U/ml,CA-125\>105 U/ml, NSE\>60 ng/ml, SCCAg\>7.5 ng/ml, CYFRA21-1\>21 ng/ml, et al.

• Measurable lesions present

• Age\>=18

• Adequate hematologic (neutrophil count \>= 1,500/uL, platelets \>= 60,000/uL,hemoglobin≥70g/L), hepatic (transaminase =\< upper normal limit(UNL)x2.5, bilirubin level =\< UNLx1.5), and renal (creatinine =\< UNL) function.

• Informed consent from patient or patient's relative.

Locations
Other Locations
China
Cancer Center, Dapping Hospital, Army Medical Center of PLA
RECRUITING
Chongqing
Contact Information
Primary
Xueqin Yang, PhD
yangxueqin@hotmail.com
15923366936
Time Frame
Start Date: 2023-11-13
Estimated Completion Date: 2028-12-31
Participants
Target number of participants: 44
Sponsors
Leads: Xueqin Yang

This content was sourced from clinicaltrials.gov