2022
DOI: 10.3892/ol.2022.13545
|View full text |Cite
|
Sign up to set email alerts
|

Meta‑analysis of the efficacy and safety of sintilimab for treating advanced non‑small cell lung cancer

Abstract: Lung cancer is the leading cause of death from malignant tumors in China, and non-small cell lung cancer (NSCLC) accounts for >80% of all types of lung cancer. Novel immunotherapeutic agents targeting programmed death protein-1 (PD-1) and its ligands [programmed death ligands (PD-L)1 and 2] have emerged as important therapeutic measures and trends in the treatment of advanced NSCLC. Sintilimab (trade name, Daboshu) is a humanized IgG4 monoclonal antibody targeting PD-1 that was developed by Innovent Biologics … Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
1
0

Year Published

2023
2023
2024
2024

Publication Types

Select...
2

Relationship

0
2

Authors

Journals

citations
Cited by 2 publications
(2 citation statements)
references
References 26 publications
(35 reference statements)
0
1
0
Order By: Relevance
“…The study by Kang et al (17) indicated that the utilization of neoadjuvant anti-PD-1 immunotherapy exhibits promising long-term efficacy in individuals diagnosed with resectable stage I-IIIA NSCLC. A phase 1b clinical trial (ChiCTR-OIC-17013726) involving patients with stage IIIB NSCLC evaluated the safety and efficacy of neoadjuvant therapy using PD-1 inhibitors, specifically sintilimab (18). Patients received two cycles of sintilimab (200 mg; intravenous injection on day 22), followed by surgical intervention between days 29 and 43.…”
Section: Discussionmentioning
confidence: 99%
“…The study by Kang et al (17) indicated that the utilization of neoadjuvant anti-PD-1 immunotherapy exhibits promising long-term efficacy in individuals diagnosed with resectable stage I-IIIA NSCLC. A phase 1b clinical trial (ChiCTR-OIC-17013726) involving patients with stage IIIB NSCLC evaluated the safety and efficacy of neoadjuvant therapy using PD-1 inhibitors, specifically sintilimab (18). Patients received two cycles of sintilimab (200 mg; intravenous injection on day 22), followed by surgical intervention between days 29 and 43.…”
Section: Discussionmentioning
confidence: 99%
“…In squamous cell carcinoma patients who don't have driver mutation, sintillimab plus paclitaxel/nab-paclitaxel plus platinum was better than sintillimab plus gemcitabine plus platinum.And the treatment was well tolerated but TREAs was more severe [7].…”
Section: Sintilimabmentioning
confidence: 96%