Impact of neoadjuvant immunotherapy on postoperative cardiac adverse events in NSCLC: insights from a bidirectional cohort.
코호트
1/5 보강
PICO 자동 추출 (휴리스틱, conf 3/4)
유사 논문P · Population 대상 환자/모집단
310 patients who received neoadjuvant therapy (nCT = 115; nCIT = 195), comprising both retrospective and prospective cases.
I · Intervention 중재 / 시술
neoadjuvant therapy (nCT = 115; nCIT = 195), comprising both retrospective and prospective cases
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
[RESULTS] Before PSM, the overall incidence of PCAEs was comparable between the nCT and nCIT groups [20.9% vs.
[BACKGROUND] The impact of neoadjuvant chemo-immunotherapy (nCIT) on perioperative cardiac safety in patients undergoing lung cancer resection remains unclear.
- 표본수 (n) 166
- p-value P < 0.001
- p-value P = 0.002
- 95% CI 0.423-2.017
- 연구 설계 cohort study
APA
Yan C, Zhang X, et al. (2026). Impact of neoadjuvant immunotherapy on postoperative cardiac adverse events in NSCLC: insights from a bidirectional cohort.. International journal of surgery (London, England). https://doi.org/10.1097/JS9.0000000000004846
MLA
Yan C, et al.. "Impact of neoadjuvant immunotherapy on postoperative cardiac adverse events in NSCLC: insights from a bidirectional cohort.." International journal of surgery (London, England), 2026.
PMID
41604535 ↗
Abstract 한글 요약
[BACKGROUND] The impact of neoadjuvant chemo-immunotherapy (nCIT) on perioperative cardiac safety in patients undergoing lung cancer resection remains unclear. This study aimed to evaluate the incidence and risk factors of postoperative cardiac adverse events (PCAEs) in patients receiving nCIT compared with neoadjuvant chemotherapy (nCT).
[METHODS] We conducted a bidirectional cohort study including 310 patients who received neoadjuvant therapy (nCT = 115; nCIT = 195), comprising both retrospective and prospective cases. Propensity score matching (PSM) at a 1:1 ratio was applied to balance baseline characteristics. Univariable and multivariable logistic regression analyses were performed to identify independent predictors of PCAEs, including clinically important perioperative atrial fibrillation, myocardial injury after non-cardiac surgery, myocardial infarction, and heart failure. Variance inflation factors were calculated to assess multicollinearity, and model goodness-of-fit was evaluated. Subgroup and sensitivity analyses were conducted to examine the robustness of findings.
[RESULTS] Before PSM, the overall incidence of PCAEs was comparable between the nCT and nCIT groups [20.9% vs. 25.6%; odds ratio (OR) 1.307, 95% confidence interval (CI) 0.759-2.300; P = 0.342]. After PSM (n = 166), no significant difference in PCAEs was observed (19.3% vs. 18.1%; OR 0.924, 95% CI 0.423-2.017; P = 0.842). Multivariable analyses confirmed that nCIT was not independently associated with increased PCAEs before (Model 3 OR 1.137, 95% CI 0.573-2.299) or after PSM (Model 3 OR 1.462, 95% CI 0.510-4.387). Hypertension (OR 11.024, 95% CI 3.518-38.380; P < 0.001) and pericardial window creation (OR 8.310, 95% CI 2.186-34.139; P = 0.002) were identified as strong independent predictors of PCAEs. Subgroup and sensitivity analyses consistently showed no elevated cardiac risk associated with nCIT across sex, hypertension status, surgical approach, ACEI/ARB use, CCB use, or treatment era.
[CONCLUSIONS] In this bidirectional cohort study, nCIT did not increase the risk of postoperative cardiac adverse events compared with nCT. Hypertension and pericardial window creation were significant independent risk factors for PCAEs. These findings support the perioperative cardiac safety of nCIT in lung cancer surgery.
[METHODS] We conducted a bidirectional cohort study including 310 patients who received neoadjuvant therapy (nCT = 115; nCIT = 195), comprising both retrospective and prospective cases. Propensity score matching (PSM) at a 1:1 ratio was applied to balance baseline characteristics. Univariable and multivariable logistic regression analyses were performed to identify independent predictors of PCAEs, including clinically important perioperative atrial fibrillation, myocardial injury after non-cardiac surgery, myocardial infarction, and heart failure. Variance inflation factors were calculated to assess multicollinearity, and model goodness-of-fit was evaluated. Subgroup and sensitivity analyses were conducted to examine the robustness of findings.
[RESULTS] Before PSM, the overall incidence of PCAEs was comparable between the nCT and nCIT groups [20.9% vs. 25.6%; odds ratio (OR) 1.307, 95% confidence interval (CI) 0.759-2.300; P = 0.342]. After PSM (n = 166), no significant difference in PCAEs was observed (19.3% vs. 18.1%; OR 0.924, 95% CI 0.423-2.017; P = 0.842). Multivariable analyses confirmed that nCIT was not independently associated with increased PCAEs before (Model 3 OR 1.137, 95% CI 0.573-2.299) or after PSM (Model 3 OR 1.462, 95% CI 0.510-4.387). Hypertension (OR 11.024, 95% CI 3.518-38.380; P < 0.001) and pericardial window creation (OR 8.310, 95% CI 2.186-34.139; P = 0.002) were identified as strong independent predictors of PCAEs. Subgroup and sensitivity analyses consistently showed no elevated cardiac risk associated with nCIT across sex, hypertension status, surgical approach, ACEI/ARB use, CCB use, or treatment era.
[CONCLUSIONS] In this bidirectional cohort study, nCIT did not increase the risk of postoperative cardiac adverse events compared with nCT. Hypertension and pericardial window creation were significant independent risk factors for PCAEs. These findings support the perioperative cardiac safety of nCIT in lung cancer surgery.
🏷️ 키워드 / MeSH
같은 제1저자의 인용 많은 논문 (5)
- [Strategies for the prevention and treatment of peritoneal metastases in large Borrmann type III and type IV gastric cancer].
- Predicting MammaPrint Recurrence Risk from Breast Cancer Pathological Images Using a Weakly Supervised Transformer.
- Utility of 3D Imaging in the Objective Evaluation of Glabellar Lines Following Botulinum Toxin Treatment.
- Single-cell RNA sequencing dissect the immunological network of immune checkpoint inhibitors-induced myocarditis.
- RAS/MEK/PI3K pathway inhibition augments response to CD40 agonism by targeting CD11b Bregs thereby overcoming melanoma PD1-resistance.