Patterns of immune-related adverse events in patients treated for various cancer types with immune checkpoint inhibitors.
1/5 보강
PICO 자동 추출 (휴리스틱, conf 2/4)
유사 논문P · Population 대상 환자/모집단
241 patients representing 262 treatment lines involving ICIs at a single institution.
I · Intervention 중재 / 시술
추출되지 않음
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
The 5.58-month difference in median time to irAE onset has important implications for monitoring protocols. Further research is needed to identify factors predicting irAE patterns and severity.
[AIMS] To investigate the association between primary cancer type and the tissues affected by immune-related adverse events (irAEs) in patients treated with immune checkpoint inhibitors (ICIs).
- p-value p = 0.00011
APA
Slaught MJ, Kaakour D, et al. (2026). Patterns of immune-related adverse events in patients treated for various cancer types with immune checkpoint inhibitors.. Future oncology (London, England), 22(1), 37-43. https://doi.org/10.1080/14796694.2025.2600910
MLA
Slaught MJ, et al.. "Patterns of immune-related adverse events in patients treated for various cancer types with immune checkpoint inhibitors.." Future oncology (London, England), vol. 22, no. 1, 2026, pp. 37-43.
PMID
41423709
Abstract
[AIMS] To investigate the association between primary cancer type and the tissues affected by immune-related adverse events (irAEs) in patients treated with immune checkpoint inhibitors (ICIs).
[PATIENTS & METHODS] A retrospective chart review was conducted on 241 patients representing 262 treatment lines involving ICIs at a single institution.
[RESULTS] No significant association was found between cancer type and tissue-specific irAEs. irAE incidence was higher with combination PD-1/CTLA-4 inhibitors vs. PD-1 inhibitors alone (61% vs. 46%, = 0.042). Median time to first irAE was 7.88 months for PD-1 monotherapy versus 2.30 months for combination therapy (log-rank p = 0.00011), a difference of 5.58 months.
[CONCLUSIONS] Primary cancer type was not significantly associated with tissue-specific irAEs in ICI-treated patients. The 5.58-month difference in median time to irAE onset has important implications for monitoring protocols. Further research is needed to identify factors predicting irAE patterns and severity.
[PATIENTS & METHODS] A retrospective chart review was conducted on 241 patients representing 262 treatment lines involving ICIs at a single institution.
[RESULTS] No significant association was found between cancer type and tissue-specific irAEs. irAE incidence was higher with combination PD-1/CTLA-4 inhibitors vs. PD-1 inhibitors alone (61% vs. 46%, = 0.042). Median time to first irAE was 7.88 months for PD-1 monotherapy versus 2.30 months for combination therapy (log-rank p = 0.00011), a difference of 5.58 months.
[CONCLUSIONS] Primary cancer type was not significantly associated with tissue-specific irAEs in ICI-treated patients. The 5.58-month difference in median time to irAE onset has important implications for monitoring protocols. Further research is needed to identify factors predicting irAE patterns and severity.
🏷️ 키워드 / MeSH
- Humans
- Immune Checkpoint Inhibitors
- Neoplasms
- Male
- Female
- Retrospective Studies
- Aged
- Middle Aged
- 80 and over
- Drug-Related Side Effects and Adverse Reactions
- Adult
- Incidence
- Programmed Cell Death 1 Receptor
- CTLA-4 Antigen
- Antineoplastic Combined Chemotherapy Protocols
- CTLA-4 inhibitors
- Immune checkpoint inhibitors
- PD-1 inhibitors
- cancer immunotherapy
- combination immunotherapy
- immune-related adverse events
- retrospective cohort study