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Re-Exposure of a PD-1 Inhibitor After Previous Immune-Related Adverse Events.

1/5 보강
Current oncology (Toronto, Ont.) 📖 저널 OA 99.6% 2021: 2/2 OA 2022: 9/9 OA 2023: 10/10 OA 2024: 22/22 OA 2025: 104/104 OA 2026: 132/133 OA 2021~2026 2026 Vol.33(4) OA
Retraction 확인
출처

PICO 자동 추출 (휴리스틱, conf 3/4)

유사 논문
P · Population 대상 환자/모집단
22 patients were included between April 2020 and December 2022 with a median age of 71 years.
I · Intervention 중재 / 시술
a different PD-(L)1 inhibitor
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
In patients receiving a different PD-(L)1 inhibitor, four (44%) developed an irAE, of which 75% were identical with the first. [CONCLUSIONS] Both an intraclass switch of PD-(L)1 inhibitor treatment and re-exposure with the same antibody after an irAE can be considered as options with a fair chance of improving therapy tolerance.

Burghaus-Zhang J, Schulz C, Ramelyte E, Mangana J, Özistanbullu D, Kleemann J

📝 환자 설명용 한 줄

[BACKGROUND] Programmed cell death protein (ligand) 1 (PD-(L)1) inhibitors are well established in the treatment of dermatological tumors.

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↓ .bib ↓ .ris
APA Burghaus-Zhang J, Schulz C, et al. (2026). Re-Exposure of a PD-1 Inhibitor After Previous Immune-Related Adverse Events.. Current oncology (Toronto, Ont.), 33(4). https://doi.org/10.3390/curroncol33040180
MLA Burghaus-Zhang J, et al.. "Re-Exposure of a PD-1 Inhibitor After Previous Immune-Related Adverse Events.." Current oncology (Toronto, Ont.), vol. 33, no. 4, 2026.
PMID 42041699 ↗

Abstract

[BACKGROUND] Programmed cell death protein (ligand) 1 (PD-(L)1) inhibitors are well established in the treatment of dermatological tumors. Mostly, they are well tolerated, but in about 9-21% of patients, grade 3/4 immune-related adverse events (irAEs) occur. As treatment options are limited, it is of interest to determine whether readministration of another or the same PD-(L)1 inhibitor is safe.

[METHODS] This is a multicenter, retrospective study on patients with metastasized dermatological tumors who were retreated with either the same or a different PD-(L)1 inhibitor after the development of irAEs. The study was conducted at centers in Heidelberg, Zurich, and Frankfurt.

[RESULTS] 22 patients were included between April 2020 and December 2022 with a median age of 71 years. A total of 13 (59%) patients were re-exposed with the same antibody and nine (41%) received a different PD-(L)1 inhibitor. Six (46%) of the patients who were re-exposed to the same antibody had an irAE, of which 67% were identical with the first. In patients receiving a different PD-(L)1 inhibitor, four (44%) developed an irAE, of which 75% were identical with the first.

[CONCLUSIONS] Both an intraclass switch of PD-(L)1 inhibitor treatment and re-exposure with the same antibody after an irAE can be considered as options with a fair chance of improving therapy tolerance.

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