Epidemiology and risk factors for the development of cutaneous toxicities in patients treated with immune-checkpoint inhibitors: A United States population-level analysis.
Epidemiology and risk factors for the development of cutaneous toxicities in patients treated with immune-checkpoint inhibitors: A United States population-level analysis.
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DOI:
10.1016/j.jaad.2021.03.094
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发表时间:
2022-03
影响因子:
13.8
通讯作者:
Semenov, Yevgeniy R.
中科院分区:
文献类型:
--
作者:
Wongvibulsin, Shannon;Pahalyants, Vartan;Kalinich, Mark;Murphy, William;Yu, Kun-Hsing;Wang, Feicheng;Chen, Steven T.;Reynolds, Kerry;Kwatra, Shawn G.;Semenov, Yevgeniy R.
关键词:
A variety of dermatoses have been reported in the growing number of patients treated with immune-checkpoint inhibitors (ICIs), but the current understanding of cutaneous immune-related adverse events (irAEs) is limited. To determine the cumulative incidence, distribution, and risk factors of cutaneous irAEs after ICI initiation. This was a retrospective cohort study of patients in a national insurance claims database including cancer patients treated with ICIs and matched controls. The study included 8637 ICI patients and 8637 matched controls. The overall incidence of cutaneous irAEs was 25.1%, with a median onset time of 113 days. The ICI group had a significantly higher incidence of pruritus, mucositis, erythroderma, maculopapular eruption, vitiligo, lichen planus, bullous pemphigoid, Grover disease, rash, other nonspecific eruptions, and drug eruption or other nonspecific drug reaction. Patients with melanoma and renal cell carcinoma and those receiving combination therapy were at a higher risk of cutaneous irAEs. Retrospective design without access to patient chart data. This study identifies cutaneous irAEs in a real-world clinical setting and highlights patient groups that are particularly at risk. The results can aid dermatologists at the bedside in the diagnosis of cutaneous irAEs and in formulating management recommendations to referring oncologists regarding the continuation of ICI therapy.
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影响因子:
10.9
作者:
Gong J;Chehrazi-Raffle A;Reddi S;Salgia R
通讯作者:
Salgia R
DOI:
10.1056/nejmoa1504030
发表时间:
2015-07-02
期刊:
The New England journal of medicine
影响因子:
--
作者:
Larkin J;Chiarion-Sileni V;Gonzalez R;Grob JJ;Cowey CL;Lao CD;Schadendorf D;Dummer R;Smylie M;Rutkowski P;Ferrucci PF;Hill A;Wagstaff J;Carlino MS;Haanen JB;Maio M;Marquez-Rodas I;McArthur GA;Ascierto PA;Long GV;Callahan MK;Postow MA;Grossmann K;Sznol M;Dreno B;Bastholt L;Yang A;Rollin LM;Horak C;Hodi FS;Wolchok JD
通讯作者:
Wolchok JD
影响因子:
13.8
作者:
Geisler AN;Phillips GS;Barrios DM;Wu J;Leung DYM;Moy AP;Kern JA;Lacouture ME
通讯作者:
Lacouture ME
影响因子:
1.7
作者:
Silva, Josenilson Antônio da;Mesquita, Kleyton de Carvalho;Campbell, Iphis Tenfuss
通讯作者:
Campbell, Iphis Tenfuss
DOI:
10.1097/pas.0000000000000900
发表时间:
2017-10
期刊:
The American journal of surgical pathology
影响因子:
--
作者:
Kaunitz GJ;Loss M;Rizvi H;Ravi S;Cuda JD;Bleich KB;Esandrio J;Sander I;Le DT;Diaz LA Jr;Brahmer JR;Drake CG;Hollmann TJ;Lacouture ME;Hellmann MD;Lipson EJ;Taube JM
通讯作者:
Taube JM