Optimizing immune checkpoint blockade in metastatic uveal melanoma: exploring the association of overall survival and the occurrence of adverse events

被引:0
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作者
Koch, Elias A. T. [1 ,2 ,3 ,4 ]
Petzold, Anne [1 ,2 ,3 ,4 ]
Dippel, Edgar [5 ]
Erdmann, Michael [1 ,2 ,3 ,4 ]
Gesierich, Anja [6 ]
Gutzmer, Ralf [7 ]
Hassel, Jessica C. [8 ,9 ,10 ]
Haferkamp, Sebastian [11 ]
Kaehler, Katharina C. [12 ]
Kreuzberg, Nicole [13 ]
Leiter, Ulrike [14 ]
Loquai, Carmen [15 ,16 ]
Meier, Friedegund [17 ,18 ,19 ]
Meissner, Markus [20 ]
Mohr, Peter [21 ]
Pfoehler, Claudia [22 ]
Rahimi, Farnaz [23 ]
Schell, Beatrice [24 ]
Terheyden, Patrick [25 ]
Thoms, Kai-Martin [26 ]
Ugurel, Selma [27 ]
Ulrich, Jens [28 ]
Utikal, Jochen [29 ,30 ,31 ]
Weichenthal, Michael [12 ]
Ziller, Fabian [32 ]
Berking, Carola [1 ,2 ,3 ,4 ]
Heppt, Markus V. [1 ,2 ,3 ,4 ]
机构
[1] Friedrich Alexander Univ Erlangen Nurnberg FAU, Dept Dermatol, Uniklinikum Erlangen, Erlangen, Germany
[2] European Metropolitan Area Nuremberg CCC ER EMN, Comprehens Canc Ctr Erlangen, Erlangen, Germany
[3] Friedrich Alexander Univ Erlangen Nurnberg FAU, Deutsch Zentrum Immuntherapie DZI, Uniklinikum Erlangen, Erlangen, Germany
[4] Friedrich Alexander Univ Erlangen Nurnberg FAU, Bavarian Canc Res Ctr BZKF, Uniklinikum Erlangen, Erlangen, Germany
[5] Ludwigshafen Med Ctr, Dept Dermatol, Ludwigshafen, Germany
[6] Univ Hosp Wurzburg, Dept Dermatol, Wurzburg, Germany
[7] Ruhr Univ Bochum Campus Minden, Skin Canc Ctr Minden, Dept Dermatol, Muhlenkreiskliniken AoR, Minden, Germany
[8] NCT Heidelberg, Dept Dermatol, Heidelberg, Germany
[9] Heidelberg Univ, Med Fac Heidelberg, Natl Ctr Tumor Dis NCT, NCT Heidelberg, Heidelberg, Germany
[10] Heidelberg Univ, Univ Hosp Heidelberg, Med Fac Heidelberg, Heidelberg, Germany
[11] Univ Hosp Regensburg, Dept Dermatol, Regensburg, Germany
[12] Univ Hosp Schleswig Holstein, Dept Dermatol, Kiel, Germany
[13] Univ Hosp Cologne, Skin Canc Ctr, Dept Dermatol & Venereol, Ctr Integrated Oncol CIO Koln Bonn, Cologne, Germany
[14] Univ Hosp Tubingen, Ctr Dermatooncol, Dept Dermatol, Tubingen, Germany
[15] Univ Med Ctr Mainz, Dept Dermatol, Mainz, Germany
[16] Klinikum Bremen Ost, Dept Dermatol, Bremen, Germany
[17] Univ Canc Ctr Dresden, Skin Canc Ctr, Dresden, Germany
[18] Natl Ctr Tumor Dis, Dresden, Germany
[19] Tech Univ Dresden, Univ Hosp Carl Gustav Carus, Dept Dermatol, Dresden, Germany
[20] Goethe Univ, Dept Dermatol Venereol & Allergol, Frankfurt, Germany
[21] Elbeklinikum, Dept Dermatol, Buxtehude, Germany
[22] Saarland Univ, Dept Dermatol, Med Sch, Homburg, Germany
[23] Munich Univ Hosp LMU, Dept Dermatol & Allergy, Munich, Germany
[24] SRH Wald Klinikum Gera, Dept Dermatol, Gera, Germany
[25] Univ Lubeck, Dept Dermatol, Lubeck, Germany
[26] Univ Med Ctr Goettingen, Dept Dermatol, Gottingen, Germany
[27] Univ Duisburg Essen, Univ Hosp Essen, Dept Dermatol, Essen, Germany
[28] Harzklinikum Dorothea Christiane Erxleben, Dept Dermatol, Quedlinburg, Germany
[29] Ruprecht Karl Univ Heidelberg, Univ Med Ctr Mannheim, German Canc Res Ctr DKFZ, Skin Canc Unit, Mannheim, Germany
[30] Ruprecht Karl Univ Heidelberg, Univ Med Ctr Mannheim, Dept Dermatol Venereol & Allergol, Mannheim, Germany
[31] Univ Med Ctr Mannheim, DKFZ Hector Canc Inst, Mannheim, Germany
[32] DRK Krankenhaus Rabenstein, Dept Dermatol, Chemnitz, Germany
来源
FRONTIERS IN IMMUNOLOGY | 2024年 / 15卷
关键词
uveal melanoma; immune checkpoint blockade; PD-1; CTLA-4; immune-related; adverse events; toxicity; NIVOLUMAB; MONOTHERAPY; IMMUNOTHERAPY; IPILIMUMAB; OUTCOMES; SAFETY; MIA;
D O I
10.3389/fimmu.2024.1395225
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Introduction Despite recent advancements in the treatment of metastatic uveal melanoma (UM), the availability of further treatment options remains limited and the prognosis continues to be poor in many cases. In addition to tebentafusp, immune checkpoint blockade (ICB, PD-1 (+/-) CTLA-4 antibodies) is commonly used for metastatic UM, in particular in HLA-A 02:01-negative patients. However, ICB comes at the cost of potentially severe immune-related adverse events (irAE). Thus, the selection of patient groups that are more likely to benefit from ICB is desirable.Methods In this analysis, 194 patients with metastatic UM undergoing ICB were included. Patients were recruited from German skin cancer sites and the ADOReg registry. To investigate the association of irAE occurrence with treatment response, progression-free survival (PFS), and overall survival (OS) two cohorts were compared: patients without irAE or grade 1/2 irAE (n=137) and patients with grade 3/4 irAE (n=57).Results In the entire population, the median OS was 16.4 months, and the median PFS was 2.8 months. Patients with grade 3/4 irAE showed more favorable survival than patients without or grade 1/2 irAE (p=0.0071). IrAE occurred in 44.7% (87/194), and severe irAE in 29.4% (57/194) of patients. Interestingly, irColitis and irHepatitis were significantly associated with longer OS (p=0.0031 and p=0.011, respectively).Conclusions This data may indicate an association between irAE and favorable survival outcomes in patients with metastatic UM undergoing ICB treatment and suggests that a reduced tolerance to tumor antigens could be linked to reduced tolerance to self-antigens.
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页数:11
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