Previous radiotherapy improves treatment responses and causes a trend toward longer time to progression among patients with immune checkpoint inhibitor-related adverse events

被引:1
|
作者
Jokimaki, Anna [1 ,2 ,3 ]
Hietala, Henna [1 ]
Lemma, Jasmiini [4 ]
Karhapaa, Hanna [4 ,5 ]
Rintala, Anna [4 ]
Kaikkonen, Jari-Pekka [6 ]
Sunela, Kaisa [7 ]
Boman, Eva [7 ]
Jukkola, Arja [6 ,7 ]
Tiainen, Satu [8 ]
Seppala, Jan [8 ]
Ronka, Aino [8 ]
Hakkarainen, Heikki [9 ]
Karna, Aarno [9 ]
Iivanainen, Sanna [1 ,3 ]
Koivunen, Jussi [1 ,3 ]
Auvinen, Paivi [8 ]
Hernberg, Micaela [4 ,5 ]
Kuusisto, Milla [3 ,10 ]
Selander, Tuomas [11 ]
Kuittinen, Outi [1 ,2 ,8 ]
机构
[1] Oulu Univ Hosp, Dept Oncol & Radiotherapy, Oulu, Finland
[2] Univ Eastern Finland, Inst Clin Med, Fac Hlth Sci, Kuopio, Finland
[3] Oulu Univ Hosp, Med Res Ctr Oulu, Oulu, Finland
[4] Helsinki Univ Hosp, Comprehens Canc Ctr, Dept Oncol, Helsinki, Finland
[5] Univ Helsinki, Helsinki, Finland
[6] Tampere Univ, Fac Med & Hlth Technol, Tampere Canc Ctr, Tampere, Finland
[7] Tampere Univ Hosp, Dept Oncol, Tampere, Finland
[8] Kuopio Univ Hosp, Ctr Oncol, Kuopio, Finland
[9] Hosp Cent Finland Nova, Dept Oncol, Jyvaskyla, Finland
[10] Oulu Univ Hosp, Dept Hematol, Oulu, Finland
[11] Kuopio Univ Hosp, Sci Serv Ctr, Kuopio, Finland
关键词
Immune checkpoint inhibitors; Immune-related adverse events; Radiotherapy; Overall response rate; CD8(+) T-CELLS; ABLATIVE RADIATION; CHEMORADIOTHERAPY; THERAPY; CANCER;
D O I
10.1007/s00262-023-03494-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundImmune-related adverse events (irAEs) are frequently encountered by patients during immune checkpoint inhibitor (ICI) treatment and are associated with better treatment outcomes. The sequencing of radiotherapy (RT) and ICIs is widely used in current clinical practice, but its effect on survival has remained unclear.MethodsIn a real-world multicenter study including 521 patients who received ICI treatment for metastatic or locally advanced cancer, RT schedules and timing, irAEs, time to progression, overall survival, and treatment responses were retrospectively reviewed.ResultsPatients who received previous RT and developed irAE (RT +/AE +) had the best overall response rate (ORR 44.0%). The ORR was 40.1% in the RT -/AE + group, 26.7% in the RT -/AE - group and 18.3% in the RT + /AE - group (p < 0.001). There was a significantly longer time to progression (TTP) in the RT + /AE + group compared to the RT -/AE - and RT + /AE - groups (log rank p = 0.001 and p < 0.001, respectively), but the trend toward longer TTP in the RT + /AE + group did not reach statistical significance in pairwise comparison to that in the RT -/AE + group. Preceding RT timing and intent had no statistically significant effect on TTP. In a multivariate model, ECOG = 0 and occurrence of irAEs remained independent positive prognostic factors for TTP (HR 0.737; 95% CI 0.582-0.935; p = 0.012, and HR 0.620; 95% CI 0.499-0.769; p < 0.001, respectively).ConclusionsBetter ORR and a trend toward longer TTP were demonstrated for patients with RT preceding ICI treatment and development of irAEs, which suggests that RT may boost the therapeutic effect of immunotherapy in patients with metastatic cancers.
引用
收藏
页码:3337 / 3347
页数:11
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