Hyperprogression of brain metastases following initiation of immune checkpoint inhibitors

被引:1
作者
Jessurun, Charissa A. C. [1 ,2 ]
Siddi, Francesca [1 ,3 ]
Nawabi, Noah L. A. [1 ]
Hulsbergen, Alexander F. C. [1 ,2 ]
Lo, Yu Tung [1 ]
Jha, Rohan [1 ]
Smith, Timothy R. [1 ]
Broekman, Marike L. D. [2 ,4 ,5 ]
机构
[1] Harvard Med Sch, Brigham & Womens Hosp, Computat Neurosci Outcomes Ctr CNOC, Dept Neurosurg, 75 Francis St, Boston, MA 02115 USA
[2] Leiden Univ, Dept Neurosurg, Med Ctr, Albinusdreef 2, NL-2333 ZA Leiden, Zuid Holland, Netherlands
[3] Univ Verona, Dept Neurosci Biomed & Movement Sci, Sect Neurosurg, Piazzale Stefani 1, I-37124 Verona, Italy
[4] Harvard Med Sch, Massachusetts Gen Hosp, Dept Neurol, 55 Fruit St, Boston, MA 02114 USA
[5] Haaglanden Med Ctr, Dept Neurosurg, Lijnbaan 32, NL-2512 VA The Hague, Netherlands
关键词
Immune-checkpoint inhibitors; Hyperprogression; Brain metastases; Small cell lung cancer; Melanoma; Tumor growth rate; CELL LUNG-CANCER; OPEN-LABEL; MELANOMA; IPILIMUMAB; IMMUNOTHERAPY; NIVOLUMAB; DISEASE; PSEUDOPROGRESSION; EFFICACY; THERAPY;
D O I
10.1007/s11060-025-04955-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Immune checkpoint inhibitors (ICI) are increasingly being administered to cancer patients, including those with brain metastases (BMs). However, in a subset of cancer patients, ICI have shown to paradoxically accelerate tumor growth. This phenomenon is known as hyperprogressive disease (HPD). The aim of this study is to investigate the occurrence of HPD following initiation of ICI in BM patients. Methods We retrospectively reviewed the charts of 60 surgically treated patients with BMs from non-small cell lung cancer or melanoma who were administered ICI at the Brigham and Women's Hospital, Boston between July 2008 and July 2018. BM tumor volumes before and after initiation of ICI were collected. HPD was defined as a 'post-immunotherapy' tumor growth rate (TGR) > 2 times 'pre-immunotherapy' TGR within three months following initiation of ICI. Results Among the 25 included patients treated with ICI, five patients showed HPD with an increase of post-immunotherapy TGR ranging from 4.9 to 207.7 times the pre-immunotherapy TGR. The median survival after initiation of ICI was was 8.0 months in the HPD cases and 13 months in the non-HPD patients. Conclusion HPD occurred in about 20% of BM patients receiving ICI. More research is necessary to prospectively analyze the occurrence of HPD and identify predictive factors for HPD in BM patients.
引用
收藏
页码:667 / 673
页数:7
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