Efficacy of immunotherapy for melanoma brain metastases in patients with concurrent corticosteroid exposure

Author:

Tringale Kathryn R1ORCID,Reiner Anne S2,Sehgal Ryka R3,Panageas Katherine2,Betof Warner Allison S4,Postow Michael A4,Moss Nelson S35ORCID

Affiliation:

1. Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA

2. Department of Epidemiology & Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA

3. Department of Neurosurgery, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA

4. Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA

5. Multidisciplinary Brain Metastasis Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA

Abstract

Aim: Immune checkpoint inhibitor (ICI) efficacy is undefined for melanoma brain metastases (MBM) with concurrent corticosteroid exposure. Materials & methods: We retrospectively evaluated patients with untreated MBM who received corticosteroids (≥1.5 mg dexamethasone equivalent) within 30 days of ICI. mRECIST criteria and Kaplan–Meier methods defined intracranial progression-free survival (iPFS). The lesion size-response association was evaluated with repeated measures modeling. Results: A total of 109 MBM were evaluated. The patient level intracranial response rate was 41%. Median iPFS was 2.3 months and overall survival was 13.4 months. Larger lesions were more likely to progress, with diameter >2.05 cm most predictive of progression (OR: 18.9; 95% CI: 2.6–139.5; p = 0.004). There was no difference in iPFS with steroid exposure pre- versus post-ICI initiation. Conclusion: In the largest reported ICI+corticosteroid cohort, we identify size dependent MBM response.

Funder

NIH/NCI Cancer Center

Publisher

Future Medicine Ltd

Subject

Neurology (clinical),Neurology

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