Specimen information:
Report ID | NOLN-210920-1 | ||
Report name | CTCL pembrolizumab | ||
Study name | Immune cell topography predicts response to PD-1 blockade in cutaneous T cell lymphoma | ||
Study authors | Nolan lab: Darci Phillips, Magdalena Matusiak, Belén Rivero Gutierrez, Salil S. Bhate, Graham L. Barlow, Sizun Jiang, Janos Demeter, Kimberly S. Smythe, Robert H. Pierce, Steven P. Fling, Nirasha Ramchurren, Martin A. Cheever, Yury Goltsev, Robert B. West, Michael S. Khodadoust, Youn H. Kim, Christian M. Schürch, and Garry P. Nolan | ||
Summary | Cutaneous T cell lymphomas (CTCL) are rare but aggressive cancers without effective treatments. While a subset of patients derive benefit from PD-1 blockade, there is a critically unmet need for predictive biomarkers of response. We performed CODEX multiplexed tissue imaging on 70 tumor regions from 14 advanced CTCL patients enrolled in a pembrolizumab clinical trial. We found no differences in the frequencies of immune or tumor cells between responders and non-responders. Instead, we identified topographical differences between effector PD-1+ CD4+ T cells, tumor cells, and immunosuppressive Tregs, from which we derived a spatial biomarker, termed the SpatialScore, that correlated strongly with pembrolizumab response. These results provide a paradigm for investigating the spatial balance of effector and suppressive T cell activity and broadly leveraging this biomarker approach to inform the clinical use of immunotherapies. |
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Specimen type | Human skin tissue | ||
Specimen ID | NOLN21097 | Case name | core002 |
Submitted by: | |
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Submitter |
Darci Phillips
(Nolan Lab, Pathology - Baxter Laboratory, Stanford) |
Last updated | 10 Jan, 2022 (Mon), 4:44 PM |
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