Publications by authors named "Sandrine Arrufat"

Article Synopsis
  • Retinoblastoma is the most common eye cancer in children, originating from developing retinal cells, but its molecular behavior is not well understood.* -
  • Researchers identified two distinct subtypes of retinoblastoma: Subtype 1 is characterized by early onset and less genetic alteration, while Subtype 2 has recurrent genetic changes, is less differentiated, and has a higher likelihood of spreading.* -
  • Understanding these two subtypes can offer new insights into the biology and treatment of retinoblastoma, with subtype 1 being less aggressive and subtype 2 showing more aggressive traits and stem cell-like features.*
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Over the last decade, various new therapies have been developed to promote anti-tumor immunity. Despite interesting clinical results in hematological malignancies, the development of bispecific killer-cell-engager antibody formats directed against tumor cells and stimulating anti-tumor T cell immunity has proved challenging, mostly due to toxicity problems. We report here the generation of trifunctional natural killer (NK) cell engagers (NKCEs), targeting two activating receptors, NKp46 and CD16, on NK cells and a tumor antigen on cancer cells.

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Hybrid oncocytic/chromophobe tumours (HOCT) are renal tumours recently described displaying histological features of both renal oncocytoma (RO) and chromophobe renal cell carcinoma (ChRCC), raising the question of their precise signification in the RO/ChRCC group. This study aimed to describe clinicopathological features of so called HOCT and to characterise their genomic profile. Five hundred and eighty-three tumours belonging to the ChRCC/RO group were retrospectively reviewed.

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Purpose: To evaluate the efficacy of endoresection after proton beam radiotherapy to prevent neovascular glaucoma (NVG) in patients treated for choroidal melanoma.

Methods: From a series of 4,867 patients treated for choroidal melanoma were prospectively recorded in the database (Macro Infermed 3.075).

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SMARCB1 germline mutations mainly predispose to rhabdoid tumors. However, less aggressive tumors with a later onset have also been reported in a context of SMARCB1 constitutional mutation-that is, schwannomatosis and meningiomatosis. No other tumor type has formally been observed in such a context thus far.

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