Diagnostic, therapeutic, and prognostic implications of the 2021 World Health Organization classification of tumors of the central nervous system

S Gritsch, TT Batchelor, LN Gonzalez Castro - Cancer, 2022 - Wiley Online Library
The 2016 revised fourth edition of the World Health Organization (WHO) classification of
central nervous system (CNS) tumors incorporated molecular features with histologic …

Invasive lobular carcinoma: an understudied emergent subtype of breast cancer

JA Mouabbi, A Hassan, B Lim, GN Hortobagyi… - Breast cancer research …, 2022 - Springer
Invasive lobular carcinoma (ILC) is the second most common histologic subtype of breast
cancer after invasive ductal carcinoma (IDC), accounting for 10–15% of all breast cancer …

MEK inhibitors for neurofibromatosis type 1 manifestations: Clinical evidence and consensus

PMK De Blank, AM Gross, S Akshintala… - Neuro …, 2022 - academic.oup.com
The wide variety of clinical manifestations of the genetic syndrome neurofibromatosis type 1
(NF1) are driven by overactivation of the RAS pathway. Mitogen-activated protein kinase …

[HTML][HTML] Targeting son of sevenless 1: the pacemaker of KRAS

D Kessler, D Gerlach, N Kraut, DB McConnell - Current Opinion in Chemical …, 2021 - Elsevier
Son of Sevenless (SOS) is a guanine nucleotide exchange factor that activates the important
cell signaling switch KRAS. SOS acts as a pacemaker for KRAS, the beating heart of cancer …

FDA approval summary: selumetinib for plexiform neurofibroma

D Casey, S Demko, A Sinha, PS Mishra-Kalyani… - Clinical Cancer …, 2021 - AACR
Abstract On April 10, 2020, the FDA approved selumetinib (KOSELUGO, AstraZeneca) for
the treatment of pediatric patients 2 years of age and older with neurofibromatosis type 1 …

Neurofibromatosis type 1: pediatric aspects and review of genotype–phenotype correlations

C Peduto, M Zanobio, V Nigro, S Perrotta, G Piluso… - Cancers, 2023 - mdpi.com
Simple Summary In the last few years, an increasing number of genotype–phenotype
correlations has been described for neurofibromatosis type 1 (NF1), impacting on the clinical …

LOGGIC/FIREFLY-2: a phase 3, randomized trial of tovorafenib vs. chemotherapy in pediatric and young adult patients with newly diagnosed low-grade glioma …

CM van Tilburg, LB Kilburn, S Perreault, R Schmidt… - BMC cancer, 2024 - Springer
Background Pediatric low-grade glioma (pLGG) is essentially a single pathway disease, with
most tumors driven by genomic alterations affecting the mitogen-activated protein …

Malignant peripheral nerve sheath tumors—a comprehensive review of pathophysiology, diagnosis, and multidisciplinary management

SWE Knight, TE Knight, T Santiago, AJ Murphy… - Children, 2022 - mdpi.com
Malignant peripheral nerve sheath tumors (MPNSTs) are aggressive soft tissue sarcomas
(STS) with nerve sheath differentiation and a tendency to metastasize. Although occurring at …

New prospectives on treatment opportunities in RASopathies

BD Gelb, ME Yohe, C Wolf… - American Journal of …, 2022 - Wiley Online Library
The RASopathies are a group of clinically defined developmental syndromes caused by
germline variants of the RAS/mitogen‐activated protein (MAPK) cascade. The prototypic …

[HTML][HTML] Novel molecular targeted therapies for patients with neurofibromatosis type 1 with inoperable plexiform neurofibromas: a comprehensive review

I Solares, D Viñal, M Morales-Conejo… - ESMO open, 2021 - Elsevier
Highlights•PNs are a major cause of morbidity in NF1.•Promising efficacy results with MEK
inhibitors and cabozantinib have been reported.•MEK inhibitors are associated with a …