Tissue-agnostic activity of BRAF plus MEK inhibitor in BRAF V600–mutant tumors

JJ Adashek, AK Menta, NK Reddy, AP Desai… - Molecular cancer …, 2022 - AACR
BRAF plus MEK inhibitor combinations are currently FDA-approved for melanoma, non–
small cell lung cancer, and anaplastic thyroid cancer. The lack of clinical benefit with BRAF …

Differential diagnoses of diaper dermatitis

R Fölster‐Holst - Pediatric dermatology, 2018 - Wiley Online Library
Diaper dermatitis is the most common contact eczema present in early childhood. The main
cause is an irritant reaction to urine and feces, which is facilitated by the occlusive conditions …

Clinical responses and persistent BRAF V600E+ blood cells in children with LCH treated with MAPK pathway inhibition

OS Eckstein, J Visser… - Blood, The Journal …, 2019 - ashpublications.org
Langerhans cell histiocytosis (LCH) is characterized by granulomatous lesions with
pathologic CD2071 dendritic cells. 1 More than 40% of children with high-risk LCH …

Langerhans cell histiocytosis: A neoplastic disorder driven by Ras-ERK pathway mutations

G Tran, TN Huynh, AS Paller - Journal of the American Academy of …, 2018 - Elsevier
Langerhans cell histiocytosis (LCH) is a disorder of myeloid neoplasia of dendritic cells that
affects 1 in 200,000 children< 15 years of age and even fewer adults. LCH presents with a …

Treatment of Langerhans cell histiocytosis and histiocytic disorders: a focus on MAPK pathway inhibitors

AV Geerlinks, O Abla - Pediatric Drugs, 2023 - Springer
Histiocytic disorders are rare diseases defined by the clonal accumulation of a macrophage
or dendritic cell origin. These disorders include Langerhans cell histiocytosis, Erdheim …

Erdheim-Chester disease: a comprehensive review from the ophthalmologic perspective

M Kanakis, P Petrou, G Lourida, I Georgalas - Survey of Ophthalmology, 2022 - Elsevier
Erdheim–Chester disease (ECD) is a rare clonal histiocytic neoplasm with less than 1200
documented cases to date. The disease is life-threatening and difficult to recognize …

[HTML][HTML] MAPK mutations and cigarette smoke promote the pathogenesis of pulmonary Langerhans cell histiocytosis

H Liu, AR Osterburg, J Flury, Z Swank, DW McGraw… - JCI insight, 2020 - ncbi.nlm.nih.gov
Pulmonary Langerhans cell histiocytosis (PLCH) is a rare smoking-related lung disease
characterized by dendritic cell (DC) accumulation, bronchiolocentric nodule formation, and …

Mitogen-activating protein kinase pathway alterations in Langerhans cell histiocytosis

F Jouenne, A Benattia, A Tazi - Current Opinion in Oncology, 2021 - journals.lww.com
Mitogen-activating protein kinase pathway alterations in Lan... : Current Opinion in Oncology
Mitogen-activating protein kinase pathway alterations in Langerhans cell histiocytosis : Current …

Efficacy and safety of vemurafenib in Langerhans cell histiocytosis (LCH): a systematic review and meta-analysis

D Mohapatra, AK Gupta, P Haldar… - Pediatric Hematology …, 2023 - Taylor & Francis
Almost half of the patients with Langerhans cell histiocytosis (LCH) are refractory to primary
induction chemotherapy or undergo reactivation. The ideal treatment modality for …

Signaling pathways, microenvironment, and targeted treatments in Langerhans cell histiocytosis

X Gao, J Li, X Cao - Cell Communication and Signaling, 2022 - Springer
Langerhans cell histiocytosis (LCH) is an inflammatory myeloid malignancy in the “L-group”
histiocytosis. Mitogen-activated protein kinase (MAPK) pathway activating mutations are …