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BIOMARKER:

ALK negative

i
Other names: NBLST3, CD246, Anaplastic Lymphoma Kinase, Anaplastic Lymphoma Kinase (Ki-1), CD246 Antigen, Mutant Anaplastic Lymphoma Kinase, ALK, ALK Receptor Tyrosine Kinase, Anaplastic Lymphoma Receptor Tyrosine Kinase, ALK Tyrosine Kinase Receptor
Entrez ID:
1d
Enrollment closed
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ALK (Anaplastic lymphoma kinase)
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ALK positive • ALK negative
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golcadomide (CC-99282)
11d
Comparative Efficacy and Safety of First-Line Immune Checkpoint Inhibitors Plus Chemotherapy with or Without Bevacizumab in Advanced Non-Squamous Non-Small Cell Lung Carcinoma. (PubMed, Curr Oncol)
Although PFS benefits were observed in certain subgroups, these were accompanied by significantly increased treatment-related toxicities. Our findings suggest that no clear subgroup has been identified where the benefit outweighs the risks, necessitating extreme clinical caution.
Clinical • Retrospective data • Journal • Checkpoint inhibition • PD(L)-1 Biomarker • IO biomarker
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EGFR (Epidermal growth factor receptor) • PD-L1 (Programmed death ligand 1) • ALK (Anaplastic lymphoma kinase)
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PD-L1 expression • PD-L1 negative • ALK negative
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Avastin (bevacizumab)
21d
Research Progress in ALK+/- Anaplastic Large Cell Lymphoma--Review (PubMed, Zhongguo Shi Yan Xue Ye Xue Za Zhi)
Understanding the subtypes and molecular characteristics of ALCL is essential for optimizing therapeutic strategies. Therefore, this review summarizes recent research advances on ALK +/- ALCL to provide insights for optimizing treatment approaches.
Review • Journal
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ALK (Anaplastic lymphoma kinase) • TNFRSF8 (TNF Receptor Superfamily Member 8) • TP63 (Tumor protein 63) • DUSP22 (Dual Specificity Phosphatase 22) • USP22 (Ubiquitin Specific Peptidase 22)
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ALK positive • TNFRSF8 positive • ALK negative
23d
UMG1 Defines a Targetable Subset of T-Cell Lymphomas and Enables Precision Immunotherapy With a First-in-Class CD3ε Bispecific Engager. (PubMed, Hematol Oncol)
Our findings suggest that the UMG1/CD3ε-BTCE selectively exerts potent anti-tumor activity against a relevant subset of TCLs. These findings support the development of a precision immunotherapy approach for patients with UMG1-expressing aggressive hematologic malignancies.
Journal • IO biomarker
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ALK (Anaplastic lymphoma kinase) • SPN (Sialophorin)
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ALK negative
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Zolinza (vorinostat)
25d
T-START-NR: T Cell Lymphoma -Stratified Therapy After Response to First-line Treatment-NR (clinicaltrials.gov)
P=N/A, N=58, Recruiting, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine
New trial
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HLA-DRB1 (Major Histocompatibility Complex, Class II, DR Beta 1) • HLA-B (Major Histocompatibility Complex, Class I, B) • HLA-C (Major Histocompatibility Complex, Class I, C)
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ALK negative
26d
FIL_BREAL: BV-CHP Real-life and Biological Evidences in Patients With sALCL (clinicaltrials.gov)
P=N/A, N=100, Not yet recruiting, Fondazione Italiana Linfomi - ETS
New trial
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ALK (Anaplastic lymphoma kinase)
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ALK positive • ALK negative
1m
Trial initiation date
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ALK (Anaplastic lymphoma kinase) • CD5 (CD5 Molecule) • DUSP22 (Dual Specificity Phosphatase 22) • USP22 (Ubiquitin Specific Peptidase 22)
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ALK negative
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Rituxan (rituximab) • cyclophosphamide • fludarabine IV
1m
Diagnostic Utility of Expression Imbalance in Idylla GeneFusion Assay for Non-Small Cell Lung Cancer. (PubMed, J Mol Diagn)
One case showed an NOL10::ALK out-of-frame fusion with negative ALK immunohistochemistry and equivocal ALK FISH results. Because the expression imbalance method can detect novel fusions, we recommend its implementation with confirmation testing.
Journal
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ALK (Anaplastic lymphoma kinase) • RET (Ret Proto-Oncogene) • ROS1 (Proto-Oncogene Tyrosine-Protein Kinase ROS) • STRN (Striatin) • SQSTM1 (Sequestosome 1) • ERC1 (ELKS/RAB6-Interacting/CAST Family Member 1)
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RET fusion • ALK fusion • ROS1 fusion • ALK negative
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Idylla™ GeneFusion Assay