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BIOMARKER:

ALK rearrangement

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:
Related tests:
3d
Delayed Postoperative Wound Healing during Alectinib Therapy for Poorly Differentiated Lung Adenocarcinoma: A Case Report. (PubMed, Case Rep Oncol)
This case highlights the possibility that alectinib may impair postoperative wound repair. Comprehensive perioperative drug evaluation, multidisciplinary collaboration, and carefully monitored treatment interruption are recommended to maintain the balance between oncologic control and effective tissue healing.
Journal
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ALK (Anaplastic lymphoma kinase)
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ALK positive • ALK rearrangement
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Alecensa (alectinib)
4d
Case report: first-line lorlatinib in metastatic lung adenocarcinoma with a novel WIPF1-ALK and EML4-ALK dual fusion. (PubMed, Transl Lung Cancer Res)
The achievement of over 24 months of disease control underscores lorlatinib's potent activity against these complex molecular profiles. Our findings highlight the importance of recognizing and targeting rare ALK fusion variants-even when coexisting with other ALK rearrangements and resistance-associated mutations and expand the therapeutic landscape of precision oncology for advanced NSCLC.
Journal
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ALK (Anaplastic lymphoma kinase) • TP53 (Tumor protein P53) • EML4 (EMAP Like 4)
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TP53 mutation • ALK rearrangement • ALK fusion
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Lorbrena (lorlatinib)
6d
When Lymph Nodes Don't Lie: Report of Three Unusual Presentations of Thoracic Tumors. (PubMed, Diagnostics (Basel))
One case harbored an ALK rearrangement, guiding effective targeted therapy with alectinib...Accurate histopathological assessment is essential to establish a correct diagnosis and guide appropriate therapy. A multidisciplinary approach remains the cornerstone of diagnostic precision in CUP cases.
Journal
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ALK (Anaplastic lymphoma kinase) • BAP1 (BRCA1 Associated Protein 1) • TTF1 (Transcription Termination Factor 1) • NKX2-1 (NK2 Homeobox 1) • NAPSA (Napsin A Aspartic Peptidase)
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ALK rearrangement
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Alecensa (alectinib)
6d
Association of Driver Oncogenic Alterations with SUVmax, Preoperative Serum Calcium, and Smoking Status in Surgically Resected Non-Small-Cell Lung Cancer: A Retrospective Single-Center Study. (PubMed, J Clin Med)
In this cohort of surgically resected NSCLC, preoperative corrected serum calcium and smoking exposure were more closely associated with tumor metabolic activity than with specific molecular alterations. These findings suggest that simple clinical and biochemical parameters may provide complementary information, although their utility for discriminating individual molecular subgroups appears limited.
Retrospective data • Journal • PD(L)-1 Biomarker • IO biomarker
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EGFR (Epidermal growth factor receptor) • PD-L1 (Programmed death ligand 1) • KRAS (KRAS proto-oncogene GTPase) • BRAF (B-raf proto-oncogene) • ALK (Anaplastic lymphoma kinase) • ROS1 (Proto-Oncogene Tyrosine-Protein Kinase ROS)
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PD-L1 expression • KRAS mutation • EGFR mutation • PD-L1 overexpression • BRAF mutation • ALK rearrangement • EGFR wild-type • ROS1 rearrangement
7d
Concordance of Actionable Driver Alterations Between Primary Lung Adenocarcinoma and Paired Thoracic Metastases: A Prospective Next-Generation Sequencing Study. (PubMed, Cancers (Basel))
This study demonstrates very high molecular concordance between primary lung adenocarcinomas and their synchronous pleural or intrapulmonary metastases. The observed 100% concordance of actionable driver alterations across paired specimens supports the clinical reliability of thoracic metastatic biopsies for baseline molecular profiling in treatment-naïve disease. Although limited by sample size, these findings support the biological stability of actionable driver alterations during early thoracic metastatic dissemination.
Journal • Next-generation sequencing
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EGFR (Epidermal growth factor receptor) • KRAS (KRAS proto-oncogene GTPase) • ALK (Anaplastic lymphoma kinase) • TP53 (Tumor protein P53)
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TP53 mutation • KRAS mutation • EGFR mutation • ALK rearrangement • ALK mutation
8d
FORTRAS: A Study of MSK-TCR5 in People With Solid Tumor Cancers (clinicaltrials.gov)
P1, N=16, Recruiting, Memorial Sloan Kettering Cancer Center
New P1 trial
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EGFR (Epidermal growth factor receptor) • HER-2 (Human epidermal growth factor receptor 2) • PD-L1 (Programmed death ligand 1) • BRAF (B-raf proto-oncogene) • ALK (Anaplastic lymphoma kinase) • MSI (Microsatellite instability)
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PD-L1 expression • BRAF V600E • EGFR mutation • MSI-H/dMMR • HER-2 amplification • BRAF V600 • HER-2 expression • ALK rearrangement • RAS mutation • ROS1 rearrangement
10d
Rare ALK-IR (Intergenic Region) Rearrangement in a Patient with Non-Small Cell Lung Cancer: A Case Report. (PubMed, Curr Cancer Drug Targets)
This first documented case demonstrates the therapeutic efficacy of crizotinib in ALK-IR rearranged NSCLC, emphasizing the importance of comprehensive molecular profiling in guiding precision oncology.
Journal
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ALK (Anaplastic lymphoma kinase) • TP53 (Tumor protein P53) • CDKN2A (Cyclin Dependent Kinase Inhibitor 2A)
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TP53 mutation • ALK positive • ALK rearrangement
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Xalkori (crizotinib)
10d
A Phase 1/2 Study of D3S-002 as Monotherapy or Combination Therapy in Adult Subjects With Advanced Solid Tumors With MAPK Pathway Mutations (clinicaltrials.gov)
P1/2, N=67, Recruiting, D3 Bio (Wuxi) Co., Ltd | Active, not recruiting --> Recruiting | Trial completion date: Apr 2028 --> Aug 2028 | Trial primary completion date: Apr 2028 --> Aug 2028
Enrollment open • Trial completion date • Trial primary completion date • First-in-human
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EGFR (Epidermal growth factor receptor) • KRAS (KRAS proto-oncogene GTPase) • BRAF (B-raf proto-oncogene) • ALK (Anaplastic lymphoma kinase) • MET (MET proto-oncogene, receptor tyrosine kinase) • ROS1 (Proto-Oncogene Tyrosine-Protein Kinase ROS) • NTRK1 (Neurotrophic tyrosine kinase, receptor, type 1) • NTRK3 (Neurotrophic tyrosine kinase, receptor, type 3) • NTRK2 (Neurotrophic tyrosine kinase, receptor, type 2)
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BRAF V600E • EGFR mutation • KRAS G12C • BRAF V600 • EGFR L858R • EGFR T790M • KRAS G12D • ALK rearrangement • MET exon 14 mutation • EGFR L861Q • ROS1 fusion • EGFR G719X • MET mutation • EGFR S768I • RET rearrangement • KRAS G12 • KRAS G12S • KRAS Q61
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D3S-002 • elisrasib (D3S-001)
11d
Enrollment closed • 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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EGFR mutation • ALK rearrangement
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balstilimab (AGEN2034) • botensilimab (AGEN1181)
12d
Uterine inflammatory myofibroblastic tumor: a clinicopathological and molecular genetic analysis of eight cases (PubMed, Zhonghua Bing Li Xue Za Zhi)
The patient was treated with the oral targeted drug crizotinib and died of multiple organ failure 18 months after surgery...UIMT and EIMS that exhibit aggressive behavior typically possess a greater number of genetic alterations. The abnormal expression of p53 or p16 protein, when combined with clinicopathological parameters, can serve as indicators for predicting the adverse biological behavior of tumors.
Journal
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ALK (Anaplastic lymphoma kinase) • TP53 (Tumor protein P53) • CCNE1 (Cyclin E1) • ANK2 (Ankyrin 2)
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TP53 mutation • ALK positive • ATM mutation • ALK rearrangement • ALK fusion
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Xalkori (crizotinib)
15d
Case report: Personalized, response-adapted neoadjuvant alectinib achieves durable remission in stage IIIB ALK-rearranged lung cancer. (PubMed, Front Pharmacol)
This case illustrates the successful personalization of neoadjuvant alectinib by employing an imaging response-adapted strategy. This strategy utilized dynamic imaging assessments to guide the scheduling of the surgical procedure, culminating in a deep pathological response and prolonged disease-free survival, thereby offering a refined perioperative paradigm for ALK-rearranged NSCLC.
Journal
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ALK (Anaplastic lymphoma kinase)
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ALK positive • ALK rearrangement
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Alecensa (alectinib)
15d
Risk Factors for Developing Venous Thromboembolism in Patients With Advanced ALK-Rearranged NSCLC. (PubMed, JTO Clin Res Rep)
Competing risk regression analysis revealed that the presence of baseline adrenal metastasis (hazard ratio [HR] = 2.92, 95% confidence interval [CI]: 1.19-7.16), leukocyte count more than 11 × 109/L (HR = 3.74, 95% CI: 1.91-7.31), and hemoglobin less than 10 g/dL (HR = 5.18, 95% CI: 2.07-12.94) significantly increased VTE risk, whereas albumin more than or equal to 3.5 g/dL reduced the risk (HR = 0.24, 95% CI: 0.10-0.56). In advanced ALK-positive NSCLC, baseline adrenal metastases, leukocytosis, and anemia were associated with increased VTE risk and may warrant heightened clinical vigilance.
Journal
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ALK (Anaplastic lymphoma kinase)
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ALK positive • ALK rearrangement