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BIOMARKER:

ALK positive

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:
24h
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)
2d
Laparoscopic Hepatectomy for Hepatic Inflammatory Myofibroblastic Tumor: A Case Report. (PubMed, Surg Case Rep)
HIMT is rare and poses significant diagnostic challenges that often mimic other liver malignancies. This case report highlights the efficacy and safety of laparoscopic hepatectomy as both a diagnostic and therapeutic strategies.
Journal
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ALK (Anaplastic lymphoma kinase)
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ALK positive
2d
Perioperative Molecular Testing in Non-small Cell Lung Cancer (PubMed, Zentralbl Chir)
The results of the ADAURA trial led to the approval of osimertinib for adjuvant treatment of completely resected, EGFR-mutated NSCLC, while the ALINA trial provided the basis for the approval of alectinib in the adjuvant treatment of ALK-positive, completely resected NSCLC. This article discusses the current evidence regarding the perioperative use of targeted therapies, the recommendations for molecular testing in non-small cell lung cancer, and the resulting therapeutic implications, as well as ongoing research efforts in this evolving field.
Journal • IO biomarker
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EGFR (Epidermal growth factor receptor) • ALK (Anaplastic lymphoma kinase)
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EGFR mutation • ALK positive
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Tagrisso (osimertinib) • Alecensa (alectinib)
2d
Vortioxetine for Cognitive Function in ALK-positive NSCLC Treated With Lorlatinib (clinicaltrials.gov)
P=N/A, N=24, Recruiting, Centro de Tratamiento e Investigación sobre Cáncer, Luis Carlos Sarmiento Angulo
New trial
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ALK (Anaplastic lymphoma kinase) • ROS1 (Proto-Oncogene Tyrosine-Protein Kinase ROS)
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ALK positive • ROS1 positive
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Lorbrena (lorlatinib)
3d
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)
4d
Transformation of ALK-translocated lung adenocarcinoma to LCNEC under alectinib treatment-a case report and mini-review. (PubMed, Oncologist)
This case adds to the limited body of evidence and underscores the importance of recognizing neuroendocrine differentiation in ALK-positive lung cancer cases which show clinical progression. Further studies are needed to elucidate the molecular drivers of this transformation and to optimize treatment strategies for affected patients.
Journal
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ALK (Anaplastic lymphoma kinase)
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ALK positive • ALK translocation
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Alecensa (alectinib)
4d
Brief Report: The Prognostic Impact of Common Molecular Alterations in Resected Lung Adenocarcinoma and Implications for the 10th Edition TNM Classification. (PubMed, J Thorac Oncol)
This study suggests that common molecular alterations in lung cancer exhibit prognostic value within specific stages, and notably, TP53, KRAS and ALK alterations hold the potential to modify the current staging system. These findings provide a valuable reference for the forthcoming 10th Edition TNM staging system.
Journal
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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 • EGFR L858R • EGFR exon 19 deletion • ALK positive • ALK fusion • ALK mutation
5d
Allogeneic Hematopoietic Cell Transplantation for Peripheral T Cell Lymphoma (clinicaltrials.gov)
P2, N=330, Recruiting, National Cancer Institute (NCI) | Trial primary completion date: Oct 2026 --> Jun 2027
Trial primary completion date
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ALK (Anaplastic lymphoma kinase) • HLA-B (Major Histocompatibility Complex, Class I, B) • HLA-C (Major Histocompatibility Complex, Class I, C)
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ALK positive
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Jakafi (ruxolitinib) • cyclophosphamide • sirolimus
6d
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)
6d
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
6d
CircRNAs derived from the tyrosine phosphatase PTPN22 impact chemosensitivity in ALK-positive T-cell lymphomas. (PubMed, Sci Rep)
Loss of CARM1 expression promoted drug tolerance in chemosensitive ALK(+) lymphoma cells. These findings identify the circPTPN22/CARM1 axis as a regulator of chemosensitivity and propose CARM1 inhibition as a potential strategy to overcome chemoresistance in patients with ALK(+) ALCL.
Journal
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ALK (Anaplastic lymphoma kinase) • PTPN22 (Protein Tyrosine Phosphatase Non-Receptor Type 22)
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ALK positive • ALK translocation
7d
New trial
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ALK (Anaplastic lymphoma kinase) • TNFRSF8 (TNF Receptor Superfamily Member 8)
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ALK positive • TNFRSF8 positive • ALK negative
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doxorubicin hydrochloride • cyclophosphamide • Adcetris (brentuximab vedotin)