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Acquired MTAP Loss Following Entrectinib Resistance in ROS1‐Rearranged NSCLC With CD74 Exon 3–ROS1 Exon 34 Fusion
by
Haraguchi Hashiguchi, Mizuha
, Yoneda, Suzuyuki
, Nakamura, Kohei
, Fukunaga, Koichi
, Asaoka, Masato
, Nishihara, Hiroshi
, Katayama, Makoto
, Tanino, Maika
, Kagyo, Junko
, Terai, Hideki
in
Antigens, Differentiation, B-Lymphocyte - genetics
/ Antimitotic agents
/ Antineoplastic agents
/ Benzamides - pharmacology
/ Benzamides - therapeutic use
/ Carcinoma, Non-Small-Cell Lung - drug therapy
/ Carcinoma, Non-Small-Cell Lung - genetics
/ Carcinoma, Non-Small-Cell Lung - pathology
/ Drug Resistance, Neoplasm - genetics
/ Exons
/ Female
/ Gene Rearrangement
/ Histocompatibility Antigens Class II - genetics
/ Humans
/ Indazoles - pharmacology
/ Indazoles - therapeutic use
/ Lung Neoplasms - drug therapy
/ Lung Neoplasms - genetics
/ Lung Neoplasms - pathology
/ Male
/ Middle Aged
/ Oncogene Proteins, Fusion - genetics
/ Protein-Tyrosine Kinases - genetics
/ Proto-Oncogene Proteins - genetics
2025
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Acquired MTAP Loss Following Entrectinib Resistance in ROS1‐Rearranged NSCLC With CD74 Exon 3–ROS1 Exon 34 Fusion
by
Haraguchi Hashiguchi, Mizuha
, Yoneda, Suzuyuki
, Nakamura, Kohei
, Fukunaga, Koichi
, Asaoka, Masato
, Nishihara, Hiroshi
, Katayama, Makoto
, Tanino, Maika
, Kagyo, Junko
, Terai, Hideki
in
Antigens, Differentiation, B-Lymphocyte - genetics
/ Antimitotic agents
/ Antineoplastic agents
/ Benzamides - pharmacology
/ Benzamides - therapeutic use
/ Carcinoma, Non-Small-Cell Lung - drug therapy
/ Carcinoma, Non-Small-Cell Lung - genetics
/ Carcinoma, Non-Small-Cell Lung - pathology
/ Drug Resistance, Neoplasm - genetics
/ Exons
/ Female
/ Gene Rearrangement
/ Histocompatibility Antigens Class II - genetics
/ Humans
/ Indazoles - pharmacology
/ Indazoles - therapeutic use
/ Lung Neoplasms - drug therapy
/ Lung Neoplasms - genetics
/ Lung Neoplasms - pathology
/ Male
/ Middle Aged
/ Oncogene Proteins, Fusion - genetics
/ Protein-Tyrosine Kinases - genetics
/ Proto-Oncogene Proteins - genetics
2025
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Acquired MTAP Loss Following Entrectinib Resistance in ROS1‐Rearranged NSCLC With CD74 Exon 3–ROS1 Exon 34 Fusion
by
Haraguchi Hashiguchi, Mizuha
, Yoneda, Suzuyuki
, Nakamura, Kohei
, Fukunaga, Koichi
, Asaoka, Masato
, Nishihara, Hiroshi
, Katayama, Makoto
, Tanino, Maika
, Kagyo, Junko
, Terai, Hideki
in
Antigens, Differentiation, B-Lymphocyte - genetics
/ Antimitotic agents
/ Antineoplastic agents
/ Benzamides - pharmacology
/ Benzamides - therapeutic use
/ Carcinoma, Non-Small-Cell Lung - drug therapy
/ Carcinoma, Non-Small-Cell Lung - genetics
/ Carcinoma, Non-Small-Cell Lung - pathology
/ Drug Resistance, Neoplasm - genetics
/ Exons
/ Female
/ Gene Rearrangement
/ Histocompatibility Antigens Class II - genetics
/ Humans
/ Indazoles - pharmacology
/ Indazoles - therapeutic use
/ Lung Neoplasms - drug therapy
/ Lung Neoplasms - genetics
/ Lung Neoplasms - pathology
/ Male
/ Middle Aged
/ Oncogene Proteins, Fusion - genetics
/ Protein-Tyrosine Kinases - genetics
/ Proto-Oncogene Proteins - genetics
2025
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Acquired MTAP Loss Following Entrectinib Resistance in ROS1‐Rearranged NSCLC With CD74 Exon 3–ROS1 Exon 34 Fusion
Journal Article
Acquired MTAP Loss Following Entrectinib Resistance in ROS1‐Rearranged NSCLC With CD74 Exon 3–ROS1 Exon 34 Fusion
2025
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Overview
This case highlights acquired MTAP loss during disease progression in ROS1‐rearranged NSCLC. Despite persistent CD74–ROS1 fusion and absence of known resistance mutations, the patient developed CNS progression after entrectinib, underscoring the value of longitudinal genomic profiling in guiding treatment decisions.
Publisher
John Wiley & Sons Australia, Ltd,John Wiley & Sons, Inc,Wiley
Subject
Antigens, Differentiation, B-Lymphocyte - genetics
/ Benzamides - therapeutic use
/ Carcinoma, Non-Small-Cell Lung - drug therapy
/ Carcinoma, Non-Small-Cell Lung - genetics
/ Carcinoma, Non-Small-Cell Lung - pathology
/ Drug Resistance, Neoplasm - genetics
/ Exons
/ Female
/ Histocompatibility Antigens Class II - genetics
/ Humans
/ Lung Neoplasms - drug therapy
/ Male
/ Oncogene Proteins, Fusion - genetics
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