Identification of a highly lethal V3+TP53+ subset in ALK+ lung adenocarcinoma
Tyrosine kinase inhibitors (TKI) have improved prognosis in metastatic anaplastic lymphoma kinase (ALK)-driven lung adenocarcinoma, but patient outcomes vary widely. We retrospectively analyzed the clinical course of all cases with assessable baseline TP53 status and/or ALK fusion variant treated at...
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| Hauptverfasser: | , , , , , , , , , , , , , , , , , , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
[1 January 2019]
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| In: |
International journal of cancer
Year: 2019, Jahrgang: 144, Heft: 1, Pages: 190-199 |
| ISSN: | 1097-0215 |
| DOI: | 10.1002/ijc.31893 |
| Online-Zugang: | Verlag, Volltext: https://doi.org/10.1002/ijc.31893 Verlag, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/ijc.31893 
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| Verfasserangaben: | P. Christopoulos, M. Kirchner, F. Bozorgmehr, V. Endris, M. Elsayed, J. Budczies, J. Ristau, R. Penzel, F.J. Herth, C.P. Heussel, M. Eichhorn, T. Muley, M. Meister, J.R. Fischer, S. Rieken, F. Lasitschka, H. Bischoff, R. Sotillo, P. Schirmacher, M. Thomas, A. Stenzinger |
MARC
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| 245 | 1 | 0 | |a Identification of a highly lethal V3+TP53+ subset in ALK+ lung adenocarcinoma |c P. Christopoulos, M. Kirchner, F. Bozorgmehr, V. Endris, M. Elsayed, J. Budczies, J. Ristau, R. Penzel, F.J. Herth, C.P. Heussel, M. Eichhorn, T. Muley, M. Meister, J.R. Fischer, S. Rieken, F. Lasitschka, H. Bischoff, R. Sotillo, P. Schirmacher, M. Thomas, A. Stenzinger |
| 246 | 3 | 3 | |a Identification of a highly lethal V3 + TP53 + subset in ALK + lung adenocarcinoma |
| 264 | 1 | |c [1 January 2019] | |
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| 500 | |a First published: 26 September 2018 | ||
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| 520 | |a Tyrosine kinase inhibitors (TKI) have improved prognosis in metastatic anaplastic lymphoma kinase (ALK)-driven lung adenocarcinoma, but patient outcomes vary widely. We retrospectively analyzed the clinical course of all cases with assessable baseline TP53 status and/or ALK fusion variant treated at our institutions (n = 102). TP53 mutations were present in 17/87 (20%) and the echinoderm microtubule-associated protein-like 4 (EML4)-ALK variant 3 (V3) in 41/92 (45%) patients. The number of metastatic sites at diagnosis was affected more by the presence of V3 than by TP53 mutations, and highest with both factors (mean 5.3, p < 0.001). Under treatment with ALK TKI, progression-free survival (PFS) was shorter with either TP53 mutations or V3, while double positive cases appeared to have an even higher risk (hazard ratio [HR] = 2.9, p = 0.015). The negative effect of V3 on PFS of TKI-treated patients was strong already in the first line (HR = 2.5, p = 0.037) and decreased subsequently, whereas a trend for PFS impairment under first-line TKI by TP53 mutations became stronger and statistically significant only when considering all treatment lines together. Overall survival was impaired more by TP53 mutations (HR = 4.9, p = 0.003) than by V3 (HR = 2.4, p = 0.018), while patients with TP53 mutated V3-driven tumors carried the highest risk of death (HR = 9.1, p = 0.02). Thus, TP53 mutations and V3 are independently associated with enhanced metastatic spread, shorter TKI responses and inferior overall survival in ALK+ lung adenocarcinoma. Both markers could assist selection of cases for more aggressive management and guide development of novel therapeutic strategies. In combination, they define a patient subset with very poor outcome. | ||
| 650 | 4 | |a ALK+ NSCLC | |
| 650 | 4 | |a EML4-ALK fusion variant | |
| 650 | 4 | |a metastasis | |
| 650 | 4 | |a overall survival | |
| 650 | 4 | |a TP53 mutation | |
| 650 | 4 | |a treatment failure | |
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