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Verfasst von:Christopoulos, Petros [VerfasserIn]   i
 Dietz, Steffen [VerfasserIn]   i
 Kirchner, Martina [VerfasserIn]   i
 Volckmar, Anna-Lena [VerfasserIn]   i
 Endris, Volker [VerfasserIn]   i
 Neumann, Olaf [VerfasserIn]   i
 Heußel, Claus Peter [VerfasserIn]   i
 Herth, Felix [VerfasserIn]   i
 Eichhorn, Martin E. [VerfasserIn]   i
 Meister, Michael [VerfasserIn]   i
 Budczies, Jan [VerfasserIn]   i
 Allgäuer, Michael [VerfasserIn]   i
 Leichsenring, Jonas [VerfasserIn]   i
 Bischoff, Helge [VerfasserIn]   i
 Schirmacher, Peter [VerfasserIn]   i
 Thomas, Michael [VerfasserIn]   i
 Sültmann, Holger [VerfasserIn]   i
 Stenzinger, Albrecht [VerfasserIn]   i
Titel:Detection of TP53 mutations in tissue or liquid rebiopsies at progression identifies ALK+ lung cancer patients with poor survival
Verf.angabe:Petros Christopoulos, Steffen Dietz, Martina Kirchner, Anna-Lena Volckmar, Volker Endris, Olaf Neumann, Simon Ogrodnik, Claus-Peter Heussel, Felix J. Herth, Martin Eichhorn, Michael Meister, Jan Budczies, Michael Allgäuer, Jonas Leichsenring, Tomasz Zemojtel, Helge Bischoff, Peter Schirmacher, Michael Thomas, Holger Sültmann, Albrecht Stenzinger
E-Jahr:2019
Jahr:21 January 2019
Umfang:9 S.
Teil:volume:11
 year:2019
 number:1
 extent:9
Fussnoten:Gesehen am 26.06.2019 ; Im Titel ist das Zeichen "+" hochgestellt
Titel Quelle:Enthalten in: Cancers
Ort Quelle:Basel : MDPI, 2009
Jahr Quelle:2019
Band/Heft Quelle:11(2019,1) Artikel-Nummer 124, 9 Seiten
ISSN Quelle:2072-6694
Abstract:Anaplastic lymphoma kinase (ALK) sequencing can identify resistance mechanisms and guide next-line therapy in ALK+ non-small-cell lung cancer (NSCLC), but the clinical significance of other rebiopsy findings remains unclear. We analysed all stage-IV ALK+ NSCLC patients with longitudinally assessable TP53 status treated in our institutions (n = 62). Patients with TP53 mutations at baseline (TP53mutbas, n = 23) had worse overall survival (OS) than patients with initially wild-type tumours (TP53wtbas, n = 39, 44 vs. 62 months in median, p = 0.018). Within the generally favourable TP53wtbas group, detection of TP53 mutations at progression defined a “converted” subgroup (TP53mutconv, n = 9) with inferior OS, similar to that of TP53mutbas and shorter than that of patients remaining TP53 wild-type (TP53wtprogr, 45 vs. 94 months, p = 0.043). Progression-free survival (PFS) under treatment with tyrosine kinase inhibitors (TKI) for TP53mutconv was comparable to that of TP53mutbas and also shorter than that of TP53wtprogr cases (5 and 8 vs. 13 months, p = 0.0039). Fewer TP53wtprogr than TP53mutbas or TP53mutconv cases presented with metastatic disease at diagnosis (67% vs. 91% or 100%, p < 0.05). Thus, acquisition of TP53 mutations at progression is associated with more aggressive disease, shorter TKI responses and inferior OS in ALK+ NSCLC, comparable to primary TP53 mutated cases.
DOI:doi:10.3390/cancers11010124
URL:Volltext ; Verlag: https://doi.org/10.3390/cancers11010124
 Volltext: https://www.mdpi.com/2072-6694/11/1/124
 DOI: https://doi.org/10.3390/cancers11010124
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:anaplastic lymphoma kinase positive (ALK+) non-small cell lung cancer (NSCLC)
 overall survival
 progression-free survival
 tumor protein p53 gene (TP53) mutation
 tyrosine kinase inhibitor
K10plus-PPN:1667973045
Verknüpfungen:→ Zeitschrift
 
 
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