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Verfasst von:Goldman, Jonathan W. [VerfasserIn]   i
 Mazieres, Julien [VerfasserIn]   i
 Barlesi, Fabrice [VerfasserIn]   i
 Dragnev, Konstantin H. [VerfasserIn]   i
 Koczywas, Marianna [VerfasserIn]   i
 Göskel, Tuncay [VerfasserIn]   i
 Cortot, Alexis B. [VerfasserIn]   i
 Girard, Nicolas [VerfasserIn]   i
 Wesseler, Claas [VerfasserIn]   i
 Bischoff, Helge [VerfasserIn]   i
 Nadal, Ernest [VerfasserIn]   i
 Park, Keunchil [VerfasserIn]   i
 Lu, Shun [VerfasserIn]   i
 Taus, Alvaro [VerfasserIn]   i
 Cobo, Manuel [VerfasserIn]   i
 Estrem, Shawn T. [VerfasserIn]   i
 Wijayawardana, Sameera R. [VerfasserIn]   i
 Turner, Kellie [VerfasserIn]   i
 Oakley, Gerard Joseph III [VerfasserIn]   i
 Hurt, Karla C. [VerfasserIn]   i
 Chiang, Alan Y. [VerfasserIn]   i
 Hossain, Anwar M. [VerfasserIn]   i
 John, William J. [VerfasserIn]   i
 Paz-Ares, Luis [VerfasserIn]   i
Titel:A randomized phase III study of abemaciclib versus erlotinib in patients with stage IV non-small cell lung cancer with a detectable KRAS mutation who failed prior platinum-based therapy
Titelzusatz:JUNIPER
Verf.angabe:Jonathan W. Goldman, Julien Mazieres, Fabrice Barlesi, Konstantin H. Dragnev, Marianna Koczywas, Tuncay Göskel, Alexis B. Cortot, Nicolas Girard, Claas Wesseler, Helge Bischoff, Ernest Nadal, Keunchil Park, Shun Lu, Alvaro Taus, Manuel Cobo, Shawn T. Estrem, Sameera R. Wijayawardana, Kellie Turner, Gerard Joseph III Oakley, Karla C. Hurt, Alan Y. Chiang, Anwar M. Hossain, William J. John and Luis Paz-Ares
E-Jahr:2020
Jahr:26 October 2020
Umfang:12 S.
Teil:volume:10
 year:2020
 elocationid:578756
 pages:1-12
 extent:12
Fussnoten:Gesehen am 19.04.2021
Titel Quelle:Enthalten in: Frontiers in oncology
Ort Quelle:Lausanne : Frontiers Media, 2011
Jahr Quelle:2020
Band/Heft Quelle:10(2020), Artikel-ID 578756, Seite 1-12
ISSN Quelle:2234-943X
Abstract:Introduction: JUNIPER compared the efficacy and safety of abemaciclib, a selective cyclin-dependent kinase 4 and 6 inhibitor, with erlotinib in patients with non-small cell lung cancer (NSCLC) harboring a Kirsten rat sarcoma (KRAS) mutation. Methods: JUNIPER was a Phase III, multicenter, randomized, open-label trial of abemaciclib versus erlotinib in patients with stage IV NSCLC and a detectable mutation in codons 12 or 13 of the KRAS oncogene, who progressed after platinum-based chemotherapy and 1 additional therapy (could include immune checkpoint inhibitor therapy). Randomized patients (3:2) received either 200 mg abemaciclib twice daily or 150 mg erlotinib once daily with best supportive care until disease progression or unacceptable toxicity. The primary endpoint was overall survival (OS); secondary endpoints included overall response rate (ORR), progression-free survival (PFS), and safety. Results: Between Dec 2014 and Apr 2017, 453 patients were randomly assigned to receive abemaciclib (N=270) or erlotinib (N=183). Median OS was 7.4 months (95% confidence interval [CI]: 6.5, 8.8) with abemaciclib and 7.8 months (95% CI: 6.4, 9.5) with erlotinib (hazard ratio [HR]=0.968 [95% CI: 0.768, 1.219]; p=.77). Median PFS was 3.6 months (95% CI: 2.8, 3.8) with abemaciclib and 1.9 months (95% CI: 1.9, 2.0) with erlotinib (HR=0.583 [95% CI: 0.470, 0.723]; p<.000001). ORR was 8.9% and 2.7% (p=.010) and the disease control rate was 54.4% and 31.7% (p<.001) with abemaciclib and erlotinib, respectively. Safety results reflected the known safety profiles of abemaciclib and erlotinib. Conclusions: In this study, the primary endpoint of OS was not met; PFS and ORR were improved with manageable toxicity in the abemaciclib arm. The increases in response rates and PFS support further investigation of abemaciclib in other NSCLC subpopulations or in combination with other agents.
DOI:doi:10.3389/fonc.2020.578756
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext ; Verlag: https://doi.org/10.3389/fonc.2020.578756
 Volltext: https://www.frontiersin.org/articles/10.3389/fonc.2020.578756/full
 DOI: https://doi.org/10.3389/fonc.2020.578756
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:Abemaciclib
 Erloitinib
 KRAS
 NSCLC
 platinum-resistant
K10plus-PPN:1755327072
Verknüpfungen:→ Zeitschrift

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