Cyclin-dependent kinase 4/6 inhibitors combined with stereotactic ablative radiotherapy in oligometastatic HR-positive/HER2-negative breast cancer patients

Cyclin-dependent kinase 4/6 inhibitors (CDK4/6i) have significantly improved the survival of patients with hormone receptor-positive HER2-negative advanced breast cancer (ABC). Although stereotactic ablative radiotherapy (SABR) is used more often in routine clinical practice, data on the safety and...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:British journal of radiology 2024-10, Vol.97 (1162), p.1627-1635
Hauptverfasser: Kubeczko, Marcin, Gabryś, Dorota, Krzywon, Aleksandra, Jarząb, Michał
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Cyclin-dependent kinase 4/6 inhibitors (CDK4/6i) have significantly improved the survival of patients with hormone receptor-positive HER2-negative advanced breast cancer (ABC). Although stereotactic ablative radiotherapy (SABR) is used more often in routine clinical practice, data on the safety and efficacy of combining SABR with CDK4/6i are lacking. Herein, we present the results of SABR combined with CDK4/6i in ABC. Patients with ABC who received CDK4/6i and SABR between 2018-2023 were analyzed. Among 384 patients treated with CDK4/6i, 34 patients received 44 courses of SABR. 2-year PFS was 63.6% (95%CI : 45.8-88.3), and the median PFS was 32 months. 3-year OS was 88.9% (95%CI : 77.7-100). 2-year local control was 92.7% [95%CI : 83.4-100]. Median OS and LC were not reached. The subgroup analysis showed the difference in survival between oligometastatic patients (OMD) and non-OMD subgroup. 2-year PFS was 69.2%(95%CI : 44.5-100) in OMD compared with 57.4% (95%CI : 36-91.7) in the non-OMD (p = 0.042). 3-year OS was 90%(95%CI : 73.2-100) in OMD compared with 86.2%(95%CI : 70-100) in the non-OMD (p = 0.67). Median PFS and OS in the non-OMD were 26 and 56 months, respectively, and were not reached in OMD. Fifteen patients required CDK4/6i dose reduction, and two discontinued treatment due to toxicity. No difference in high-grade toxicity was observed between the sequential and concurrent SABR. The addition of SABR to CDK4/6i seems to be safe and effective, especially in patients with oligometastatic disease. In advanced breast cancer patients treated with CDK4/6i, SABR provides a high local control and may provide additional benefit in an oligometastatic setting.
ISSN:0007-1285
1748-880X
1748-880X
DOI:10.1093/bjr/tqae138