Abstract | BACKGROUND: METHODS: The authors retrospectively identified 361 patients who received palbociclib combined with ET. Progression-free survival (PFS) and overall survival (OS) were analyzed based on subsequent treatments and HER2 status (PFSsub and OSsub, respectively). PFS1 and OS1 were calculated from palbociclib administration to disease progression/death and death from any cause, respectively. PFSsub and OSsub were calculated from subsequent treatment initiation. RESULTS: The median PFS1 and OS1 were 10.2 and 39.9 months, respectively. The median PFSsub and OSsub of 111 patients (54.7%) who received chemotherapy were 4.9 months and 20.0 months, respectively, whereas those of 89 patients (43.8%) who received endocrine backbone therapy were 5.9 months and 29.3 months, respectively. Among them, 31 patients (15.3%) who received abemaciclib combined with new ET showed better PFSsub and OSsub (12.2 months and not reached, respectively). The median PFS1 was significantly shorter in the HER2-low subgroup than in the HER2-zero subgroup among patients who received second-line or later palbociclib (6.1 vs. 7.8 months; p = .040) but did not differ among patients who received first-line palbociclib. CONCLUSIONS: Various regimens after palbociclib use were received. An improvement was noted in PFS among patients who received endocrine backbone therapy relative to chemotherapy, which may have been secondary to the receipt of chemotherapy by patients with more aggressive disease. HER2 status was not related to the effect of first-line palbociclib, but it may play a role in later lines.
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Authors | Xu Liang, Linhui Zhang, Xinyu Gui, Lijun Di, Huiping Li, Guohong Song |
Journal | Cancer
(Cancer)
Vol. 130
Issue S8
Pg. 1476-1487
(Apr 15 2024)
ISSN: 1097-0142 [Electronic] United States |
PMID | 38198366
(Publication Type: Journal Article)
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Copyright | © 2024 The Authors. Cancer published by Wiley Periodicals LLC on behalf of American Cancer Society. |
Chemical References |
- palbociclib
- Pyridines
- Receptor, ErbB-2
- Piperazines
|
Topics |
- Humans
- Female
- Breast Neoplasms
(pathology)
- Retrospective Studies
- Antineoplastic Combined Chemotherapy Protocols
(therapeutic use)
- Pyridines
- Receptor, ErbB-2
(metabolism)
- Piperazines
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