Vollständiger Abstract
Worum geht es in dieser Arbeit?
<h4>Background</h4>Dalpiciclib shows satisfactory efficacy and safety in patients with hormone receptor-positive (HR + )/human epidermal growth factor receptor 2-negative (HER2 - ) advanced breast cancer. Nevertheless, relevant real-world evidence is inadequate, particularly in elderly patients. This real-world study intended to explore the efficacy and safety of dalpiciclib plus endocrine therapy in elderly patients with HR + /HER2 - advanced breast cancer.<h4>Methods</h4>This single-center retrospective study analyzed the data of 70 elderly patients (≥65 years) with HR + /HER2 - advanced breast cancer receiving dalpiciclib combined with endocrine therapy. The median (range) follow-up duration was 13.5 (1.7-29.4) months.<h4>Results</h4>The objective response rate (ORR) was 14.3%, and the disease control rate was 94.3%. The ORR was higher in patients with first-line dalpiciclib-based therapy than in those with second-line therapy or above (24.4% vs. 0.0%) (<i>P</i> = 0.004). A total of 39 (55.7%) progression-free survival (PFS) events were recorded. The median (95% confidence interval) PFS was 17.0 (14.6-19.4) months after dalpiciclib plus endocrine therapy. The multivariate Cox regression model disclosed that Eastern Cooperative Oncology Group performance status score 2 (vs. 0) [hazard ratio (HR): 4.010, <i>P</i> = 0.028], lines of dalpiciclib-based therapy (HR: 4.161, <i>P</i> = 0.041), cross-line dalpiciclib (HR: 3.362, <i>P</i> = 0.046), and endocrine resistance (HR: 2.728, <i>P</i> = 0.047) were associated with shorter PFS. The most common adverse events were leukopenia (97.1%) and neutropenia (95.7%), which were predominantly grade 2 or 3. Grade 4 adverse events included leukopenia (2.9%), neutropenia (7.1%), and thrombopenia (1.4%).<h4>Conclusion</h4>Dalpiciclib plus endocrine therapy possesses acceptable efficacy and safety for the treatment of elderly patients with HR + /HER2 - advanced breast cancer.
Abstract: PubMed · Datensatz
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- CrossRef Listing of Deleted DOIs
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- 2000-01-01
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- 0849-6757
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(2000). 10.3389/fpsyg.2012.00132. CrossRef Listing of Deleted DOIs. https://doi.org/10.3389/fonc.2026.1789316