Akademik Veri Yönetim Sistemi
Supportive Care in Cancer, cilt.33, sa.12, 2025 (SCI-Expanded, Scopus)
Background: The treatment goal in early-stage breast cancer (ESBC) is disease-free survival, but toxicity should not be ignored as it will affect the quality of life of patients in the later period. Paclitaxel-induced peripheral neuropathy (PIPN) is one of the most significant dose-limiting toxicities in early-stage breast cancer. The incidence of PIPN in patients receiving paclitaxel chemotherapy reaches 64–84%, and > 30% of patients may experience chronic peripheral neuropathy. Although PIPN is a common toxicity, it is unclear which patient group is most frequently affected in ESBC. Furthermore, sarcopenia is known to increase the toxicity of chemotherapeutic agents. In this study, we aimed to evaluate the relationship between sarcopenia and neuropathy. Methods: This prospective observational study was conducted between November 2024 and May 2025. ESBC patients receiving paclitaxel at a weekly dose of 80 mg/m via a 3-h infusion were included in the study. SMI was calculated by measuring L3 muscle volume from the computed tomography (CT) images taken for staging purposes at the time of diagnosis and adjusting it according to height squared. Sex-specific cutoffs for L3 SMI were used for the diagnosis of sarcopenia. Neuropathy complaints were assessed with the EORTC QLQ-CIPN20 questionnaire before starting paclitaxel treatment and after the completion of treatment. The relationship between sarcopenia and neuropathy as well as other toxicities was evaluated. Results: Sarcopenia was detected in 29 (27.4%) patients. Overall, 50 patients (47.1%) developed paclitaxel-induced peripheral neuropathy (PIPN), including 18 (17.0%) with grade 3, 16 (15.1%) with grade 2, and 16 (15.1%) with grade 1 neuropathy. Five patients (4.7%) were unable to complete 12 weeks of treatment due to grade 3 neuropathy. A significant association was found between age (< 65 vs ≥ 65) (OR 5.2; 95% CI 1.8–15.0; p = 0.002), sarcopenia (OR: 6.5; 95% CI 2.3–18.2; p < 0.001), and neuropathy; no significant association was found between diabetes and concomitant carboplatin use and neuropathy. Conclusions: This study found a significant association between sarcopenia and geriatric age and PIPN. Toxicity and quality of life are crucial in ESBC patients due to their long-life expectancy. Prospective randomized studies with personalized dosing are needed to minimize the risk of PIPN in this patient group. NCT number: NCT06996548