Abstract 349P
Background
Peripheral neuropathy is one of the long-term complications of diabetes. In breast cancer diabetic patients, this condition can worsen neurotoxic symptoms induced by taxane-based therapy administration. Chemotherapy induced peripheral neuropathy (CIPN) and its influence on patient’s quality of life (QoL) is evaluated through certified questionnaires (NCI-CTC, EORTC QLQ-CIPN20, FACT-TAXANE).
Methods
Data from stage I-III breast cancer patients treated with taxane-based therapy between 2018 and 2022 were retrospectively analyzed at the Medical Oncology of the University Hospital of Cagliari. 300 patients, median age 57 years (32-85), followed a schedule of PCT 80mg/m2 ± 30 weekly per maximum 12 administrations; 43 patients had diabetes (14,3%). Peripheral neuropathy was evaluated by the NCI-CTC scale at every drug administration. QLQ-CIPN20 and FACT-TAXANE questionnaires were collected at baseline, at 4 and 12 weeks of treatment. Kruskal-Wallis test was used to assess relation between neurotoxicity grade and QoL; ANOVA for repeated measures was used to test differences at different timing. Student’s T-test was used to analyze differences in diabetic and non-diabetic population.
Results
Neurotoxicity influenced QoL, in both populations, at cycle IV (p<0.001) and cycle XII (p=0.008). Patients with grade 0, 1 and 2 neurotoxicity reported a QLQ-CIPN20 median score of 32, 34 and 43 at cycle IV respectively, and a median value of 27, 33 and 34 at cycle XII respectively. ANOVA test showed a significant worsening of QLQ-CIPN20 and FACT-TAXANE scores at 4 and 12 weeks vs. baseline (p<0.001 for both). Values of QLQ-CIPN20 remained significantly higher in comparison to baseline also at 3 (p<0.001), 6 (p<0.001) and 12 months (p<0.001) follow up. In diabetic population, scores were significantly higher (p<0.05) in all neurotoxicity questionnaires, but no difference in QoL was highlighted by FACT-TAXANE, compared to non diabetic patients.
Conclusions
The use of QLQ-CIPN20 and FACT-TAXANE questionnaires identified neurotoxicity onset and its correlation to QoL, yet at an initial phase of treatment. Diabetic patients presented more severe neurotoxicity, without influencing overall QoL.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
371P - Adherence to standardized and structured electronic symptom reporting (ePRO) via mobile app in HER2-positive breast cancer treated with HER2 biosimilar trastuzumab
Presenter: Andreas Trojan
Session: Poster session 03
372P - Prevalence of BRCA1 and BRCA2 mutation among Indian breast cancer patients: A multicentre cross-sectional study
Presenter: Shona Nag
Session: Poster session 03
374P - Evaluation of symptom severity, tolerability, and physical function in the I-SPY2 trial
Presenter: Amrita Basu
Session: Poster session 03
375TiP - A phase I, 2-part, multicenter, first-in-human dose-escalation and dose-expansion study of DS-1103a with trastuzumab deruxtecan (T-DXd) in patients with advanced solid tumors
Presenter: Ludimila Cavalcante
Session: Poster session 03
388P - Subgroup analysis of patients (pts) with HER2-low metastatic breast cancer (mBC) with brain metastases (BMs) at baseline from DESTINY-Breast04, a randomized phase III study of trastuzumab deruxtecan (T-DXd) vs treatment of physician’s choice (TPC)
Presenter: Junji Tsurutani
Session: Poster session 03
391P - Detrimental effect on overall survival of CDK4/6 inhibitor dose reduction if immortal time bias is considered
Presenter: Andreas Bjerrum
Session: Poster session 03
392P - The prognostic impact of BMI in patients with HR+/HER2- advanced breast cancer on first-line endocrine therapy with or without a CDK 4/6 inhibitor
Presenter: Senna Lammers
Session: Poster session 03