Abstract 1871P
Background
Chemotherapy-induced peripheral neuropathy (CIPN) is a common adverse effect of taxane (Paclitaxel, nab-Paclitaxel, Docetaxel). CIPN could reduce long-term quality of life (Blackley et al, 2019) and result in dose delays, reductions or treatment discontinuations. Temperature-controlled hand-foot cooling (Hilotherapy®) prevents CIPN (Oneda et al. 2020&2021, Coolbrandt et al. 2022). Prospectively collected data of 151 breast cancer patients showed that cooling using 1st generation cuffs with 30 minutes post-cooling prevents CIPN ≥ 2° in 93,4% of patients undergoing taxane-based chemotherapy (Schaper et al. in prep.). The development of 2nd generation, combined cooling-compression cuffs, ensures even more effective skin cooling. This raises the question, whether cooling time could be safely reduced.
Methods
We used prophylactic cooling with 2nd generation cuffs as standard of care during chemotherapy without the recommended 30 minutes post-cooling, due to capacity issues, and investigated the efficacy of the 2nd generation cuffs regarding prevention of CIPN through surveys. Patients were stratified according to dosing schedule (q1w vs q3w). Follow-up data will be collected to report the sustainability of the results.
Results
181 breast cancer patients completed their taxane-based chemotherapy using 2nd generation cuffs without post-cooling. 169 (93,4%) patients showed symptoms of CIPN 0-1° and 12 (6,6%) of CIPN 2°. No patient reported grade 3 toxicity. Data collection is still in process and follow-up will be updated to examine the sustainability of the results.
Conclusions
Prophylactic temperature-controlled hand-foot cooling combined with compression (Hilotherapy® 2nd generation) without the recommended 30 minutes post-cooling effectively prevents the development of severe CIPN ≥ 2°.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
ISI e.V. - International Senology Initiativ.
Disclosure
A. Kostara: Non-Financial Interests, Personal and Institutional, Advisory Board, Study Equipment funding: Hilotherm GmbH. All other authors have declared no conflicts of interest.
Resources from the same session
1874P - Time to vomiting after chemotherapy in association with number of emetic risk factors among breast cancer patients receiving highly emetogenic chemotherapy
Presenter: Winnie Yeo
Session: Poster session 12
1875P - Real-world evidence of ribociclib induced liver toxicity in patients with breast cancer: A multi-center experience
Presenter: Onur Bas
Session: Poster session 12
1877P - Adverse effects (AEs) of trastuzumab deruxtecan (T-DXd) in solid tumours: A meta-analysis
Presenter: Neha Pathak
Session: Poster session 12
1878P - Efficacy of surgical gloves (SG) as compression therapy to prevent oxaliplatin-induced peripheral neuropathy (PN): The ELEGANT trial
Presenter: Aurélia JOUREAU-CHABERT
Session: Poster session 12
1879P - Effectiveness of intravenous fosnetupitant & palonosetron for cinv prophylaxis in patients receiving highly emetogenic chemotherapy regimens: Subgroup analysis from a phase IV Indian study
Presenter: Arun Kumar Verma
Session: Poster session 12
1880P - Antiemetic prophylaxis during chemoradiation: Sub-study of the GAND-emesis trial identifying dosimetric predictors for vomiting
Presenter: Anika Johannsdottir
Session: Poster session 12
1881P - Enhancing chemotherapy-induced nausea and vomiting management: Insights into guideline adherence and patient outcomes
Presenter: Suresh Attili
Session: Poster session 12
1882P - Awareness of chemotherapy induced nausea and vomiting and adherence to guidelines: A multinational and multicenter survey
Presenter: Ricardo Caponero
Session: Poster session 12
1883P - Impact of geriatrician-implemented Interventions on chemotherapy (CT) delivery in vulnerable elderly patients with early or advanced solid tumors: The GIVE trial
Presenter: Emanuela Risi
Session: Poster session 12
1884P - Development and validation of a prediction tool for severe treatment-related toxicities in older cancer patients on systemic treatment (TR-TRM)
Presenter: Wendy Chan
Session: Poster session 12