Limb compression therapy and chemotherapy-induced peripheral neuropathy in women with gynecologic cancers: A prospective self-controlled study (NEURO-GLOVE Trial)—Updated long-term analysis.
Abstract
5545 Background: No established strategy prevents taxane-induced CIPN. We evaluated if dual-site mechanical compression reduces CIPN severity at 3 and 6 months post-treatment. Methods: In this prospective, self-controlled study (Dec 2023–Dec 2024), 76 women receiving carboplatin–paclitaxel were enrolled. During infusions, compression was applied to the non-dominant hand (two surgical gloves) and ipsilateral foot (Class II stocking); contralateral limbs served as controls. The primary endpoint was the incidence of Grade ≥2 sensory/motor neuropathy (CTCAE v5.0) at End-of-Treatment (EOT), 3 months, and 6 months. Results: Among 76 patients (median age 61), Grade ≥2 CIPN was lower in compression vs control limbs at Cycle 3 (27/76 [35.5%] vs 41/76 [53.9%]; P=.001) and EOT (45/76 [59.2%] vs 53/76 [69.7%]; P=.021). Benefits persisted at 3 months (22/76 [28.9%] vs 40/76 [52.6%]; P=.015) and 6 months (15/74 [20.3%] vs 25/74 [33.8%]; P=.002). Longitudinal analysis showed significant time-by-limb interactions for hand sensory (P=.003), foot sensory (P=.018), and motor domains (P=.041). EORTC QLQ-CIPN20 sensory scores showed high accuracy (AUC 0.92 at Cycle 3; 0.97 at EOT). Conclusions: Compression significantly reduces acute and persistent CIPN. Sustained benefits at 3 and 6 months suggest prevention of irreversible damage, supporting compression as an effective neuroprotective strategy. Clinical trial information: NCT07105553 . Limb-specific incidence of moderate-to-severe chemotherapy-induced peripheral neuropathy by EORTC QLQ–CIPN20 across time. Time point Limb Moderate–severe CIPN†, n/N (%) Discordant cases ‡, n McNemar p (compression vs control) RD %, Control–Compression (95% CI) P value vs baseline § Baseline CompressionControl 0/76 (0.0)0/76 (0.0) – – – – Cycle 3 Compression Control 27/76 (35.5)41/76 (53.9) Compression only: 2Control only: 16 0.001 +18.4% (4.5 to 32.4) <0.001 <0.001 EOT Compression Control 45/76 (59.2)53/76 (69.7) Compression only: 1Control only: 9 0.021 +10.5% (3.5 to 24.5) <0.001 <0.001 3-month follow-up Compression Control 22/76 (28.9)40/76 (52.6) Compression only: 2Control only: 20 0.015 +23.7% (10.0 to 37.4 <0.001 <0.001 6-month follow-up Compression Control 15/74 ** (20.3)25/74 (33.8) Compression only: 0Control only: 10 0.002 +13.5% (1.5 to 25.4) <0.001 <0.001
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (10)
Kadriye Başkurt
Etlik City Hospital, Department of Medical Oncology, Ankara, Turkey
Galip Can Uyar
Enes Yeşi̇lbaş
Etlik City Hospital, Department of Medical Oncology, Ankara, Turkey
Fatma Zehra Altunc
Etlik City Hospital, Department of Neurology, Ankara, Turkey
Damla Emirhan Cevik
Etlik City Hospital, Department of Neurology, Ankara, Turkey
Ismet Murat Melek
Etlik City Hospital, Department of Neurology, Ankara, Turkey
Yasemin Eren
Etlik City Hospital, Department of Neurology, Ankara, Turkey
Omur Berna Cakmak Oksuzoglu
Etlik City Hospital, Department of Medical Oncology, Ankara, Turkey
Kadriye Bir Yucel
Etlik City Hospital, Department of Medical Oncology, Ankara, Turkey
Osman Sütcüoglu
Orhun Akdogan, MD; Ahmet Ozet, MD; Ozan Yazıcı, MD; Nuriye Ozdemir, MD; and Osman Sütcüoglu, MD, Department of Medical Oncology, Gazi University, Ankara, Turkey