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Social Support and Chemotherapy-Induced Peripheral Neuropathy in Breast Cancer: A Full Mediation Dual-Pathway Model Through Physical Activity and Psychological Distress.

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Psycho-oncology 📖 저널 OA 61.2% 2024: 0/1 OA 2025: 11/14 OA 2026: 29/51 OA 2024~2026 2026 Vol.35(4) p. e70470 Cancer Treatment and Pharmacology
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PubMed DOI OpenAlex 마지막 보강 2026-05-01
OpenAlex 토픽 · Cancer Treatment and Pharmacology Cancer-related cognitive impairment studies Cancer survivorship and care

Wei H, He W

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[BACKGROUND] Chemotherapy-induced peripheral neuropathy (CIPN) is a debilitating toxicity.

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APA Huijie Wei, Wubin He (2026). Social Support and Chemotherapy-Induced Peripheral Neuropathy in Breast Cancer: A Full Mediation Dual-Pathway Model Through Physical Activity and Psychological Distress.. Psycho-oncology, 35(4), e70470. https://doi.org/10.1002/pon.70470
MLA Huijie Wei, et al.. "Social Support and Chemotherapy-Induced Peripheral Neuropathy in Breast Cancer: A Full Mediation Dual-Pathway Model Through Physical Activity and Psychological Distress.." Psycho-oncology, vol. 35, no. 4, 2026, pp. e70470.
PMID 41999611 ↗
DOI 10.1002/pon.70470

Abstract

[BACKGROUND] Chemotherapy-induced peripheral neuropathy (CIPN) is a debilitating toxicity. While social support is protective, its precise mechanisms remain unclear.

[AIMS] To test whether social support influences CIPN symptoms through physical activity and psychological distress, and if mediation is full or partial.

[METHODS] A prospective cohort of 240 breast cancer patients was enrolled and assessed longitudinally at three time points: baseline, 6 weeks, and 12 weeks. Using structural equation modeling, a partial mediation model (with a direct social support-CIPN path) was compared to a full mediation model (path constrained) via a likelihood ratio test. Indirect effects were tested with bootstrapping.

[RESULTS] Model comparison supported the full mediation (Δχ(1) = 0.22, p = 0.639). Higher baseline social support was associated with greater week-6 physical activity (β = 0.668) and lower week-6 psychological distress (β = -0.602). These mediators subsequently predicted week-12 CIPN symptoms (physical activity: β = -0.403; psychological distress: β = 0.361). Significant indirect effects were found for both the physical activity pathway (β = -0.271) and the psychological distress pathway (β = -0.219). The model explained 47.6% of the variance in CIPN symptoms.

[CONCLUSIONS] The protective effect of social support on CIPN symptoms operates predominantly by promoting physical activity and buffering psychological distress. These findings support integrated, mechanism-informed interventions leveraging social resources to mitigate a debilitating burden of treatment-related symptoms.

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