Updates in the Treatment of Chemotherapy-Induced Peripheral Neuropathy.
Updates in the Treatment of Chemotherapy-Induced Peripheral Neuropathy.
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DOI:
10.1007/s11864-021-00926-0
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发表时间:
2022-01
影响因子:
4.3
通讯作者:
Lustberg MB
中科院分区:
文献类型:
--
作者:
Mezzanotte JN;Grimm M;Shinde NV;Nolan T;Worthen-Chaudhari L;Williams NO;Lustberg MB
Chemotherapy-induced peripheral neuropathy (CIPN) is a common toxicity associated with treatment with platinum-based agents, taxanes, vinca alkaloids, and other specific agents. The long-term consequences of this condition can result in decreased patient quality of life and can lead to reduced dose intensity, which can negatively impact disease outcomes. There are currently no evidence-based preventative strategies for CIPN and only limited options for treatment. However, there are several strategies that can be utilized to improve patient experience and outcomes as more data are gathered in the prevention and treatment setting. Before treatment, patient education on the potential side effects of chemotherapy is key, and although trials have been limited, recommending exercise and a healthy lifestyle before and while undergoing chemotherapy may provide some overall benefit. In patients who develop painful CIPN, our approach is to offer duloxetine and titrate up to 60mg daily. Chemotherapy doses may also need to be reduced if intolerable symptoms develop during treatment. Some patients may also try acupuncture and physical therapy to help address their symptoms, although this can be limited by cost, time commitment, and patient motivation. Additionally, data on these modalities are currently limited, as studies are ongoing. Overall, approaching each patient on an individual level and tailoring treatment options for them based on overall physical condition, their disease burden, goals of care and co-morbid health conditions, and willingness to trial different approaches is necessary when addressing CIPN.
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影响因子:
5.2
作者:
Caillaud M;Patel NH;Toma W;White A;Thompson D;Mann J;Tran TH;Roberts JL;Poklis JL;Bigbee JW;Fang X;Gewirtz DA;Damaj MI
通讯作者:
Damaj MI
影响因子:
2.9
作者:
Ben-Horin I;Kahan P;Ryvo L;Inbar M;Lev-Ari S;Geva R
通讯作者:
Geva R
影响因子:
3.1
作者:
Gewandter, J. S.;Fan, L.;Mohile, S. G.
通讯作者:
Mohile, S. G.
影响因子:
3.8
作者:
Courneya, Kerry S.;McKenzie, Donald C.;Segal, Roanne J.
通讯作者:
Segal, Roanne J.
影响因子:
3.1
作者:
Gewandter, Jennifer S.;Mohile, Supriya G.;Heckler, Charles E.;Ryan, Julie L.;Kirshner, Jeffrey J.;Flynn, Patrick J.;Hopkins, Judith O.;Morrow, Gary R.
通讯作者:
Morrow, Gary R.