Department of Gastrointestinal Surgical Oncology, Affiliated Cancer Hospital and Institute of Guangzhou Medical University, Guangzhou, China.
Department of General Surgery, the Fifth Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Ann Palliat Med. 2021 Mar;10(3):3009-3017. doi: 10.21037/apm-21-61.
This study sought to test the effectiveness of EVOSKIN®Palm and sole moisturizing cream (PSMC) in preventing and treating hand-foot syndrome (HFS) during capecitabine chemotherapy.
Stage II/III colorectal cancer patients receiving capecitabine adjuvant chemotherapy were randomly allocated to receive either EVOSKINPSMC or physiological saline treatments for their hands and feet. Treatment was initiated along with adjuvant chemotherapy and continued till the end of chemotherapy. Participants' skin responses were evaluated every 3 weeks.
During the study, 51 participants in the EVOSKIN PSMC group and 54 participants in the physiological saline group completed at least three cycles of capecitabine chemotherapy. The total incidence of HFS in the EVOSKIN PSMC group was lower than that in the physiological saline group (56.8% vs. 75.9%, P=0.006), as was the incidence of Grade 3/4 HFS (6.0% vs. 18.5%, P=0.011). The incidence of HFS became significant after 6weeks of chemotherapy. Further, the incidence of severe HFS was significant from as early as 3weeks after the commencement of chemotherapy despite the use of EVOSKIN PSMC to manage the condition. Notably, the incidence of Grade 1/2 HFS was not statistically significant between the two groups (26/51 vs. 32/54, 52.0% vs. 59.2%, P=0.194).
The incidence of severe HFS among individuals using oral capecitabine can be reduced by the prophylactic treatment of EVOSKIN PSMC, this treatment is reasonable and acceptable for patients with capecitabine chemotherapy.
本研究旨在测试 EVOSKIN®手掌和足底保湿霜(PSMC)在预防和治疗卡培他滨化疗期间手足综合征(HFS)的有效性。
接受卡培他滨辅助化疗的 II/III 期结直肠癌患者被随机分配接受 EVOSKIN PSMC 或生理盐水治疗其手部和足部。治疗从辅助化疗开始,持续到化疗结束。每 3 周评估一次参与者的皮肤反应。
在研究期间,EVOSKIN PSMC 组的 51 名参与者和生理盐水组的 54 名参与者至少完成了三个周期的卡培他滨化疗。EVOSKIN PSMC 组 HFS 的总发生率低于生理盐水组(56.8%比 75.9%,P=0.006),3/4 级 HFS 的发生率也较低(6.0%比 18.5%,P=0.011)。HFS 的发生率在化疗 6 周后变得显著。此外,尽管使用 EVOSKIN PSMC 来管理 HFS,但在化疗开始后 3 周时 HFS 的严重程度就变得显著。值得注意的是,两组间 HFS 的严重程度发生率无统计学差异(26/51 比 32/54,52.0%比 59.2%,P=0.194)。
预防性使用 EVOSKIN PSMC 可降低使用口服卡培他滨的个体发生严重 HFS 的风险,这种治疗方法对于接受卡培他滨化疗的患者是合理且可接受的。