Watanabe Kazuteru, Ishibe Atsushi, Watanabe Jun, Ota Mitsuyoshi, Fujii Shoichi, Ichikawa Yasushi, Oba Mari S, Endo Itaru
Department of Gastroenterological Surgery, Yokohama City University, Yokohama, Japan.
Department of Gastroenterological Center, Yokohama City University Medical center, Yokohama, Japan.
Indian J Gastroenterol. 2020 Apr;39(2):204-210. doi: 10.1007/s12664-020-01039-6. Epub 2020 May 13.
Eppikajututo (TJ-28, a Kampo medicine) is effective against rheumatoid arthritis and eczema. We conducted a randomized comparative trial to assess the efficacy of TJ-28 for preventing hand-foot syndrome (HFS) as a complication of adjuvant chemotherapy using capecitabine.
The present study was a multi-institutional randomized-controlled trial (UMIN000005899). Colorectal cancer patients scheduled to receive capecitabine chemotherapy as adjuvant therapy were randomly assigned to receive TJ-28 (7500 mg/day) or oral pyridoxine (60 mg/day). Patients were monitored for the development of grade ≥ 2 HFS according to the National Cancer Institute Common Toxicity Criteria until chemotherapy completion.
Twenty-two patients were enrolled in this study. The relative dose intensity of capecitabine was 76.2% in the TJ-28 group and 68.2% in the pyridoxine group. Grade ≥ 2 HFS developed in 6 (50.0%) of 12 TJ-28 patients and in 4 (40.0%) of 10 pyridoxine patients. Chemotherapy treatment failure was observed in seven patients, mainly due to HFS, liver dysfunction, diarrhea, and neutropenia. Chemotherapy treatment failure due to HFS occurred in none of the TJ-28 group and 2 patients (20.0%) in the pyridoxine group (p = 0.114).
Capecitabine-associated HFS was not markedly prevented by TJ-28 compared with pyridoxine. However, TJ-28 might support the continuation of chemotherapy with capecitabine. Further studies are warranted to clarify the benefits of TJ-28.
Eppikajututo(TJ - 28,一种汉方药物)对类风湿性关节炎和湿疹有效。我们进行了一项随机对照试验,以评估TJ - 28预防卡培他滨辅助化疗并发症手足综合征(HFS)的疗效。
本研究为多机构随机对照试验(UMIN000005899)。计划接受卡培他滨化疗作为辅助治疗的结直肠癌患者被随机分配接受TJ - 28(7500毫克/天)或口服吡哆醇(60毫克/天)。根据美国国立癌症研究所通用毒性标准监测患者≥2级HFS的发生情况,直至化疗结束。
本研究共纳入22例患者。卡培他滨的相对剂量强度在TJ - 28组为76.2%,在吡哆醇组为68.2%。12例TJ - 28患者中有6例(50.0%)发生≥2级HFS,10例吡哆醇患者中有4例(40.0%)发生。7例患者出现化疗治疗失败,主要原因是HFS、肝功能障碍、腹泻和中性粒细胞减少。TJ - 28组未发生因HFS导致的化疗治疗失败,吡哆醇组有2例患者(20.0%)发生(p = 0.114)。
与吡哆醇相比,TJ - 28未能显著预防卡培他滨相关的HFS。然而,TJ - 28可能有助于卡培他滨化疗的持续进行。有必要进一步研究以阐明TJ - 28的益处。