Department of Gastroenterological Surgery, St. Marianna University Hospital, St. Marianna University School of Medicine, 2-16-1 Sugao, Miyamae-ku, Kawasaki 216-8511, Japan.
Int J Clin Oncol. 2011 Jun;16(3):257-63. doi: 10.1007/s10147-010-0176-0. Epub 2011 Jan 18.
Chemotherapy-associated hepatotoxicity is a common cause of postoperative complications after major hepatectomy. Splenomegaly may indicate portal hypertension due to chemotherapy. To identify chemotherapy-naïve patients with liver damage, the splenic volume (SV) and aspartate aminotransferase to platelet ratio (APR) were investigated.
Seventy-one patients receiving FOLFIRI, FOLFOX, or FOLFOX plus bevacizumab as first-line chemotherapy were included in this study. The SV measurement was performed by helical computed tomography volumetry, and the SV index (SVI) was calculated during 6 cycles of chemotherapy. The APR was used as an indicator of liver injury and the APR index (APRI) was calculated.
The SVI and APRI were significantly higher in the FOLFOX group than in the FOLFIRI group. In the FOLFOX group, the maximum APR during FOLFOX administration was significantly higher in the subjects with SVI ≥ +30% than in those with SVI < +30% (p < 0.01). The incidences of grade 3 or 4 adverse events and grade 2 or greater histopathological sinusoidal injury were significantly higher in the SVI ≥ +30% than in the SVI < +30% group. Interestingly, the SVI was significantly higher in the group with APR ≥ 0.17 before FOLFOX than in the subjects with an APR < 0.17 before FOLFOX (p < 0.05).
Splenomegaly due to FOLFOX-associated hepatotoxicity can be predicted if the APR before FOLFOX is 0.17 or higher.
化疗相关肝毒性是肝大部切除术后术后并发症的常见原因。脾肿大可能提示化疗引起的门脉高压。为了确定无化疗肝损伤的患者,研究人员检测了脾脏体积(SV)和天冬氨酸转氨酶与血小板比值(APR)。
本研究纳入了 71 例接受 FOLFIRI、FOLFOX 或 FOLFOX 联合贝伐珠单抗作为一线化疗的患者。通过螺旋 CT 容积测量法进行 SV 测量,并在 6 个周期的化疗期间计算 SV 指数(SVI)。APR 用于评估肝损伤,计算 APR 指数(APRI)。
FOLFOX 组的 SVI 和 APRI 显著高于 FOLFIRI 组。在 FOLFOX 组中,FOLFOX 治疗期间,SVI≥+30%的患者最大 APR 显著高于 SVI<+30%的患者(p<0.01)。SVI≥+30%的患者 3 级或 4 级不良事件和 2 级或更严重的组织病理学窦状隙损伤发生率显著高于 SVI<+30%的患者。有趣的是,在 FOLFOX 之前 APR≥0.17 的患者中,SVI 显著高于 APR<0.17 的患者(p<0.05)。
如果 FOLFOX 前的 APR 为 0.17 或更高,则可预测与 FOLFOX 相关的肝毒性引起的脾肿大。