Department of Gastrointestinal Oncology, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Peking University Cancer Hospital and Institute, Beijing 100142, China.
World J Gastroenterol. 2018 Jan 14;24(2):266-273. doi: 10.3748/wjg.v24.i2.266.
To investigate predictive and prognostic value of serum alpha-fetoprotein (AFP) level and its dynamic changes in patients with advanced gastric cancer with elevated serum AFP (AFPAGC).
One hundred and five patients with AFPAGC were enrolled in the study, and all of them underwent at least one cycle of systemic chemotherapy at our institute and had serum AFP ≥ 20 ng/mL at diagnosis or recurrence. Clinicopathologic features, serum AFP level at diagnosis and changes during treatment, first-line chemotherapy regimens, efficacy and toxicity, and survival information were collected. A Person's χ or Fisher's exact test was used to measure the differences between variables. Survival prognostic factors were investigated using the Kaplan-Meier method and Cox regression.
Median serum AFP level was 161.7 ng/mL (range, 22.9-2557110 ng/mL). Objective response rates (ORR) was significantly lower in the AFP ≥ 160 ng/mL group than in the AFP < 160 ng/mL group (30.4% 68.3%, < 0.001). ORR to doublet regimens was significantly lower in the AFP ≥ 160 ng/mL group, whereas ORR to triplet regimens was similar between the two groups. Liver metastasis rate was significantly higher in the AFP ≥ 160 ng/mL group than in the AFP < 160 ng/mL (69.8% 50.0%, < 0.001). Overall survival (OS) in the two cohorts did not show any significant difference ( = 0.712). Dynamic changes of AFP were consistent with response to chemotherapy, and median OS of patients with a serum AFP decline ≥ 50% and those with a serum AFP decline < 50% was 17.5 m and 10.0 m, respectively ( = 0.003). Hepatic ( = 0.005), peritoneal ( < 0.001), non-regional lymph node metastasis ( < 0.001), and portal vein tumor thrombus (PVTT) ( = 0.042) were identified as independent prognostic factors for AFPAGC.
Real-time examination of AFP has great predictive and prognostic value for managing AFPAGC. For those with markedly elevated AFP, triplet regimens may be a better choice.
研究血清甲胎蛋白(AFP)水平及其在血清 AFP 升高的晚期胃癌(AFPAGC)患者中的动态变化的预测和预后价值。
本研究纳入了 105 例 AFPAGC 患者,他们均在我院至少接受了一个周期的系统化疗,且在诊断或复发时血清 AFP≥20ng/mL。收集了临床病理特征、诊断时的血清 AFP 水平及治疗过程中的变化、一线化疗方案、疗效和毒性以及生存信息。采用 Pearson χ 或 Fisher 确切概率检验比较变量间的差异。采用 Kaplan-Meier 法和 Cox 回归分析生存预后因素。
中位血清 AFP 水平为 161.7ng/mL(范围,22.9-2557110ng/mL)。AFP≥160ng/mL 组的客观缓解率(ORR)明显低于 AFP<160ng/mL 组(30.4% 68.3%,<0.001)。AFP≥160ng/mL 组对双联方案的 ORR 明显较低,而两组对三联方案的 ORR 相似。AFP≥160ng/mL 组的肝转移率明显高于 AFP<160ng/mL 组(69.8% 50.0%,<0.001)。两组患者的总生存期(OS)无显著差异(=0.712)。AFP 的动态变化与化疗反应一致,血清 AFP 下降≥50%和血清 AFP 下降<50%的患者中位 OS 分别为 17.5m 和 10.0m(=0.003)。肝转移(=0.005)、腹膜转移(<0.001)、非区域性淋巴结转移(<0.001)和门静脉癌栓(PVTT)(=0.042)被确定为 AFPAGC 的独立预后因素。
实时检查 AFP 对 AFPAGC 的管理具有重要的预测和预后价值。对于 AFP 明显升高的患者,三联方案可能是更好的选择。