Treatment efficacy of ramucirumab-containing chemotherapy in patients with alpha-fetoprotein producing gastric cancer

被引:2
|
作者
Kamiimabeppu, Daisaku [1 ]
Wakatsuki, Takeru [1 ]
Takahari, Daisuke [1 ]
Fukuda, Naoki [1 ]
Shimozaki, Keitaro [1 ]
Osumi, Hiroki [1 ]
Nakayama, Izuma [1 ]
Ogura, Mariko [1 ]
Ooki, Akira [1 ]
Shinozaki, Eiji [1 ]
Chin, Keisho [1 ]
Yamaguchi, Kensei [1 ]
机构
[1] Japanese Fdn Canc Res, Canc Inst Hosp, Dept Gastrointestinal Med Oncol, Koto Ku, 3-8-31 Ariake, Tokyo 1358550, Japan
关键词
Alpha-fetoprotein; AFP-producing gastric cancer; Ramucirumab; Target therapy; DOUBLE-BLIND; CLINICOPATHOLOGICAL FEATURES; SERUM AFP; PLACEBO; ADENOCARCINOMA; CARCINOMA; PROTEIN; MULTICENTER; EXPRESSION; THERAPY;
D O I
10.1007/s10147-022-02263-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Alpha-Fetoprotein Producing Gastric Cancer (AFPGC) is an aggressive subgroup of gastric cancer. Recently ramucirumab has shown survival benefits in hepatocellular carcinoma, but only in those with higher Alpha-Fetoprotein (AFP) levels. However, the efficacy of ramucirumab-containing chemotherapy in AFPGC remains unclear. Methods We retrospectively assessed 352 patients who received ramucirumab-containing chemotherapy between June 2015 and December 2019. AFPGC was defined when serum AFP levels were elevated at diagnosis and correlated with the disease state during treatment. Non-AFPGC was defined when serum AFP levels were normal at diagnosis. Results Among the 352 patients, 28 patients were defined as AFPGC and 246 patients were defined as non-AFPGC. AFPGC was characterized by high frequency of liver metastasis and low frequency of peritoneal metastasis compared to non-AFPGC. Ramucirumab containing chemotherapy showed higher response rates in AFPGC (39.1% vs 24.8%, p = 0.198) and disease control rates (86.9% vs 61.5%, p = 0.028) than those of non-AFPGC, respectively. Median progression-free survival (PFS) was 5.5 months (95%CI 3.9-7.1) in AFPGC and 4.0 months (95%CI 3.6-4.6) in non-AFPGC (HR: 0.91, 95% CI 0.61-1.36, p = 0.66), and median overall survival (OS) was 10.7 months (95% CI 7.4-20.8) in AFPGC and 9.2 months (95% CI 8.1-10.4) in non-AFPGC (HR: 0.72, 95% CI 0.48-1.08, p = 0.11), respectively. In multivariate analysis, AFPGC was not a negative prognostic factor both for PFS and OS. Conclusion Ramucirumab containing chemotherapy showed higher response and comparable survival in AFPGC compared to those of non-AFPGC. Considering the generally poor prognosis of AFPGC, ramucirumab-containing chemotherapy might be a promising treatment option in AFPGC.
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页码:121 / 129
页数:9
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