Jiang Huici, Shao Dongxuan, Zhao Peiyu, Wu Yupeng
Department of Obstetrics and Gynecology, Shanghai Tenth People's Hospital, Shanghai, China.
Department of Obstetrics and Gynecology, Shanghai Eighth People's Hospital, Shanghai, China.
Front Oncol. 2021 Feb 23;11:631995. doi: 10.3389/fonc.2021.631995. eCollection 2021.
To evaluate the predictive and guidance value of signet-ring cell carcinoma for chemotherapy response in stage II/III colon cancer.
Eligible patients were recruited from the Surveillance, Epidemiology and End Results (SEER) database. The differences between adenocarcinoma (AD) and SRCC groups in the incidence of patients' demographic and clinical characteristics were analyzed by Pearson's chi-squared (×2) test. Survival was analyzed using the Kaplan-Meier method, and the differences were determined by the log-rank test. Some Cox regression models were built to assess hazard ratios (HRs) of different variables with 95% confidence intervals (95% CIs).
In stage II AD, it was found that the receipt of chemotherapy had significantly 12.6% decreased risk of cancer-specific mortality (HR = 0.874, 95% CI = 0.825-0.927, P < 0.001). In stage II SRCC, however, the receipt of chemotherapy had significantly 70.00% increased risk of cancer-specific mortality (HR = 1.700, 95% CI = 1.032-2.801, P = 0.037). In stage III AD, it was found that the receipt of chemotherapy had significantly 45.3% decreased risk of cancer-specific mortality (HR = 0.547, 95% CI = 0.530-0.564, P < 0.001). In stage III SRCC, the receipt of chemotherapy had significantly 24.6% decreased risk of cancer-specific mortality (HR = 0.754, 95% CI = 0.632-0.900, P = 0.002).
The cancer-specific survival (CSS) difference between AD and SRCC was not statistically significant in stage II colon cancer. We provided the first compelling evidence that chemotherapy should not be treated in stage II SRCC, while stage III SRCC should be treated with chemotherapy.
评估印戒细胞癌对Ⅱ/Ⅲ期结肠癌化疗反应的预测及指导价值。
从监测、流行病学与最终结果(SEER)数据库招募符合条件的患者。采用Pearson卡方(×2)检验分析腺癌(AD)组和印戒细胞癌(SRCC)组患者人口统计学和临床特征发生率的差异。采用Kaplan-Meier法分析生存情况,通过对数秩检验确定差异。构建一些Cox回归模型以评估不同变量的风险比(HR)及95%置信区间(95%CI)。
在Ⅱ期AD中,发现接受化疗可使癌症特异性死亡风险显著降低12.6%(HR = 0.874,95%CI = 0.825 - 0.927,P < 0.001)。然而,在Ⅱ期SRCC中,接受化疗可使癌症特异性死亡风险显著增加70.00%(HR = 1.700,95%CI = 1.032 - 2.801,P = 0.037)。在Ⅲ期AD中,发现接受化疗可使癌症特异性死亡风险显著降低45.3%(HR = 0.547,95%CI = 0.530 - 0.564,P < 0.001)。在Ⅲ期SRCC中,接受化疗可使癌症特异性死亡风险显著降低24.6%(HR = 0.754,95%CI = 0.632 - 0.900,P = 0.002)。
Ⅱ期结肠癌中AD和SRCC之间的癌症特异性生存(CSS)差异无统计学意义。我们提供了首个有力证据,即Ⅱ期SRCC不应接受化疗,而Ⅲ期SRCC应接受化疗。