第8版和第7版TNM分期在分化型甲状腺癌患者死亡率、顽固性疾病和治疗反应方面的比较。

Golnaz Gholami, Atena Aghaee, Susan Shafiei, Bashir Rasoulian, Emran Askari, Samira Zare Namdar, Seyed Rasoul Zakavi
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摘要

目的比较第八版和第七版TNM分期(TNM-8和TNM-7)对分化型甲状腺癌(DTC)患者疾病相关死亡率、持续性疾病和治疗反应的影响:我们对平均年龄为 40.93±14.11 岁的 400 名 DTC 患者(79% 为女性)进行了研究。根据第 7 版和第 8 版记录 TNM 分期,对患者进行至少 1 年的随访,并根据 ATA 反应分类记录治疗反应:平均随访时间为(42.5±15.24)个月。总体而言,108 名患者(27%)使用 TNM-8 进行了降期,主要是由于年龄分界线(14.5%)、N(9.25%)和 T 分类(3.25%)的变化。所有Ⅲ期和82.8%的Ⅳ期患者都进行了降期。与TNM-7相比,TNM-8中III期和IV期患者的平均Tg水平明显更高。随访期间共记录到四例与疾病相关的死亡病例,根据TNM-7标准均为IV期,而根据TNM-8标准则为II期。治疗一年后,根据第 7 版和第 8 版,分别有 12% 和 77% 的 III 期患者发现疾病持续存在(P= 0.04)。同样,根据第 7 版和第 8 版,治疗一年后生化反应不完全的 III 期患者分别占 7.3% 和 87%(P=0.006),最后一次就诊时分别降至 2.4% 和 22%(P=0.04):结论:与TNM-7版相比,TNM-8版中的III期和IV期患者更容易出现疾病持续存在和治疗反应不完全的情况。第八版TNM更能预测III期和IV期的持续性疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparison of 8th and 7th editions of TNM staging in terms of mortality, persistent disease, and response to treatment in patients with differentiated thyroid cancer.

Objective: To compare the eighth and seventh editions of TNM staging (TNM-8 and TNM-7) on disease-related mortality, persistent disease, and response to treatment in patients with differentiated thyroid cancer (DTC).

Methods and materials: We studied 400 patients (79% female) with DTC with a mean age of 40.93±14.11 years. TNM staging was recorded according to the 7th and 8th editions and patients were followed for at least 1 year and response to therapy was recorded according to ATA response categorization.

Results: The mean follow up time was 42.5±15.24 months. Overall, 108 patients (27%) were down-staged using the TNM-8, mainly due to the changes in the age cut-off (14.5%), N (9.25%), and T categorization (3.25%). All patients in stage III and 82.8% in stage IV were down-staged. The mean Tg levels were significantly higher in stages III and IV in TNM-8 compared to TNM-7. Four disease-related death were recorded during follow up, all in stage IV according to TNM-7, while one was in stage II according to TNM-8. One year after treatment, persistent disease was detected in 12% and 77% of patients in stage III according to the 7th and 8th editions, respectively (P= 0.04). Similarly, biochemical incomplete response one year after treatment was seen in 7.3% and 87% in stage III disease using 7th and 8th editions (P = 0.006) that fell to 2.4% and 22% in the last visit respectively (P = 0.04).

Conclusion: Persistent disease and incomplete response to therapy were more common in stages III and IV in TNM-8 compared to TNM-7. The eighth edition was a better predictor of persistent disease in stages III and IV disease.

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