Three timepoint perioperative CEA levels are a prognostic factor for recurrence after adjuvant chemotherapy in patients with Stage II and III colorectal cancer

被引:0
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作者
Mizuno, Shodai [1 ]
Shigeta, Kohei [1 ]
Hara, Ryosuke [1 ]
Sakamoto, Kyoko [1 ]
Nakadai, Jumpei [2 ]
Baba, Hideo [2 ]
Kikuchi, Hiroto [3 ]
Adachi, Yoko [4 ]
Shimada, Takehiro [4 ]
Suzumura, Hirofumi [5 ]
Sugiura, Kiyoaki [6 ]
Matsui, Shimpei [1 ]
Seishima, Ryo [1 ]
Okabayashi, Koji [1 ]
Kitagawa, Yuko [1 ]
机构
[1] Keio Univ, Dept Surg, Sch Med, 35 Shinano Machi,Shinjuku Ku, Tokyo 1608582, Japan
[2] Saitama City Hosp, Dept Surg, Saitama, Japan
[3] Hiratsuka City Hosp, Dept Surg, Hiratsuka, Kanagawa, Japan
[4] Natl Hosp Org, Dept Surg, Tokyo Med Ctr, Tokyo, Japan
[5] Saiseikai Utsunomiya Hosp, Dept Surg, Utsunomiya, Japan
[6] Eiju Hosp, Dept Surg, Tokyo, Japan
关键词
adjuvant chemotherapy; CEA; colorectal cancer; multi-institutional study; recurrence; AMERICAN-SOCIETY; TUMOR-MARKERS; COLON; SURVEILLANCE; GUIDELINES; RECOMMENDATIONS; RADIATION; OUTCOMES; UPDATE; RISK;
D O I
10.1002/ags3.12886
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AimTo investigate the relationship between the three timepoint perioperative CEA (ttpCEA) calculated at three timepoints and recurrence during the perioperative period in Stage II and III colorectal cancer (CRC) patients. MethodsWe performed a multi-institutional retrospective analysis of patients with Stage II and III CRC who underwent surgery and adjuvant chemotherapy from 2010 to 2020. Patient data from three facilities were used as training data, and data from three other facilities were used as validation data. The primary endpoint was the time to recurrence (TTR). ResultsA total of 538 patients were included for the training data. To validate the feasibility of ttpCEA, 329 patients were included for the validation data. Training data patients were categorized as ttpCEA low (n = 365) and ttpCEA high (n = 173). The 5-y TTR was significantly greater in the ttpCEA-low subgroup than in the ttpCEA-high subgroup (84.3% vs. 69.6%, respectively; p < 0.001). Validation data patients were categorized as ttpCEA low (n = 221) and ttpCEA high (n = 108). The 5-y TTR was significantly greater in the ttpCEA-low subgroup than in the ttpCEA-high subgroup (82.9% vs. 68.7%, respectively; p = 0.003). ConclusionThe ttpCEA calculated from perioperative CEA levels at different timepoints was a prognostic factor for recurrence in Stage II and III CRC patients who underwent adjuvant chemotherapy according to both the training and validation data.
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