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논문 기본 정보

자료유형
학술저널
저자정보
Seong-A Jeong (University of Ulsan College of Medicine) In Ja Park (University of Ulsan College of Medicine) Seung Mo Hong (University of Ulsan College of Medicine) Jun Woo Bong (University of Ulsan College of Medicine) Hye Yoon Choi (University of Ulsan College of Medicine) Ji Hyun Seo (University of Ulsan College of Medicine) Hyong Eun Kim (University of Ulsan College of Medicine) Seok-Byung Lim (University of Ulsan College of Medicine) Chang Sik Yu (University of Ulsan College of Medicine) Jin Cheon Kim (University of Ulsan College of Medicine)
저널정보
대한외과학회 Annals of Surgical Treatment and Research Annals of Surgical Treatment and Research Vol.96 No.2
발행연도
2019.2
수록면
78 - 85 (8page)

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Purpose: Insistence that total regression of primary tumor would not represent long-term oncologic outcomes has been raised. Therefore, this study aimed to evaluate the outcomes of these patients after preoperative chemoradiotherapy (PCRT) and radical surgery and to evaluate the associated risk factors.
Methods: We included 189 patients with rectal cancer who showed total regression of the primary tumor after PCRT, followed by radical resection, between 2001 and 2012. Recurrence-free survival (RFS) was calculated using the Kaplan- Meier method, and the results were compared with 77 patients with Tis rectal cancer who received only radical resection. Factors associated with RFS were evaluated using Cox regression analysis.
Results: Sphincter-saving resection was performed for 146 patients (77.2%). Adjuvant chemotherapy was administered to 168 patients (88.9%). During the follow-up period, recurrence occurred in 17 patients (9%). The 5-year RFS was 91.3%, which was significantly lower than that of patients with Tis rectal cancer without PCRT (P = 0.005). In univariate analysis, preoperative CEA and histologic differentiation were associated with RFS. However, no factors were found to be associated with RFS.
Conclusion: RFS was lower in patients with total regression of primary rectal cancer after PCRT than in those with Tis rectal cancer without PCRT, and it would not be considered as the same entity with early rectal cancer or “disappeared tumor” status.

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INTRODUCTION
METHODS
RESULTS
DISCUSSION
REFERENCES

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UCI(KEPA) : I410-ECN-0101-2019-514-000442142