Oncologic outcomes after neoadjuvant chemoradiation followed by curative resection with tumor-specific mesorectal excision for fixed locally advanced rectal cancer - Impact of postirradiated pathologic downstaging on local recurrence and survival

被引:124
作者
Kim, Nam Kyu [1 ]
Baik, Seung Hyuk
Seong, Jin Sil
Kim, Hoguen
Roh, Jae Kyung
Lee, Kang Young
Sohn, Seung Kook
Cho, Chang Hwan
机构
[1] Yonsei Univ, Coll Med, Dept Surg, Div Colorectal Surg, Seoul, South Korea
[2] Yonsei Univ, Coll Med, Dept Med Oncol, Seoul, South Korea
[3] Yonsei Univ, Coll Med, Dept Radiat Oncol, Seoul, South Korea
[4] Yonsei Univ, Coll Med, Dept Pathol, Seoul, South Korea
[5] Yonsei Univ, Med Ctr, Colorectal Canc Clin, Severance Hosp, Seoul 120749, South Korea
关键词
D O I
10.1097/01.sla.0000225360.99257.73
中图分类号
R61 [外科手术学];
学科分类号
摘要
Objective: The purpose of this study was to deter-mine the oncologic Outcomes and clinical factors affecting survival in patients who underwent neoadjuvant chemoradiotherapy following tumor specific mesorectal excision for locally advanced, fixed rectal cancer. Summary Background Data: Neoadjuvant chemoradiation therapy has resulted in significant tumor downstaging, which enhances curative resection and subsequently improves local disease control for rectal cancer. However, oncologic outcomes, according to clinical factors, have not yet been fully understood in locally advanced and fixed rectal cancer. Methods: A total of 114 patients who had undergone neoadjuvant chemoradiation for advanced rectal cancer (T3 or T4 and node positive) were investigated retrospectively. Chemotherapy was administered intravenously with 5-FU and leucovorin during weeks 1 and 5 of radiotherapy. The total radiation dose was 5040 cGY in 25 fractions delivered over 5 weeks. Tumor-specific mesorectal excision was done 4 to 6 weeks after the completion of neoadjuvant chemoradiation. Survival and recurrence rates, according to the pathologic stage, were evaluated. Moreover, factors affecting survival were investigated. Results: The 5-year survival rates according to pathologic stage were: 100% in pathologic complete remission (n = 10), 80% in stage I (n = 23), 56.8% in stage II (n = 34), and 42.3% in stage III (n = 47) (P = 0.0000). Local, systemic, and combined recurrence rates were 11.4%, 22.8%, and 3.5%, respectively. Multivariate analysis showed that the pathologic N stage and operation method were the independent factors affecting survival rate. Conclusion: Pathologic complete remission showed excellent oncologic outcomes, and the pathologic N stage was the most important factor for oncologic outcomes.
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页码:1024 / 1030
页数:7
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