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<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="1.3" xml:lang="en" article-type="research-article"><?properties open_access?><processing-meta base-tagset="archiving" mathml-version="3.0" table-model="xhtml" tagset-family="jats"><restricted-by>pmc</restricted-by></processing-meta><front><journal-meta><journal-id journal-id-type="nlm-ta">Ann Surg Treat Res</journal-id><journal-id journal-id-type="iso-abbrev">Ann Surg Treat Res</journal-id><journal-id journal-id-type="publisher-id">ASTR</journal-id><journal-title-group><journal-title>Annals of Surgical Treatment and Research</journal-title></journal-title-group><issn pub-type="ppub">2288-6575</issn><issn pub-type="epub">2288-6796</issn><publisher><publisher-name>The Korean Surgical Society</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">35071118</article-id><article-id pub-id-type="pmc">8753379</article-id><article-id pub-id-type="doi">10.4174/astr.2022.102.1.36</article-id><article-categories><subj-group subj-group-type="heading"><subject>Original Article</subject></subj-group></article-categories><title-group><article-title>Short- and long-term outcomes of local excision with adjuvant radiotherapy in high-risk T1 rectal cancer patients</article-title></title-group><contrib-group><contrib contrib-type="author"><contrib-id authenticated="true" contrib-id-type="orcid">https://orcid.org/0000-0001-6030-1508</contrib-id><name><surname>Al-Sawat</surname><given-names>Abdullah</given-names></name><xref rid="A1-astr-102-36" ref-type="aff">1</xref></contrib><contrib contrib-type="author"><contrib-id authenticated="true" contrib-id-type="orcid">https://orcid.org/0000-0002-7598-2825</contrib-id><name><surname>Bae</surname><given-names>Jung Hoon</given-names></name><xref rid="A2-astr-102-36" ref-type="aff">2</xref></contrib><contrib contrib-type="author"><contrib-id authenticated="true" contrib-id-type="orcid">https://orcid.org/0000-0001-6194-7300</contrib-id><name><surname>Kim</surname><given-names>Hyun Ho</given-names></name><xref rid="A3-astr-102-36" ref-type="aff">3</xref></contrib><contrib contrib-type="author"><contrib-id authenticated="true" contrib-id-type="orcid">https://orcid.org/0000-0002-4859-3015</contrib-id><name><surname>Lee</surname><given-names>Chul Seung</given-names></name><xref rid="A2-astr-102-36" ref-type="aff">2</xref></contrib><contrib contrib-type="author"><contrib-id authenticated="true" contrib-id-type="orcid">https://orcid.org/0000-0002-7362-3888</contrib-id><name><surname>Han</surname><given-names>Seung Rim</given-names></name><xref rid="A2-astr-102-36" ref-type="aff">2</xref></contrib><contrib contrib-type="author"><contrib-id authenticated="true" contrib-id-type="orcid">https://orcid.org/0000-0002-1849-2774</contrib-id><name><surname>Lee</surname><given-names>Yoon Suk</given-names></name><xref rid="A2-astr-102-36" ref-type="aff">2</xref></contrib><contrib contrib-type="author"><contrib-id authenticated="true" contrib-id-type="orcid">https://orcid.org/0000-0002-7183-2838</contrib-id><name><surname>Cho</surname><given-names>Hyeon-Min</given-names></name><xref rid="A3-astr-102-36" ref-type="aff">3</xref></contrib><contrib contrib-type="author"><contrib-id authenticated="true" contrib-id-type="orcid">https://orcid.org/0000-0003-0326-272X</contrib-id><name><surname>Jang</surname><given-names>Hong Seok</given-names></name><xref rid="A4-astr-102-36" ref-type="aff">4</xref></contrib><contrib contrib-type="author" corresp="yes"><contrib-id authenticated="true" contrib-id-type="orcid">https://orcid.org/0000-0001-9074-5214</contrib-id><name><surname>Lee</surname><given-names>In Kyu</given-names></name><xref rid="A2-astr-102-36" ref-type="aff">2</xref></contrib></contrib-group><aff id="A1-astr-102-36"><label>1</label>Department of Surgery, College of Medicine, Taif University, Taif, <country>Saudi Arabia</country>.</aff><aff id="A2-astr-102-36"><label>2</label>Division of Colorectal Surgery, Department of Surgery, Seoul St. Mary&#x2019;s Hospital, College of Medicine, The Catholic University of Korea, Seoul, <country>Korea</country>.</aff><aff id="A3-astr-102-36"><label>3</label>Division of Colorectal Surgery, Department of Surgery, St. Vincent Hospital, College of Medicine, The Catholic University of Korea, Seoul, <country>Korea</country>.</aff><aff id="A4-astr-102-36"><label>4</label>Department of Radiation Oncology, Seoul St. Mary&#x2019;s Hospital, College of Medicine, The Catholic University of Korea, Seoul, <country>Korea</country>.</aff><author-notes><corresp>Corresponding Author: In Kyu Lee. Division of Colorectal Surgery, Department of Surgery, Seoul St. Mary&#x2019;s Hospital, College of Medicine, The Catholic University of Korea, 222 Banpo-daero, Seocho-gu, Seoul 06591, Korea. Tel: +82-2-2258-6104, Fax: +82-2-595-2822, <email>cmcgslee@catholic.ac.kr</email></corresp></author-notes><pub-date pub-type="ppub"><month>1</month><year>2022</year></pub-date><pub-date pub-type="epub"><day>03</day><month>1</month><year>2022</year></pub-date><volume>102</volume><issue>1</issue><fpage>36</fpage><lpage>45</lpage><history><date date-type="received"><day>07</day><month>10</month><year>2021</year></date><date date-type="rev-recd"><day>28</day><month>10</month><year>2021</year></date><date date-type="accepted"><day>12</day><month>11</month><year>2021</year></date></history><permissions><copyright-statement>Copyright &#xA9; 2022, the Korean Surgical Society</copyright-statement><copyright-year>2022</copyright-year><copyright-holder>The Korean Surgical Society</copyright-holder><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/" specific-use="textmining" content-type="ccbynclicense">https://creativecommons.org/licenses/by-nc/4.0/</ali:license_ref><license-p>Annals of Surgical Treatment and Research is an Open Access Journal. All articles are distributed under the terms of the Creative Commons Attribution Non-Commercial License (<ext-link ext-link-type="uri" xlink:href="https://creativecommons.org/licenses/by-nc/4.0/">http://creativecommons.org/licenses/by-nc/4.0/</ext-link>) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p></license></permissions><abstract><sec><title>Purpose</title><p>The standard of care for early rectal cancer is radical surgery; however, it carries high postoperative morbidity. This study aimed to assess the short-term and oncological outcomes of local excision and adjuvant radiotherapy in patients with high-risk pathological stage (p) T1 rectal cancer.</p></sec><sec><title>Methods</title><p>Fifty-five patients underwent local excision with adjuvant radiotherapy or radical resection for high-risk T1 rectal cancer. Patients with adenocarcinoma within 10 cm from the anal verge; pT1 with high-risk features (grade 3&#x2013;4); a tumor size of &#x2265;3 cm; a positive margin; a lymphovascular or perineural invasion; or a submucosal invasion depth of &#x2265;SM2 were included.</p></sec><sec><title>Results</title><p>The rates of postoperative complications and stoma formation were higher in the radical surgery group (P = 0.021 and P = 0.003, respectively). No significant differences were observed in the overall survival and disease-free survival (DFS) between the 2 groups (P = 0.301 and P = 0.076, respectively). Vascular invasion was a significantly poor prognostic factor for DFS (P = 0.033). The presence of 3 or more high-risk features was associated with a poor DFS (P = 0.002).</p></sec><sec><title>Conclusion</title><p>Local excision with adjuvant radiotherapy significantly reduces the risk of complications and stoma formation. It is also an alternative option for patients with fewer than 3 high-risk features.</p></sec></abstract><kwd-group><kwd>Lymphatic metastasis</kwd><kwd>Margins of excision</kwd><kwd>Rectal neoplasms</kwd><kwd>Risk factors</kwd></kwd-group></article-meta></front><body><sec sec-type="intro"><title>INTRODUCTION</title><p>The standard of care for early rectal cancer is radical surgery, namely, total mesorectal excision (TME), which carries a high risk of postoperative morbidities and influences the patients&#x2019; quality of life [<xref rid="B1-astr-102-36" ref-type="bibr">1</xref>]. Low anterior resection syndrome and stoma formation can negatively affect bowel function [<xref rid="B2-astr-102-36" ref-type="bibr">2</xref><xref rid="B3-astr-102-36" ref-type="bibr">3</xref>], along with various aspects of sexual dysfunction, urological difficulties, and psychological disturbances [<xref rid="B1-astr-102-36" ref-type="bibr">1</xref>].</p><p>Local excision for early rectal cancer was restricted to patients with contraindications to radical surgery or to accept procedure-related recurrence and death [<xref rid="B4-astr-102-36" ref-type="bibr">4</xref>]. However, with the advancements in early rectal cancer assessment modalities, the improvements in the techniques used to perform local excision and adjuvant therapy for selected patients, and the decreased postoperative morbidity and incidence of stoma formation, local excision has become an alternative to radical surgery [<xref rid="B5-astr-102-36" ref-type="bibr">5</xref><xref rid="B6-astr-102-36" ref-type="bibr">6</xref>]. However, with the advances in early rectal cancer assessment modalities, some centers perform transanal endoscopic microsurgery (TEM) for full-thickness assessment due to the uncertainty of the preoperative diagnosis and staging [<xref rid="B7-astr-102-36" ref-type="bibr">7</xref>].</p><p>Several studies have reported a relatively high recurrence rate after transanal local excision (TLE) for early rectal cancer [<xref rid="B8-astr-102-36" ref-type="bibr">8</xref><xref rid="B9-astr-102-36" ref-type="bibr">9</xref><xref rid="B10-astr-102-36" ref-type="bibr">10</xref>]. The primary concern associated with disease recurrence is the presence of high-risk histopathological features, which increases the risk of lymph node involvement and recurrence. This concern has been studied extensively over the past few decades. Researchers have reported that cancer type, lymphovascular invasion (LVI), depth, and invasion width carry a high recurrence risk [<xref rid="B11-astr-102-36" ref-type="bibr">11</xref><xref rid="B12-astr-102-36" ref-type="bibr">12</xref>]. However, adjuvant chemoradiotherapy significantly decreases the incidence of local recurrence [<xref rid="B13-astr-102-36" ref-type="bibr">13</xref>]; to achieve this low recurrence rate, multidisciplinary treatment is needed for selected patients and an intensive surveillance program must be implemented [<xref rid="B14-astr-102-36" ref-type="bibr">14</xref><xref rid="B15-astr-102-36" ref-type="bibr">15</xref>]. Interestingly, Borstlap et al. [<xref rid="B16-astr-102-36" ref-type="bibr">16</xref>] reported in their meta-analysis that the local recurrence rates in T1 rectal cancer between patients with TLE with adjuvant therapy and those who underwent radical surgery were comparable.</p><p>As only a few studies in the literature have addressed the usefulness of radiotherapy after local excision for early rectal cancer, we aimed to assess the postoperative complications and morbidity rates of radiation therapy following local excision in pathological stage (p) T1 rectal adenocarcinoma patients with unfavorable histological features, and compare the oncological outcomes with those of the radical resection group.</p></sec><sec sec-type="methods"><title>METHODS</title><p>A retrospective analysis of the medical records of 78 early rectal cancer patients who underwent local excision followed by adjuvant radiotherapy or radical surgery for T1 rectal cancer with high-risk histological features was performed from April 2010 to July 2020 at Yeouido St. Mary&#x2019;s Hospital, Seoul St. Mary&#x2019;s Hospital, and St. Vincent Hospitals. This study was approved by the Institutional Review Board of the College of Medicine, The Catholic University of Korea (No. KC21RASI0391). It was performed in accordance with the Declaration of Helsinki and written informed consent was waived due to its retrospective nature.</p><sec><title>Patient selection</title><p>Patients with a histologically confirmed adenocarcinoma within 10 cm from the anal verge (AV); pT1 high-risk features, including a poorly or undifferentiated adenocarcinoma; a tumor size of &#x2265;3 cm; a positive resection margin; a lymphatic, vascular, or perineural invasion; or a submucosal invasion of &#x2265;SM2 were included in our study. Patients who had low-risk T1 rectal cancer, carcinoma <italic toggle="yes">in situ</italic> (Tis), another primary cancer, upper rectal cancer, or refusing adjuvant radiotherapy after TLE were excluded from our analysis (<xref rid="F1-astr-102-36" ref-type="fig">Fig. 1</xref>).</p></sec><sec><title>Local excision</title><p>Endoscopic biopsy, polypectomy, endoscopic mucosal resection, or endoscopic submucosal dissection (ESD) was performed prior to attempting local excision. We reviewed the histopathological results of biopsy specimens to obtain an accurate diagnosis and to assess for unfavorable features. Clinical and radiological assessments were performed, including digital rectal examination and proctoscopy, to identify the lesion size, location, and accessibility for transanal excision plus abdominopelvic CT and pelvic MRI for staging. Therefore, local excision is considered for both diagnostic and therapeutic purposes. However, some patients underwent upfront radical resection due to patient&#x2019;s preference or surgeon&#x2019;s experience (<xref rid="F2-astr-102-36" ref-type="fig">Fig. 2</xref>).</p></sec><sec><title>Post local excision follow-up</title><p>A multidisciplinary team reviewed the final histopathological results of local excision to determine whether the patient was suitable for adjuvant radiotherapy or radical surgery according to the histopathological features and comorbidity, considering the patient&#x2019;s preference and surgeon&#x2019;s experience.</p></sec><sec><title>Surveillance</title><p>After 3 months, the patients who underwent local excision and adjuvant radiotherapy underwent follow-up sigmoidoscopy and abdominopelvic CT. When there are no signs of recurrence, the patients underwent sigmoidoscopy and abdominopelvic CT every 3 months for the first 3 years, every 6 months for the next 2 years, and then annually. Clinical and endoscopic evaluation, plus carcinoembryonic antigen testing, abdominopelvic CT, or pelvic MRI were carried out at each visit.</p></sec><sec><title>Outcomes</title><p>Data on patient&#x2019;s demographic characteristics (sex, age, and body mass index [BMI]); tumor size; distance from the AV; margin and submucosal invasion; histological types; lymphatic, vascular, and perineural invasion; duration of follow-up; recurrence; postoperative complications; and stoma status were obtained.</p><p>Short-term outcomes were defined as morbidity that occurred during the first 30 days postoperatively. Meanwhile, long-term outcomes referred to the oncological outcomes, including recurrence and metastasis. Overall survival (OS) was defined as the period from the date of surgery to the time of death. Patients were censored at the date that they were last known to be alive (last clinic or investigation attendance). Disease-free survival (DFS) was defined as the period from the date of surgery to the time of disease recurrence (local or distant).</p></sec><sec><title>Statistics</title><p>Categorical variables were analyzed using the chi-square test. Continuous variables were expressed as mean &#xB1; standard deviation and were compared using the Student t-test. Patients&#x2019; characteristics and follow-up results were compared between the local and radical groups; the DFS was analyzed using the Kaplan-Meier curve. Statistical significance was set at P &lt; 0.05. Statistical analyses were performed using IBM SPSS Statistics ver. 24.0 (IBM Corp., Armonk, NY, USA).</p></sec></sec><sec sec-type="results"><title>RESULTS</title><sec><title>Patients&#x2019; characteristics</title><p>Fifty-five patients were enrolled in this study and were divided into the radical resection group (37 patients) and local excision group (18 patients). Their mean age was 61.98 &#xB1; 9.97 years; of the total participants, 65.5% were male and 34.5% were female. No difference was found in the baseline characteristics (age, sex, and BMI). The mean tumor distances from the AV were 7.24 &#xB1; 2.5 cm and 4.83 &#xB1; 2.5 cm in the radical group and local excision group, respectively, which showed a significant difference (P &lt; 0.002). In the radical group, 1 patient underwent an abdominoperineal resection (APR), 4 underwent an intersphincteric resection, and 32 underwent a low anterior resection (<xref rid="T1-astr-102-36" ref-type="table">Table 1</xref>). In the local excision group, 12 patients underwent a TEM, 4 underwent a TLE, and 2 underwent an ESD. No difference was found in the baseline characteristics among the different approaches of local excision (<xref rid="T2-astr-102-36" ref-type="table">Table 2</xref>).</p></sec><sec><title>Pathology</title><p>The high-risk features were measured; no significant difference was found between the radical and local excision groups. Furthermore, no difference was observed in the high-risk features in contrast to the different local excision approaches. One patient with a positive resection margin was identified (5.6%) in the local excision group after TLE; however, the difference was not significant compared with the radical resection group. No difference was found in the histological types. The LVI in the local excision group was insignificant compared with that in the radical resection group, which had seven patients with positive lymphatic invasion and five with vascular invasion. With regard to the submucosal depth of invasion, a significant difference was observed between the 2 groups. In the radical resection group, 2 patients (5.4%) had SM2 invasion, while 33 (89.2%) had SM3 invasion. In the local excision group, 10 patients (55.6%) had SM2 and 8 (44.4%) had SM3 invasion (P &lt; 0.001) (<xref rid="T1-astr-102-36" ref-type="table">Table 1</xref>).</p></sec><sec><title>Postoperative morbidity and mortality</title><p>Within the 30-day postoperative period, 10 patients (27.0%) in the radical surgery group developed some complications (ileostomy prolapse, 1; anastomotic leakage, 1; anastomotic stricture, 1; left ureteric injury, 1; ileus, 2; wound infection, 1; neuropathic bladder, 1; erectile dysfunction, 1; and fecal incontinence due to high stool frequency, 1). However, no complications were reported in the local excision group, indicating a significant difference between the 2 groups (P = 0.021). Moreover, the rates of stoma formation were significantly higher in the radical surgery group than in the local excision group (P = 0.003). A total of 17 patients (45.9%) had a temporary stoma in the radical surgery group, while none in the local excision group. By contrast, one patient in each group had a permanent stoma. Meanwhile, none of the patients in either group died 30 days after the surgery.</p></sec><sec><title>Oncological outcomes</title><p>The overall median follow-up was 52.78 &#xB1; 34.46 months (60.68 &#xB1; 33.40 months in the radical group and 36.56 &#xB1; 31.53 months in the local excisional group, P = 0.013). Clinical recurrence was not significantly different between radical excision and local excision with adjuvant therapy (P = 0.103). However, 2 patients who underwent local excision experienced disease recurrence. Specifically, recurrence occurred in the TLE subgroup but not after undergoing TEM. One patient had distant metastasis after 41 months of follow-up, while 1 patient had local recurrence with distant metastasis after 14 months of follow-up. The patient who had local recurrence underwent salvage radical resection with a permanent stoma, and the other patient with distant metastasis received palliative chemotherapy. These 2 patients had 3 high-risk features based on their histopathological reports. One patient had submucosal (SM3) depth invasion, vascular invasion, and mucinous component. The second patient had positive excisional margins, lymphatic invasion, and vascular invasion (<xref rid="T2-astr-102-36" ref-type="table">Table 2</xref>).</p><p>The OS rate was similar in both groups (P = 0.301). With regard to the DFS, the analysis showed that the radical group had a superior tendency compared with the local excision group, but the difference was not significant (P = 0.076) (<xref rid="T3-astr-102-36" ref-type="table">Table 3</xref>). Vascular invasion was a significantly poor prognostic factor for DFS (P = 0.033). Presence of 3 or more high-risk features was associated with poor DFS (P = 0.002) (<xref rid="F3-astr-102-36" ref-type="fig">Fig. 3</xref>).</p></sec></sec><sec sec-type="discussion"><title>DISCUSSION</title><p>The management of rectal cancer has improved over the past few decades, and TME without neoadjuvant or adjuvant therapy remains the cornerstone of therapy for early rectal cancer, associated with a decreased incidence of local recurrence and subsequent improvements in patient&#x2019;s survival. Thus, our data showed no recurrence of unfavorable T1 rectal cancer in the radical resection group. Mellgren et al. [<xref rid="B17-astr-102-36" ref-type="bibr">17</xref>] reported that within the 5-year follow-up, 18% of the patients in the local excision group and none in the radical resection group developed local recurrence. Nevertheless, rectal preservation benefits, low morbidity, less operative time, and the reduced length of hospital stay have made a clinical shift toward less invasive approaches [<xref rid="B18-astr-102-36" ref-type="bibr">18</xref>].</p><p>As no conclusive criteria have been established yet, the selection of patients who will undergo local excision or radical resection remains a challenge during the preoperative period. After conducting an endoscopic biopsy, we aimed to implement local excision in any patient with clinical and radiological T1 rectal cancer to determine the underlying pathology. We revised the criteria used for selecting patients for undergoing local excision and adjuvant radiotherapy. However, clinicians should carefully select the suitable patients and educate them regarding the possible interventions that would be implemented and the complications that might occur, as the oncological outcomes for salvage radical resection after local excision are poorer than those of the initial radical resection [<xref rid="B8-astr-102-36" ref-type="bibr">8</xref>].</p><p>The different techniques for local excision applied in this study depend on the surgeon&#x2019;s experience and preference. Approximately 12 of the patients from the local excision group (66.7%) underwent TEM performed by the same surgeon. Indeed, TEM is more effective in obtaining negative excisional margins and better DFS than TLE. A meta-analysis [<xref rid="B19-astr-102-36" ref-type="bibr">19</xref>] of 11 studies included 1,191 patients, who were divided into the TEM group (514 patients), radical resection group (291 patients), and the TLE group (386 patients). Results of the meta-analysis showed that radical resection was more superior in obtaining a negative margin; moreover, TLE was reported to be inferior to TEM. The TLE subgroup&#x2019;s recurrence rate in the present study was consistent with that in the previous studies, which reported a higher recurrence rate after conducting a TLE [<xref rid="B8-astr-102-36" ref-type="bibr">8</xref>].</p><p>Despite the recent advances in local excision techniques, unfavorable histological features are associated with the risk of lymph node metastasis and local recurrence. Therefore, the assessment of regional lymph nodes after a local excision remains challenging. Nascimbeni et al. [<xref rid="B11-astr-102-36" ref-type="bibr">11</xref>] reported that the depth of invasion and LVI were associated with a significant risk of lymph node metastasis. On the contrary, Kikuchi et al.&#x2019;s study [<xref rid="B20-astr-102-36" ref-type="bibr">20</xref>] showed that lymph node metastasis was related to the depth of submucosal invasion, unlike LVI. In comparison, Min et al. [<xref rid="B21-astr-102-36" ref-type="bibr">21</xref>] reported LVI and SM2 invasion as risk factors for local recurrence. However, several studies have concluded that the rate of lymph node metastasis and local recurrence is higher in patients with early rectal cancer than in those with colonic cancer [<xref rid="B20-astr-102-36" ref-type="bibr">20</xref><xref rid="B22-astr-102-36" ref-type="bibr">22</xref><xref rid="B23-astr-102-36" ref-type="bibr">23</xref>]. In our study, we found that vascular invasion had a clinical significance (P = 0.033). Interestingly, the 2 patients who experienced a recurrence were found to have 3 high-risk features. The first patient had a lower third submucosal invasion (SM3), vascular invasion, and mucinous component, while the second patient had positive resection margins, lymphatic invasion, and vascular invasion.</p><p>In this study, patients who underwent local excision received adjuvant radiotherapy either alone or in combination with concurrent chemotherapy-accepting a higher recurrence rate after local excision against the morbidity of radical resection. A previous meta-analysis [<xref rid="B16-astr-102-36" ref-type="bibr">16</xref>] showed that the recurrence rate after a local excision with adjuvant radiotherapy for high-risk early rectal cancer is 2-fold higher than that after radical resection. Therefore, an intensive surveillance program for these patients is crucial. Nevertheless, recent studies have shown promising results regarding the effectiveness of radiotherapy when combined with TEM [<xref rid="B24-astr-102-36" ref-type="bibr">24</xref>]. Duek et al. [<xref rid="B25-astr-102-36" ref-type="bibr">25</xref>] found no recurrence at a median follow-up of 3 years after TEM with adjuvant radiotherapy in 12 patients with early rectal cancer. Balyasnikova et al. [<xref rid="B5-astr-102-36" ref-type="bibr">5</xref>] found no recurrence at a median follow-up of 4 years in 18 patients with high-risk rectal cancer after undergoing a local excision with adjuvant radiotherapy. Our data also showed no recurrence at a median follow-up of 3 years in the TEM subgroup treated with adjuvant radiotherapy.</p><p>Recently, there has been an increasing interest in the nonoperative &#x201C;watch and wait&#x201D; approach. However, before implementing this approach, the possible oncological outcomes must be determined. These patients have the chance to achieve excellent results with very low recurrence rates with neoadjuvant therapy and radical resection. The primary challenge and pitfall of this strategy are that it may leave a viable residual tumor in the rectum of a patient who achieved a complete clinical response but not a complete pathological response. Habr-Gama et al. [<xref rid="B26-astr-102-36" ref-type="bibr">26</xref>] reported that the risk of locoregional treatment failure of the watch and wait approach was approximately 30%. Other studies have shown a 50%&#x2013;60% risk of locoregional treatment failure [<xref rid="B27-astr-102-36" ref-type="bibr">27</xref><xref rid="B28-astr-102-36" ref-type="bibr">28</xref>]. A meta-analysis concluded that a universal criterion for response assessment needs to be established to evaluate the safety of this strategy [<xref rid="B29-astr-102-36" ref-type="bibr">29</xref>]. Considering that this strategy is used in advanced cancer, local excision followed by adjuvant radiotherapy may be an alternative treatment option for patients with early cancer with high-risk features.</p><p>The short-term benefits of local excision must be counter-balanced with its oncological outcomes. Uncertainty persists concerning the oncological appropriateness of local excision for rectal cancer. In our study, no complications were reported following the different local excision techniques or temporary stoma maturation (P = 0.021 and P = 0.003, respectively). However, a permanent stoma was made in the local excision group due to local recurrence, which was managed with APR. By contrast, recurrence occurred in 2 patients from the TLE subgroup who had more than 2 high-risk features in their final histopathological evaluation. The first patient experienced local recurrence detected during surveillance and was managed with radical resection. Later, the patient developed distant metastasis to the lungs, ribs, and vertebrae and underwent palliative chemotherapy. The second patient had lung metastasis on follow-up and received systemic chemotherapy. Thus, the group who had radical resection showed a superior tendency to develop recurrence compared with the group who had local excision with radiotherapy, but the difference was not significant (P = 0.076). This result is consistent with that of previously published studies.</p><p>The present study has some limitations. First, our review was retrospective in nature. Second, the surgical intervention depends on the surgeon&#x2019;s experience and patient preference; therefore, the potential of selection bias exists. Third, it has a limited sample size. Lastly, we defined SM1 as tumor invasion in the submucosa of less than 1,000 &#xB5;m, SM2 as equal to 1,000 &#xB5;m or more but less than 2,000 &#xB5;m, and SM3 as equal to 2,000 &#xB5;m or more. Thus, the pathological results of the 3 hospitals were not standardized. However, the results are promising for patients with less than 3 high-risk T1 rectal cancer features who prefer local excision and adjuvant radiotherapy instead of radical resection to avoid procedure morbidity and improve the quality of life; in order to achieve an acceptable low risk of recurrence, a meticulous surveillance must be mandated.</p><p>Our study concludes that local excision with adjuvant radiotherapy is a better treatment option to avoid complications and stoma formation. Furthermore, local excision with adjuvant radiotherapy is an alternative option for patients with T1 rectal cancer with fewer than 3 high-risk features.</p></sec></body><back><fn-group><fn fn-type="COI-statement"><p><bold>Conflict of Interest:</bold> No potential conflict of interest relevant to this article was reported.</p></fn><fn fn-type="con"><p><bold>Author Contribution:</bold>
<list list-type="simple"><list-item><p><bold>Conceptualization:</bold> JHB, HHK, IKL.</p></list-item><list-item><p><bold>Formal Analysis:</bold> AAS, HHK, JHB.</p></list-item><list-item><p><bold>Investigation:</bold> HHK, JHB.</p></list-item><list-item><p><bold>Methodology:</bold> AAS, HHK.</p></list-item><list-item><p><bold>Project Administration:</bold> CSL, SRH, YSL, HMC, HSJ, IKL.</p></list-item><list-item><p><bold>Writing &#x2013; Original Draft:</bold> AAS, JHB.</p></list-item><list-item><p><bold>Writing &#x2013; Review &amp; Editing:</bold> All authors.</p></list-item></list>
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</person-group><article-title>A watch-and-wait approach for locally advanced rectal cancer after a clinical complete response following neoadjuvant chemoradiation: a systematic review and meta-analysis</article-title><source>Lancet Gastroenterol Hepatol</source><year>2017</year><volume>2</volume><fpage>501</fpage><lpage>513</lpage><pub-id pub-id-type="pmid">28479372</pub-id></element-citation></ref></ref-list></back><floats-group><fig position="float" id="F1-astr-102-36"><label>Fig. 1</label><caption><title>A flowchart of the research. A total of 78 patients were enrolled in the study, 23 patients were excluded; 37 patients (67.3%) underwent radical resection, and 18 patients (32.7%) had local excision with adjuvant radiotherapy. pT1, pathological stage T1.</title></caption><graphic xlink:href="astr-102-36-g001" position="float"/></fig><fig position="float" id="F2-astr-102-36"><label>Fig. 2</label><caption><title>After reviewing colonoscopic biopsy, patients underwent local excision or upfront radical resection depending on patients&#x2019; preference and surgeon experience. EMR, endoscopic mucosal resection; ESD, endoscopic submucosal dissection; TEM, transanal endoscopic microsurgery; TLE, transanal local excision; MDT, multidisciplinary team.</title></caption><graphic xlink:href="astr-102-36-g002" position="float"/></fig><fig position="float" id="F3-astr-102-36"><label>Fig. 3</label><caption><title>Disease-free survival (DFS) for (A) local excision and radical resection groups, (B) vascular invasion as a risk factor, and (C) numbers of high-risk features factors.</title></caption><graphic xlink:href="astr-102-36-g003" position="float"/></fig><table-wrap position="float" id="T1-astr-102-36"><label>Table 1</label><caption><title>Patients&#x2019; characteristics</title></caption><graphic xlink:href="astr-102-36-i001" position="float"/><table-wrap-foot><fn><p>Values are presented as number only, number (%), or mean &#xB1; standard deviation.</p><p>APR, abdominoperineal resection; LATA, laparoscopic abdominal transanal proctosigmoidectomy; LAR, low anterior resection; TEM, transanal endoscopic microsurgery; TLE, transanal local excision; ESD, endoscopic submucosal dissection; SM, submucosa; CCRT, concurrent chemoradiation therapy.</p></fn></table-wrap-foot></table-wrap><table-wrap position="float" id="T2-astr-102-36"><label>Table 2</label><caption><title>Local excision approaches</title></caption><graphic xlink:href="astr-102-36-i002" position="float"/><table-wrap-foot><fn><p>Values are presented as number (%).</p><p>TEM, transanal endoscopic microsurgery; TLE, transanal local excision; ESD, endoscopic submucosal dissection; SM, submucosa; NA, not applicable; CCRT, concurrent chemoradiation therapy; EMR, endoscopic mucosal resection.</p></fn></table-wrap-foot></table-wrap><table-wrap position="float" id="T3-astr-102-36"><label>Table 3</label><caption><title>Univariate analysis</title></caption><graphic xlink:href="astr-102-36-i003" position="float"/><table-wrap-foot><fn><p>CI, confidence interval; APR, abdominoperineal resection; LATA, laparoscopic abdominal transanal proctosigmoidectomy; LAR, low anterior resection; TEM, transanal endoscopic microsurgery; TLE, transanal local excision; ESD, endoscopic submucosal dissection.</p></fn></table-wrap-foot></table-wrap></floats-group></article>
