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Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_1073_Библиотеки_им_академика_М_И_Перельмана

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M. L. Westfal and M. G. Mutch
and this has been studied in clinical trials but remains controversial [28, 4042]. Taira etal. looked at the prognosis of patients with T1 rectal cancer stratied by pre-operative chemo-radiation therapy. In 86 patients there was no signicant dif­ference in relapse-free survival but they did nd that in a multivariate analysis, tumor location within 5cm from the anal verge was a signicant risk factor associ­ated with a poor relapse-free survival [43].
In terms of adjuvant therapy, Minsky etal. concluded that post-operative radia­tion therapy is not needed after local excision in patients with T1 tumors and nega­tive prognostic features [44]. On the other hand, Taylor etal [45] and Lamont etal. [46] reported that adjuvant radiation therapy improved both recurrence rate and survival in their patient cohorts. Paty etal. [47] reported that local recurrence was delayed in patient that received adjuvant pelvic radiation. Finally, Borstlap et al. concluded that local recurrence rates in T1 rectal cancer between patients with local excision with adjuvant therapy and those who underwent radical surgery were com­parable [48].
When patients with high-risk T1 lesions refuse radical resection or prioritize sphincter preservation, adjuvant chemoradiation in combination with local excision has been considered. A systematic review of patients with T1/T2 rectal lesions removed by local excision compared the patients who received adjuvant chemora­diation with those that underwent radical resection. The authors report a 10% recur­rence rate after local excision with adjuvant therapy versus a 6% recurrence rate after radical resection of T1 tumors [49]. Oostendorp et al. performed a meta­analysis of 73 studies and showed a local recurrence rate of 6.7% for low risk T1 tumors with local excision alone and no local recurrences in patients treated with adjuvant pelvic radiation and concurrent chemotherapy. High risk T1 tumors had a local recurrence rate of 13.6% compared to 3.9% with LE alone versus adjuvant therapy, therefore the authors concluded that local excision with adjuvant chemo­radiation therapy may provide an alternative approach to radical surgery for patients with high-risk features. In a small study, Balyasnikova etal. found no recurrence at a median follow-up of 4years in 18 patients with high-risk rectal cancer after under­going local excision with adjuvant radiotherapy [50]. Al-Sawat etal. concluded that local excision with adjuvant radiotherapy is a better treatment option to avoid com­plications and stoma formation compared with radical excision and is a safe alterna­tive for patients with T1 rectal cancer with fewer than three high-risk features [51]. Finally, Swanton etal. found similar results and concluded that local excision fol­lowed by adjuvant pelvic radiation is feasible, safe and yields good locoregional control in T1 rectal cancers, thereby avoiding denitive surgery and the morbidity associated with LAR or APR. [52]
In summary, the NCCN guidelines8 recommend that for node negative T1 rectal cancer, lesions can be treated with trans-abdominal resection or trans-anal resection as appropriate. If pathology review after local excision reveals no high-risk features, then no further treatment is required. However, if pathology shows poorly differen­tiated histology, positive margins, invasion into the deepest third of the submucosa (sm3), LVI or PNI, then additional treatment is required. Trans-abdominal resection is the preferred next step in management followed by adjuvant therapy based on
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pathologic stage. If patients instead undergo adjuvant chemoradiation therapy after local excision, additional treatment will be determined by whether there is evidence of residual disease. If there is no evidence of disease, observation or additional che­motherapy can be considered based the patient’s risk factors. If there is evidence of disease, then trans-abdominal resection should be performed with or without adju­vant chemotherapy. It is imperative that the patient undergo careful surveillance if they forego trans-abdominal resection.
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Surveillance
Whether or not patients with T1N0M0 rectal cancer require further surveillance remains controversial. ASCRS and NCCN guidelines both recommend surveillance for stage 1 rectal cancer with a regular history and exam, CEA, exible sigmoidos­copy/proctoscopy and colonoscopy. There is no role for routine imaging for these patients [1, 8]. On the other hand the Cancer Care Ontario (CCO) and the American Society of Clinical Oncology (ASCO) do not recommend surveillance for stage I patients for colon or rectal cancer [53]. The decision regarding surveillance for patients with T1 rectal cancer should be made on an individual basis based on the patient’s risk factors.
Outcomes
Local Recurrence
The risk of local recurrence for patients undergoing local excision remains unknown. One retrospective study by Nash etal. showed that in 282 patients undergoing either transanal local excision or radical resection for T1 rectal cancer, the respective local recurrence rates were 13.2% and 2.7% respectively [23]. A similar retrospective study by You etal. showed local recurrence rates of 12.5% for transanal excision patients and 6.9% for radical resection patients [27]. Rates of local control follow­ing local excision have been shown to be favorable in T1 sm1–2 tumors [54], while prognostic factors for increased local recurrence rates include high grade tumors, LVI, PNI, tumor budding, sm3 tumors, mucinous type tumors, and positive resec­tion margins [36, 37, 55]. Overall, several studies have found recurrence rates of 10–30% for patients undergoing local resection for T1 rectal cancer [45, 5658].
In high-risk patients the risk of local recurrence is higher. One meta-analysis looking at local recurrence in patients with high-risk T1 and T2 rectal cancer who did not receive additional therapy showed a substantial risk of local recurrence. Completion TME or adjuvant chemoradiation for T1 patient was found to mitigate that risk. This provides support for using full thickness local excision as a guide to denitive management. Another meta-analysis reported a substantial risk of local recurrence in patients with high-risk T1 and T2 rectal cancer who received no addi­tional therapy following local excision. The authors conclude that neo-adjuvant
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chemoradiation therapy followed by local excision may be safe and effective alter­native for patients with any T stage of cancer who refuse or are unt for transab­dominal resection but understand that further studies are needed to explore this management suggestion [59].
Finally, Madbouly etal [60] showed that the 5-year recurrence rate after trans­anal excision was 29.4%. 5-year cancer specic and overall survival were 89% and 75% respectively. Nearly all patients with a recurrence underwent salvage treatment with a 56.3% ve-year survival rate. They concluded that although overall cancer survival rates might be regarded as satisfactory, the high recurrence and low salvage rate raises the issue about the role of transanal excision alone for early rectal cancer and the potential need to consider adjuvant therapy for these patients.
M. L. Westfal and M. G. Mutch
Metastasis
Lymph node (LN) metastasis occurs in 2–35% of T1 lesions. When looking at the depth of tumor involvement into the submucosa and LN metastasis in T1 rectal cancer, the rates of LN metastasis for sm1, sm2 and sm3 tumors was 2%, 9%, and 35% respectively [25]. Additionally, Kitajima etal. established the method for mea­suring submucosal invasion depth (SID) and found that lesions with SID less than 1000 micrometers had no evidence of lymph node metastasis. The clinical guide­lines of the Japanese Society for Cancer of the Colon and Rectum describe the method of measuring an SID and advise additional surgical resection with lymph node dissection after endoscopic treatment for lesions with SID greater than 1000 micrometers. This “1000 micrometer rule” is recommended as a criterion for addi­tional resection in many previous papers [34, 61, 62] and is used as a gold-standard indicator for endoscopic diagnoses, such as magnifying endoscopy or image­enhanced endoscopy [63]. As endoscopic techniques progress, endoscopic treat­ment is becoming more widely acceptable for lesions with SID greater than or equal to 1000 micrometers [61, 64, 65].
Disease Free andOverall Survival
Although limited, some data suggests that TEM may have similar oncologic outcomes in patients with T1N0M0 rectal cancer compared with radical resection, while addi­tionally offering patients the benets of local resection [66, 67]. Additionally, Lu etal. showed that although the local recurrence rate after TEM was higher than that after TME, distant metastasis, overall survival and disease-free survival rates did not differ between these groups [68]. Clancy etal. performed a meta-analysis in 2015 and found that TEM provides superior oncologic outcomes compared to transanal local excision as it had a higher rate of negative microscopic margins, reduced rate of specimen fragmentation, and reduced rate of lesion recurrence [69]. Endreseth etal. completed a prospective study from the Norwegian Rectal Cancer Project looking at 291 patients with T1 rectal cancer treated with radical resection or trans-anal excision. They found
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that the 5-year survival for trans-anal excision was 70% compared to 80% in the radi­cal resection group [55]. Hyun etal. performed a retrospective review from multi­center data and used propensity score matching to form two groups of patients who underwent local excision and compared them to patients who underwent TME for T1 rectal cancer. They found that although patients who underwent local excision had higher local recurrence rates, there was no difference in disease-free survival or over­all survival [70]. Several other studies found that there was not a signicant difference in overall survival rate between patients undergoing local excision versus TME with T1 rectal cancer [27, 57, 71].
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Quality ofLife
Local excision is associated with improved quality of life secondary to overall decreased morbidity in terms of bowel function, sexual function, and micturition function. In the NSABP R-04 trial, patients who had an APR reported worse body image, worse mic­turition symptoms, and less sexual enjoyment at 1year post- surgery compared to those who had sphincter-sparing surgery [8]. An extra-levator APR may have benets over a conventional APR approach, including lower rates of intra-operative perforation, CRM involvement and local recurrence although the data remains varied [72, 73]. Further studies comparing the quality of life of patients after radical resection and local exci­sion are needed to further delineate these outcomes in more detail.
Conclusion
In patients found to have T1 rectal cancer, a careful review of the pathology as well was local and distant staging is necessary in order to determine if a local excision or a radical resection is appropriate. All resected specimens should undergo pathologic review to assess for high-risk features because presence of these features are associ­ated with an increased likelihood of mesorectal lymph node involvement and there­fore a radical resection with TME would be warranted in this setting. If the patient has signicant co-morbidities and is not a candidate for radical resection, then a local excision should be considered. Although this is the safer approach from an operative standpoint in terms of morbidity, mortality and sphincter function, there is a possible increased risk of local and distant failure. For patients that opt for a local excision, close surveillance is necessary in order to identify local recurrence quickly should it occur. The use of either neo-adjuvant and/or adjuvant chemoradiation therapy remains controversial but may provide better outcomes for patients opting to undergo local excision. A multi-disciplinary clinical team should be utilized in order to review each case on an individual basis and provide the patient with all pos­sible options for the management of T1 rectal cancer. Overall, it is important to match the treatment plan approach to the individual patient and all risk factors must be explained to the patient in order to allow them to make an informed decision that considers short and long-term risks and benets.
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References
1. You YN, Hardiman KM, Bafford A, etal. The American Society of Colon and Rectal Surgeons clinical practice guidelines for the Management of Rectal Cancer. Dis Colon Rectum. 2020;63(9):1191–222.
2. Kudo S, Tamegai Y, Yamano H, etal. Endoscopic mucosal resection of the colon: the Japanese technique. Gastrointest Endosc Clin N Am. 2001;11(3):519–35.
3. Marijnen CA, Kapiteijn E, van de Velde CJ, etal. Acute side effects and complications after short-term preoperative radiotherapy combined with total mesorectal excision in primary rec­tal cancer: report of a multicenter randomized trial. J Clin Oncol. 2002;20(3):817–25.
4. Snijders HS, Wouters MW, van Leersum NJ, etal. Meta-analysis of the risk for anastomotic leakage, the postoperative mortality caused by leakage in relation to the overall postoperative mortality. Eur J Surg Oncol. 2012;38(11):1013–9.
5. Guillou PJ, Quirke P, Thorpe H, etal. Short-term endpoints of conventional versus laparoscopic­assisted surgery in patients with colorectal cancer (MRC CLASICC trial): multicentre, ran­domised controlled trial. Lancet. 2005;365(9472):1718–26.
6. Hamilton S.Carcinoma of the colon and rectum. Pathology and genetics of tumours of the digestive system. 2000:103–43.
7. Cooper HS, Deppisch LM, Gourley WK, etal. Endoscopically removed malignant colorectal polyps: clinicopathologic correlations. Gastroenterology. 1995;108(6):1657–65.
8. Benson AB, Venook AP, Al-Hawary MM, etal. Rectal cancer, version 2.2022, NCCN clinical practice guidelines in oncology. J Natl Compr Cancer Netw. 2022;20(10):1139–67.
9. Yoshii S, Nojima M, Nosho K, etal. Factors associated with risk for colorectal cancer recurrence after endoscopic resection of T1 tumors. Clin Gastroenterol Hepatol. 2014;12(2):292–302 e293.
10. Tarantino I, Warschkow R, Worni M, etal. Elevated preoperative CEA is associated with worse survival in stage I-III rectal cancer patients. Br J Cancer. 2012;107(2):266–74.
11. Adloff M, Arnaud JP, Bergamaschi R, Schloegel M.Synchronous carcinoma of the colon and rectum: prognostic and therapeutic implications. Am J Surg. 1989;157(3):299–302.
12. Barillari P, Ramacciato G, De Angelis R, et al. Effect of preoperative colonoscopy on the incidence of synchronous and metachronous neoplasms. Acta Chir Scand. 1990;156(2):163–6.
13. Bat L, Neumann G, Shemesh E.The association of synchronous neoplasms with occluding colorectal cancer. Dis Colon Rectum. 1985;28(3):149–51.
14. Isler JT, Brown PC, Lewis FG, Billingham RP. The role of preoperative colonoscopy in colorectal cancer. Dis Colon Rectum. 1987;30(6):435–9.
15. Beets-Tan RGH, Lambregts DMJ, Maas M, etal. Magnetic resonance imaging for clinical management of rectal cancer: updated recommendations from the 2016 European Society of Gastrointestinal and Abdominal Radiology (ESGAR) consensus meeting. Eur Radiol. 2018;28(4):1465–75.
16. Lahaye MJ, Engelen SM, Nelemans PJ, et al. Imaging for predicting the risk factors—the circumferential resection margin and nodal disease—of local recurrence in rectal cancer: a meta-analysis. Semin Ultrasound CT MR. 2005;26(4):259–68.
17. Faletti R, Gatti M, Arezzo A, etal. Preoperative staging of rectal cancer using magnetic reso­nance imaging: comparison with pathological staging. Minerva Chir. 2018;73(1):13–9.
18. Klessen C, Rogalla P, Taupitz M.Local staging of rectal cancer: the current role of MRI.Eur Radiol. 2007;17(2):379–89.
19. Benson AB, Venook AP, Al-Hawary MM, etal. Rectal cancer, version 2.2018, NCCN clinical practice guidelines in oncology. J Natl Compr Cancer Netw. 2018;16(7):874–901.
20. Xie H, Zhou X, Zhuo Z, etal. Effectiveness of MRI for the assessment of mesorectal fascia involvement in patients with rectal cancer: a systematic review and meta-analysis. Dig Surg. 2014;31(2):123–34.
21. Chaudhri S, Brown L, Hassan I, Horgan AF.Preoperative intensive, community-based vs. tra­ditional stoma education: a randomized, controlled trial. Dis Colon Rectum. 2005;48(3):504–9.
22. Crooks S.Foresight that leads to improved outcome: stoma care nurses’ role in siting stomas. Prof Nurse. 1994;10(2):89–92.
21 Management ofT1 Rectal Cancer
https://t.me/medicina_free
23. Nash GM, Weiser MR, Guillem JG, etal. Long-term survival after transanal excision of T1 rectal cancer. Dis Colon Rectum. 2009;52(4):577–82.
24. Berger NF, Sylla P. The role of Transanal endoscopic surgery for early rectal cancer. Clin Colon Rectal Surg. 2022;35(2):113–21.
25. Nascimbeni R, Burgart LJ, Nivatvongs S, Larson DR.Risk of lymph node metastasis in T1 carcinoma of the colon and rectum. Dis Colon Rectum. 2002;45(2):200–6.
26. Rogers AC, Winter DC, Heeney A, etal. Systematic review and meta-analysis of the impact of tumour budding in colorectal cancer. Br J Cancer. 2016;115(7):831–40.
27. You YN, Baxter NN, Stewart A, Nelson H.Is the increasing rate of local excision for stage I rectal cancer in the United States justied?: a nationwide cohort study from the National Cancer Database. Ann Surg. 2007;245(5):726–33.
28. Shaikh I, Askari A, Ouru S, etal. Oncological outcomes of local excision compared with radi­cal surgery after neoadjuvant chemoradiotherapy for rectal cancer: a systematic review and meta-analysis. Int J Color Dis. 2015;30(1):19–29.
29. Heald RJ, Husband EM, Ryall RD. The mesorectum in rectal cancer surgery—the clue to pelvic recurrence? Br J Surg. 1982;69(10):613–6.
30. Lindsetmo RO, Joh YG, Delaney CP.Surgical treatment for rectal cancer: an international perspective on what the medical gastroenterologist needs to know. World J Gastroenterol. 2008;14(21):3281–9.
31. Baxter NN, Garcia-Aguilar J. Organ preservation for rectal cancer. J Clin Oncol. 2007;25(8):1014–20.
32. Yamamoto S, Watanabe M, Hasegawa H, et al. The risk of lymph node metastasis in T1 colorectal carcinoma. Hepato-Gastroenterology. 2004;51(58):998–1000.
33. Seitz U, Bohnacker S, Seewald S, etal. Is endoscopic polypectomy an adequate therapy for malignant colorectal adenomas? Presentation of 114 patients and review of the literature. Dis Colon Rectum. 2004;47(11):1789–96. discussion 1796–1787
34. Ueno H, Mochizuki H, Hashiguchi Y, etal. Risk factors for an adverse outcome in early inva­sive colorectal carcinoma. Gastroenterology. 2004;127(2):385–94.
35. Volk EE, Goldblum JR, Petras RE, Carey WD, Fazio VW.Management and outcome of patients with invasive carcinoma arising in colorectal polyps. Gastroenterology. 1995;109(6):1801–7.
36. Maeda K, Koide Y, Katsuno H.When is local excision appropriate for "early" rectal cancer? Surg Today. 2014;44(11):2000–14.
37. Bach SP, Hill J, Monson JR, etal. A predictive model for local recurrence after transanal endo­scopic microsurgery for rectal cancer. Br J Surg. 2009;96(3):280–90.
38. Baron PL, Enker WE, Zakowski MF, Urmacher C.Immediate vs. salvage resection after local treatment for early rectal cancer. Dis Colon Rectum. 1995;38(2):177–81.
39. Friel CM, Cromwell JW, Marra C, etal. Salvage radical surgery after failed local excision for early rectal cancer. Dis Colon Rectum. 2002;45(7):875–9.
40. Garcia-Aguilar J, Renfro LA, Chow OS, etal. Organ preservation for clinical T2N0 distal rectal cancer using neoadjuvant chemoradiotherapy and local excision (ACOSOG Z6041): results of an open-label, single-arm, multi-institutional, phase 2 trial. Lancet Oncol. 2015;16(15):1537–46.
41. Rullier E, Vendrely V, Asselineau J, etal. Organ preservation with chemoradiotherapy plus local excision for rectal cancer: 5-year results of the GRECCAR 2 randomised trial. Lancet Gastroenterol Hepatol. 2020;5(5):465–74.
42. Lezoche E, Baldarelli M, Lezoche G, etal. Randomized clinical trial of endoluminal locore­gional resection versus laparoscopic total mesorectal excision for T2 rectal cancer after neoad­juvant therapy. Br J Surg. 2012;99(9):1211–8.
43. Taira T, Nozawa H, Kawai K, etal. Oncological outcomes of pathological T1 lower rectal can­cer patients with or without preoperative Chemoradiotherapy. In Vivo. 2020;34(6):3559–64.
44. Minsky BD. Conservative treatment of rectal cancer with local excision and postoperative radiation therapy. Eur J Cancer. 1995;31A(7–8):1343–6.
45. Taylor RH, Hay JH, Larsson SN.Transanal local excision of selected low rectal cancers. Am J Surg. 1998;175(5):360–3.
253
254
https://t.me/medicina_free
46. Lamont JP, McCarty TM, Digan RD, et al. Should locally excised T1 rectal cancer receive adjuvant chemoradiation? Am J Surg. 2000;180(6):402–5. discussion 405–406
47. Paty PB, Nash GM, Baron P, etal. Long-term results of local excision for rectal cancer. Ann Surg. 2002;236(4):522–9. discussion 529–530
48. Borstlap WAA, van Oostendorp SE, Klaver CEL, etal. Organ preservation in rectal cancer: a synopsis of current guidelines. Color Dis. 2017;
49. Borstlap WA, Tanis PJ, Koedam TW, etal. A multi-centred randomised trial of radical surgery versus adjuvant chemoradiotherapy after local excision for early rectal cancer. BMC Cancer. 2016;16:513.
50. Balyasnikova S, Read J, Tait D, etal. The results of local excision with or without postopera­tive adjuvant chemoradiotherapy for early rectal cancer among patients choosing to avoid radi­cal surgery. Color Dis. 2017;19(2):139–47.
51. Al-Sawat A, Bae JH, Kim HH, et al. Short- and long-term outcomes of local excision with adjuvant radiotherapy in high-risk T1 rectal cancer patients. Ann Surg Treat Res. 2022;102(1):36–45.
52. Swanton C, Marcus S, Jayamohan J, etal. Can adjuvant pelvic radiation therapy after local excision or polypectomy for T1 and T2 rectal cancer offer an alternative option to radical sur­gery? Clin Transl Radiat Oncol. 2021;31:97–101.
53. Meyerhardt JA, Mangu PB, Flynn PJ, etal. Follow-up care, surveillance protocol, and sec­ondary prevention measures for survivors of colorectal cancer: American Society of Clinical Oncology clinical practice guideline endorsement. J Clin Oncol. 2013;31(35):4465–70.
54. Morino M, Risio M, Bach S, etal. Early rectal cancer: the European Association for Endoscopic Surgery (EAES) clinical consensus conference. Surg Endosc. 2015;29(4):755–73.
55. Endreseth BH, Myrvold HE, Romundstad P, etal. Transanal excision vs. major surgery for T1 rectal cancer. Dis Colon Rectum. 2005;48(7):1380–8.
56. Garcia-Aguilar J, Mellgren A, Sirivongs P, etal. Local excision of rectal cancer without adju­vant therapy: a word of caution. Ann Surg. 2000;231(3):345–51.
57. Mellgren A, Sirivongs P, Rothenberger DA, Madoff RD, Garcia-Aguilar J.Is local excision adequate therapy for early rectal cancer? Dis Colon Rectum. 2000;43(8):1064–71. discussion 1071–1064
58. Chorost MI, Petrelli NJ, McKenna M, Kraybill WG, Rodriguez-Bigas MA.Local excision of rectal carcinoma. Am Surg. 2001;67(8):774–9.
59. van Oostendorp SE, Smits LJH, Vroom Y, etal. Local recurrence after local excision of early rectal cancer: a meta-analysis of completion TME, adjuvant (chemo)radiation, or no additional treatment. Br J Surg. 2020;107(13):1719–30.
60. Madbouly KM, Remzi FH, Erkek BA, etal. Recurrence after transanal excision of T1 rectal cancer: should we be concerned? Dis Colon Rectum. 2005;48(4):711–9. discussion 719–721
61. Tanaka S, Asayama N, Shigita K, et al. Towards safer and appropriate application of endo­scopic submucosal dissection for T1 colorectal carcinoma as total excisional biopsy: future perspectives. Dig Endosc. 2015;27(2):216–22.
62. Kawachi H, Eishi Y, Ueno H, etal. A three-tier classication system based on the depth of sub­mucosal invasion and budding/sprouting can improve the treatment strategy for T1 colorectal cancer: a retrospective multicenter study. Mod Pathol. 2015;28(6):872–9.
63. Kitajima K, Fujimori T, Fujii S, etal. Correlations between lymph node metastasis and depth of submucosal invasion in submucosal invasive colorectal carcinoma: a Japanese collaborative study. J Gastroenterol. 2004;39(6):534–43.
64. Asayama N, Oka S, Tanaka S, et al. Endoscopic submucosal dissection as total excisional biopsy for clinical T1 colorectal carcinoma. Digestion. 2015;91(1):64–9.
65. Saito Y, Sakamoto T, Nakajima T, Matsuda T.Colorectal ESD: current indications and latest technical advances. Gastrointest Endosc Clin N Am. 2014;24(2):245–55.
66. Kidane B, Chadi SA, Kanters S, Colquhoun PH, Ott MC. Local resection compared with radical resection in the treatment of T1N0M0 rectal adenocarcinoma: a systematic review and meta-analysis. Dis Colon Rectum. 2015;58(1):122–40.
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67. Sajid MS, Farag S, Leung P, et al. Systematic review and meta-analysis of published trials comparing the effectiveness of transanal endoscopic microsurgery and radical resection in the management of early rectal cancer. Color Dis. 2014;16(1):2–14.
68. Lu JY, Lin GL, Qiu HZ, et al. Comparison of Transanal endoscopic microsurgery and Total Mesorectal excision in the treatment of T1 rectal cancer: a meta-analysis. PLoS One. 2015;10(10):e0141427.
69. Clancy C, Burke JP, Albert MR, O’Connell PR, Winter DC.Transanal endoscopic micro­surgery versus standard transanal excision for the removal of rectal neoplasms: a systematic review and meta-analysis. Dis Colon Rectum. 2015;58(2):254–61.
70. Hyun JH, Alhanafy MK, Park HC, etal. Initial local excision for clinical T1 rectal cancer showed comparable overall survival despite high local recurrence rate: a propensity-matched analysis. Ann Coloproctol. 2022;38(2):166–75.
71. Bentrem DJ, Okabe S, Wong WD, etal. T1 adenocarcinoma of the rectum: transanal excision or radical surgery? Ann Surg. 2005;242(4):472–7. discussion 477–479
72. Huang A, Zhao H, Ling T, et al. Oncological superiority of extralevator abdominoperineal resection over conventional abdominoperineal resection: a meta-analysis. Int J Color Dis. 2014;29(3):321–7.
73. Negoi I, Hostiuc S, Paun S, Negoi RI, Beuran M.Extralevator vs conventional abdomino­perineal resection for rectal cancer-a systematic review and meta-analysis. Am J Surg. 2016;212(3):511–26.
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Can Total Mesorectal Excision
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BeAvoided inT2 Rectal Cancer?
AnthonyLoria andFergalJ.Fleming
Introduction
In 2020, there were approximately 43,000 incident cases of rectal cancer in the United States and over 700,000 incident cases worldwide [1, 2]. Patients with clini­cal stage one rectal cancer (T1–2N0) represent approximately 25–30% of incident cases at the population level [3]. For patients with T2N0 disease, total mesorectal excision (TME) is the standard of care due to durable oncologic outcomes [4]. However TME can be associated with considerable morbidity. Balancing the risk of undertreatment with minimizing surgical morbidity has prompted a growing inter­est in using local excision among patients with T2N0 rectal cancer. Moreover, recent data on neoadjuvant chemoradiation followed by local excision is challeng­ing the paradigm that TME is associated with superior oncologic outcomes in patients with T2N0 disease. This chapter aims to articulate the rationale for seeking alternatives to TME, weigh the contemporary evidence, and provide expert opinion on the rapidly advancing management of early (T1-T2, node-negative) rectal cancer.
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Search Strategy
For this narrative review, a comprehensive literature search of PubMed identied studies comparing local excision with TME published between 2002 and 2023 (Table22.1). Local excision in the context of early rectal (T1–2N0) cancer refers to transanal endoscopic microsurgery (TEMS) or transanal minimally invasive surgery
A. Loria · F. J. Fleming (*) Division of Colorectal Surgery, Department of Surgery, University of Rochester Medical Center, Rochester, NY, USA e-mail: anthony_loria@urmc.rochester.edu; fergal_eming@urmc.rochester.edu
© The Author(s), under exclusive license to Springer Nature Switzerland AG 2023 K. Umanskiy, N. Hyman (eds.), Difcult Decisions in Colorectal Surgery, Difcult Decisions in Surgery: An Evidence-Based Approach,
https://doi.org/10.1007/978-3-031-42303-1_22
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Table 22.1 PICO
P (patients) T2N0 rectal cancer TME Local excision
I (intervention) C (comparison)
(TEMS, TAMIS)
A. Loria and F. J. Fleming
O (outcomes) Morbidity (short-term)
Survival (overall, disease free) Patient reported
(TAMIS). The search included “rectal neoplasms,” “natural orice endoscopic sur­gery,” “microsurgery,” “minimally invasive surgical procedures,” or “watchful wait­ing” [5]. Representative title or abstract limited terms included “early rectal cancer,” “T1 rectal cancer,” “T2 rectal cancer,” “TEM,” “local excision,” “TAMIS,” “EMR,” among others. Non-English and non-comparative studies were excluded. The refer­ences were reviewed to identify additional studies not captured in the primary search.
Results
Difculties in accurately staging early rectal cancer must be acknowledged. Tumor invasion (T) and nodal involvement (N) are assessed by either endorectal ultrasound (EUS) or magnetic resonance imaging (MRI) [4]. Unfortunately, for T2 lesions, MRI over stages 42% and EUS over stages 18% [68]. Similarly, accurately detect­ing nodal involvement is a diagnostic challenge. A meta-analysis found that the sensitivity and specicity for accurately detecting nodal involvement of EUS were 67% and 78%, and for MRI, they were 66% and 76% [6]. Consequently, European guidelines focus heavily on the area where MRI excels, tumor involvement of the circumferential resection margin [9].
TME Works: Why Replace it?
Benchmarking the short-term morbidity, functional, and oncologic outcomes asso­ciated with TME and local excision is essential. Expectedly, the short-term morbid­ity prole favors local excision. In a large retrospective study of 2124 patients with Stage I (T1–2N0) disease, 5.6% of patients who underwent local excision experi­enced a 30-day complication compared to 14.6% following TME (p<0.001) [10]. Neoadjuvant therapy was less common in the era of those retrospective data, how­ever, multi-institutional, randomized controlled trials suggest the postoperative morbidity following TME alone is higher than patients who receive neoadjuvant chemoradiation and local excision (50.6% vs. 20.7%, p<0.001) [11]. Similarly, in a trial comparing neoadjuvant short-course radiation (SCRT) followed by local excision to TME alone, the rates of serious adverse events among the TME group were signicantly higher than those who had SCRT followed by local excision (39% vs. 15%) [12]. Contemporary 30-day mortality rates following TME are low (approximately 1–1.5%), but it is notable that at 3-months post-TME, the mortality rate in four European nations ranged from 5.6–8.3% among patients 80years or older with stage I rectal cancer [13, 14].