Endoscopic Local Excision (ELE) with Knife-Assisted Resection (KAR) Techniques Followed by Adjuvant Radiotherapy and/or Chemotherapy for Invasive (T1bsm2,3/T2) Early Rectal Cancer: A Multicenter Retrospective Cohort
Abstract
:1. Introduction
2. Materials and Methods
Statistical Analysis
3. Results
4. Discussion
5. Conclusions
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Conflicts of Interest
References
- Kapiteijn, E.K.K.E. Total Mesorectal Excision (TME) with or without Preoperative Radiotherapy in the Treatment of Primary Rectal Cancer: Prospective Randomised Trial with Standard Operative and Histopathological Techniques. Br. J. Surg. 1999, 165, 410–420. [Google Scholar] [CrossRef]
- Kusters, M.; Marijnen, C.; van de Velde, C.; Rutten, H.; Lahaye, M.; Kim, J.; Beets-Tan, R.; Beets, G. Patterns of local recurrence in rectal cancer; a study of the Dutch TME trial. Eur. J. Surg. Oncol. (EJSO) 2010, 36, 470–476. [Google Scholar] [CrossRef] [PubMed]
- Borstlap, W.A.A.; Tanis, P.J.; Koedam, T.W.A.; Marijnen, C.A.M.; Cunningham, C.; Dekker, E.; van Leerdam, M.E.; Meijer, G.; van Grieken, N.; Nagtegaal, I.D.; 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. [Google Scholar] [CrossRef] [PubMed]
- Stijns, R.C.H.; de Graaf, E.J.R.; Punt, C.J.A.; Nagtegaal, I.D.; Nuyttens, J.J.M.E.; van Meerten, E.; Tanis, P.J.; de Hingh, I.H.J.T.; van der Schelling, G.P.; Acherman, Y.; et al. Long-term Oncological and Functional Outcomes of Chemoradiotherapy Followed by Organ-Sparing Transanal Endoscopic Microsurgery for Distal Rectal Cancer. JAMA Surg. 2019, 154, 47–54. [Google Scholar] [CrossRef]
- Rullier, E.; Vendrely, V.; Asselineau, J.; Rouanet, P.; Tuech, J.-J.; Valverde, A.; de Chaisemartin, C.; Rivoire, M.; Trilling, B.; Jafari, M.; 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, 465–474. [Google Scholar] [CrossRef]
- Bach, S.P.; Gilbert, A.; Brock, K.; Korsgen, S.; Geh, I.; Hill, J.; Gill, T.; Hainsworth, P.; Tutton, M.G.; Khan, J.; et al. Radical surgery versus organ preservation via short-course radiotherapy followed by transanal endoscopic microsurgery for early-stage rectal cancer (TREC): A randomised, open-label feasibility study. Lancet Gastroenterol. Hepatol. 2020, 6, 92–105. [Google Scholar] [CrossRef]
- Gilbert, A.; Homer, V.; Brock, K.; Korsgen, S.; Geh, I.; Hill, J.; Gill, T.; Hainsworth, P.; Tutton, M.; Khan, J.; et al. Quality-of-life outcomes in older patients with early-stage rectal cancer receiving organ-preserving treatment with hypofractionated short-course radiotherapy followed by transanal endoscopic microsurgery (TREC): Non-randomised registry of patients unsuitable for total mesorectal excision. Lancet Health Longev. 2022, 3, e825–e838. [Google Scholar] [CrossRef]
- Dossa, F.; Acuna, S.A.; Baxter, N.N. Local excision after preoperative chemoradiation for T2 and T3 rectal cancers: Is the wait over? Lancet Gastroenterol. Hepatol. 2020, 5, 422–424. [Google Scholar] [CrossRef]
- Pimentel-Nunes, P.; Libânio, D.; Bastiaansen, B.A.J.; Bhandari, P.; Bisschops, R.; Bourke, M.J.; Esposito, G.; Lemmers, A.; Maselli, R.; Messmann, H.; et al. Endoscopic submucosal dissection for superficial gastrointestinal lesions: European Society of Gastrointestinal Endoscopy (ESGE) Guideline—Update 2022. Endoscopy 2022, 54, 591–622. [Google Scholar] [CrossRef]
- Zwager, L.W.; Bastiaansen, B.A.; Montazeri, N.S.; Hompes, R.; Barresi, V.; Ichimasa, K.; Kawachi, H.; Machado, I.; Masaki, T.; Sheng, W.; et al. Deep Submucosal Invasion Is Not an Independent Risk Factor for Lymph Node Metastasis in T1 Colorectal Cancer: A Meta-Analysis. Gastroenterology 2022, 163, 174–189. [Google Scholar] [CrossRef]
- Morino, M.; Risio, M.; Bach, S.; Beets-Tan, R.; Bujko, K.; Panis, Y.; Quirke, P.; Rembacken, B.; Rullier, E.; Saito, Y.; et al. Early rectal cancer: The European Association for Endoscopic Surgery (EAES) clinical consensus conference. Surg. Endosc. 2015, 29, 755–773. [Google Scholar] [CrossRef] [PubMed]
- Tribonias, G.; Komeda, Y.; Leontidis, N.; Anagnostopoulos, G.; Palatianou, M.; Mpellou, G.; Pantoula, P.; Manola, M.-E.; Paspatis, G.; Tzouvala, M.; et al. Endoscopic intermuscular dissection (EID) for removing early rectal cancers and benign fibrotic rectal lesions. Tech. Coloproctology 2023, 27, 1393–1400. [Google Scholar] [CrossRef] [PubMed]
- Meier, B.; Stritzke, B.; Kuellmer, A.; Zervoulakos, P.; Huebner, G.H.; Repp, M.; Walter, B.; Meining, A.; Gutberlet, K.; Wiedbrauck, T.; et al. Efficacy and Safety of Endoscopic Full-Thickness Resection in the Colorectum: Results from the German Colonic FTRD Registry. Am. J. Gastroenterol. 2020, 115, 1998–2006. [Google Scholar] [CrossRef] [PubMed]
- Kim, M.; Bareket, R.; Eleftheriadis, N.P.; Kedia, P.; Seewald, S.; Groth, S.; Nieto, J.; Kumta, N.A.; Deshmukh, A.A.; Katz, J.; et al. Endoscopic Submucosal Dissection (ESD) Offers a Safer and More Cost-effective Alternative to Transanal Endoscopic Microsurgery (TEM). J. Clin. Gastroenterol. 2022, 57, 486–489. [Google Scholar] [CrossRef]
- Leung, G.; Nishimura, M.; Hingorani, N.; Lin, I.-H.; Weiser, M.R.; Garcia-Aguilar, J.; Pappou, E.P.; Paty, P.B.; Schattner, M.A. Technical feasibility of salvage endoscopic submucosal dissection after chemoradiation for locally advanced rectal adenocarcinoma. Gastrointest. Endosc. 2022, 96, 359–367. [Google Scholar] [CrossRef]
- von Elm, E.; Altman, D.G.; Egger, M.; Pocock, S.J.; Gotzsche, P.C.; Vandenbroucke, J.P. The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) Statement: Guidelines for reporting observational studies. BMJ 2007, 335, 806–808. [Google Scholar] [CrossRef]
- Critical Peak Pricing-San Diego Gas & Electric. Available online: https://www.sdge.com/businesses/savings-center/energy-management-programs/demand-response/critical-peak-pricing (accessed on 4 March 2022).
- World Medical Association. Declaration of Helsinki, Ethical Principles for Scientific Requirements and Research Protocols. Bull. World Health Organ. 2013, 79, 373. [Google Scholar]
- Wolters, U.; Wolf, T.; Stützer, H.; Schröder, T. ASA classification and perioperative variables as predictors of postoperative outcome. Br. J. Anaesth. 1996, 77, 217–222. [Google Scholar] [CrossRef]
- Swanton, C.; Marcus, S.; Jayamohan, J.; Pathma-Nathan, N.; El-Khoury, T.; Wong, M.; Nagrial, A.; Latty, D.; Sundaresan, P. 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. [Google Scholar] [CrossRef]
- Al-Sawat, A.; Bae, J.H.; Kim, H.H.; Lee, C.S.; Han, S.R.; Lee, Y.S.; Cho, H.-M.; Jang, H.S.; Lee, I.K. Short- and long-term outcomes of local excision with adjuvant radiotherapy in high-risk T1 rectal cancer patients. Ann. Surg. Treat. Res. 2022, 102, 36–45. [Google Scholar] [CrossRef]
- Cutting, J.E.; Hallam, S.E.; Thomas, M.G.; Messenger, D.E. A systematic review of local excision followed by adjuvant therapy in early rectal cancer: Are pT1 tumours the limit? Color. Dis. 2018, 20, 854–863. [Google Scholar] [CrossRef] [PubMed]
- Binda, C.; Secco, M.; Tuccillo, L.; Coluccio, C.; Liverani, E.; Jung, C.F.M.; Fabbri, C.; Gibiino, G. Early Rectal Cancer and Local Excision: A Narrative Review. J. Clin. Med. 2024, 13, 2292. [Google Scholar] [CrossRef] [PubMed]
- Participants in the Paris Workshop. The Paris endoscopic classification of superficial neoplastic lesions: Esophagus, stomach, and colon: November 30 to December 1, 2002. Gastrointest. Endosc. 2003, 58, S3–S43. [Google Scholar] [CrossRef] [PubMed]
- Horiuchi, Y.; Chino, A.; Matsuo, Y.; Kishihara, T.; Uragami, N.; Fujimoto, Y.; Ueno, M.; Tamegai, Y.; Hoshino, E.; Igarashi, M. Diagnosis of laterally spreading tumors (LST) in the rectum and selection of treatment: Characteristics of each of the subclassifications of LST in the rectum. Dig. Endosc. 2013, 25, 608–614. [Google Scholar] [CrossRef]
- Komeda, Y.; Kashida, H.; Sakurai, T.; Asakuma, Y.; Tribonias, G.; Nagai, T.; Kono, M.; Minaga, K.; Takenaka, M.; Arizumi, T.; et al. Magnifying Narrow Band Imaging (NBI) for the Diagnosis of Localized Colorectal Lesions Using the Japan NBI Expert Team (JNET) Classification. Oncology 2017, 93, 49–54. [Google Scholar] [CrossRef]
- Moon, J.Y.; Lee, M.R.; Ha, G.W. Long-term oncologic outcomes of transanal TME compared with transabdominal TME for rectal cancer: A systematic review and meta-analysis. Surg. Endosc. 2021, 36, 3122–3135. [Google Scholar] [CrossRef]
- Donohue, K.; Rossi, A.; Deek, M.P.; Feingold, D.; Patel, N.M.; Jabbour, S.K. Local Excision for Early-Stage Rectal Adenocarcinomas. Cancer J. 2024, 30, 245–250. [Google Scholar] [CrossRef]
- Gondal, G.; Grotmol, T.; Hofstad, B.; Bretthauer, M.; Eide, T.J.; Hoff, G. Biopsy of Colorectal Polyps Is Not Adequate for Grading of Neoplasia. Endoscopy 2005, 37, 1193–1197. [Google Scholar] [CrossRef]
- MERCURY Study Group. Diagnostic accuracy of preoperative magnetic resonance imaging in predicting curative resection of rectal cancer: Prospective observational study. BMJ 2006, 333, 779. [Google Scholar] [CrossRef]
- Detering, R.; Oostendorp, S.E.; Meyer, V.M.; Dieren, S.; Bos, A.C.R.K.; Dekker, J.W.T.; Reerink, O.; Waesberghe, J.H.T.M.; Marijnen, C.A.M.; Moons, L.M.G.; et al. MRI cT1–2 rectal cancer staging accuracy: A population-based study. Br. J. Surg. 2020, 107, 1372–1382. [Google Scholar] [CrossRef]
- Miranda, J.; Tan, G.X.V.; Fernandes, M.C.; Yildirim, O.; Sims, J.A.; Araujo-Filho, J.d.A.B.; Machado, F.A.d.M.; Assuncao, A.N., Jr.; Nomura, C.H.; Horvat, N. Rectal MRI radiomics for predicting pathological complete response: Where we are. Clin. Imaging 2021, 82, 141–149. [Google Scholar] [CrossRef] [PubMed]
- Suresh, R.S.; Garcia, L.E.; Gearhart, S.L. Young-Onset Rectal Cancer. Adv. Surg. 2024, 58, 275–291. [Google Scholar] [CrossRef]
- Tamraz, M.; Al Ghossaini, N.; Temraz, S. Optimization of colorectal cancer screening strategies: New insights. World J. Gastroenterol. 2024, 30, 3361–3366. [Google Scholar] [CrossRef] [PubMed]
- Ebbehøj, A.L.; Jørgensen, L.N.; Krarup, P.-M.; Smith, H.G. Histopathological risk factors for lymph node metastases in T1 colorectal cancer: Meta-analysis. Br. J. Surg. 2021, 108, 769–776. [Google Scholar] [CrossRef]
- van Oostendorp, S.E.; Smits, L.J.H.; Vroom, Y.; Detering, R.; Heymans, M.W.; Moons, L.M.G.; Tanis, P.J.; de Graaf, E.J.R.; Cunningham, C.; Denost, Q.; 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, 1719–1730. [Google Scholar] [CrossRef] [PubMed]
- Junginger, T.; Goenner, U.; Trinh, T.T.; Heintz, A.; Lollert, A.; Blettner, M.; Wollschlaeger, D. The Link Between Local Recurrence and Distant Metastases in Patients with Rectal Cancer. Anticancer. Res. 2019, 39, 3079–3088. [Google Scholar] [CrossRef]
- Brink, M.v.D.; Stiggelbout, A.M.; Hout, W.B.v.D.; Kievit, J.; Kranenbarg, E.K.; Marijnen, C.A.; Nagtegaal, I.D.; Rutten, H.J.; Wiggers, T.; van de Velde, C.J. Clinical Nature and Prognosis of Locally Recurrent Rectal Cancer After Total Mesorectal Excision with or Without Preoperative Radiotherapy. J. Clin. Oncol. 2004, 22, 3958–3964. [Google Scholar] [CrossRef]
- Nascimbeni, R.; Burgart, L.J.; Nivatvongs, S.; Larson, D.R. Risk of Lymph Node Metastasis in T1 Carcinoma of the Colon and Rectum. Dis. Colon Rectum 2002, 45, 200–206. [Google Scholar] [CrossRef]
- Wang, L.; Zhang, X.-Y.; Zhao, Y.-M.; Li, S.-J.; Li, Z.-W.; Sun, Y.-S.; Wang, W.-H.; Wu, A.-W.; on behalf of the Rectal Cancer Cooperative Group of Peking University Cancer Hospital. Intentional Watch and Wait or Organ Preservation Surgery Following Neoadjuvant Chemoradiotherapy Plus Consolidation CAPEOX for MRI-defined Low-risk Rectal Cancer. Ann. Surg. 2022, 277, 647–654. [Google Scholar] [CrossRef]
- Broc, G.; Gana, K.; Denost, Q.; Quintard, B. Decision-making in rectal and colorectal cancer: Systematic review and qualitative analysis of surgeons’ preferences. Psychol. Health Med. 2016, 22, 434–448. [Google Scholar] [CrossRef]
- Gerard, J.-P.; Barbet, N.; Schiappa, R.; Magné, N.; Martel, I.; Mineur, L.; Deberne, M.; Zilli, T.; Dhadda, A.; Myint, A.S. Neoadjuvant chemoradiotherapy with radiation dose escalation with contact x-ray brachytherapy boost or external beam radiotherapy boost for organ preservation in early cT2–cT3 rectal adenocarcinoma (OPERA): A phase 3, randomised controlled trial. Lancet Gastroenterol. Hepatol. 2023, 8, 356–367. [Google Scholar] [CrossRef]
- Bach, S.P.; STAR-TREC Collaborative. Can we Save the rectum by watchful waiting or TransAnal surgery following (chemo)Radiotherapy versus Total mesorectal excision for early REctal Cancer (STAR-TREC)? Protocol for the international, multicentre, rolling phase II/III partially randomized patient preference trial evaluating long-course concurrent chemoradiotherapy versus short-course radiotherapy organ preservation approaches. Colorectal Dis. 2022, 24, 639–651. [Google Scholar] [CrossRef] [PubMed] [PubMed Central]
- Lynn, P.B.; Van der Valk, M.J.M.; Claassen, Y.H.M.; Shi, Q.; Widmar, M.; Bastiaannet, E.; Van de Velde, C.J.H.; Garcia-Aguilar, J. Chemoradiation and Local Excision Versus Total Mesorectal Excision for T2N0 Rectal Cancer: Comparison of Short- and Long-Term Outcomes from 2 Prospective Studies. Ann Surg. 2023, 277, e96–e102. [Google Scholar] [CrossRef] [PubMed] [PubMed Central]
- Teste, B.; Rouanet, P.; Tuech, J.J.; Valverde, A.; Lelong, B.; Rivoire, M.; Faucheron, J.L.; Jafari, M.; Portier, G.; Meunier, B.; et al. Early and late morbidity of local excision after chemoradiotherapy for rectal cancer. BJS Open 2021, 5, zrab043. [Google Scholar] [CrossRef] [PubMed] [PubMed Central]
- Pacevicius, J.; Petrauskas, V.; Pilipavicius, L.; Dulskas, A. Local Excision ± Chemoradiotherapy vs. Total Mesorectal Excision for Early Rectal Cancer: Case-Matched Analysis of Long-Term Results. Front Surg. 2021, 8, 746784. [Google Scholar] [CrossRef] [PubMed] [PubMed Central]
Variable | N = 51 |
---|---|
Age (mean ± SD) | 65.0 ± 11.1 |
Sex | |
Female | 21 (41.2%) |
Male | 30 (58.8%) |
ASA score | |
1 | 16 (31.4%) |
2 | 23 (45.1%) |
3 | 11 (21.6%) |
4 | 1 (2.0%) |
Reason for endoscopic resection | |
Diagnosis/Staging | 38 (74.5%) |
Patient preference | 9 (17.6%) |
Unsuitable for surgery | 4 (7.8%) |
Antiplatelet or anticoagulation | 6 (11.8%) |
Characteristic | N = 51 1 |
---|---|
Distance to the dentate line (cm) | 3.9 ± 3.6 |
Part of the rectum | |
Lower rectum | 30 (58.8%) |
Middle rectum | 13 (25.5%) |
Upper rectum | 8 (15.7%) |
Location | |
Anterior | 35 (68.6%) |
Posterior | 16 (31.4%) |
Lesion Size (mm) | 44.9 ± 25.9 |
Histology prior resection | |
LGD adenoma | 4 (7.8%) |
HGD adenoma | 19 (37.3%) |
Intramucosal cancer | 12 (23.5%) |
Infiltrative cancer | 4 (7.8%) |
No biopsy | 12 (23.5%) |
Paris-Classification | |
IIa | 7 (13.7%) |
IIa + c | 10 (19.6%) |
IIa + Is | 22 (43.1%) |
Is | 12 (23.5%) |
LST-Classification | |
G-type Homogenous | 8 (15.7%) |
G-type Mixed | 24 (47.1%) |
NG-type Flat-elevated | 2 (3.9%) |
NG-type Pseudodepressed | 7 (13.7%) |
non LST | 10 (19.6%) |
JNET-Classification | |
2A | 6 (11.8%) |
2B | 35 (68.6%) |
3 | 10 (19.6%) |
Depression | 16 (31.4%) |
Ulceration | 8 (15.7%) |
Characteristic | N = 51 1 |
---|---|
Duration (min) | 185.8 ± 135.7 |
Method of resection | |
ESD | 39 (76.5%) |
EID | 8 (15.7%) |
Partial EFTR | 1 (2.0%) |
Complete EFTR | 3 (5.9%) |
Plane of resection | |
Submucosal | 39 (76.5%) |
Intermuscular | 8 (15.7%) |
Partial full-thickness | 1 (2.0%) |
Complete full-thickness | 3 (5.9%) |
Type of knife | |
Needle-type knife (Dual knife, Flush knife, Hybrid knife) | 39 (76.5%) |
Needle-type + Hook knife | 7 (13.7%) |
Needle-type + IT knife | 5 (9.8%) |
Resected specimen size (mm) | 61.1 ± 28.4 |
Macroscopic complete—En bloc resection | 50 (98%) |
Histological type | |
Classical adenocarcinoma | 47 (92.2%) |
Mucinous adenocarcinoma | 2 (3.9%) |
Signet-ring carcinoma | 2 (3.9%) |
Histology-stage | |
pT1bSM1 | 8 (15.7%) |
pT1bSM2 | 20 (39.2%) |
pT1bSM3 | 13 (25.5%) |
Superficial pT2 | 8 (15.7%) |
Deep pT2 | 2 (3.9%) |
Lymphovascular invasion | 16 (31.4%) |
Perineural Invasion | 3 (5.9%) |
Budding score | |
Bd1 | 29 (56.9%) |
Bd2 | 11 (21.6%) |
Bd3 | 11 (21.6%) |
Differentiation | |
G1 | 10 (19.6%) |
G2 | 30 (58.8%) |
G3 | 10 (19.6%) |
G4 | 1 (2.0%) |
Type of resection | |
R0 | 31 (60.8%) |
R1 | 19 (37.3%) |
R2 | 1 (2.0%) |
Lateral margins | |
Clear | 48 (94.1%) |
Positive-adenoma | 2 (3.9%) |
Positive-carcinoma | 1 (2.0%) |
Vertical margins | |
Clear | 32 (62.7%) |
Positive-adenoma | 8 (15.7%) |
Positive-carcinoma | 11 (21.6%) |
Depth of invasion from muscularis mucosa (μm) | 2175.6 ± 932.3 |
Complications | 9 (17.6%) |
Characteristic | N = 51 1 |
---|---|
Follow up (months) | 20.6 ± 15.8 |
Endoscopic recurrence | 7 (13.7%) |
Type of endoscopic recurrence | |
Adenoma | 3 (5.9%) |
Carcinoma | 4 (7.8%) |
No recurrence | 44 (86.3%) |
Treatment of endoscopic recurrence | |
Endoscopic follow-up | 1 (2.0%) |
Endoscopic resection | 5 (9.8%) |
Surgery | 1 (2.0%) |
No recurrence | 44 (86.3%) |
Time of recurrence (months) | |
3 | 3 (42.8%) |
4 | 1 (14.3%) |
6 | 1 (14.3%) |
19 | 1 (14.3%) |
24 | 1 (14.3%) |
MRI-rectum protocol in follow-up | |
Clear | 23 (45.1%) |
Not performed | 23 (45.1%) |
Recurrence | 5 (9.8%) |
Abdomen CT-scan in follow-up | |
Clear | 35 (68.6%) |
Distant metastasis | 2 (3.9%) |
Lymph-node metastasis | 1 (2.0%) |
Not performed | 13 (25.5%) |
Adjuvant treatment options | |
Chemotherapy | 6 (11.8%) |
Combined CRT | 20 (39.2%) |
Radiotherapy | 25 (49.0%) |
Adjuvant chemotherapy | 26 (51.0%) |
Type of chemotherapy | |
5-FU | 4 (7.8%) |
5-FU with Leucovorin | 5 (9.8%) |
Capecitabine | 15 (29.4%) |
Capecitabine→FOLFIRI | 1 (2.0%) |
Capecitabine→FOLFIRI + Bevacizumab | 1 (2.0%) |
None | 25 (49.0%) |
Adjuvant Radiotherapy | 45 (88.2%) |
Type of radiotherapy (Gy dosage) | 48 ± 1.5 |
Complication from adjuvant therapy | |
No | 47 (92%) |
Radiation proctitis | 2 (3.9%) |
Bleeding | 1 (2.0%) |
Stricture | 1 (2.0%) |
Reason for no surgical treatment | |
MDT proposal due to comorbidities | 22 (43.1%) |
Patient willingness | 29 (56.9%) |
Endoscopic Recurrence | |||
---|---|---|---|
Variable | No, N = 44 1 | Yes, N = 7 1 | p-Value 2 |
Reason for endoscopic resection | 0.089 | ||
Diagnosis/Staging | 33 (75%) | 5 (71%) | |
Patient preference | 9 (20%) | 0 (0%) | |
Unsuitable for surgery | 2 (4.5%) | 2 (29%) | |
Type of knife | 0.001 | ||
Needle-type + Hook knife | 7 (16%) | 0 (0%) | |
Needle-type + IT knife | 1 (2.3%) | 4 (57%) | |
Needle-type knife (Dual knife, Flush knife, etc.) | 36 (82%) | 3 (43%) | |
Paris-Classification | 0.068 | ||
IIa | 4 (9.1%) | 3 (43%) | |
IIa + c | 10 (23%) | 0 (0%) | |
IIa + Is | 20 (45%) | 2 (29%) | |
Is | 10 (23%) | 2 (29%) | |
Preoperative MRI rectal-protocol staging | 0.087 | ||
cT1 | 8 (18%) | 0 (0%) | |
Superficial cT2 | 8 (18%) | 2 (29%) | |
Deep cT2 | 2 (4.5%) | 0 (0%) | |
cT3a | 1 (2.3%) | 2 (29%) | |
Not performed | 25 (57%) | 3 (43%) | |
Budding score | 0.023 | ||
Bd1 | 28 (64%) | 1 (14%) | |
Bd2 | 8 (18%) | 3 (43%) | |
Bd3 | 8 (18%) | 3 (43%) | |
Lateral margins | 0.046 | ||
Clear | 43 (98%) | 5 (71%) | |
Positive-adenoma | 1 (2.3%) | 1 (14%) | |
Positive-carcinoma | 0 (0%) | 1 (14%) | |
MRI-rectum protocol in follow-up | <0.001 | ||
Clear | 22 (50%) | 1 (14%) | |
Not performed | 22 (50%) | 1 (14%) | |
Recurrence | 0 (0%) | 5 (71%) | |
Abdomen CT-scan in follow-up | 0.025 | ||
Clear | 30 (68%) | 5 (71%) | |
Distant metastasis | 1 (2.3%) | 1 (14%) | |
Lymph-node metastasis | 0 (0%) | 1 (14%) | |
Not performed | 13 (30%) | 0 (0%) | |
Adjuvant chemotherapy | 20 (45%) | 6 (86%) | 0.10 |
Adjuvant Radiotherapy | 39 (89%) | 6 (86%) | >0.9 |
Adjuvant treatment options | 0.10 | ||
Chemotherapy | 5 (11%) | 1 (14%) | |
CRT | 15 (34%) | 5 (71%) | |
Radiotherapy | 24 (55%) | 1 (14%) | |
Lesion Size (mm) | 0.011 | ||
40 or more | 20 (45%) | 7 (100%) | |
Less than 40 | 24 (55%) | 0 (0%) |
Variable | OR | p-Value |
---|---|---|
Clear vertical margins | 1 | |
Positive margins for adenoma | 0.003 | 1 |
Positive margins for carcinoma | 0.000 | 1 |
Depth of invasion more than 2000 μm | 0.718 | 0.83 |
R0 resection | 0.001 | 1 |
Budding (Bd1) | 0.56 | |
Budding (Bd2) | 9.351 | 0.22 |
Budding (Bd3) | 19.081 | 0.16 |
Differentiation (G1) | 0.88 | |
Differentiation (G2) | 0.260 | 0.58 |
Differentiation (G3) | 0.138 | 0.42 |
Differentiation (G4) | 0.000 | 1 |
Lymphovascular invasion | 0.359 | 0.53 |
pT1bSM1 | 0.99 | |
pT1bSM2 | 0.756 | 0.89 |
pT1bSM3 | 1.163 | 0.95 |
Superficial pT2 | 0.000 | 0.99 |
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Tribonias, G.; Papaefthymiou, A.; Zormpas, P.; Seewald, S.; Zachou, M.; Barbaro, F.; Kahaleh, M.; Andrisani, G.; Elkholy, S.; El-Sherbiny, M.; et al. Endoscopic Local Excision (ELE) with Knife-Assisted Resection (KAR) Techniques Followed by Adjuvant Radiotherapy and/or Chemotherapy for Invasive (T1bsm2,3/T2) Early Rectal Cancer: A Multicenter Retrospective Cohort. J. Clin. Med. 2024, 13, 6951. https://doi.org/10.3390/jcm13226951
Tribonias G, Papaefthymiou A, Zormpas P, Seewald S, Zachou M, Barbaro F, Kahaleh M, Andrisani G, Elkholy S, El-Sherbiny M, et al. Endoscopic Local Excision (ELE) with Knife-Assisted Resection (KAR) Techniques Followed by Adjuvant Radiotherapy and/or Chemotherapy for Invasive (T1bsm2,3/T2) Early Rectal Cancer: A Multicenter Retrospective Cohort. Journal of Clinical Medicine. 2024; 13(22):6951. https://doi.org/10.3390/jcm13226951
Chicago/Turabian StyleTribonias, George, Apostolis Papaefthymiou, Petros Zormpas, Stefan Seewald, Maria Zachou, Federico Barbaro, Michel Kahaleh, Gianluca Andrisani, Shaimaa Elkholy, Mohamed El-Sherbiny, and et al. 2024. "Endoscopic Local Excision (ELE) with Knife-Assisted Resection (KAR) Techniques Followed by Adjuvant Radiotherapy and/or Chemotherapy for Invasive (T1bsm2,3/T2) Early Rectal Cancer: A Multicenter Retrospective Cohort" Journal of Clinical Medicine 13, no. 22: 6951. https://doi.org/10.3390/jcm13226951
APA StyleTribonias, G., Papaefthymiou, A., Zormpas, P., Seewald, S., Zachou, M., Barbaro, F., Kahaleh, M., Andrisani, G., Elkholy, S., El-Sherbiny, M., Komeda, Y., Yarlagadda, R., Tziatzios, G., Essam, K., Haggag, H., Paspatis, G., & Mavrogenis, G. (2024). Endoscopic Local Excision (ELE) with Knife-Assisted Resection (KAR) Techniques Followed by Adjuvant Radiotherapy and/or Chemotherapy for Invasive (T1bsm2,3/T2) Early Rectal Cancer: A Multicenter Retrospective Cohort. Journal of Clinical Medicine, 13(22), 6951. https://doi.org/10.3390/jcm13226951