Surgical Outcomes, Long-Term Recurrence Rate, and Resource Utilization in a Prospective Cohort of 165 Patients Treated by Transanal Total Mesorectal Excision for Distal Rectal Cancer
Abstract
:Simple Summary
Abstract
1. Introduction
2. Materials and Methods
2.1. Statistical Analysis
2.2. Perioperative Management
2.3. Surgery
2.4. Histological Evaluation
2.5. Economic Evaluation
3. Results
3.1. Demographics
3.2. Surgical Outcomes
3.3. Histologic Outcomes
3.4. Oncologic Outcomes
3.5. Resource Utilization
4. Discussion
5. Conclusions
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Acknowledgments
Conflicts of Interest
References
- Sung, H.; Ferlay, J.; Siegel, R.L.; Laversanne, M.; Soerjomataram, I.; Jemal, A.; Bray, F. Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries. CA Cancer J. Clin. 2021, 71, 209–249. [Google Scholar] [CrossRef] [PubMed]
- Ferlay, J.; Colombet, M.; Soerjomataram, I.; Dyba, T.; Randi, G.; Bettio, M.; Gavin, A.; Visser, O.; Bray, F. Cancer incidence and mortality patterns in Europe: Estimates for 40 countries and 25 major cancers in 2018. Eur. J. Cancer 2018, 103, 356–387. [Google Scholar] [CrossRef] [PubMed]
- Heald, R.J.; Ryall, R.D. Recurrence and survival after total mesorectal excision for rectal cancer. Lancet 1986, 1, 1479–1482. [Google Scholar] [CrossRef]
- Tilney, H.S.; Rasheed, S.; Northover, J.M.; Tekkis, P.P. The influence of circumferential resection margins on long-term outcomes following rectal cancer surgery. Dis. Colon Rectum. 2009, 52, 1723–1729. [Google Scholar] [CrossRef] [PubMed]
- Planellas, P.; Salvador, H.; Cornejo, L.; Buxo, M.; Farres, R.; Molina, X.; Maroto, A.; Ortega, N.; Rodriguez-Hermosa, J.I.; Codina-Cazador, A. Risk factors for suboptimal laparoscopic surgery in rectal cancer patients. Langenbecks Arch. Surg. 2021, 406, 309–318. [Google Scholar] [CrossRef]
- Stevenson, A.R.L.; Solomon, M.J.; Brown, C.S.B.; Lumley, J.W.; Hewett, P.; Clouston, A.D.; Gebski, V.J.; Wilson, K.; Hague, W.; Simes, J.; et al. Disease-free Survival and Local Recurrence After Laparoscopic-assisted Resection or Open Resection for Rectal Cancer: The Australasian Laparoscopic Cancer of the Rectum Randomized Clinical Trial. Ann. Surg. 2019, 269, 596–602. [Google Scholar] [CrossRef] [PubMed]
- Fleshman, J.; Branda, M.E.; Sargent, D.J.; Boller, A.M.; George, V.V.; Abbas, M.A.; Peters, W.R., Jr.; Maun, D.C.; Chang, G.J.; Herline, A.; et al. Disease-free Survival and Local Recurrence for Laparoscopic Resection Compared With Open Resection of Stage II to III Rectal Cancer: Follow-up Results of the ACOSOG Z6051 Randomized Controlled Trial. Ann. Surg. 2019, 269, 589–595. [Google Scholar] [CrossRef]
- Veltcamp Helbach, M.; Koedam, T.W.A.; Knol, J.J.; Diederik, A.; Spaargaren, G.J.; Bonjer, H.J.; Tuynman, J.B.; Sietses, C. Residual mesorectum on postoperative magnetic resonance imaging following transanal total mesorectal excision (TaTME) and laparoscopic total mesorectal excision (LapTME) in rectal cancer. Surg. Endosc. 2019, 33, 94–102. [Google Scholar] [CrossRef]
- Jayne, D.; Pigazzi, A.; Marshall, H.; Croft, J.; Corrigan, N.; Copeland, J.; Quirke, P.; West, N.; Rautio, T.; Thomassen, N.; et al. Effect of Robotic-Assisted vs Conventional Laparoscopic Surgery on Risk of Conversion to Open Laparotomy Among Patients Undergoing Resection for Rectal Cancer: The ROLARR Randomized Clinical Trial. JAMA 2017, 318, 1569–1580. [Google Scholar] [CrossRef]
- Simillis, C.; Lal, N.; Thoukididou, S.N.; Kontovounisios, C.; Smith, J.J.; Hompes, R.; Adamina, M.; Tekkis, P.P. Open Versus Laparoscopic Versus Robotic Versus Transanal Mesorectal Excision for Rectal Cancer: A Systematic Review and Network Meta-analysis. Ann. Surg. 2019, 270, 59–68. [Google Scholar] [CrossRef]
- Dhanani, N.H.; Olavarria, O.A.; Bernardi, K.; Lyons, N.B.; Holihan, J.L.; Loor, M.; Haynes, A.B.; Liang, M.K. The Evidence Behind Robot-Assisted Abdominopelvic Surgery: A Systematic Review. Ann. Intern. Med. 2021, 174, 1110–1117. [Google Scholar] [CrossRef]
- Balciscueta, Z.; Uribe, N.; Caubet, L.; Lopez, M.; Torrijo, I.; Tabet, J.; Martin, M.C. Impact of the number of stapler firings on anastomotic leakage in laparoscopic rectal surgery: A systematic review and meta-analysis. Tech. Coloproctol. 2020, 24, 919–925. [Google Scholar] [CrossRef]
- Sylla, P.; Rattner, D.W.; Delgado, S.; Lacy, A.M. NOTES transanal rectal cancer resection using transanal endoscopic microsurgery and laparoscopic assistance. Surg. Endosc. 2010, 24, 1205–1210. [Google Scholar] [CrossRef]
- Lacy, A.M.; Tasende, M.M.; Delgado, S.; Fernandez-Hevia, M.; Jimenez, M.; De Lacy, B.; Castells, A.; Bravo, R.; Wexner, S.D.; Heald, R.J. Transanal Total Mesorectal Excision for Rectal Cancer: Outcomes after 140 Patients. J. Am. Coll. Surg. 2015, 221, 415–423. [Google Scholar] [CrossRef] [PubMed]
- Lelong, B.; de Chaisemartin, C.; Meillat, H.; Cournier, S.; Boher, J.M.; Genre, D.; Karoui, M.; Tuech, J.J.; Delpero, J.R.; French Research Group of Rectal Cancer Surgery (GRECCAR). A multicentre randomised controlled trial to evaluate the efficacy, morbidity and functional outcome of endoscopic transanal proctectomy versus laparoscopic proctectomy for low-lying rectal cancer (ETAP-GRECCAR 11 TRIAL): Rationale and design. BMC Cancer 2017, 17, 253. [Google Scholar] [CrossRef] [PubMed]
- Deijen, C.L.; Velthuis, S.; Tsai, A.; Mavroveli, S.; de Lange-de Klerk, E.S.; Sietses, C.; Tuynman, J.B.; Lacy, A.M.; Hanna, G.B.; Bonjer, H.J. COLOR III: A multicentre randomised clinical trial comparing transanal TME versus laparoscopic TME for mid and low rectal cancer. Surg. Endosc. 2016, 30, 3210–3215. [Google Scholar] [CrossRef] [PubMed]
- Keller, D.S.; de Lacy, F.B.; Hompes, R. Education and Training in Transanal Endoscopic Surgery and Transanal Total Mesorectal Excision. Clin. Colon. Rectal. Surg. 2021, 34, 163–171. [Google Scholar] [CrossRef] [PubMed]
- Dickson, E.A.; Penna, M.; Cunningham, C.; Ratcliffe, F.M.; Chantler, J.; Crabtree, N.A.; Tuynman, J.B.; Albert, M.R.; Monson, J.R.T.; Hompes, R.; et al. Carbon Dioxide Embolism Associated With Transanal Total Mesorectal Excision Surgery: A Report From the International Registries. Dis. Colon. Rectum. 2019, 62, 794–801. [Google Scholar] [CrossRef]
- Sylla, P.; Knol, J.J.; D'Andrea, A.P.; Perez, R.O.; Atallah, S.B.; Penna, M.; Hompes, R.; Wolthuis, A.; Rouanet, P.; Fingerhut, A.; et al. Urethral Injury and Other Urologic Injuries During Transanal Total Mesorectal Excision: An International Collaborative Study. Ann. Surg. 2021, 274, e115–e125. [Google Scholar] [CrossRef] [PubMed]
- Penna, M.; Hompes, R.; Arnold, S.; Wynn, G.; Austin, R.; Warusavitarne, J.; Moran, B.; Hanna, G.B.; Mortensen, N.J.; Tekkis, P.P.; et al. Incidence and Risk Factors for Anastomotic Failure in 1594 Patients Treated by Transanal Total Mesorectal Excision: Results From the International TaTME Registry. Ann. Surg. 2019, 269, 700–711. [Google Scholar] [CrossRef]
- Roodbeen, S.X.; Penna, M.; van Dieren, S.; Moran, B.; Tekkis, P.; Tanis, P.J.; Hompes, R.; on behalf of the International TaTME Registry Collaborative. Local Recurrence and Disease-Free Survival After Transanal Total Mesorectal Excision: Results From the International TaTME Registry. J. Natl. Compr. Canc. Netw. 2021. [Google Scholar] [CrossRef] [PubMed]
- Adamina, M.; Buchs, N.C.; Penna, M.; St. Hompes, R. Gallen consensus on safe implementation of transanal total mesorectal excision. Surg Endosc 2018, 32, 1091–1103. [Google Scholar] [CrossRef] [PubMed]
- TaTME Guidance Group representing the ESCP, in collaboration with ASCRS, ACPGBI, ECCO, EAES, ESSO, CSCRS, CNSCRS, CSLES, CSSANZ, JSES, SACP, SAGES, SBCP, Swiss-MIS. International expert consensus guidance on indications, implementation and quality measures for transanal total mesorectal excision. Colorectal Dis. 2020, 22, 749–755. [Google Scholar] [CrossRef]
- Roodbeen, S.X.; Spinelli, A.; Bemelman, W.A.; Di Candido, F.; Cardepont, M.; Denost, Q.; D'Hoore, A.; Houben, B.; Knol, J.J.; Martin-Perez, B.; et al. Local Recurrence After Transanal Total Mesorectal Excision for Rectal Cancer: A Multicenter Cohort Study. Ann. Surg. 2020. [Google Scholar] [CrossRef]
- Clavien, P.A.; Barkun, J.; de Oliveira, M.L.; Vauthey, J.N.; Dindo, D.; Schulick, R.D.; de Santibanes, E.; Pekolj, J.; Slankamenac, K.; Bassi, C.; et al. The Clavien-Dindo classification of surgical complications: Five-year experience. Ann. Surg. 2009, 250, 187–196. [Google Scholar] [CrossRef] [PubMed]
- Rahbari, N.N.; Weitz, J.; Hohenberger, W.; Heald, R.J.; Moran, B.; Ulrich, A.; Holm, T.; Wong, W.D.; Tiret, E.; Moriya, Y.; et al. Definition and grading of anastomotic leakage following anterior resection of the rectum: A proposal by the International Study Group of Rectal Cancer. Surgery 2010, 147, 339–351. [Google Scholar] [CrossRef]
- Glynne-Jones, R.; Wyrwicz, L.; Tiret, E.; Brown, G.; Rodel, C.; Cervantes, A.; Arnold, D. Rectal cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann. Oncol. 2017, 28 Suppl 4, iv22–iv40. [Google Scholar] [CrossRef]
- Nagtegaal, I.D.; van de Velde, C.J.; van der Worp, E.; Kapiteijn, E.; Quirke, P.; van Krieken, J.H.; Cooperative Clinical Investigators of the Dutch Colorectal Cancer, G. Macroscopic evaluation of rectal cancer resection specimen: Clinical significance of the pathologist in quality control. J. Clin. Oncol. 2002, 20, 1729–1734. [Google Scholar] [CrossRef]
- Dworak, O.; Keilholz, L.; Hoffmann, A. Pathological features of rectal cancer after preoperative radiochemotherapy. Int. J. Colorectal Dis. 1997, 12, 19–23. [Google Scholar] [CrossRef]
- Stevenson, A.R.; Solomon, M.J.; Lumley, J.W.; Hewett, P.; Clouston, A.D.; Gebski, V.J.; Davies, L.; Wilson, K.; Hague, W.; Simes, J.; et al. Effect of Laparoscopic-Assisted Resection vs Open Resection on Pathological Outcomes in Rectal Cancer: The ALaCaRT Randomized Clinical Trial. JAMA 2015, 314, 1356–1363. [Google Scholar] [CrossRef]
- Lee, L.; Kelly, J.; Nassif, G.J.; deBeche-Adams, T.C.; Albert, M.R.; Monson, J.R.T. Defining the learning curve for transanal total mesorectal excision for rectal adenocarcinoma. Surg. Endosc. 2020, 34, 1534–1542. [Google Scholar] [CrossRef] [PubMed]
- Wasmuth, H.H.; Faerden, A.E.; Myklebust, T.A.; Pfeffer, F.; Norderval, S.; Riis, R.; Olsen, O.C.; Lambrecht, J.R.; Korner, H.; Larsen, S.G.; et al. Transanal total mesorectal excision for rectal cancer has been suspended in Norway. Br. J. Surg. 2020, 107, 121–130. [Google Scholar] [CrossRef] [PubMed]
- Veltcamp Helbach, M.; van Oostendorp, S.E.; Koedam, T.W.A.; Knol, J.J.; Stockmann, H.; Oosterling, S.J.; Vuylsteke, R.; de Graaf, E.J.R.; Doornebosch, P.G.; Hompes, R.; et al. Structured training pathway and proctoring; multicenter results of the implementation of transanal total mesorectal excision (TaTME) in the Netherlands. Surg. Endosc. 2020, 34, 192–201. [Google Scholar] [CrossRef] [PubMed]
- Hol, J.C.; Burghgraef, T.A.; Rutgers, M.L.W.; Crolla, R.; van Geloven, N.A.W.; Hompes, R.; Leijtens, J.W.A.; Polat, F.; Pronk, A.; Smits, A.B.; et al. Comparison of laparoscopic versus robot-assisted versus transanal total mesorectal excision surgery for rectal cancer: A retrospective propensity score-matched cohort study of short-term outcomes. Br. J. Surg. 2021, 108, 1380–1387. [Google Scholar] [CrossRef]
- Ryan, O.K.; Ryan, E.J.; Creavin, B.; Rausa, E.; Kelly, M.E.; Petrelli, F.; Bonitta, G.; Kennelly, R.; Hanly, A.; Martin, S.T.; et al. Surgical approach for rectal cancer: A network meta-analysis comparing open, laparoscopic, robotic and transanal TME approaches. Eur. J. Surg. Oncol. 2021, 47, 285–295. [Google Scholar] [CrossRef]
- An, Y.; Roodbeen, S.X.; Talboom, K.; Tanis, P.J.; Bemelman, W.A.; Hompes, R. A systematic review and meta-analysis on complications of transanal total mesorectal excision. Colorectal Dis. 2021, 23, 2527–2538. [Google Scholar] [CrossRef]
- Roodbeen, S.X.; de Lacy, F.B.; van Dieren, S.; Penna, M.; Ris, F.; Moran, B.; Tekkis, P.; Bemelman, W.A.; Hompes, R. Predictive Factors and Risk Model for Positive Circumferential Resection Margin Rate After Transanal Total Mesorectal Excision in 2653 Patients With Rectal Cancer. Ann. Surg. 2019, 270, 884–891. [Google Scholar] [CrossRef]
- Marks, J.H.; Myers, E.A.; Zeger, E.L.; Denittis, A.S.; Gummadi, M.; Marks, G.J. Long-term outcomes by a transanal approach to total mesorectal excision for rectal cancer. Surg. Endosc. 2017, 31, 5248–5257. [Google Scholar] [CrossRef]
- Ezeokoli, E.U.; Hilli, R.; Wasvary, H.J. Index cost comparison of laparoscopic vs robotic surgery in colon and rectal cancer resection: A retrospective financial investigation of surgical methodology innovation at a single institution. Tech. Coloproctol 2023, 27, 63–68. [Google Scholar] [CrossRef]
- Lau, S.Y.C.; Choy, K.T.; Yang, T.W.W.; Heriot, A.; Warrier, S.K.; Guest, G.D.; Kong, J.C. Defining the learning curve of transanal total mesorectal excision: A systematic review and meta-analysis. ANZ J. Surg. 2021. [Google Scholar] [CrossRef]
- Persiani, R.; Agnes, A.; Belia, F.; D'Ugo, D.; Biondi, A. The learning curve of TaTME for mid-low rectal cancer: A comprehensive analysis from a five-year institutional experience. Surg Endosc 2021, 35, 6190–6200. [Google Scholar] [CrossRef] [PubMed]
- Diers, J.; Baum, P.; Wagner, J.C.; Matthes, H.; Pietryga, S.; Baumann, N.; Uttinger, K.; Germer, C.T.; Wiegering, A. Hospital volume following major surgery for gastric cancer determines in-hospital mortality rate and failure to rescue: A nation-wide study based on German billing data (2009-2017). Gastric Cancer 2021, 24, 959–969. [Google Scholar] [CrossRef] [PubMed]
- Guller, U.; Warschkow, R.; Ackermann, C.J.; Schmied, B.; Cerny, T.; Ess, S. Lower hospital volume is associated with higher mortality after oesophageal, gastric, pancreatic and rectal cancer resection. Swiss. Med. Wkly 2017, 147, w14473. [Google Scholar] [CrossRef]
- Francis, N.; Penna, M.; Carter, F.; Mortensen, N.J.; Hompes, R.; ACPGBI Pilot National TaTME Training Initiative Steering Group. Development and early outcomes of the national training initiative for transanal total mesorectal excision in the UK. Colorectal Dis. 2020, 22, 756–767. [Google Scholar] [CrossRef] [PubMed]
- Caycedo-Marulanda, A.; Lee, L.; Chadi, S.A.; Verschoor, C.P.; Crosina, J.; Ashamalla, S.; Brown, C.J.; Canadian taTME Expert Collaboration. Association of Transanal Total Mesorectal Excision With Local Recurrence of Rectal Cancer. JAMA Netw Open 2021, 4, e2036330. [Google Scholar] [CrossRef]
- Klein, M.F.; Seiersen, M.; Bulut, O.; Bech-Knudsen, F.; Jansen, J.E.; Gogenur, I. Short-term outcomes after transanal total mesorectal excision for rectal cancer in Denmark - a prospective multicentre study. Colorectal Dis. 2021, 23, 834–842. [Google Scholar] [CrossRef]
- Laurencet, F.L.; Bussmann, W.D. Value of mechanography in the diagnosis of aortic isthmic stenosis. Arch. Mal. Coeur. Vaiss 1970, 63, 532–538. [Google Scholar]
- Falz, R.; Bischoff, C.; Thieme, R.; Lassing, J.; Mehdorn, M.; Stelzner, S.; Busse, M.; Gockel, I. Effects and duration of exercise-based prehabilitation in surgical therapy of colon and rectal cancer: A systematic review and meta-analysis. J. Cancer Res. Clin. Oncol. 2022, 148, 2187–2213. [Google Scholar] [CrossRef]
Variable | Overall (n = 165) | One-Team (n = 55) | Two-Team (n = 110) | p-Value |
---|---|---|---|---|
Gender, n (%) | 0.816 | |||
Female | 55 (33) | 19 (35) | 36 (33) | |
Male | 110 (67) | 36 (65) | 74 (67) | |
Median age, years (IQR) | 64 (55–76) | 69 (58–76) | 62 (53–73) | 0.030 |
Median body mass index, kg/m2 (IQR) | 26 (23–29) | 26 (23–29) | 26 (22–29) | 0.946 |
ASA risk classification, n (%) | 0.481 | |||
ASA 1–2 | 88 (53) | 32 (58) | 56 (51) | |
ASA 3–4 | 77 (47) | 23 (42) | 54 (49) | |
Median tumor distance to anal verge by rigid proctoscopy, cm (IQR) | 7 (5–10) | 7 (5–9) | 7 (5–10) | 0.749 |
Preoperative circumferential resection margin in MRI, n (%) | 0.450 | |||
Positive | 42 (25) | 16 (22) | 26 (24) | |
Negative | 123 (75) | 39 (78) | 84 (76) | |
Neoadjuvant radio-chemotherapy, n (%) | 0.204 | |||
Yes | 124 (75) | 38 (69) | 86 (78) | |
No | 41 (25) | 17 (31) | 24 (22) |
Variable | Overall (n = 165) | One-Team (n = 55) | Two-Team (n = 110) | p-Value |
---|---|---|---|---|
Median operative time, minutes (IQR) | 348 (293–425) | 422 (353–492) | 320 (276–373) | <0.001 |
Median height of anastomosis from anal verge, cm (IQR) | 6 (4–8) | 6 (4–8) | 6 (4–8) | 0.715 |
Rate of conversion, n (%) | 1 (1) | 0 | 1 (1) | 0.480 |
Highest complication grade at 90 days, Clavien–Dindo grading (%) | 0.030 | |||
0 | 74 (45) | 21 (38) | 53 (48) | |
1 | 23 (14) | 3 (5) | 20 (18) | |
2 | 32 (19) | 14 (26) | 18 (16) | |
3a | 22 (13) | 11 (20) | 11 (10) | |
3b | 7 (4) | 3 (5) | 4 (4) | |
4a | 4 (2) | 2 (4) | 2 (2) | |
4b | 0 | 0 | 0 | |
5 | 3 (2) | 1 (2) | 2 (2) | |
Most frequent complications, n (%) | ||||
Anastomotic leakage | 12 (7) | 5 (9) | 7 (6) | 0.526 |
Pelvic collection | 7 (4) | 1 (2) | 6 (6) | 0.276 |
Bleeding | 3 (2) | 3 (6) | 0 | 0.014 |
Urinary retention | 18 (11) | 10 (18) | 8 (7) | 0.035 |
Paralytic ileus | 23 (14) | 9 (16) | 14 (13) | 0.526 |
LOS, days (IQR) | 9 (7–13) | 11 (9–14) | 9 (7–11) | 0.002 |
Mortality at 30 days, n (%) | 2 (1) | 0 | 2 (2) | 0.316 |
Reoperation rate at 30 days, n (%) | 13 (8) | 5 (9) | 8 (7) | 0.684 |
Mortality at 90 days, n (%) | 3 (2) | 1 (2) | 2 (2) | 1.000 |
Reoperation rate at 90 days, n (%) | 14 (9) | 6 (11) | 8 (7) | 0.410 |
Reversal of ileostomy, n (%) | 142 (86) | 46 (84) | 96 (87) | 0.727 |
Variable | OR (95% CI) | p-Value |
---|---|---|
Male sex | 5.589 (0.6–49.0) | 0.120 |
High ASA grade (≥3) | 5.655 (1.1–29.2) | 0.039 |
Age ≥ 65 years | 1.463 (0.3–6.3) | 0.608 |
Obesity (body mass index ≥ 30 kg/m2) | 0.409 (0.1–2.3) | 0.310 |
Neoadjuvant chemotherapy | 0.387 (0.1–1.6) | 0.192 |
Low anastomosis (≤6 cm from anal verge) | 0.298 (0.1–1.3) | 0.104 |
Two-team approach | 1.387 (0.3–6.6) | 0.682 |
Long operation time (>75th percentile) | 7.045 (1.2–41.6) | 0.031 |
Variable | Overall (n = 165) | One-Team (n = 55) | Two-Team (n = 110) | p-Value |
---|---|---|---|---|
Mesorectal resection quality in Quirke grade, n (%) | 0.788 | |||
Grade 1, incomplete | 5 (3) | 0 | 5 (5) | |
Grade 2, nearly complete | 11 (7) | 6 (11) | 5 (5) | |
Grade 3, complete | 149 (90) | 49 (89) | 100 (90) | |
T-stage, n (%) | 0.289 | |||
0 | 31 (19) | 9 (16) | 22 (20) | |
1 | 18 (11) | 4 (7) | 14 (13) | |
2 | 43 (26) | 15 (28) | 28 (25) | |
3 | 73 (44) | 27 (49) | 46 (42) | |
4 | 0 | 0 | 0 | |
N-stage, n (%) | 0.723 | |||
Negative | 126 (76) | 41 (75) | 85 (77) | |
Positive | 39 (24) | 14 (25) | 25 (23) | |
Lymph nodes harvested, median (IQR) | 27 (20–38) | 26 (20–38) | 27 (20–38) | 0.864 |
cM-stage, n (%) | 0.737 | |||
0 | 145 (88) | 49 (89) | 96 (87) | |
1 | 20 (12) | 6 (11) | 14 (13) | |
L-stage, n (%) | 0.358 | |||
0 | 155 (94) | 53 (96) | 102 (93) | |
1 | 10 (6) | 2 (4) | 8 (7) | |
V-stage, n (%) | 0.518 | |||
0 | 139 (84) | 45 (82) | 94 (86) | |
1 | 26 (16) | 10 (18) | 16 (14) | |
Pn-stage, n (%) | 0.865 | |||
0 | 152 (92) | 51 (93) | 101 (92) | |
1 | 13 (8) | 4 (7) | 9 (8) | |
Resection margin, n (%) | 1.000 | |||
Negative | 159 (96) | 53 (96) | 106 (96) | |
Positive | 6 (4) | 2 (4) | 4 (4) | |
Distal resection margin, mm (IQR) | 16 (10–30) | 15 (9–25) | 18 (10–30) | 0.383 |
Circumferential resection margin, mm (IQR) | 10 (5–15) | 9 (4–15) | 9 (5–16) | 0.417 |
Dvorak tumor regression grade, n (%) | 0.663 | |||
1 | 32 (19) | 12 (22) | 21 (19) | |
2 | 71 (43) | 21 (38) | 49 (45) | |
3 | 21 (13) | 9 (16) | 12 (11) | |
4 | 41 (25) | 13 (24) | 28 (25) |
Variable | OR (95% CI) | p-Value |
---|---|---|
Male sex | 0.768 (0.1–4.8) | 0.778 |
Obesity (body mass index (≥30 kg/m2) | 0.244 (<0.1–3.2) | 0.283 |
Low anastomosis (≤6 cm from anal verge) | 0.548 (0.1–3.7) | 0.537 |
High T-stage (≥3) | 1.571 (0.2–10.5) | 0.641 |
Positive N-stage | 0.829 (0.1–5.5) | 0.846 |
Two-team approach | 1.785 (0.2–13.5) | 0.574 |
Long operation time (>75th percentile) | 6.003 (0.6–62.3) | 0.133 |
Positive distal resection margin | 29.565 (2.1–418.1) | 0.012 |
Positive circumferential margin | 3.283 (0.3–33.5) | 0.316 |
Anastomotic leakage | 0.908 (0.1–15.6) | 0.947 |
Variable | OR (95% CI) | p-Value |
---|---|---|
Male sex | 1.982 (0.7–5.3) | 0.174 |
Obesity (body mass index (≥30 kg/m2) | 0.434 (0.1–1.5) | 0.188 |
Low anastomosis (≤6 cm from anal verge) | 1.432 (0.6–3.7) | 0.454 |
High T-stage (≥3) | 1.270 (0.5–3.2) | 0.614 |
Positive N-stage | 3.189 (1.3–7.9) | 0.012 |
Two-team approach | 0.490 (0.2–1.4) | 0.169 |
Long operation time (>75th percentile) | 0.366 (0.1–1.4) | 0.144 |
Positive distal resection margin | 0.737 (0.1–6.7) | 0.787 |
Positive circumferential margin | 2.855 (0.6–14.4) | 0.204 |
Anastomotic leakage | 2.664 (0.6–11.6) | 0.192 |
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Gloor, S.; Pozza, G.; Troller, R.; Wehrli, M.; Adamina, M. Surgical Outcomes, Long-Term Recurrence Rate, and Resource Utilization in a Prospective Cohort of 165 Patients Treated by Transanal Total Mesorectal Excision for Distal Rectal Cancer. Cancers 2023, 15, 1190. https://doi.org/10.3390/cancers15041190
Gloor S, Pozza G, Troller R, Wehrli M, Adamina M. Surgical Outcomes, Long-Term Recurrence Rate, and Resource Utilization in a Prospective Cohort of 165 Patients Treated by Transanal Total Mesorectal Excision for Distal Rectal Cancer. Cancers. 2023; 15(4):1190. https://doi.org/10.3390/cancers15041190
Chicago/Turabian StyleGloor, Severin, Gioia Pozza, Rebekka Troller, Markus Wehrli, and Michel Adamina. 2023. "Surgical Outcomes, Long-Term Recurrence Rate, and Resource Utilization in a Prospective Cohort of 165 Patients Treated by Transanal Total Mesorectal Excision for Distal Rectal Cancer" Cancers 15, no. 4: 1190. https://doi.org/10.3390/cancers15041190
APA StyleGloor, S., Pozza, G., Troller, R., Wehrli, M., & Adamina, M. (2023). Surgical Outcomes, Long-Term Recurrence Rate, and Resource Utilization in a Prospective Cohort of 165 Patients Treated by Transanal Total Mesorectal Excision for Distal Rectal Cancer. Cancers, 15(4), 1190. https://doi.org/10.3390/cancers15041190