Skip to main content
Log in

Current Status of the Management of Stage I Rectal Cancer

  • Gastrointestinal Cancers (J Meyer, Section Editor)
  • Published:
Current Oncology Reports Aims and scope Submit manuscript

Abstract

Purpose of Review

To summarize the current available treatments for stage I rectal cancer and the evidence that supports them.

Recent Findings

Radical surgery, or total mesorectal excision (TME) without neoadjuvant therapy, reports excellent oncologic outcomes, with 5-year disease-free survival of approximately 95%. Alternative therapies include local excision, which has acceptable long-term outcomes in some low-risk T1 tumors; but overall local excision, with or without additional chemotherapy or radiation, generally reports 5-year disease-free survival less than TME alone. New research is showing complete clinical response rates of 67% with chemoradiation combined with additional consolidation chemotherapy in T2 lesions, making watch and wait a potential strategy for stage I tumors.

Summary

Owing to its superior oncologic outcomes, radical surgery remains the mainstay of treatment for stage I tumors. Both local excision and watch and wait have advantages that may make them useful in individual patients and should be considered under the right circumstances.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1

Similar content being viewed by others

References

Papers of particular interest, published recently, have been highlighted as: • Of importance •• Of major importance

  1. Wang X, Cao W, Zheng C, Hu W, Liu C. Marital status and survival in patients with rectal cancer: an analysis of the Surveillance, Epidemiology and End Results (SEER) database. Cancer Epidemiol. 2018;54:119–24.

    Article  Google Scholar 

  2. Wang H, Fu CG, Chai R, Cao FA, Yu ED, Zhang W, et al. Lymph node metastasis and its risk factors in T1-2 staging invasive rectal carcinoma. Zhonghua Wai Ke Za Zhi. 2010;48(13):968–71.

    PubMed  Google Scholar 

  3. Al-Sukhni E, Milot L, Fruitman M, Beyene J, Victor JC, Schmocker S, et al. Diagnostic accuracy of MRI for assessment of T category, lymph node metastases, and circumferential resection margin involvement in patients with rectal cancer: a systematic review and meta-analysis. Ann Surg Oncol. 2012;19(7):2212–23.

    Article  Google Scholar 

  4. Zhang G, Cai YZ, Xu GH. Diagnostic accuracy of MRI for assessment of T category and circumferential resection margin involvement in patients with rectal cancer: a meta-analysis. Dis Colon Rectum. 2016;59(8):789–99.

    Article  Google Scholar 

  5. Zhou Y, Shao W, Lu W. Diagnostic value of endorectal ultrasonography for rectal carcinoma: a meta-analysis. J Cancer Res Ther. 2014;10(Suppl):319–22.

    Article  Google Scholar 

  6. Dehal A, Graff-Baker AN, Vuong B, Nelson D, Chang SC, Goldfarb M, et al. Current imaging modalities understage one-third of patients with stage I rectal cancer: implications for treatment selection. Am Surg. 2018;84(10):1589–94.

    PubMed  Google Scholar 

  7. Oien K, Mjorud Forsmo H, Rosler C, Nylund K, Waage JE, Pfeffer F. Endorectal ultrasound and magnetic resonance imaging for staging of early rectal cancers: how well does it work in practice? Acta Oncol. 2019;58(sup1):S49–54.

    Article  Google Scholar 

  8. Kraima AC, West NP, Treanor D, Magee DR, Rutten HJ, Quirke P, et al. Whole mount microscopic sections reveal that Denonvilliers’ fascia is one entity and adherent to the mesorectal fascia; implications for the anterior plane in total mesorectal excision? Eur J Surg Oncol. 2015;41(6):738–45.

    Article  CAS  Google Scholar 

  9. Fitzgerald TL, Brinkley J, Zervos EE. Pushing the envelope beyond a centimeter in rectal cancer: oncologic implications of close, but negative margins. J Am Coll Surg. 2011;213(5):589–95.

    Article  Google Scholar 

  10. Kitaguchi D, Sasaki T, Nishizawa Y, Tsukada Y, Ito M. Long-term outcomes and lymph node metastasis in patients receiving radical surgery for pathological T1 lower rectal cancer. World J Surg. 2019;43(2):649–56.

    Article  Google Scholar 

  11. Fleshman J, Branda M, Sargent DJ, Boller AM, George V, Abbas M, et al. Effect of laparoscopic-assisted resection vs open resection of stage II or III rectal cancer on pathologic outcomes: the ACOSOG Z6051 randomized clinical trial. JAMA. 2015;314(13):1346–55.

    Article  CAS  Google Scholar 

  12. Stevenson AR, Solomon MJ, Lumley JW, Hewett P, Clouston AD, Gebski VJ, et al. Effect of laparoscopic-assisted resection vs open resection on pathological outcomes in rectal cancer: the ALaCaRT randomized clinical trial. JAMA. 2015;314(13):1356–63.

    Article  CAS  Google Scholar 

  13. • Bonjer HJ, Deijen CL, Haglind E, Group CIS. A randomized trial of laparoscopic versus open surgery for rectal cancer. N Engl J Med. 2015;373(2):194 COLOR II is the only laparoscopic versus open trial of rectal cancer to include stage I patients. It is also the only trial to show equivalence between the two surgical modalities, and as such applies best to this population of patients.

    PubMed  Google Scholar 

  14. Sammour T, Malakorn S, Bednarski BK, Kaur H, Shin US, Messick C, et al. Oncological outcomes after robotic proctectomy for rectal cancer: analysis of a prospective database. Ann Surg. 2018;267(3):521–6.

    Article  Google Scholar 

  15. de Lacy FB, van Laarhoven J, Pena R, Arroyave MC, Bravo R, Cuatrecasas M, et al. Transanal total mesorectal excision: pathological results of 186 patients with mid and low rectal cancer. Surg Endosc. 2018;32(5):2442–7.

    Article  Google Scholar 

  16. Jayne D, Pigazzi A, Marshall H, Croft J, Corrigan N, Copeland J, 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(16):1569–80.

    Article  Google Scholar 

  17. European Society of Coloproctology collaborating g. An international multicentre prospective audit of elective rectal cancer surgery; operative approach versus outcome, including transanal total mesorectal excision (TaTME). Colorectal Dis. 2018;20(Suppl 6):33–46.

    Article  Google Scholar 

  18. Rubinkiewicz M, Zarzycki P, Witowski J, Pisarska M, Gajewska N, Torbicz G, et al. Functional outcomes after resections for low rectal tumors: comparison of transanal with laparoscopic total mesorectal excision. BMC Surg. 2019;19(1):79.

    Article  Google Scholar 

  19. Battersby NJ, Juul T, Christensen P, Janjua AZ, Branagan G, Emmertsen KJ, et al. Predicting the risk of bowel-related quality-of-life impairment after restorative resection for rectal cancer: a multicenter cross-sectional study. Dis Colon Rectum. 2016;59(4):270–80.

    Article  Google Scholar 

  20. Tan WS, Tang CL, Shi L, Eu KW. Meta-analysis of defunctioning stomas in low anterior resection for rectal cancer. Br J Surg. 2009;96(5):462–72.

    Article  CAS  Google Scholar 

  21. Blok RD, Stam R, Westerduin E, Borstlap WAA, Hompes R, Bemelman WA, et al. Impact of an institutional change from routine to highly selective diversion of a low anastomosis after TME for rectal cancer. Eur J Surg Oncol. 2018;44(8):1220–5.

    Article  CAS  Google Scholar 

  22. Nash GM, Weiser MR, Guillem JG, Temple LK, Shia J, Gonen M, et al. Long-term survival after transanal excision of T1 rectal cancer. Dis Colon Rectum. 2009;52(4):577–82.

    Article  Google Scholar 

  23. 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.

    Article  Google Scholar 

  24. Wawok P, Polkowski W, Richter P, Szczepkowski M, Oledzki J, Wierzbicki R, et al. Preoperative radiotherapy and local excision of rectal cancer: long-term results of a randomised study. Radiother Oncol. 2018;127(3):396–403.

    Article  Google Scholar 

  25. Rackley TP, Ma RM, Brown CJ, Hay JH. Transanal local excision for patients with rectal cancer: can radiation compensate for what is perceived as a nondefinitive surgical approach? Dis Colon Rectum. 2016;59(3):173–8.

    Article  Google Scholar 

  26. •• Garcia-Aguilar J, Renfro LA, Chow OS, Shi Q, Carrero XW, Lynn PB, 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 This is a multi-institutional randomized trial demonstrating the results of chemoradiotherapy and local excision are close to mesorectal excision. In addition, functional results were excellent, making neoadjuvant chemoradiation followed by local excision a potential therapeutic option for appropriate patients.

    Article  Google Scholar 

  27. Tyler Ellis C, Charlton ME, Stitzenberg KB. Patient-reported roles, preferences, and expectations regarding treatment of stage I rectal cancer in the cancer care outcomes research and surveillance consortium. Dis Colon Rectum. 2016;59(10):907–15.

    Article  CAS  Google Scholar 

  28. Fazio VW, Zutshi M, Remzi FH, Parc Y, Ruppert R, Furst A, et al. A randomized multicenter trial to compare long-term functional outcome, quality of life, and complications of surgical procedures for low rectal cancers. Ann Surg. 2007;246(3):481–8 discussion 8-90.

    Article  Google Scholar 

  29. Atallah S, Albert M, Larach S. Transanal minimally invasive surgery: a giant leap forward. Surg Endosc. 2010;24(9):2200–5.

    Article  Google Scholar 

  30. Warren CD, Hamilton AER, Stevenson ARL. Robotic transanal minimally invasive surgery (TAMIS) for local excision of rectal lesions with the da Vinci Xi (dVXi): technical considerations and video vignette. Tech Coloproctol. 2018;22(7):529–33.

    Article  CAS  Google Scholar 

  31. Habr-Gama A, Perez RO, Proscurshim I, Campos FG, Nadalin W, Kiss D, et al. Patterns of failure and survival for nonoperative treatment of stage c0 distal rectal cancer following neoadjuvant chemoradiation therapy. J Gastrointest Surg. 2006;10(10):1319–28 discussion 28-9.

    Article  Google Scholar 

  32. Habr-Gama A, Sao Juliao GP, Vailati BB, Fernandez LM, Ortega CD, Figueiredo N, et al. Organ preservation among patients with clinically node-positive rectal cancer: is it really more dangerous? Dis Colon Rectum. 2019;62(6):675–83.

    Article  Google Scholar 

  33. Creavin B, Ryan E, Martin ST, Hanly A, O’Connell PR, Sheahan K, et al. Organ preservation with local excision or active surveillance following chemoradiotherapy for rectal cancer. Br J Cancer. 2017;116(2):169–74.

    Article  CAS  Google Scholar 

  34. Habr-Gama A, Gama-Rodrigues J, Sao Juliao GP, Proscurshim I, Sabbagh C, Lynn PB, et al. Local recurrence after complete clinical response and watch and wait in rectal cancer after neoadjuvant chemoradiation: impact of salvage therapy on local disease control. Int J Radiat Oncol Biol Phys. 2014;88(4):822–8.

    Article  Google Scholar 

  35. Li J, Li L, Yang L, Yuan J, Lv B, Yao Y, et al. Wait-and-see treatment strategies for rectal cancer patients with clinical complete response after neoadjuvant chemoradiotherapy: a systematic review and meta-analysis. Oncotarget. 2016;7(28):44857–70.

    PubMed  PubMed Central  Google Scholar 

  36. Martens MH, Maas M, Heijnen LA, Lambregts DM, Leijtens JW, Stassen LP, et al. Long-term outcome of an organ preservation program after neoadjuvant treatment for rectal cancer. J Natl Cancer Inst. 2016;108(12). https://doi.org/10.1093/jnci/djw171.

  37. Habr-Gama A, Sao Juliao GP, Gama-Rodrigues J, Vailati BB, Ortega C, Fernandez LM, et al. Baseline T classification predicts early tumor regrowth after nonoperative management in distal rectal cancer after extended neoadjuvant chemoradiation and initial complete clinical response. Dis Colon Rectum. 2017;60(6):586–94.

    Article  Google Scholar 

  38. •• Habr-Gama A, Sao Juliao GP, Vailati BB, Sabbaga J, Aguilar PB, Fernandez LM, et al. Organ preservation in cT2N0 rectal cancer after neoadjuvant chemoradiation therapy: the impact of radiation therapy dose-escalation and consolidation chemotherapy. Ann Surg. 2019;269(1):102–7 This study demonstrates truly remarkable results without surgery for the treatment of stage I rectal cancer. By adding additional consolidation chemotherapy, the authors were able to increase the rate of clinical complete response to 67%, making organ preservation a potentially viable first approach in the treatment of rectal cancer.

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Craig Howard Olson.

Ethics declarations

Conflict of Interest

The author declares that he has no conflict of interest.

Human and Animal Rights and Informed Consent

This article does not contain any studies with human or animal subjects performed by any of the authors.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

This article is part of the Topical Collection on Gastrointestinal Cancers

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Olson, C.H. Current Status of the Management of Stage I Rectal Cancer. Curr Oncol Rep 22, 40 (2020). https://doi.org/10.1007/s11912-020-00905-y

Download citation

  • Published:

  • DOI: https://doi.org/10.1007/s11912-020-00905-y

Keywords

Navigation