Grass F and Mathis K. Novelties in treatment of locally advanced rectal cancer [version 1; peer review: 3 approved]. F1000Research 2018, 7(F1000 Faculty Rev):1868 (https://doi.org/10.12688/f1000research.16194.1)
NOTE: it is important to ensure the information in square brackets after the title is included in all citations of this article.
Treatment of locally advanced rectal cancer is evolving through surgical innovation and paradigm shifts in neoadjuvant treatment. Whereas local recurrence was a significant concern before the systematic implementation of neoadjuvant chemoradiation therapy and surgery according to total mesorectal excision principles, distant relapse remains a major drawback. Hence, efforts in recent years have focused on delivering preoperative chemotherapy regimens to overcome compliance issues with adjuvant administration. In parallel, new surgical techniques, including transanal video-assisted total mesorectal excision and robot-assisted surgery, emerged to face the challenge to navigate in the deep and narrow spaces of the pelvis. Furthermore, patients experiencing a complete response after neoadjuvant treatment might even escape surgery within a close surveillance strategy. This novel “watch and wait” concept has gained interest to improve quality of life in highly selected patients. This review summarizes recent evidence and controversies and provides an overview on timely and innovative aspects in the treatment of locally advanced rectal cancer.
Keywords
Rectal cancer, treatment, surgery, neoadjuvant, watch and wait
During the last decades, new surgical and medical treatment strategies for stage II and III locally advanced rectal cancer (LARC) emerged and challenged classic treatment schemes1. Laparoscopic surgery according to the principles of total mesorectal excision (TME) is now widely established as standard in well-resourced countries. However, this approach is technically demanding for low-rectal cancers in patients with unfavorable baseline conditions and narrow pelvises. In recent years, robot-assisted surgery and the transanal video-assisted approach (TaTME) have been described as modern alternatives for overcoming these difficulties2,3.
In parallel, the standard concept of neoadjuvant fractioned long-course chemoradiation therapy (CRT) followed by surgical resection six weeks later and adjuvant chemotherapy has been questioned4. Distant relapse has become more of a concern than local recurrence, which is significantly better controlled since the systematic implementation of preoperative chemoradiation and surgery carried out according to the TME principles5. On the other hand, adjuvant systemic treatments may be delayed or even omitted in up to 50% of patients as a consequence of major surgery with potential complications, slow recovery, and interference with loop ileostomy reversal6–8; hence, administration of systemic chemotherapy before the actual surgical resection has been suggested to overcome these drawbacks9,10.
One of the most debated treatment concepts today is the “watch and wait” approach, which implies a non-operative surveillance strategy in patients with complete clinical response to neoadjuvant treatment11. This approach notably gained interest after observing equivalent long-term results in patients with clinical stage 0 disease undergoing surgery as compared with patients within a close surveillance strategy12. In this review, recent developments and controversies in surgical management, neoadjuvant strategies, and non-operative management of LARC are summarized and discussed.
Surgical innovations
Laparoscopic surgery
Laparoscopy has been established as the standard approach for colorectal resections in most developed countries because of advantages regarding postoperative pain, return of bowel function, and length of hospital stay without compromising oncological safety13–15. Particularly for rectal cancer, the plane of surgery has been identified as an important predictive factor of local recurrence16, and principles of TME with sharp dissection of the mesorectal fascia are now considered standard17,18. However, laparoscopic dissection of a deep-situated LARC might be challenging and has raised concerns regarding long-term oncologic outcome. Several randomized controlled trials compared oncological outcomes between open and laparoscopic resections. The large COLOR II trial, which randomly assigned 1044 patients, found no difference in locoregional recurrence at three years, which was 5% in both groups19. One interesting finding was that circumferential resection margins (CRMs) were more often compromised in the laparoscopic group for mid-rectal cancers, whereas for low-rectal cancers, CRM was more often positive after open surgery. This latter finding, however, was explained by the particular challenge of abdominoperineal resections. The COREAN trial, which looked at three-year disease-free survival in mid- and low-rectal cancers, found similar outcomes, thus justifying a wide adoption of the laparoscopic approach20. However, heterogeneity of endpoints as well as differences in disease stages, tumor location, and neoadjuvant chemotherapy impede uncritical comparisons of the results of these studies and potentially lead to misinterpretations. On the other hand, two other randomized trials, published in 2015, raised concerns about the safety of a laparoscopic approach for LARC since they failed to demonstrate non-inferiority of the laparoscopic approach using pathological endpoints21,22. The first was a multicenter North American study that included only experienced, credentialed surgeons; a composite pathological endpoint to determine surgical quality was chosen21. The second was a similarly designed Australasian trial that reproduced these results22. As a common conclusion of the trials, routine use of the laparoscopic approach could not be recommended beyond doubt. However, all trials, including the formerly conducted CLASICC trial, acknowledged advantages of the laparoscopic approach regarding improved surgical and functional recovery and decreased length of stay23–25.
In summary, despite favorable short-term outcomes, ambiguous results regarding oncological long-term outcome after laparoscopy probably emphasize the importance of surgical expertise and dexterity when choosing one approach over another. Long-term oncologic results of the North American and Australasian trials are anxiously awaited.
Transanal total mesorectal excision
Low LARC needing sphincter-sparing resection can be challenging because of narrow pelvic anatomy, especially in male patients and in patients with a high body mass index and fatty mesorectum26. Notably, clean distal resection margins can be difficult to achieve because of visibility issues27. To overcome these challenges, a new approach has been described in recent years, taking advantage of the magnification of a laparoscope to allow better visualization of the lower mesorectum and endangered structures through the anus. A recent meta-analysis of seven studies showed encouraging outcomes regarding completeness of specimens and postoperative complications. However, individual study quality was modest (retrospective case control trials), the approach was barely standardized, and all studies were conducted in high-volume expert centers. Hence, confirmation of these results in less experienced centers might not be achievable right away. Two randomized trials of the GRECCAR and COLOR study groups are recruiting patients28. Furthermore, a recent expert consensus statement provided guidance for optimal clinical practice29. Several questions remain unanswered, in particular whether a one- or two-team approach is preferable and to what extent surgical experience and proper training are required to overcome the significant learning curve30,31. Obviously, at this stage, long-term functional and oncological outcomes are not yet available.
Robotic surgery
The robotic platform da Vinci (Intuitive Surgical, Sunnyvale, CA, USA) entered the market in 2001 and was applied mainly for urologic and gynecologic surgery. Even though robot-assisted laparoscopic prostatectomy was not superior to open retropubic prostatectomy regarding short-term postoperative outcomes in a recent randomized controlled phase 3 study32, the robotic approach is widely established in the urologic field in well-resourced countries33. It was estimated that up to 80% of radical prostatectomies will be performed robotically in the US by 202034.
In recent years, robot-assisted surgery gained interest for rectal cancer resections because of its optimal visualization and improved navigation in the narrow pelvic space. However, meta-analyses did not show any advantage over laparoscopic surgery, except for decreased conversion rates2. Mainly retrospective case series demonstrated similar completeness of TME, similar rates of CRM positivity, and equal short-term oncological outcomes35,36, whereas a smaller study suggested improved quality of the specimen after robotic TME37. The most important study in the field was published recently: The ROLARR study, an international multicenter prospective trial, randomly assigned 471 patients to either conventional laparoscopic or robotic-assisted resections38. The study failed to demonstrate significant benefits of robotic surgery regarding the main outcomes of CRM positivity, TME quality, intra- and postoperative complications, and 30-day mortality. However, the wide range of experience among operating surgeons was criticized.
In conclusion, it probably comes down to a matter of experience and dexterity with either approach, and no clear recommendation can be made based on the available evidence.
Neoadjuvant strategies
The guidelines of the National Comprehensive Cancer Network (NCCN) for LARC recommend a multidisciplinary approach with neoadjuvant CRT, surgery according to TME principles, and adjuvant chemotherapy39. Neoadjuvant CRT was defined as standard mainly because of its potential to decrease 5- and 10-year pelvic recurrence rates40. However, whether long- or short-course radiotherapy is preferable remains matter of debate; in the US, the overwhelming majority of radiation oncologists still favor long-course CRT41. Classically, preoperative chemotherapeutic agents act as radiosensitizers. Although 5-fluorouracil (5-FU) is widely accepted, the oral 5-FU prodrug capecitabine was identified as a valid treatment alternative more recently42.
Neoadjuvant chemotherapy
The concept of neoadjuvant CRT was re-evaluated recently. Although local recurrence was better controlled, facing the estimated five-year distal relapse rate of 35% became the primary target43. Administration of systemic chemotherapy in the neoadjuvant setting, before or after CRT, gained interest to face the drawback of low compliance in the adjuvant setting6,44. Neoadjuvant chemotherapy further allows timely identification of non-responders and treatment of occult micro-metastases several months preoperatively4,45. A wide range of drugs, including oxaliplatin as an adjunct to CRT, failed to demonstrate clear benefits in several high-quality studies and this was due mainly to increased toxicity46,47. However, more recent data showed improved disease-free survival when adding oxaliplatin to both preoperative CRT and postoperative chemotherapy48. Several further phase II trials showed similar promising results without jeopardizing planned CRT or increasing surgical complications9,49–51, labelling the concept of total neoadjuvant chemotherapy as safe and feasible. Splitting of adjuvant chemotherapy by delivering at least some cycles before CRT and the remaining post-surgery has also been described as an alternative52,53. A randomized trial in North America (NRG GI002) is accruing patients for a total neoadjuvant approach.
Despite these encouraging results, systemic chemotherapy is still administered primarily in the adjuvant setting. Fluoropyrimidine-based regimens for four months are recommended by consensus guidelines, even though the value of the regimens was debated because of incongruent results when administered to all patients, independent of pathologic tumor stage54,55.
Selective preoperative radiotherapy
Given the drawback of long-term morbidity with pelvic irradiation and widespread application of TME principles to decrease local recurrence, a subset of patients may be eligible to avoid preoperative radiation and to undergo solely neoadjuvant systemic chemotherapy. However, only relatively small single-arm studies are available to date and results are promising: radiographic down-staging was achieved in 25 to 70% of patients, and local recurrence rates were not increased in these highly selected patients56–58. Large studies are ongoing44 and today this approach is used primarily in trial settings. The randomized phase III PROSPECT (Preoperative Radiation or Selective Preoperative Radiation and Evaluation Before Chemotherapy and TME) trial is assessing this strategy in patients with uncompromised CRM (ClinicalTrials.gov Identifier: NCT01515787).
Watch and wait
Surgery for LARC has a significant impact on the patient, and severe complications occur in up to 22% of patients21. Quality of life might be significantly impaired postoperatively, especially since sphincter preservation is possible in only 50% of patients with low-rectal cancer59. Organ-preserving strategies thus gained interest in patients with a complete clinical response to neoadjuvant treatment12. The most critical aspect when considering organ preservation is the accuracy in assessing tumor response. Optimal timing of the assessment is crucial since tumor regression after CRT appears to be time-dependent. Although non-responding tumors should be re-assessed within six to eight weeks, responders might benefit from at least a 12-week interval, according to a Brazilian pioneer group of this approach60. A large British study assessed oncological outcomes in 259 patients with clinical complete response to CRT through a propensity score–matched cohort analysis. No difference in three-year disease-free survival was noted, and permanent colostomy could be avoided in 74% of patients in the surveillance group61. A recent systematic review and pooled analysis described an overall complete clinical response rate to neoadjuvant CRT of 22.4%62. Seventeen studies reported on 692 patients with complete clinical response and were retained in this systematic review; most studies were relatively small retrospective cohort studies. Whereas 68% of patients presented with cT3 tumors, 50% were node-positive on pre-treatment staging. The time to response assessment varied widely, from 3 to 24 weeks. Most studies (67%), however, re-assessed treatment response after a minimum of eight weeks. Treatment response was assessed through triple assessment (digital rectal examination, endoscopic, and radiological) in 88% of studies. Tumor regrowth within the three-year observation period was noted in 22.1% of patients and 68% of these patients relapsed during the first year of surveillance.
Taken together, the vast majority of patients who received current neoadjuvant CRT did not achieve a complete response. In recent years, intense molecular biology research aimed to identify reliable biomarkers to predict complete response. Several recent studies described extramural vascular invasion as a promising prognostic factor on high-resolution magnetic resonance imaging (MRI) to assess risks of metastatic disease after CRT63–65. Furthermore, MRI-based texture parameters have been investigated more recently as potential predictors of long-term survival in LARC66,67. Accuracy of re-assessment of tumor response is of utmost importance. A recent meta-analysis described a sensitivity of 77% and a specificity of 94% of MRI in predicting CRM involvement68. The highly cited MERCURY trial found that MRI involvement of the CRM was the only preoperative staging parameter for predicting local recurrence and survival69. Thus, high-resolution MRI has become an indispensable tool to confirm clinical and endoscopic findings of a complete clinical response. Patients within a watch-and-wait strategy should adhere to a strict follow-up program, ideally with a prospective registry, to allow successful salvage surgery if deemed necessary70.
Further considerations and perspectives
A particular challenge represents the management of LARC in frail patients and the elderly. Preoperative frailty and nutritional assessment together with quality-of-life considerations are of utmost importance when defining surgical and oncologic strategies71,72. Importantly, radical surgery should be considered only after careful case-by-case evaluation involving caregivers, patients, and their family through shared decision making to aim for the best possible outcomes and quality of life73–75.
Promising results can be expected from studies focusing on disease monitoring by genomics, such as target sequencing of circulating tumor DNA76,77 or apoptosis-related genes, including the p53-signaling pathway78,79. Findings of these innovative research fields will likely further impact treatment strategies of LARC in the future.
Conclusions
Classic concepts of neoadjuvant and surgical treatment for LARC are being challenged. Modern surgical concepts aim to facilitate surgical navigation in the pelvis, but the ideal approach has not yet been described. In particular, robotic surgery has not yet provided the expected breakthrough.
An individualized oncological approach for selected patients is about to replace the classic tri-modality treatment scheme, according to numerous high-quality multicenter randomized trials, and several ongoing multicenter trials may liven the debate for years to come.
The author(s) declared that no grants were involved in supporting this work.
F1000 recommended
References
1.
Minsky BD:
Chemoradiation for rectal cancer: rationale, approaches, and controversies.
Surg Oncol Clin N Am.
2010; 19(4): 803–18. PubMed Abstract
2.
Lorenzon L, Bini F, Balducci G, et al.:
Laparoscopic versus robotic-assisted colectomy and rectal resection: a systematic review and meta-analysis.
Int J Colorectal Dis.
2016; 31(2): 161–73. PubMed Abstract
| Publisher Full Text
| F1000 Recommendation
3.
Sylla P, Rattner DW, Delgado S, et al.:
NOTES transanal rectal cancer resection using transanal endoscopic microsurgery and laparoscopic assistance.
Surg Endosc.
2010; 24(5): 1205–10. PubMed Abstract
| Publisher Full Text
5.
Benson AB 3rd, Bekaii-Saab T, Chan E, et al.:
Rectal Cancer.
J Natl Compr Canc Netw.
2012; 10(12): 1528–64. PubMed Abstract
| Publisher Full Text
6.
Bosset JF, Calais G, Mineur L, et al.:
Fluorouracil-based adjuvant chemotherapy after preoperative chemoradiotherapy in rectal cancer: long-term results of the EORTC 22921 randomised study.
Lancet Oncol.
2014; 15(2): 184–90. PubMed Abstract
| Publisher Full Text
7.
Rödel C, Liersch T, Becker H, et al.:
Preoperative chemoradiotherapy and postoperative chemotherapy with fluorouracil and oxaliplatin versus fluorouracil alone in locally advanced rectal cancer: initial results of the German CAO/ARO/AIO-04 randomised phase 3 trial.
Lancet Oncol.
2012; 13(7): 679–87. PubMed Abstract
| Publisher Full Text
| F1000 Recommendation
8.
Hayden DM, Pinzon MC, Francescatti AB, et al.:
Hospital readmission for fluid and electrolyte abnormalities following ileostomy construction: preventable or unpredictable?
J Gastrointest Surg.
2013; 17(2): 298–303. PubMed Abstract
| Publisher Full Text
9.
Maréchal R, Vos B, Polus M, et al.:
Short course chemotherapy followed by concomitant chemoradiotherapy and surgery in locally advanced rectal cancer: a randomized multicentric phase II study.
Ann Oncol.
2012; 23(6): 1525–30. PubMed Abstract
| Publisher Full Text
10.
Schou JV, Larsen FO, Rasch L, et al.:
Induction chemotherapy with capecitabine and oxaliplatin followed by chemoradiotherapy before total mesorectal excision in patients with locally advanced rectal cancer.
Ann Oncol.
2012; 23(10): 2627–33. PubMed Abstract
| Publisher Full Text
11.
Habr-Gama A, São Julião GP, Perez RO:
Nonoperative management of rectal cancer: identifying the ideal patients.
Hematol Oncol Clin North Am.
2015; 29(1): 135–51. PubMed Abstract
| Publisher Full Text
12.
Habr-Gama A, Perez RO, Nadalin W, et al.:
Operative Versus Nonoperative Treatment for Stage 0 Distal Rectal Cancer Following Chemoradiation Therapy: Long-term Results.
Trans Meet Am Surg Assoc Am Surg Assoc.
2004; 122: 309–16. Publisher Full Text
13.
Goh BK:
Impact of laparoscopic resection for colorectal cancer on operative outcomes and survival.
Ann Surg.
2007; 246(2): 338–9; author reply 339–40. PubMed Abstract
| Publisher Full Text
| Free Full Text
14.
Bonjer HJ, Hop WC, Nelson H, et al.:
Laparoscopically assisted vs open colectomy for colon cancer: a meta-analysis.
Arch Surg.
2007; 142(3): 298–303. PubMed Abstract
| Publisher Full Text
15.
Jackson TD, Kaplan GG, Arena G, et al.:
Laparoscopic versus open resection for colorectal cancer: a metaanalysis of oncologic outcomes.
J Am Coll Surg.
2007; 204(3): 439–46. PubMed Abstract
| Publisher Full Text
16.
Quirke P, Steele R, Monson J, et al.:
Effect of the plane of surgery achieved on local recurrence in patients with operable rectal cancer: a prospective study using data from the MRC CR07 and NCIC-CTG CO16 randomised clinical trial.
Lancet.
2009; 373(9666): 821–8. PubMed Abstract
| Publisher Full Text
| Free Full Text
| F1000 Recommendation
17.
Martling A, Holm T, Rutqvist LE, et al.:
Impact of a surgical training programme on rectal cancer outcomes in Stockholm.
Br J Surg.
2005; 92(2): 225–9. PubMed Abstract
| Publisher Full Text
18.
Kapiteijn E, Marijnen CA, Nagtegaal ID, et al.:
Preoperative radiotherapy combined with total mesorectal excision for resectable rectal cancer.
N Engl J Med.
2001; 345(9): 638–46. PubMed Abstract
| Publisher Full Text
19.
Bonjer HJ, Deijen CL, Abis GA, et al.:
A randomized trial of laparoscopic versus open surgery for rectal cancer.
N Engl J Med.
2015; 372(14): 1324–32. PubMed Abstract
| Publisher Full Text
20.
Jeong SY, Park JW, Nam BH, et al.:
Open versus laparoscopic surgery for mid-rectal or low-rectal cancer after neoadjuvant chemoradiotherapy (COREAN trial): survival outcomes of an open-label, non-inferiority, randomised controlled trial.
Lancet Oncol.
2014; 15(7): 767–74. PubMed Abstract
| Publisher Full Text
21.
Fleshman J, Branda M, Sargent DJ, 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. PubMed Abstract
| Publisher Full Text
| Free Full Text
22.
Stevenson AR, Solomon MJ, Lumley JW, 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. PubMed Abstract
| Publisher Full Text
23.
Jayne DG, Thorpe HC, Copeland J, et al.:
Five-year follow-up of the Medical Research Council CLASICC trial of laparoscopically assisted versus open surgery for colorectal cancer.
Br J Surg.
2010; 97(11): 1638–45. PubMed Abstract
| Publisher Full Text
24.
Kang SB, Park JW, Jeong SY, et al.:
Open versus laparoscopic surgery for mid or low rectal cancer after neoadjuvant chemoradiotherapy (COREAN trial): short-term outcomes of an open-label randomised controlled trial.
Lancet Oncol.
2010; 11(7): 637–45. PubMed Abstract
| Publisher Full Text
25.
van der Pas MH, Haglind E, Cuesta MA, et al.:
Laparoscopic versus open surgery for rectal cancer (COLOR II): short-term outcomes of a randomised, phase 3 trial.
Lancet Oncol.
2013; 14(3): 210–8. PubMed Abstract
| Publisher Full Text
26.
Rouanet P, Mourregot A, Azar CC, et al.:
Transanal endoscopic proctectomy: an innovative procedure for difficult resection of rectal tumors in men with narrow pelvis.
Dis Colon Rectum.
2013; 56(4): 408–15. PubMed Abstract
| Publisher Full Text
27.
Penninckx F, Kartheuser A, Van de Stadt J, et al.:
Outcome following laparoscopic and open total mesorectal excision for rectal cancer.
Br J Surg.
2013; 100(10): 1368–75. PubMed Abstract
| Publisher Full Text
28.
Deijen CL, Velthuis S, Tsai A, et al.:
COLOR III: a multicentre randomised clinical trial comparing transanal TME versus laparoscopic TME for mid and low rectal cancer.
Surg Endosc.
2016; 30(8): 3210–5. PubMed Abstract
| Publisher Full Text
| Free Full Text
30.
Atallah S, Albert M, Monson JR:
Critical concepts and important anatomic landmarks encountered during transanal total mesorectal excision (taTME): toward the mastery of a new operation for rectal cancer surgery.
Tech Coloproctol.
2016; 20(7): 483–94. PubMed Abstract
| Publisher Full Text
31.
Abbott SC, Stevenson ARL, Bell SW, et al.:
An assessment of an Australasian pathway for the introduction of transanal total mesorectal excision (taTME).
Colorectal Dis.
2018; 20(1): O1–O6. PubMed Abstract
| Publisher Full Text
| F1000 Recommendation
32.
Yaxley JW, Coughlin GD, Chambers SK, et al.:
Robot-assisted laparoscopic prostatectomy versus open radical retropubic prostatectomy: early outcomes from a randomised controlled phase 3 study.
Lancet.
2016; 388(10049): 1057–66. PubMed Abstract
| Publisher Full Text
| F1000 Recommendation
34.
Porpiglia F, Morra I, Lucci Chiarissi M, et al.:
Randomised controlled trial comparing laparoscopic and robot-assisted radical prostatectomy.
Eur Urol.
2013; 63(4): 606–14. PubMed Abstract
| Publisher Full Text
35.
Baek JH, McKenzie S, Garcia-Aguilar J, et al.:
Oncologic outcomes of robotic-assisted total mesorectal excision for the treatment of rectal cancer.
Ann Surg.
2010; 251(5): 882–6. PubMed Abstract
| Publisher Full Text
36.
Pigazzi A, Luca F, Patriti A, et al.:
Multicentric study on robotic tumor-specific mesorectal excision for the treatment of rectal cancer.
Ann Surg Oncol.
2010; 17(6): 1614–20. PubMed Abstract
| Publisher Full Text
37.
Allemann P, Duvoisin C, Di Mare L, et al.:
Robotic-Assisted Surgery Improves the Quality of Total Mesorectal Excision for Rectal Cancer Compared to Laparoscopy: Results of a Case-Controlled Analysis.
World J Surg.
2016; 40(4): 1010–6. PubMed Abstract
| Publisher Full Text
| F1000 Recommendation
38.
Jayne D, Pigazzi A, Marshall H, 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. PubMed Abstract
| Publisher Full Text
| Free Full Text
| F1000 Recommendation
39.
Petersen SH, Harling H, Kirkeby LT, et al.:
Postoperative adjuvant chemotherapy in rectal cancer operated for cure.
Cochrane Database Syst Rev.
2012; (3): CD004078. PubMed Abstract
| Publisher Full Text
40.
Sauer R, Liersch T, Merkel S, et al.:
Preoperative versus postoperative chemoradiotherapy for locally advanced rectal cancer: results of the German CAO/ARO/AIO-94 randomized phase III trial after a median follow-up of 11 years.
J Clin Oncol.
2012; 30(16): 1926–33. PubMed Abstract
| Publisher Full Text
41.
Mowery YM, Salama JK, Zafar SY, et al.:
Neoadjuvant long-course chemoradiation remains strongly favored over short-course radiotherapy by radiation oncologists in the United States.
Cancer.
2017; 123(8): 1434–41. PubMed Abstract
| Publisher Full Text
| F1000 Recommendation
42.
Hofheinz RD, Wenz F, Post S, et al.:
Chemoradiotherapy with capecitabine versus fluorouracil for locally advanced rectal cancer: a randomised, multicentre, non-inferiority, phase 3 trial.
Lancet Oncol.
2012; 13(6): 579–88. PubMed Abstract
| Publisher Full Text
| F1000 Recommendation
43.
Gollins S, Sebag-Montefiore D:
Neoadjuvant Treatment Strategies for Locally Advanced Rectal Cancer.
Clin Oncol (R Coll Radiol).
2016; 28(2): 146–51. PubMed Abstract
| Publisher Full Text
44.
Franke AJ, Parekh H, Starr JS, et al.:
Total Neoadjuvant Therapy: A Shifting Paradigm in Locally Advanced Rectal Cancer Management.
Clin Colorectal Cancer.
2018; 17(1): 1–12. PubMed Abstract
| Publisher Full Text
| F1000 Recommendation
45.
Glynne-Jones R, Grainger J, Harrison M, et al.:
Neoadjuvant chemotherapy prior to preoperative chemoradiation or radiation in rectal cancer: should we be more cautious?
Br J Cancer.
2006; 94(3): 363–71. PubMed Abstract
| Publisher Full Text
| Free Full Text
46.
Aschele C, Cionini L, Lonardi S, et al.:
Primary tumor response to preoperative chemoradiation with or without oxaliplatin in locally advanced rectal cancer: pathologic results of the STAR-01 randomized phase III trial.
J Clin Oncol.
2011; 29(20): 2773–80. PubMed Abstract
| Publisher Full Text
| F1000 Recommendation
47.
Allegra CJ, Yothers G, O'Connell MJ, et al.:
Neoadjuvant 5-FU or Capecitabine Plus Radiation With or Without Oxaliplatin in Rectal Cancer Patients: A Phase III Randomized Clinical Trial.
J Natl Cancer Inst.
2015; 107(11): pii: djv248. PubMed Abstract
| Publisher Full Text
| Free Full Text
48.
Rödel C, Graeven U, Fietkau R, et al.:
Oxaliplatin added to fluorouracil-based preoperative chemoradiotherapy and postoperative chemotherapy of locally advanced rectal cancer (the German CAO/ARO/AIO-04 study): final results of the multicentre, open-label, randomised, phase 3 trial.
Lancet Oncol.
2015; 16(8): 979–89. PubMed Abstract
| Publisher Full Text
49.
Perez K, Safran H, Sikov W, et al.:
Complete Neoadjuvant Treatment for Rectal Cancer: The Brown University Oncology Group CONTRE Study.
Am J Clin Oncol.
2017; 40(3): 283–7. PubMed Abstract
| Publisher Full Text
| F1000 Recommendation
50.
Dewdney A, Cunningham D, Tabernero J, et al.:
Multicenter randomized phase II clinical trial comparing neoadjuvant oxaliplatin, capecitabine, and preoperative radiotherapy with or without cetuximab followed by total mesorectal excision in patients with high-risk rectal cancer (EXPERT-C).
J Clin Oncol.
2012; 30(14): 1620–7. PubMed Abstract
| Publisher Full Text
| F1000 Recommendation
51.
Chua YJ, Barbachano Y, Cunningham D, et al.:
Neoadjuvant capecitabine and oxaliplatin before chemoradiotherapy and total mesorectal excision in MRI-defined poor-risk rectal cancer: a phase 2 trial.
Lancet Oncol.
2010; 11(3): 241–8. PubMed Abstract
| Publisher Full Text
| F1000 Recommendation
52.
Chau I, Brown G, Cunningham D, et al.:
Neoadjuvant capecitabine and oxaliplatin followed by synchronous chemoradiation and total mesorectal excision in magnetic resonance imaging-defined poor-risk rectal cancer.
J Clin Oncol.
2006; 24(4): 668–74. PubMed Abstract
| Publisher Full Text
53.
Fernández-Martos C, Pericay C, Aparicio J, et al.:
Phase II, randomized study of concomitant chemoradiotherapy followed by surgery and adjuvant capecitabine plus oxaliplatin (CAPOX) compared with induction CAPOX followed by concomitant chemoradiotherapy and surgery in magnetic resonance imaging-defined, locally advanced rectal cancer: Grupo cancer de recto 3 study.
J Clin Oncol.
2010; 28(5): 859–65. PubMed Abstract
| Publisher Full Text
54.
Kiran RP, Kirat HT, Burgess AN, et al.:
Is adjuvant chemotherapy really needed after curative surgery for rectal cancer patients who are node-negative after neoadjuvant chemoradiotherapy?
Ann Surg Oncol.
2012; 19(4): 1206–12. PubMed Abstract
| Publisher Full Text
55.
Bujko K, Glynne-Jones R, Bujko M:
Does adjuvant fluoropyrimidine-based chemotherapy provide a benefit for patients with resected rectal cancer who have already received neoadjuvant radiochemotherapy? A systematic review of randomised trials.
Ann Oncol.
2010; 21(9): 1743–50. PubMed Abstract
| Publisher Full Text
56.
Uehara K, Hiramatsu K, Maeda A, et al.:
Neoadjuvant oxaliplatin and capecitabine and bevacizumab without radiotherapy for poor-risk rectal cancer: N-SOG 03 Phase II trial.
Jpn J Clin Oncol.
2013; 43(10): 964–71. PubMed Abstract
| Publisher Full Text
57.
Schrag D, Weiser MR, Goodman KA, et al.:
Neoadjuvant chemotherapy without routine use of radiation therapy for patients with locally advanced rectal cancer: a pilot trial.
J Clin Oncol.
2014; 32(6): 513–8. PubMed Abstract
| Publisher Full Text
| Free Full Text
58.
Hasegawa J, Nishimura J, Mizushima T, et al.:
Neoadjuvant capecitabine and oxaliplatin (XELOX) combined with bevacizumab for high-risk localized rectal cancer.
Cancer Chemother Pharmacol.
2014; 73(5): 1079–87. PubMed Abstract
| Publisher Full Text
59.
Battersby NJ, How P, Moran B, et al.:
Prospective Validation of a Low Rectal Cancer Magnetic Resonance Imaging Staging System and Development of a Local Recurrence Risk Stratification Model: The MERCURY II Study.
Ann Surg.
2016; 263(4): 751–60. PubMed Abstract
| Publisher Full Text
| F1000 Recommendation
60.
Perez RO, Habr-Gama A, São Julião GP, et al.:
Rectal sparing approach after preoperative radio- and/or chemotherapy (RESARCH) in patients with rectal cancer: potential pitfalls of a multicentre observational study.
Tech Coloproctol.
2018; 22(2): 141–2. PubMed Abstract
| Publisher Full Text
| F1000 Recommendation
61.
Renehan AG, Malcomson L, Emsley R, et al.:
Watch-and-wait approach versus surgical resection after chemoradiotherapy for patients with rectal cancer (the OnCoRe project): a propensity-score matched cohort analysis.
Lancet Oncol.
2016; 17(2): 174–83. PubMed Abstract
| Publisher Full Text
| F1000 Recommendation
62.
Dattani M, Heald RJ, Goussous G, et al.:
Oncological and Survival Outcomes in Watch and Wait Patients With a Clinical Complete Response After Neoadjuvant Chemoradiotherapy for Rectal Cancer: A Systematic Review and Pooled Analysis.
Ann Surg.
2018; 268(6): 955–967. PubMed Abstract
| Publisher Full Text
| F1000 Recommendation
63.
Chand M, Evans J, Swift RI, et al.:
The prognostic significance of postchemoradiotherapy high-resolution MRI and histopathology detected extramural venous invasion in rectal cancer.
Ann Surg.
2015; 261(3): 473–9. PubMed Abstract
| Publisher Full Text
65.
Battersby NJ, Dattani M, Rao S, et al.:
A rectal cancer feasibility study with an embedded phase III trial design assessing magnetic resonance tumour regression grade (mrTRG) as a novel biomarker to stratify management by good and poor response to chemoradiotherapy (TRIGGER): study protocol for a randomised controlled trial.
Trials.
2017; 18(1): 394. PubMed Abstract
| Publisher Full Text
| Free Full Text
| F1000 Recommendation
66.
Jalil O, Afaq A, Ganeshan B, et al.:
Magnetic resonance based texture parameters as potential imaging biomarkers for predicting long-term survival in locally advanced rectal cancer treated by chemoradiotherapy.
Colorectal Dis.
2017; 19(4): 349–62. PubMed Abstract
| Publisher Full Text
| F1000 Recommendation
67.
De Cecco CN, Ganeshan B, Ciolina M, et al.:
Texture analysis as imaging biomarker of tumoral response to neoadjuvant chemoradiotherapy in rectal cancer patients studied with 3-T magnetic resonance.
Invest Radiol.
2015; 50(4): 239–45. PubMed Abstract
| Publisher Full Text
68.
Al-Sukhni E, Milot L, Fruitman M, 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. PubMed Abstract
| Publisher Full Text
69.
Taylor FG, Quirke P, Heald RJ, et al.:
Preoperative magnetic resonance imaging assessment of circumferential resection margin predicts disease-free survival and local recurrence: 5-year follow-up results of the MERCURY study.
J Clin Oncol.
2014; 32(1): 34–43. PubMed Abstract
| Publisher Full Text
71.
PACE participants, Audisio RA, Pope D, et al.:
Shall we operate? Preoperative assessment in elderly cancer patients (PACE) can help. A SIOG surgical task force prospective study.
Crit Rev Oncol Hematol.
2008; 65(2): 156–63. PubMed Abstract
| Publisher Full Text
74.
Rao C, Sun Myint A, Athanasiou T, et al.:
Avoiding Radical Surgery in Elderly Patients With Rectal Cancer Is Cost-Effective.
Dis Colon Rectum.
2017; 60(1): 30–42. PubMed Abstract
| Publisher Full Text
| F1000 Recommendation
75.
Smith FM, Rao C, Oliva Perez R, et al.:
Avoiding radical surgery improves early survival in elderly patients with rectal cancer, demonstrating complete clinical response after neoadjuvant therapy: results of a decision-analytic model.
Dis Colon Rectum.
2015; 58(2): 159–71. PubMed Abstract
| Publisher Full Text
76.
Hsu HC, Lapke N, Wang CW, et al.:
Targeted Sequencing of Circulating Tumor DNA to Monitor Genetic Variants and Therapeutic Response in Metastatic Colorectal Cancer.
Mol Cancer Ther.
2018; 17(10): 2238–47. PubMed Abstract
| Publisher Full Text
| F1000 Recommendation
79.
Slattery ML, Mullany LE, Wolff RK, et al.:
The p53-signaling pathway and colorectal cancer: Interactions between downstream p53 target genes and miRNAs.
Genomics.
2018; pii: S0888-7543(18)30036-3. PubMed Abstract
| Publisher Full Text
| F1000 Recommendation
Grass F and Mathis K. Novelties in treatment of locally advanced rectal cancer [version 1; peer review: 3 approved] F1000Research 2018, 7(F1000 Faculty Rev):1868 (https://doi.org/10.12688/f1000research.16194.1)
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Faculty Reviews are commissioned and written by members of the prestigious Faculty Opinions Faculty, and are edited as a service to our readers. In order to make these reviews as comprehensive and accessible as possible, we seek the reviewers’ input before publication. The reviewers’ names and any additional comments they may have are published alongside the review, as is usual on F1000Research.
I confirm that I have read this submission and believe that I have an appropriate level of expertise to confirm that it is of an acceptable scientific standard.
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Competing Interests: No competing interests were disclosed.
Faculty Reviews are commissioned and written by members of the prestigious Faculty Opinions Faculty, and are edited as a service to our readers. In order to make these reviews as comprehensive and accessible as possible, we seek the reviewers’ input before publication. The reviewers’ names and any additional comments they may have are published alongside the review, as is usual on F1000Research.
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