Evidence map›Paper›PMID 30973610›Full record

Trial reportJAMA oncology2019

Safety and Feasibility of Using Magnetic Resonance Imaging Criteria to Identify Patients With "Good Prognosis" Rectal Cancer Eligible for Primary Surgery: The Phase 2 Nonrandomized QuickSilver Clinical Trial.

Erin D Kennedy, Marko Simunovic, Kartik Jhaveri, Richard Kirsch, Jim Brierley, Sébastien Drolet, Carl Brown, Patrick M Vos, Wei Xiong, Tony MacLean and 28 more

Abstract readClinical Trial, Phase II
In one paragraph

Trial report in JAMA oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

57 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. Trial
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Early-Onset Colorectal Cancer: From Genetic Discovery to Clinical Innovation.American Society of Clinical Oncology educational book. American Society of Clinical Oncology. Annual Meeting · 2025
    Review
  11. MRI for Rectal Cancer: Updates and Controversies-AJR. American journal of roentgenology · 2025
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

38 authors.

Erin D KennedyDivision of General Surgery, Department of Surgery, Mount Sinai Hospital, Toronto, Ontario, Canada.
Marko SimunovicDepartment of Surgery, Faculty of Health Sciences, McMaster University, Hamilton, Ontario, Canada.
Kartik JhaveriJoint Department of Medical Imaging, University Health Network, Mount Sinai Hospital, Toronto, Ontario, Canada.
Richard KirschDepartment of Pathology and Laboratory Medicine, Mount Sinai Hospital, Toronto, Ontario, Canada.
Jim BrierleyDepartment of Radiation Oncology, Princess Margaret Cancer Centre, Toronto, Ontario, Canada.
Sébastien DroletDepartment of Surgery, Centre Hospitalier Universitaire (CHU) de Quebec, Laval University, Quebec City, Quebec, Canada.
Carl BrownDepartment of Surgery, St Paul's Hospital, Providence Health Care, Vancouver, British Columbia, Canada.
Patrick M VosDepartment of Radiology, St Paul's Hospital, Providence Health Care, Vancouver, British Columbia, Canada.
Wei XiongDepartment of Pathology & Laboratory Medicine, St Paul's Hospital, Vancouver, British Columbia, Canada.
Tony MacLeanDepartment of Surgery, Foothills Medical Centre, University of Calgary, Calgary, Alberta, Canada.
Selliah KanthanDepartment of Surgery, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
Peter StotlandDepartment of Surgery, North York General Hospital, Toronto, Ontario, Canada.
Simon RaphaelDepartment of Pathology and Laboratory Medicine, North York General Hospital, Toronto, Ontario, Canada.
Gil ChowDepartment of Medical Imaging, North York General Hospital, Toronto, Ontario, Canada.
Catherine A O'BrienDepartment of Surgery, University Health Network, Toronto, Ontario, Canada.
Charles ChoDepartment of Radiation Oncology, Southlake Regional Health Centre, Newmarket, Ontario, Canada.
Cathy StreutkerDepartment of Pathology and Laboratory Medicine, St Michael's Hospital, Toronto, Ontario, Canada.
Raimond WongDepartment of Radiation Oncology, McMaster University, Juravinski Cancer Centre, Hamilton, Ontario, Canada.
Selina SchmockerDivision of General Surgery, Department of Surgery, Mount Sinai Hospital, Toronto, Ontario, Canada.
Sender LibermanDepartment of Surgery, McGill University Health Centre (MUHC)-Montreal General Hospital, Montreal, Quebec, Canada.
Caroline ReinholdDepartment of Diagnostic Radiology, MUHC-Montreal General Hospital, Montreal, Quebec, Canada.
Neil KopekDepartment of Radiation Oncology, MUHC-Montreal General Hospital, Montreal, Quebec, Canada.
Victoria MarcusDepartment of Pathology and Laboratory Medicine, MUHC-Montreal General Hospital, Montreal, Quebec, Canada.
Alexandre BouchardDepartment of Surgery, CHU de Quebec, Laval University, Quebec City, Quebec, Canada.
Caroline LavoieDepartment of Radiation Oncology, CHU de Quebec, Laval University, Quebec City, Quebec, Canada.
Stanislas MorinDepartment of Medical Imaging, CHU de Quebec, Laval University, Quebec City, Quebec, Canada.
Martine PérignyDepartment of Pathology and Laboratory Medicine, CHU de Quebec, Laval University, Quebec City, Quebec, Canada.
Ann WrightDepartment of Surgery, Centre Hospitalier Universitaire (CHU) de Quebec, Laval University, Quebec City, Quebec, Canada.
Katerina NeumannDepartment of Surgery, Queen Elizabeth II Health Sciences Centre, Halifax, Nova Scotia, Canada.
Sharon ClarkeDepartment of Diagnostic Radiology, Queen Elizabeth II Health Sciences Centre, Halifax, Nova Scotia, Canada.
Nikhilesh G PatilDepartment of Radiation Oncology, Queen Elizabeth II Health Sciences Centre, Halifax, Nova Scotia, Canada.
Thomas ArnasonDepartment of Pathology & Laboratory Medicine, Queen Elizabeth II Health Sciences Centre, Halifax, Nova Scotia, Canada.
Lara WilliamsDepartment of Surgery, The Ottawa Hospital, Ottawa, Ontario, Canada.
Robin McLeodDepartment of Surgery, University of Toronto, Toronto, Ontario, Canada.
Gina BrownDepartment of Radiology, The Royal Marsden Hospital National Health Service (NHS) Foundation Trust, Surrey, England, United Kingdom.
Alex MathiesonDepartment of Surgery, Eastern Health Authority, Memorial University, St John's, Newfoundland, Canada.
Amandeep PooniDivision of General Surgery, Department of Surgery, Mount Sinai Hospital, Toronto, Ontario, Canada.
Nancy N BaxterDepartment of Surgery, University of Toronto, Toronto, Ontario, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

importanceChemoradiotherapy (CRT), followed by surgery, is the recommended approach for stage II and III rectal cancer. While CRT decreases the risk of local recurrence, it does not improve survival and leads to poorer functional outcomes than surgery alone. Therefore, new approaches to better select patients for CRT are important.

objectiveTo conduct a phase 2 study to evaluate the safety and feasibility of using magnetic resonance imaging (MRI) criteria to select patients with "good prognosis" rectal tumors for primary surgery. DESIGN, SETTING, AND

participantsProspective nonrandomized phase 2 study at 12 high-volume colorectal surgery centers across Canada. From September 30, 2014, to October 21, 2016, a total of 82 patients were recruited for the study. Participants were patients newly diagnosed as having rectal cancer with MRI-predicted good prognosis rectal cancer. The MRI criteria for good prognosis tumors included distance to the mesorectal fascia greater than 1 mm; definite T2, T2/early T3, or definite T3 with less than 5 mm of extramural depth of invasion; and absent or equivocal extramural venous invasion.

interventionsPatients with rectal cancer with MRI-predicted good prognosis tumors underwent primary surgery. MAIN OUTCOMES AND MEASURES: The primary outcome was the proportion of patients with a positive circumferential resection margin (CRM) rate. Assuming a 10% baseline probability of a positive CRM, a sample size of 75 was estimated to yield a 95% CI of ±6.7%.

resultsEighty-two patients (74% male) participated in the study. The median age at the time of surgery was 66 years (range, 37-89 years). Based on MRI, most tumors were midrectal (65% [n = 53]), T2/early T3 (60% [n = 49]), with no suspicious lymph nodes (63% [n = 52]). On final pathology, 91% (n = 75) of tumors were T2 or greater, 29% (n = 24) were node positive, and 59% (n = 48) were stage II or III. The positive CRM rate was 4 of 82 (4.9%; 95% CI, 0.2%-9.6%). CONCLUSIONS AND RELEVANCE: The use of MRI criteria to select patients with good prognosis rectal cancer for primary surgery results in a low rate of positive CRM and suggests that CRT may not be necessary for all patients with stage II and III rectal cancer.

trial registrationISRCTN.com identifier: ISRCTN05107772.

Indexed as

Magnetic Resonance ImagingAdultAgedAged, 80 and overDigestive System Surgical ProceduresFemaleHumansMaleMiddle AgedPrognosisRectal Neoplasms

Identifiers

PMID30973610
PMCPMC6583831

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.