Evidence map›Paper›PMID 30629084›Full record

ArticleJAMA oncology2019

Assessment of a Watch-and-Wait Strategy for Rectal Cancer in Patients With a Complete Response After Neoadjuvant Therapy.

J Joshua Smith, Paul Strombom, Oliver S Chow, Campbell S Roxburgh, Patricio Lynn, Anne Eaton, Maria Widmar, Karuna Ganesh, Rona Yaeger, Andrea Cercek and 19 more

2 registry-linked trialsOpen access · bronzeAbstract read
In one paragraph

Article in JAMA oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 261 papers, 9 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
261citing papers in PubMed, 9 pooled it
26.9field-weighted citation impact, top 1% of its field
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.

NCT05338866 enrolling by invitationnot on this mapstarted 2022, after this paper: background citation

Chemotherapy Combined With High-dose Radiotherapy for Low Rectal Cancer Using Magnetic Resonance Guided Radiotherapy Linear Accelerator:A Prospective Phase 2 Trial

TypeobservationalSponsorSun Yat-sen UniversityRan2022 to 2033Enrolled58ConditionsRectal CancerArmsMagnetic resonance guided radiotherapy, Chemotherapy
NCT07404228 not yet recruitingnot on this mapstarted 2026, after this paper: background citation

Multidimensional Study Designed to Develop a Methodological Framework Based on MRI Data to Predict Pathological Complete Response (pCR) in Patients With Locally Advanced Rectal Cancer After Neoadjuvant Treatment

TypeobservationalSponsorInstitut du Cancer de Montpellier - Val d'AurelleRan2026 to 2029Enrolled115ConditionsRectal Cancer, Chemoradiotherapy, MriArmsquestionnaire completion
3 · Its place in the literature

Who cites it

261 citing papers in PubMed, 9 syntheses or guidelines pooled it, 583 citations in OpenAlex.

  1. Guideline
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  13. Patient-Reported Outcomes During and After Treatment for Locally Advanced Rectal Cancer in the PROSPECT Trial (Alliance N1048).Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2023
    Trial
  14. Neoadjuvant Chemotherapy, Excision, and Observation for Early Rectal Cancer: The Phase II NEO Trial (CCTG CO.28) Primary End Point Results.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2023
    Trial
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  19. Clinical target volume radiomics from planning CT for pretreatment response prediction  in rectal cancer undergoing chemoradiotherapy.Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al] · 2026
    Article
  20. Conversations in rectal cancer treatment: a qualitative study of multidisciplinary clinician perspective into non-operative management decision-making discussions.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2026
    Article

201 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

29 authors at 2 institutions in 2 countries.

J Joshua SmithDepartment of Surgery, Memorial Sloan Kettering Cancer Center, New York, New York.
Paul StrombomDepartment of Surgery, Memorial Sloan Kettering Cancer Center, New York, New York.
Oliver S ChowDepartment of Surgery, Memorial Sloan Kettering Cancer Center, New York, New York.
Campbell S RoxburghDepartment of Surgery, Memorial Sloan Kettering Cancer Center, New York, New York.
Patricio LynnDepartment of Surgery, Memorial Sloan Kettering Cancer Center, New York, New York.
Anne EatonDepartment of Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York.
Maria WidmarDepartment of Surgery, Memorial Sloan Kettering Cancer Center, New York, New York.
Karuna GaneshDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
Rona YaegerDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
Andrea CercekDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
Martin R WeiserDepartment of Surgery, Memorial Sloan Kettering Cancer Center, New York, New York.
Garrett M NashDepartment of Surgery, Memorial Sloan Kettering Cancer Center, New York, New York.
Jose G GuillemDepartment of Surgery, Memorial Sloan Kettering Cancer Center, New York, New York.
Larissa K F TempleDepartment of Surgery, Memorial Sloan Kettering Cancer Center, New York, New York.
Sree B ChalasaniDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
James L FuquaDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, New York.
Iva PetkovskaDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, New York.
Abraham J WuDepartment of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, New York.
Marsha ReyngoldDepartment of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, New York.
Efsevia VakianiDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Jinru ShiaDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Neil H SegalDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
James D SmithDepartment of Surgery, Memorial Sloan Kettering Cancer Center, New York, New York.
Christopher CraneDepartment of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, New York.
Marc J GollubDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, New York.
Mithat GonenDepartment of Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York.
Leonard B SaltzDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
Julio Garcia-AguilarDepartment of Surgery, Memorial Sloan Kettering Cancer Center, New York, New York.
Philip B PatyDepartment of Surgery, Memorial Sloan Kettering Cancer Center, New York, New York.
Memorial Sloan Kettering Cancer Center · USUniversity of Glasgow · GB

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Investigating L1CAM-dependent stem cell regeneration in metastasisK08CA230213 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI GANESH, KARUNA · 2018 to 2022
$1.3M
National Cancer Institute K08 CA230213National Cancer Institute P30 CA008748NCI NIH HHS K08 CA230213NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

importanceThe watch-and-wait (WW) strategy aims to spare patients with rectal cancer unnecessary resection.

objectiveTo analyze the outcomes of WW among patients with rectal cancer who had a clinical complete response to neoadjuvant therapy. DESIGN, SETTING, AND

participantsThis retrospective case series analysis conducted at a comprehensive cancer center in New York included patients who received a diagnosis of rectal adenocarcinoma between January 1, 2006, and January 31, 2015. The median follow-up was 43 months. Data analyses were conducted from June 1, 2016, to October 1, 2018. EXPOSURES: Patients had a clinical complete response after completing neoadjuvant therapy and agreed to a WW strategy of active surveillance and possible salvage surgery (n = 113), or patients underwent total mesorectal excision and were found to have a pathologic complete response (pCR) at resection (n = 136). MAIN OUTCOMES AND MEASURES: Kaplan-Meier estimates were used for analyses of local regrowth and 5-year rates of overall survival, disease-free survival, and disease-specific survival.

resultsCompared with the 136 patients in the pCR group, the 113 patients in the WW group were older (median [range], 67.2 [32.1-90.9] vs 57.3 [25.0-87.9] years, P < .001) with cancers closer to the anal verge (median [range] height from anal verge, 5.5 [0.0-15.0] vs 7.0 [0.0-13.0] cm). All 22 local regrowths in the WW group were detected on routine surveillance and treated by salvage surgery (20 total mesorectal excisions plus 2 transanal excisions). Pelvic control after salvage surgery was maintained in 20 of 22 patients (91%). No pelvic recurrences occurred in the pCR group. Rectal preservation was achieved in 93 of 113 patients (82%) in the WW group (91 patients with no local regrowths plus 2 patients with local regrowths salvaged with transanal excision). At 5 years, overall survival was 73% (95% CI, 60%-89%) in the WW group and 94% (95% CI, 90%-99%) in the pCR group; disease-free survival was 75% (95% CI, 62%-90%) in the WW group and 92% (95% CI, 87%-98%) in the pCR group; and disease-specific survival was 90% (95% CI, 81%-99%) in the WW group and 98% (95% CI, 95%-100%) in the pCR group. A higher rate of distant metastasis was observed among patients in the WW group who had local regrowth vs those who did not have local regrowth (36% vs 1%, P < .001). CONCLUSIONS AND RELEVANCE: A WW strategy for select rectal cancer patients who had a clinical complete response after neoadjuvant therapy resulted in excellent rectal preservation and pelvic tumor control; however, in the WW group, worse survival was noted along with a higher incidence of distant progression in patients with local regrowth vs those without local regrowth.

Indexed as

Neoadjuvant TherapyWatchful WaitingAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedNeoplasm Recurrence, LocalRectal NeoplasmsRemission InductionRetrospective StudiesTreatment Outcome

Identifiers

PMID30629084
PMCPMC6459120
OpenAlexW2910132967

What OpenQuestion holds

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Registered trials

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.