Evidence map›Paper›PMID 30830296›Full record

Trial reportJournal of cancer research and clinical oncology2019

Neoadjuvant chemoradiotherapy delivered with helical tomotherapy under daily image guidance for rectal cancer patients: efficacy and safety in a large, multi-institutional series.

Berardino De Bari, Alessandra Franzetti-Pellanda, Asma Saidi, Maira Biggiogero, Dieter Hahnloser, Michael Montemurro, Jean Bourhis, Michele Zeverino, Mahmut Ozsahin

Erratum issuedAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in Journal of cancer research and clinical oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

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

  1. Pooled it
  2. Review
  3. Review
  4. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Berardino De BariRadiation Oncology Department, Centre Hospitalier Universitaire Vaudois, CHUV, 46 rue du Bugnon, 1011, Lausanne, Switzerland. bdebari@chu-besancon.fr.ORCID http://orcid.org/0000-0003-0117-3360
Alessandra Franzetti-PellandaRadiation Oncology Department, Clinica Luganese, 6900, Lugano, Switzerland.
Asma SaidiRadiation Oncology Department, Centre Hospitalier Universitaire Vaudois, CHUV, 46 rue du Bugnon, 1011, Lausanne, Switzerland.
Maira BiggiogeroRadiation Oncology Department, Clinica Luganese, 6900, Lugano, Switzerland.
Dieter HahnloserSurgery Department, Centre Hospitalier Universitaire Vaudois, 1011, Lausanne, Switzerland.
Michael MontemurroMedical Oncology Department, Centre Hospitalier Universitaire Vaudois, 1011, Lausanne, Switzerland.
Jean BourhisRadiation Oncology Department, Centre Hospitalier Universitaire Vaudois, CHUV, 46 rue du Bugnon, 1011, Lausanne, Switzerland.
Michele ZeverinoMedical Physics Department, Centre Hospitalier Universitaire Vaudois, 1011, Lausanne, Switzerland.
Mahmut OzsahinRadiation Oncology Department, Centre Hospitalier Universitaire Vaudois, CHUV, 46 rue du Bugnon, 1011, Lausanne, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeHelical tomotherapy (HT) has been recently introduced in the neoadjuvant treatment of locally advanced rectal cancer. Aim of this study is to report the toxicity and local control rates of a large series of locally advanced rectal cancer patients treated with neoadjuvant chemotherapy and HT under daily image guidance followed by surgery.

methodsData from 117 locally advanced rectal cancer patients treated at two Swiss Radiotherapy departments were collected and analyzed. Radiotherapy consisted of 45 Gy (1.8 Gy/fraction, 5 fractions/week delivered in 5 weeks) to the regional pelvic lymph nodes. Seventy patients also received a simultaneous integrated boost (SIB) up to 50 Gy to the tumor and involved nodes (2 Gy/fraction, 5 fractions/week delivered in 5 weeks). Chemotherapy consisted of capecitabine 825 mg/m

resultsMedian follow-up was 45 months (range 4-90 months). The overall rate of acute grade 2-4 toxicity was 18.8% (n = 22). Four patients (3.4%) presented a grade 3 dermatitis (n = 1) or diarrhea (n = 3), and 1 (0.8%) demonstrated grade 4 rectal toxicity. No patients presented with grade ≥ 3 hematologic toxicity. Six patients (5.1%) had late grade 3 gastrointestinal toxicity. The 4-year local control rate was 88.4% (95% CI 87.5-88.5%).

conclusionsNeoadjuvant chemoradiotherapy delivered with HT under daily image guidance is well tolerated and shows a high 4-year local control rates.

Indexed as

AdultAgedAged, 80 and overAntimetabolites, AntineoplasticCapecitabineChemoradiotherapy, AdjuvantFemaleHumansMaleMiddle AgedNeoadjuvant TherapyNeoplasm StagingRadiotherapy, Image-GuidedRectal NeoplasmsTomography, X-Ray ComputedWhole Body ImagingAntimetabolites, AntineoplasticCapecitabineHelical tomotherapyImage-guided radiotherapyNeoadjuvant chemoradiotherapyRectal cancerToxicity

Identifiers

PMID30830296
PMCPMC6584215

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Registered trials

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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.