Evidence map›Paper›PMID 26711129›Full record

ArticleSurgery today2016

(18)F-Fluorodeoxyglucose positron emission tomography ((18)F-FDG PET) for the early detection of response to neoadjuvant chemotherapy for locally advanced rectal cancer.

Junichi Nishimura, Junichi Hasegawa, Yoji Ogawa, Hideaki Miwa, Mamoru Uemura, Naotsugu Haraguchi, Taishi Hata, Hirofumi Yamamoto, Ichiro Takemasa, Tsunekazu Mizushima and 3 more

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Article in Surgery today, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 33% 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.

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

2 citing papers in PubMed, 9 citations in OpenAlex.

  1. Trial
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 2 institutions in 1 country.

Junichi NishimuraDepartment of Gastroenterological Surgery, Osaka University, Graduate School of Medicine, Suita, Osaka, Japan.
Junichi HasegawaDepartment of Surgery, Osaka Rosai Hospital, Sakai, Osaka, Japan. j-hasegawa@orh.go.jp.
Yoji OgawaDepartment of Diagnostic Radiology, Hanwa Intelligent Medical Center, Sakai, Osaka, Japan.
Hideaki MiwaDepartment of Pathology, Osaka Rosai Hospital, Sakai, Osaka, Japan.
Mamoru UemuraDepartment of Gastroenterological Surgery, Osaka University, Graduate School of Medicine, Suita, Osaka, Japan.
Naotsugu HaraguchiDepartment of Gastroenterological Surgery, Osaka University, Graduate School of Medicine, Suita, Osaka, Japan.
Taishi HataDepartment of Gastroenterological Surgery, Osaka University, Graduate School of Medicine, Suita, Osaka, Japan.
Hirofumi YamamotoDepartment of Gastroenterological Surgery, Osaka University, Graduate School of Medicine, Suita, Osaka, Japan.
Ichiro TakemasaDepartment of Gastroenterological Surgery, Osaka University, Graduate School of Medicine, Suita, Osaka, Japan.
Tsunekazu MizushimaDepartment of Gastroenterological Surgery, Osaka University, Graduate School of Medicine, Suita, Osaka, Japan.
Riichiro NezuDepartment of Surgery, Osaka Rosai Hospital, Sakai, Osaka, Japan.
Yuichiro DokiDepartment of Gastroenterological Surgery, Osaka University, Graduate School of Medicine, Suita, Osaka, Japan.
Masaki MoriDepartment of Gastroenterological Surgery, Osaka University, Graduate School of Medicine, Suita, Osaka, Japan.
Osaka University · JPOsaka Rosai Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeEarly detection of a response to neoadjuvant chemotherapy for locally advanced rectal cancer may spare patients from additional toxic but ineffective chemotherapy. Using (18)F-fluorodeoxyglucose positron emission tomography ((18)F-FDG PET), we evaluated tumor response prospectively in the early course of preoperative chemotherapy.

methodsThe subjects were 15 patients who received neoadjuvant chemotherapy (XELOX or XELOX plus bevacizumab) for locally advanced rectal cancer. Patients underwent (18)F-FDG PET before chemotherapy, at the end of the first cycle of chemotherapy, and before surgical resection. Magnetic resonance imaging (MRI) was performed before chemotherapy, after the second cycle of chemotherapy, and before resection. After resection, the SUVmax and diameter were compared and graded according to the tumor regression grade (TRG).

resultsThe TRG was assessed as TRG1 in one patient, TRG2 in five patients, and TRG3 in nine patients. We divided the patients into two groups: non-responders (NR) included the TRG1 and TRG2 patients, and responders (R) included the TRG3 patients. The tumor size before surgery was significantly smaller in the R group than in the NR group. The SUVmax at the end of the first cycle of chemotherapy and before surgical resection was significantly lower in the R group than in the NR group.

conclusionPerforming (18)F-FDG PET at the end of the first cycle of chemotherapy allowed us to predict the pathological response of locally advanced rectal cancer.

Indexed as

Chemotherapy, AdjuvantFluorine RadioisotopesFluorodeoxyglucose F18Neoadjuvant TherapyPositron-Emission TomographyPreoperative CareRadiopharmaceuticalsAgedDigestive System Surgical ProceduresFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedNeoplasm StagingProspective StudiesFluorine RadioisotopesFluorodeoxyglucose F18RadiopharmaceuticalsFDG-PETNeoadjuvant chemotherapyRectal cancer

Identifiers

PMID26711129
OpenAlexW2202304535

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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.