Evidence map›Paper›PMID 21830087›Full record

ArticleInternational journal of clinical oncology2012

18F-fluorodeoxyglucose positron emission tomography optimizes neoadjuvant chemotherapy for primary breast cancer to achieve pathological complete response.

Shigeto Ueda, Toshiaki Saeki, Takashi Shigekawa, Jiro Omata, Tomoyuki Moriya, Junji Yamamoto, Akihiko Osaki, Nobuko Fujiuchi, Misono Misumi, Hideki Takeuchi and 8 more

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Article in International journal of clinical oncology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 21% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 27 citations in OpenAlex.

  1. The accuracy ofEuropean radiology · 2017
    Pooled it
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  4. [La Radiologia medica · 2026
    Review
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  6. Observational
  7. Glycolytic activity with 18F-FDG PET/CT predicts final neoadjuvant chemotherapy response in breast cancer.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2014
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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

18 authors at 5 institutions in 1 country.

Shigeto UedaMedical Service School, National Defense Force, 1-2-24 Ikejiri, Setagaya-ku, Tokyo, 154-0001, Japan.
Toshiaki Saeki
Takashi Shigekawa
Jiro Omata
Tomoyuki Moriya
Junji Yamamoto
Akihiko Osaki
Nobuko Fujiuchi
Misono Misumi
Hideki Takeuchi
Takaki Sakurai
Hitoshi Tsuda
Katsumi Tamura
Jiro Ishida
Yoshiyuki Abe
Etsuko Imabayashi
Ichiei Kuji
Hiroshi Matsuda
Saitama Medical University · JPNational Defense Medical College · JPNational Defense Medical College Hospital · JPSaitama Medical University Hospital · JPTokyo National Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTo assess the usefulness of positron emission tomography combined with computed tomography using (18)F-fluorodeoxyglucose (FDG PET/CT) for optimizing chemotherapy during neoadjuvant chemotherapy for primary breast cancer.

methodsOne hundred and eight patients (110 tumors) with breast cancer (≥2 cm, stages II and III) received neoadjuvant chemotherapy consisting of an anthracycline-based regimen and taxane. The maximal value of the baseline standardized uptake value (SUV) and the change in SUV after four cycles of an anthracycline-based regimen relative to baseline SUV were assessed for predicting pathological complete response (pCR) after sequential taxane.

resultsTumors with pCR had significantly higher baseline SUV (9.3 ± 3.7 SD) compared to those with non-pCR (7.2 ± 3.8 SD) (p = 0.02), but there was a considerable overlap between two groups. On PET scan after four cycles of chemotherapy, thirty-three patients (33.7%) with a 72.1% or greater reduction in SUV were considered as responders and the performance in predicting pCR had a sensitivity of 88.9% and specificity of 78.7%.

conclusionThe baseline SUV could not be a useful indicator for predicting pCR due to the wide range in sensitivity. On the other hand, a relative change in SUV after completion of an anthracycline-based regimen could be useful for predicting pCR.

Indexed as

Fluorodeoxyglucose F18RadiopharmaceuticalsAntineoplastic AgentsBreast NeoplasmsBridged-Ring CompoundsFemaleHumansMiddle AgedNeoadjuvant TherapyPositron-Emission TomographyProspective StudiesTaxoidsTomography, X-Ray ComputedAntineoplastic AgentsBridged-Ring CompoundsFluorodeoxyglucose F18RadiopharmaceuticalstaxaneTaxoids

Identifiers

PMID21830087
OpenAlexW2006745136

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.