Evidence map›Paper›PMID 36119824›Full record

ArticleAmerican journal of cancer research2022

Improving the prognostic ability of PET/CT SUVmax to identify follicular lymphoma with early treatment failure.

Xin Wan, Wei Guo, Xingtong Wang, Jia Li, Yangzhi Zhao, Xiaomeng Feng, Ken H Young, Ou Bai

Abstract read
In one paragraph

Article in American journal of cancer research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–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. Article
  2. Prognostic value ofQuantitative imaging in medicine and surgery · 2024
    Article
  3. Duodenal-type follicular lymphoma inAmerican journal of nuclear medicine and molecular imaging · 2023
    Article
  4. Article
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

8 authors.

Xin WanDepartment of Hematology, The First Hospital of Jilin University Jilin, China.
Wei GuoDepartment of Hematology, The First Hospital of Jilin University Jilin, China.
Xingtong WangDepartment of Hematology, The First Hospital of Jilin University Jilin, China.
Jia LiDepartment of Hematology, The First Hospital of Jilin University Jilin, China.
Yangzhi ZhaoDepartment of Hematology, The First Hospital of Jilin University Jilin, China.
Xiaomeng FengDepartment of Hematology, The First Hospital of Jilin University Jilin, China.
Ken H YoungDivision of Hematopathology, Department of Pathology, Duke University Medical Center and Duke Cancer Institute Durham, NC, USA.
Ou BaiDepartment of Hematology, The First Hospital of Jilin University Jilin, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Follicular lymphoma (FL) has a high degree of heterogeneity both clinically and molecularly. Early treatment failure (ETF), progression or relapse within 24 months of frontline immunochemotherapy is associated with a poor prognosis in FL. However, the clinical utility of ETF at diagnosis is limited. The maximum standardized uptake value (SUVmax) is a metabolic parameter for positron emission tomography/computed tomography (PET/CT); nevertheless, the relationship between SUVmax and ETF remains unclear. Thus, identifying early biomarkers that incorporate SUVmax and other clinical correlative variables could be helpful in identifying patients at high risk of ETF. A nomogram consisted of three independent variables, including SUVmax ≥ 12, beta-2 microglobulin > 3 mg/L, and Ki67 > 40%, was established to predict ETF in 127 patients with grade 1, 2, or 3a FL from the First Hospital of Jilin University (training cohort) and was validated using data from the Duke University Medical Center (validation cohort, n=95). The nomogram demonstrated prognostic accuracy in predicting ETF (sensitivity 70.8% and specificity 83.5% in the training cohort; sensitivity 84.2% and specificity 68.4% in the validation cohort). The patients were stratified into three groups: low-, intermediate-, and high-risk. In the training cohort, the corresponding 5-year progression-free survival (PFS) rates were 81.7%, 73.4%, and 34.9%, and the 5-year overall survival (OS) rates were 97.4%, 87.4%, and 62.3%, respectively. In the validation cohort, the 5-year PFS rates were 77.7%, 52.9%, and 34.8%, and the 5-year OS rates were 96.4%, 94.1%, and 73.7%, respectively. This was the first study to use a nomogram with SUVmax to predict ETF in FL to identify a subset of patients who might benefit from individualized targeted therapy.

Indexed as

early treatment failureFollicular lymphomanomogramPET/CTSUVmax

Identifiers

PMID36119824
PMCPMC9442020

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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.