Evidence map›Paper›PMID 25888612›Full record

ArticleAnnals of oncology : official journal of the European Society for Medical Oncology2015

A refined risk stratification scheme for clinical stage 1 NSGCT based on evaluation of both embryonal predominance and lymphovascular invasion.

C A Lago-Hernandez, H Feldman, E O'Donnell, B A Mahal, V Perez, S Howard, M Rosenthal, S C Cheng, P L Nguyen, C Beard and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Annals of oncology : official journal of the European Society for Medical Oncology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 4 pooled it
3.8field-weighted citation impact, top 7% 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

16 citing papers in PubMed, 4 syntheses or guidelines pooled it, 45 citations in OpenAlex.

  1. SEOM-GG clinical guidelines for the management of germ-cell testicular cancer (2023).Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2024
    Guideline
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Article
  6. Article
  7. Testicular Germ-Cell Tumors with Spermatic Cord Involvement: A Retrospective International Multi-Institutional Experience.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2022
    Article
  8. Pathological predictors of metastatic disease in testicular non-seminomatous germ cell tumors: which tumor-node-metastasis staging system?Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2021
    Article
  9. Review
  10. Improving outcomes in germ cell cancers using miRNA.Therapeutic advances in medical oncology · 2021
    Review
  11. Article
  12. Review
  13. Article
  14. Testicular cancer.Nature reviews. Disease primers · 2018
    Review
  15. Review
  16. 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

12 authors at 5 institutions in 2 countries.

C A Lago-HernandezHarvard Medical School, Boston Department of Medical Oncology-Genitourinary Division, Dana-Farber Cancer Institute, Boston.
H FeldmanAlbert Einstein College of Medicine, New York Department of Medical Oncology-Genitourinary Division, Dana-Farber Cancer Institute, Boston.
E O'DonnellDepartment of Medical Oncology-Genitourinary Division, Dana-Farber Cancer Institute, Boston.
B A MahalHarvard Medical School, Boston Department of Radiation Oncology, Dana-Farber Cancer Institute, Boston.
V PerezUniversity of Puerto Rico Medical School, San Juan PR.
S HowardDepartments of Imaging, Dana-Farber Cancer Institute, Boston, USA.
M RosenthalDepartments of Imaging, Dana-Farber Cancer Institute, Boston, USA.
S C ChengBiostatistics/Computational Biology, Dana-Farber Cancer Institute, Boston, USA.
P L NguyenDepartment of Radiation Oncology, Dana-Farber Cancer Institute, Boston.
C BeardDepartment of Radiation Oncology, Dana-Farber Cancer Institute, Boston.
A V D'AmicoDepartment of Radiation Oncology, Dana-Farber Cancer Institute, Boston.
C J SweeneyDepartment of Medical Oncology-Genitourinary Division, Dana-Farber Cancer Institute, Boston christopher_sweeney@dfci.harvard.edu.
Dana-Farber Cancer Institute · USBoston University · USHarvard University · USAlbert Einstein College of Medicine · USUniversity of Puerto Rico, Medical Sciences Campus · PR

Funding

Physician Scientist Training in Cancer ResearchT32CA009172 · NCI · DANA-FARBER CANCER INSTITUTE · PI Jennifer R Brown, James A. DeCaprio · 1985 to 2026
$17.1M
NCI NIH HHS T32 CA009172
6 · The paper itself

Abstract

backgroundActive surveillance is an increasingly accepted approach for managing patients with germ-cell tumors (GCTs) after an orchiectomy. Here we investigate a time-to-relapse stratification scheme for clinical stage 1 (CS1) nonseminoma GCT (NSGCT) patients according to factors associated with relapse and identify a group of patients with a lower frequency and longer time-to-relapse who may require an alternative surveillance strategy. PATIENTS AND

methodsWe analyzed 266 CS1 GCT patients from the IRB-approved DFCI GCT database that exclusively underwent surveillance following orchiectomy from 1997 to 2013. We stratified NSGCT patients according to predominance of embryonal carcinoma (EmbP) and lymphovascular invasion (LVI), using a 0, 1, and 2 scoring system. Cox regression and conditional risk analysis were used to compare each NSGCT group to patients in the seminomatous germ-cell tumor (SGCT) category. Median time-to-relapse values were then calculated among those patients who underwent relapse. Relapse-free survival curves were generated using the Kaplan-Meier method.

resultsFifty (37%) NSGCT and 20 (15%) SGCT patients relapsed. The median time-to-relapse was 11.5 versus 6.3 months for the SGCT and NSGCT groups, respectively. For NSGCT patients, relapse rates were higher and median time-to-relapse faster with increasing number of risk factors (RFs). Relapse rates (%) and median time-to-relapse (months) were 25%/8.5 months, 41%/6.8 months and 78%/3.8 months for RF0, RF1 and RF2, respectively. We found a statistically significant difference between SGCT and patients with one or two RFs (P < 0.001) but not between SGCT and NSGCT RF0 (P = 0.108).

conclusionNSGCT patients grouped by a risk score system based on EmbP and LVI yielded three groups with distinct relapse patterns -and patients with neither EmbP nor LVI appear to behave similar to SGCT.

Indexed as

Risk AssessmentAdolescentAdultAgedCarcinoma, EmbryonalFollow-Up StudiesHumansLymph NodesMaleMiddle AgedNeoplasm InvasivenessNeoplasm Recurrence, LocalNeoplasms, Germ Cell and EmbryonalNeoplasm StagingPopulation SurveillancePrognosisactive surveillanceclinical stage 1embryonal predominancelymphovascular invasionnonseminoma germ-cell tumorrelapse

Identifiers

PMID25888612
PMCPMC4553701
OpenAlexW2138169452

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.