Evidence map›Paper›PMID 39507757›Full record

ReviewFrontiers in oncology2024

Establishment of a clinical cancer genetics program for breast cancer in a resource-limited country; challenges and opportunities.

Hikmat Abdel-Razeq, Baha Sharaf, Faris Tamimi, Hira Bani Hani, Osama Alsmadi, Hanan Khalil, Mahmoud Abunasser, Sarah Edaily, Asem Mansour

Abstract readReview
In one paragraph

Review in Frontiers in oncology, 2024. 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. Review
  2. Article
  3. Review
  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

9 authors.

Hikmat Abdel-RazeqDepartment of Internal Medicine, King Hussein Cancer Center, Amman, Jordan.
Baha SharafDepartment of Internal Medicine, King Hussein Cancer Center, Amman, Jordan.
Faris TamimiDepartment of Internal Medicine, King Hussein Cancer Center, Amman, Jordan.
Hira Bani HaniDepartment of Internal Medicine, King Hussein Cancer Center, Amman, Jordan.
Osama AlsmadiDepartment of Cell Therapy and Applied Genomics, King Hussein Cancer Center, Amman, Jordan.
Hanan KhalilDepartment of Internal Medicine, King Hussein Cancer Center, Amman, Jordan.
Mahmoud AbunasserDepartment of Internal Medicine, King Hussein Cancer Center, Amman, Jordan.
Sarah EdailyDepartment of Internal Medicine, King Hussein Cancer Center, Amman, Jordan.
Asem MansourDepartment of Radiology, King Hussein Cancer Center, Amman, Jordan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast cancer is the most common cancer among women worldwide, and its incidence rate is still increasing, especially among younger women. Nationally, it constitutes one-fifth of all cancer cases and almost 40% of all female cancers. With a median age of 51 years, breast cancer is diagnosed at least a decade earlier, and at more advanced stages compared to Western societies. Hereditary cancers account for 10% or more of all cancer burden worldwide. With expanded indications, increased number of genes tested, and significant decline in cost of testing, such proportion will probably increase. Individuals with pathogenic variants of

Indexed as

BRCAclinical cancer genetics programgermline mutationinherited breast cancerlow-income countries

Identifiers

PMID39507757
PMCPMC11537866

What OpenQuestion holds

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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.