Evidence map›Paper›PMID 39874007›Full record

ArticleAsian Pacific journal of cancer prevention : APJCP2025

Analyzing Secondary Cancer Risk: A Machine Learning Approach.

Erfan Hatamabadi Farahani, Hossein Sadeghi, Fatemeh Seif, Mahdi Azad Marzabadi, Reza Rezaee

Abstract read
In one paragraph

Article in Asian Pacific journal of cancer prevention : APJCP, 2025. 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

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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.

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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

5 authors.

Erfan Hatamabadi FarahaniDepartment of Physics, Faculty of Sciences, Arak University, Arak, Iran.
Hossein SadeghiDepartment of Physics, Faculty of Sciences, Arak University, Arak, Iran.
Fatemeh SeifDepartment of Radiotherapy and Medical Physics, Arak University of Medical Sciences and Khansari Hospital, Arak, Iran.
Mahdi Azad MarzabadiDepartment of Physics, Faculty of Sciences, Arak University, Arak, Iran.
Reza RezaeeDepartment of Physics, Faculty of Sciences, Arak University, Arak, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveAddressing the rising cancer rates through timely diagnosis and treatment is crucial. Additionally, cancer survivors need to understand the potential risk of developing secondary cancer (SC), which can be influenced by several factors including treatment modalities, lifestyle choices, and habits such as smoking and alcohol consumption. This study aims to establish a novel relationship using linear regression models between dose and the risk of SC, comparing different prediction methods for lung, colon, and breast cancer.

methodsMachine learning (ML) models have demonstrated their usefulness in forecasting the likelihood of SC risks based on effective doses in the organ. Linear regression analysis is a widely utilized technique for examining the relationship between predictor variables and continuous responses, particularly in scenarios with limited sample sizes. This study employs linear regression models to analyze the relationship between effective dose and the risk of SC, comparing different prediction methods across lung, colon, and breast cancer.

resultThe results indicate that the risk of SC increases with the effective dose in the organ. The linear regression model provides coefficients that mirror the radiation sensitivity of the specific organ, demonstrating the model's effectiveness in predicting SC risk based on dose.

conclusionThe study highlights the significance of using linear regression models to predict the risk of SC based on effective doses in the organ. The findings underscore the importance of considering the radiation sensitivity of specific organs in SC risk prediction, which can aid in better understanding and managing the long-term health of cancer survivors.

Indexed as

Breast NeoplasmsColonic NeoplasmsLung NeoplasmsMachine LearningNeoplasms, Second PrimaryCancer SurvivorsFemaleHumansLinear ModelsPrognosisRisk AssessmentRisk FactorsDecision treesMachine LearningPrecision medicineRadiation dosage

Identifiers

PMID39874007
PMCPMC12082399

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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.