Recent Advances in Pediatric Cancer Predisposition Syndromes

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60

authors

12

articles

Recent Advances in Pediatric Cancer Predisposition Syndromes

144.3K

views

60

authors

12

articles

Editorial

08 March 2021

Editorial: Recent Advances in Pediatric Cancer Predisposition Syndromes

Angela Mastronuzzi

,

Luigi Boccuto

and

Riccardo Masetti

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1 citations

Editors

3

Angela Mastronuzzi

Bambino Gesù Children's Hospital (IRCCS)

Luigi Boccuto

Clemson University

Riccardo Masetti

University of Bologna

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Up to 10% of cancers occur through the inherited mutation of a group of genes called cancer predisposition genes. Individuals who carry a mutant allele of these genes have an increased susceptibility to cancer. A growing number of cancer susceptibility genes are being identified, and the physiopathology of germline mutation-based cancer development is also being elucidated with accumulating clinical and molecular data. More importantly, the identification of familial mutations has become routine practice, which is a perfect example of bench-to-bed translational medicine.

Incorporation of these variants into clinical management algorithms will help refine patient management, and that this will be further improved by the inclusion of other germline variants, such as those that determine the likelihood of benefit or toxicity from anti-neoplastic therapy. Such integrated patient and tumor profiling will be essential if we are to deliver truly precision medicine for cancer patients, but in a similar way to rare germline mutations, we must ensure that we identify and utilize rare somatic mutations with strong predictive and prognostic effects.

Recently, other clinical applications of predisposition genes have been exploited, especially as efficient biomarkers predicting prognosis or response to treatment. This Research Topic will cover all the aspects of pediatrics cancer predisposition syndromes. We welcome the submission of original research articles focusing on:
(i) Strategies to identify germline predisposing variants in familial and sporadic cases, including identification of non-coding and structural variants;
(ii) Approaches to assign significance to variants using in silico and experimental methods;
(iii) Clinical management of variant identification;
(iv) Advancing new concepts in genetic approach for cancer;
(v) Novel diagnostic approaches;
(vi) New potential targeted therapies;
(vii) Clinical trials.

We also welcome the submission of review articles on the use of narrative medicine in pediatric cancer predisposition syndrome within this Research Topic. Translational papers covering different tumors and/or therapeutic strategies will be preferred.

We would like to acknowledge Dr. Giada Del Baldo and Dr. Mariachiara Lodi from IRCCS Bambino Gesù Children’s Hospital have acted as coordinator and have contributed to the preparation of the proposal for this Research Topic.

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Editors

Angela Mastronuzzi

Bambino Gesù Children's Hospital (IRCCS)

Luigi Boccuto

Clemson University

Riccardo Masetti

University of Bologna

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144,258 Total views

114,504 Article views

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Published In

Frontiers in Pediatrics

Pediatric Oncology

Frontiers in Oncology

Pediatric Oncology

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