Radiation‐induced sarcoma of head and neck: Clinical characteristics and molecular signatures
Background Radiation‐induced sarcoma of the head and neck (RISHN) is a rare yet devastating potential complication of radiotherapy treatment. We aimed to evaluate the clinicopathological characteristics and molecular signatures of RISHN in patients who underwent radiotherapy for head and neck cancer...
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Published in | Head & neck Vol. 45; no. 3; pp. 638 - 646 |
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Main Authors | , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Hoboken, USA
John Wiley & Sons, Inc
01.03.2023
Wiley Subscription Services, Inc |
Subjects | |
Online Access | Get full text |
ISSN | 1043-3074 1097-0347 1097-0347 |
DOI | 10.1002/hed.27279 |
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Abstract | Background
Radiation‐induced sarcoma of the head and neck (RISHN) is a rare yet devastating potential complication of radiotherapy treatment. We aimed to evaluate the clinicopathological characteristics and molecular signatures of RISHN in patients who underwent radiotherapy for head and neck cancer (HNC) to identify high‐risk patients and enable earlier cancer detection.
Methods
This study retrospectively evaluated 24 sarcoma patients who received radiotherapy for HNC between 1994 and 2019. Patients were divided into two groups based on RISHN latency period. Patient demographics, initial tumor staging, risk factors, and survival between groups were analyzed, and whole‐exome sequencing (WES) of selected samples was performed.
Results
The median age at diagnosis of RISHN was 54 years, and the male‐to‐female ratio was 2:1. The latency period ranged from 0.8 to 64.4 years (median 6.5 years), with a median survival of 21.5 months. Primary cancer in the oral cavity, treatment with alkylating agents, alcohol consumption, betel nut chewing, and smoking were identified as risk factors for short (<5 years) latency periods. The majority of RISHN cases occurred in the oral cavity (58.3%). WES analysis showed that tumor necrosis factor and cell cycle checkpoint pathways were differentially involved in both patient groups.
Conclusions
Although case numbers were small, our cohort represents the largest case series of RISHN from a single institution to date. Clinicians must be aware of factors affecting RISHN development and latency, and risk factor identification may lead to earlier detection and prevention in the future. |
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AbstractList | Background
Radiation‐induced sarcoma of the head and neck (RISHN) is a rare yet devastating potential complication of radiotherapy treatment. We aimed to evaluate the clinicopathological characteristics and molecular signatures of RISHN in patients who underwent radiotherapy for head and neck cancer (HNC) to identify high‐risk patients and enable earlier cancer detection.
Methods
This study retrospectively evaluated 24 sarcoma patients who received radiotherapy for HNC between 1994 and 2019. Patients were divided into two groups based on RISHN latency period. Patient demographics, initial tumor staging, risk factors, and survival between groups were analyzed, and whole‐exome sequencing (WES) of selected samples was performed.
Results
The median age at diagnosis of RISHN was 54 years, and the male‐to‐female ratio was 2:1. The latency period ranged from 0.8 to 64.4 years (median 6.5 years), with a median survival of 21.5 months. Primary cancer in the oral cavity, treatment with alkylating agents, alcohol consumption, betel nut chewing, and smoking were identified as risk factors for short (<5 years) latency periods. The majority of RISHN cases occurred in the oral cavity (58.3%). WES analysis showed that tumor necrosis factor and cell cycle checkpoint pathways were differentially involved in both patient groups.
Conclusions
Although case numbers were small, our cohort represents the largest case series of RISHN from a single institution to date. Clinicians must be aware of factors affecting RISHN development and latency, and risk factor identification may lead to earlier detection and prevention in the future. Radiation-induced sarcoma of the head and neck (RISHN) is a rare yet devastating potential complication of radiotherapy treatment. We aimed to evaluate the clinicopathological characteristics and molecular signatures of RISHN in patients who underwent radiotherapy for head and neck cancer (HNC) to identify high-risk patients and enable earlier cancer detection. This study retrospectively evaluated 24 sarcoma patients who received radiotherapy for HNC between 1994 and 2019. Patients were divided into two groups based on RISHN latency period. Patient demographics, initial tumor staging, risk factors, and survival between groups were analyzed, and whole-exome sequencing (WES) of selected samples was performed. The median age at diagnosis of RISHN was 54 years, and the male-to-female ratio was 2:1. The latency period ranged from 0.8 to 64.4 years (median 6.5 years), with a median survival of 21.5 months. Primary cancer in the oral cavity, treatment with alkylating agents, alcohol consumption, betel nut chewing, and smoking were identified as risk factors for short (<5 years) latency periods. The majority of RISHN cases occurred in the oral cavity (58.3%). WES analysis showed that tumor necrosis factor and cell cycle checkpoint pathways were differentially involved in both patient groups. Although case numbers were small, our cohort represents the largest case series of RISHN from a single institution to date. Clinicians must be aware of factors affecting RISHN development and latency, and risk factor identification may lead to earlier detection and prevention in the future. Radiation-induced sarcoma of the head and neck (RISHN) is a rare yet devastating potential complication of radiotherapy treatment. We aimed to evaluate the clinicopathological characteristics and molecular signatures of RISHN in patients who underwent radiotherapy for head and neck cancer (HNC) to identify high-risk patients and enable earlier cancer detection.BACKGROUNDRadiation-induced sarcoma of the head and neck (RISHN) is a rare yet devastating potential complication of radiotherapy treatment. We aimed to evaluate the clinicopathological characteristics and molecular signatures of RISHN in patients who underwent radiotherapy for head and neck cancer (HNC) to identify high-risk patients and enable earlier cancer detection.This study retrospectively evaluated 24 sarcoma patients who received radiotherapy for HNC between 1994 and 2019. Patients were divided into two groups based on RISHN latency period. Patient demographics, initial tumor staging, risk factors, and survival between groups were analyzed, and whole-exome sequencing (WES) of selected samples was performed.METHODSThis study retrospectively evaluated 24 sarcoma patients who received radiotherapy for HNC between 1994 and 2019. Patients were divided into two groups based on RISHN latency period. Patient demographics, initial tumor staging, risk factors, and survival between groups were analyzed, and whole-exome sequencing (WES) of selected samples was performed.The median age at diagnosis of RISHN was 54 years, and the male-to-female ratio was 2:1. The latency period ranged from 0.8 to 64.4 years (median 6.5 years), with a median survival of 21.5 months. Primary cancer in the oral cavity, treatment with alkylating agents, alcohol consumption, betel nut chewing, and smoking were identified as risk factors for short (<5 years) latency periods. The majority of RISHN cases occurred in the oral cavity (58.3%). WES analysis showed that tumor necrosis factor and cell cycle checkpoint pathways were differentially involved in both patient groups.RESULTSThe median age at diagnosis of RISHN was 54 years, and the male-to-female ratio was 2:1. The latency period ranged from 0.8 to 64.4 years (median 6.5 years), with a median survival of 21.5 months. Primary cancer in the oral cavity, treatment with alkylating agents, alcohol consumption, betel nut chewing, and smoking were identified as risk factors for short (<5 years) latency periods. The majority of RISHN cases occurred in the oral cavity (58.3%). WES analysis showed that tumor necrosis factor and cell cycle checkpoint pathways were differentially involved in both patient groups.Although case numbers were small, our cohort represents the largest case series of RISHN from a single institution to date. Clinicians must be aware of factors affecting RISHN development and latency, and risk factor identification may lead to earlier detection and prevention in the future.CONCLUSIONSAlthough case numbers were small, our cohort represents the largest case series of RISHN from a single institution to date. Clinicians must be aware of factors affecting RISHN development and latency, and risk factor identification may lead to earlier detection and prevention in the future. BackgroundRadiation‐induced sarcoma of the head and neck (RISHN) is a rare yet devastating potential complication of radiotherapy treatment. We aimed to evaluate the clinicopathological characteristics and molecular signatures of RISHN in patients who underwent radiotherapy for head and neck cancer (HNC) to identify high‐risk patients and enable earlier cancer detection.MethodsThis study retrospectively evaluated 24 sarcoma patients who received radiotherapy for HNC between 1994 and 2019. Patients were divided into two groups based on RISHN latency period. Patient demographics, initial tumor staging, risk factors, and survival between groups were analyzed, and whole‐exome sequencing (WES) of selected samples was performed.ResultsThe median age at diagnosis of RISHN was 54 years, and the male‐to‐female ratio was 2:1. The latency period ranged from 0.8 to 64.4 years (median 6.5 years), with a median survival of 21.5 months. Primary cancer in the oral cavity, treatment with alkylating agents, alcohol consumption, betel nut chewing, and smoking were identified as risk factors for short (<5 years) latency periods. The majority of RISHN cases occurred in the oral cavity (58.3%). WES analysis showed that tumor necrosis factor and cell cycle checkpoint pathways were differentially involved in both patient groups.ConclusionsAlthough case numbers were small, our cohort represents the largest case series of RISHN from a single institution to date. Clinicians must be aware of factors affecting RISHN development and latency, and risk factor identification may lead to earlier detection and prevention in the future. |
Author | Leu, Chih‐Yu Lin, Mei‐Chun Tsai, Mong‐Hsun Chen, Chun‐Nan Yang, Tsung‐Lin Liao, Yu‐Hao Lai, Shih‐Fan Hsieh, Min‐Shu Huang, Yen‐Lin Hsu, Chia‐Lang Lou, Pei‐Jen Chen, Tseng‐Cheng Wang, Cheng‐Ping |
Author_xml | – sequence: 1 givenname: Yu‐Hao surname: Liao fullname: Liao, Yu‐Hao organization: National Taiwan University Hospital Hsin‐Chu Biomedical Park Branch – sequence: 2 givenname: Chia‐Lang surname: Hsu fullname: Hsu, Chia‐Lang organization: National Taiwan University Hospital – sequence: 3 givenname: Chih‐Yu surname: Leu fullname: Leu, Chih‐Yu organization: National Taiwan University – sequence: 4 givenname: Shih‐Fan surname: Lai fullname: Lai, Shih‐Fan organization: National Taiwan University Hospital – sequence: 5 givenname: Yen‐Lin surname: Huang fullname: Huang, Yen‐Lin organization: National Taiwan University Cancer Center – sequence: 6 givenname: Min‐Shu surname: Hsieh fullname: Hsieh, Min‐Shu organization: National Taiwan University Hospital – sequence: 7 givenname: Tseng‐Cheng orcidid: 0000-0002-3360-0382 surname: Chen fullname: Chen, Tseng‐Cheng organization: National Taiwan University Hospital and College of Medicine, National Taiwan University – sequence: 8 givenname: Chun‐Nan orcidid: 0000-0001-9240-0631 surname: Chen fullname: Chen, Chun‐Nan organization: National Taiwan University Hospital and College of Medicine, National Taiwan University – sequence: 9 givenname: Cheng‐Ping surname: Wang fullname: Wang, Cheng‐Ping organization: National Taiwan University Hospital and College of Medicine, National Taiwan University – sequence: 10 givenname: Tsung‐Lin surname: Yang fullname: Yang, Tsung‐Lin organization: National Taiwan University Hospital and College of Medicine, National Taiwan University – sequence: 11 givenname: Mong‐Hsun surname: Tsai fullname: Tsai, Mong‐Hsun organization: Bioinformatics and Biostatistics Core, Center of Genomic and Precision Medicine, National Taiwan University – sequence: 12 givenname: Mei‐Chun orcidid: 0000-0003-1133-6741 surname: Lin fullname: Lin, Mei‐Chun email: mayandjean@gmail.com organization: National Taiwan University Hospital and College of Medicine, National Taiwan University – sequence: 13 givenname: Pei‐Jen orcidid: 0000-0002-3383-8593 surname: Lou fullname: Lou, Pei‐Jen email: pjlou@ntu.edu.tw organization: National Taiwan University Hospital and College of Medicine, National Taiwan University |
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CitedBy_id | crossref_primary_10_1016_j_oraloncology_2025_107216 crossref_primary_10_3389_fonc_2024_1474536 crossref_primary_10_3389_fonc_2024_1413610 |
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Snippet | Background
Radiation‐induced sarcoma of the head and neck (RISHN) is a rare yet devastating potential complication of radiotherapy treatment. We aimed to... Radiation-induced sarcoma of the head and neck (RISHN) is a rare yet devastating potential complication of radiotherapy treatment. We aimed to evaluate the... BackgroundRadiation‐induced sarcoma of the head and neck (RISHN) is a rare yet devastating potential complication of radiotherapy treatment. We aimed to... |
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SubjectTerms | Alkylating agents Cancer Cell cycle Female Head & neck cancer head and neck cancer Head and Neck Neoplasms - complications Head and Neck Neoplasms - genetics Head and Neck Neoplasms - radiotherapy Humans Latency Male Neoplasm Staging Neoplasms, Radiation-Induced - genetics Oral cancer Oral carcinoma Oral cavity Patients Radiation therapy radiation‐induced sarcoma Retrospective Studies Risk factors Sarcoma Soft Tissue Neoplasms - pathology whole exome sequencing |
Title | Radiation‐induced sarcoma of head and neck: Clinical characteristics and molecular signatures |
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