Salivary Dysfunctions and Conséquences After RadioiodineTreatment for Thyroid Cancer: Protocol for a Self-Controlled Study(START Study)

Background: Following radioiodine (131I) therapy of differentiated thyroid cancer, salivary glands may become inflamed, leading to dysfunctions, then leading to decreases in patients’ nutrition and quality of life. The incidence of these dysfunctions after 131I-therapy is poorly known, and no clinic...

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Veröffentlicht in:JMIR research protocols 2022-07, Vol.11
Hauptverfasser: Baudin, Clemence, Lussey-Lepoutre, Charlotte, Bressand, Alice, Buffet, Camille, Menegaux, Fabrice, Soret, Marine, Broggio, David, Bassinet, Celine, Huet, Christelle, Armengol, Gemma, Leenhardt, Laurence, Bernier, Marie Odile
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container_title JMIR research protocols
container_volume 11
creator Baudin, Clemence
Lussey-Lepoutre, Charlotte
Bressand, Alice
Buffet, Camille
Menegaux, Fabrice
Soret, Marine
Broggio, David
Bassinet, Celine
Huet, Christelle
Armengol, Gemma
Leenhardt, Laurence
Bernier, Marie Odile
description Background: Following radioiodine (131I) therapy of differentiated thyroid cancer, salivary glands may become inflamed, leading to dysfunctions, then leading to decreases in patients’ nutrition and quality of life. The incidence of these dysfunctions after 131I-therapy is poorly known, and no clinical or genetic factors have been identified to date to define patients at risk, allowing the delivered activity to be adapted to the expected risk of salivary dysfunctions.Objective: this study aims to estimate the incidence of salivary dysfunctions after 131I-therapy, to characterize patients at risk of developing post-treatment dysfunctions using clinical, biomolecular and biochemical factors, and to validate a dosimetric method to calculate the dose received at the salivary gland level in order to analyze the dose response relationship between absorbed doses to salivary glands and salivary dysfunctions.Methods: This prospective cohort aims to include patients for whom a 131I-therapy is indicated within the treatment of their differentiated thyroid cancer in a Paris hospital (40 and 80 patients in a 1.1 GBq and a 3.7 GBq groups respectively). The follow-up is based on 3 scheduled visits: at inclusion (T0, immediately before 131I-therapy), 6 months (T6) and 18 months (T18) after treatment. For each visit, questionnaires on salivary dysfunctions (validated French tool), quality of life (HAD-scale, MOS-SF-36), and nutritional status are administered by a trained clinical research associate. At T0 and at T6, saliva samples and individual measurement of the salivary flow, without and with salivary glands stimulation, are performed. External thermoluminescent dosimeters are positioned on the skin opposite the salivary glands and at the sternal fork immediately before radioiodine administration and removed 5 days after treatment. From dosimeters, an estimation of the dose received at the salivary glands will be performed using physical and computational phantoms.Genetic and epigenetic analyses will be performed in order to look for potential biomarkers of predisposition to develop salivary dysfunctions after 131I-therapy.Results: 139 patients (71% women, mean age=47.4 (±14.3) years old) were included between September 2020 and April 2021 (45 and 94 patients in 1.1GBq and 3.7GBq groups respectively). The 6-months follow-up is still ongoing, and the 18-months follow-up will start in February 2022. Statistical analyses will study the links between salivary dysfunctions a
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The incidence of these dysfunctions after 131I-therapy is poorly known, and no clinical or genetic factors have been identified to date to define patients at risk, allowing the delivered activity to be adapted to the expected risk of salivary dysfunctions.Objective: this study aims to estimate the incidence of salivary dysfunctions after 131I-therapy, to characterize patients at risk of developing post-treatment dysfunctions using clinical, biomolecular and biochemical factors, and to validate a dosimetric method to calculate the dose received at the salivary gland level in order to analyze the dose response relationship between absorbed doses to salivary glands and salivary dysfunctions.Methods: This prospective cohort aims to include patients for whom a 131I-therapy is indicated within the treatment of their differentiated thyroid cancer in a Paris hospital (40 and 80 patients in a 1.1 GBq and a 3.7 GBq groups respectively). The follow-up is based on 3 scheduled visits: at inclusion (T0, immediately before 131I-therapy), 6 months (T6) and 18 months (T18) after treatment. For each visit, questionnaires on salivary dysfunctions (validated French tool), quality of life (HAD-scale, MOS-SF-36), and nutritional status are administered by a trained clinical research associate. At T0 and at T6, saliva samples and individual measurement of the salivary flow, without and with salivary glands stimulation, are performed. External thermoluminescent dosimeters are positioned on the skin opposite the salivary glands and at the sternal fork immediately before radioiodine administration and removed 5 days after treatment. From dosimeters, an estimation of the dose received at the salivary glands will be performed using physical and computational phantoms.Genetic and epigenetic analyses will be performed in order to look for potential biomarkers of predisposition to develop salivary dysfunctions after 131I-therapy.Results: 139 patients (71% women, mean age=47.4 (±14.3) years old) were included between September 2020 and April 2021 (45 and 94 patients in 1.1GBq and 3.7GBq groups respectively). The 6-months follow-up is still ongoing, and the 18-months follow-up will start in February 2022. Statistical analyses will study the links between salivary dysfunctions and absorbed doses to the salivary glands, taking into account associated factors. In addition, impacts on the patients' quality of life will be analyzed.Conclusions: To our knowledge, this study is the first to investigate the risk of salivary dysfunctions (using both objective and subjective indicators) in relation to organ (salivary glands) doses, based on individual dosimeter records and dose reconstructions. 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The incidence of these dysfunctions after 131I-therapy is poorly known, and no clinical or genetic factors have been identified to date to define patients at risk, allowing the delivered activity to be adapted to the expected risk of salivary dysfunctions.Objective: this study aims to estimate the incidence of salivary dysfunctions after 131I-therapy, to characterize patients at risk of developing post-treatment dysfunctions using clinical, biomolecular and biochemical factors, and to validate a dosimetric method to calculate the dose received at the salivary gland level in order to analyze the dose response relationship between absorbed doses to salivary glands and salivary dysfunctions.Methods: This prospective cohort aims to include patients for whom a 131I-therapy is indicated within the treatment of their differentiated thyroid cancer in a Paris hospital (40 and 80 patients in a 1.1 GBq and a 3.7 GBq groups respectively). The follow-up is based on 3 scheduled visits: at inclusion (T0, immediately before 131I-therapy), 6 months (T6) and 18 months (T18) after treatment. For each visit, questionnaires on salivary dysfunctions (validated French tool), quality of life (HAD-scale, MOS-SF-36), and nutritional status are administered by a trained clinical research associate. At T0 and at T6, saliva samples and individual measurement of the salivary flow, without and with salivary glands stimulation, are performed. External thermoluminescent dosimeters are positioned on the skin opposite the salivary glands and at the sternal fork immediately before radioiodine administration and removed 5 days after treatment. From dosimeters, an estimation of the dose received at the salivary glands will be performed using physical and computational phantoms.Genetic and epigenetic analyses will be performed in order to look for potential biomarkers of predisposition to develop salivary dysfunctions after 131I-therapy.Results: 139 patients (71% women, mean age=47.4 (±14.3) years old) were included between September 2020 and April 2021 (45 and 94 patients in 1.1GBq and 3.7GBq groups respectively). The 6-months follow-up is still ongoing, and the 18-months follow-up will start in February 2022. Statistical analyses will study the links between salivary dysfunctions and absorbed doses to the salivary glands, taking into account associated factors. In addition, impacts on the patients' quality of life will be analyzed.Conclusions: To our knowledge, this study is the first to investigate the risk of salivary dysfunctions (using both objective and subjective indicators) in relation to organ (salivary glands) doses, based on individual dosimeter records and dose reconstructions. The results will allow the identification of patients at risk of salivary dysfunctions, and thus to propose to clinicians a more adapted follow-up and/or countermeasures to adverse effects.</description><subject>Life Sciences</subject><issn>1929-0748</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNqVjk1OwzAQhS0kJCrIHbyki0ASkzhhFxVQF12gxvtoFNuqkesB26mUG3AVzsHFMD8XYDbz6c17T0NIVhY3Vdk1t6yum_qMrMqu6vKC37UXJAvhpUjTct5VzYq8D2DNCfxCH5agZzdFgy5QcJJuEnx-vM3KTSrQXkfl6R6kQYPSOCW8gnhULlKNnorD4tGkECS3v6fPHiNOaH-OQAdldZ4Ko0drlaRDnOVyPYh-L355fUXONdigsr99SdZPj2KzzQ9gx1dvjunHEcGM2343fmsF4w1rGT-V7D_eL6YgWs0</recordid><startdate>202207</startdate><enddate>202207</enddate><creator>Baudin, Clemence</creator><creator>Lussey-Lepoutre, Charlotte</creator><creator>Bressand, Alice</creator><creator>Buffet, Camille</creator><creator>Menegaux, Fabrice</creator><creator>Soret, Marine</creator><creator>Broggio, David</creator><creator>Bassinet, Celine</creator><creator>Huet, Christelle</creator><creator>Armengol, Gemma</creator><creator>Leenhardt, Laurence</creator><creator>Bernier, Marie Odile</creator><general>JMIR publications</general><scope>1XC</scope><scope>VOOES</scope><orcidid>https://orcid.org/0000-0002-5642-2208</orcidid><orcidid>https://orcid.org/0000-0001-8118-8268</orcidid><orcidid>https://orcid.org/0000-0001-5807-4596</orcidid><orcidid>https://orcid.org/0000-0002-2240-1548</orcidid><orcidid>https://orcid.org/0000-0002-0097-7765</orcidid><orcidid>https://orcid.org/0000-0002-4037-5048</orcidid><orcidid>https://orcid.org/0000-0001-5807-4596</orcidid><orcidid>https://orcid.org/0000-0002-0097-7765</orcidid><orcidid>https://orcid.org/0000-0002-5642-2208</orcidid><orcidid>https://orcid.org/0000-0002-4037-5048</orcidid><orcidid>https://orcid.org/0000-0001-8118-8268</orcidid><orcidid>https://orcid.org/0000-0002-2240-1548</orcidid></search><sort><creationdate>202207</creationdate><title>Salivary Dysfunctions and Conséquences After RadioiodineTreatment for Thyroid Cancer: Protocol for a Self-Controlled Study(START Study)</title><author>Baudin, Clemence ; Lussey-Lepoutre, Charlotte ; Bressand, Alice ; Buffet, Camille ; Menegaux, Fabrice ; Soret, Marine ; Broggio, David ; Bassinet, Celine ; Huet, Christelle ; Armengol, Gemma ; Leenhardt, Laurence ; Bernier, Marie Odile</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-hal_primary_oai_HAL_hal_03763837v13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Life Sciences</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Baudin, Clemence</creatorcontrib><creatorcontrib>Lussey-Lepoutre, Charlotte</creatorcontrib><creatorcontrib>Bressand, Alice</creatorcontrib><creatorcontrib>Buffet, Camille</creatorcontrib><creatorcontrib>Menegaux, Fabrice</creatorcontrib><creatorcontrib>Soret, Marine</creatorcontrib><creatorcontrib>Broggio, David</creatorcontrib><creatorcontrib>Bassinet, Celine</creatorcontrib><creatorcontrib>Huet, Christelle</creatorcontrib><creatorcontrib>Armengol, Gemma</creatorcontrib><creatorcontrib>Leenhardt, Laurence</creatorcontrib><creatorcontrib>Bernier, Marie Odile</creatorcontrib><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><jtitle>JMIR research protocols</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Baudin, Clemence</au><au>Lussey-Lepoutre, Charlotte</au><au>Bressand, Alice</au><au>Buffet, Camille</au><au>Menegaux, Fabrice</au><au>Soret, Marine</au><au>Broggio, David</au><au>Bassinet, Celine</au><au>Huet, Christelle</au><au>Armengol, Gemma</au><au>Leenhardt, Laurence</au><au>Bernier, Marie Odile</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Salivary Dysfunctions and Conséquences After RadioiodineTreatment for Thyroid Cancer: Protocol for a Self-Controlled Study(START Study)</atitle><jtitle>JMIR research protocols</jtitle><date>2022-07</date><risdate>2022</risdate><volume>11</volume><eissn>1929-0748</eissn><abstract>Background: Following radioiodine (131I) therapy of differentiated thyroid cancer, salivary glands may become inflamed, leading to dysfunctions, then leading to decreases in patients’ nutrition and quality of life. The incidence of these dysfunctions after 131I-therapy is poorly known, and no clinical or genetic factors have been identified to date to define patients at risk, allowing the delivered activity to be adapted to the expected risk of salivary dysfunctions.Objective: this study aims to estimate the incidence of salivary dysfunctions after 131I-therapy, to characterize patients at risk of developing post-treatment dysfunctions using clinical, biomolecular and biochemical factors, and to validate a dosimetric method to calculate the dose received at the salivary gland level in order to analyze the dose response relationship between absorbed doses to salivary glands and salivary dysfunctions.Methods: This prospective cohort aims to include patients for whom a 131I-therapy is indicated within the treatment of their differentiated thyroid cancer in a Paris hospital (40 and 80 patients in a 1.1 GBq and a 3.7 GBq groups respectively). The follow-up is based on 3 scheduled visits: at inclusion (T0, immediately before 131I-therapy), 6 months (T6) and 18 months (T18) after treatment. For each visit, questionnaires on salivary dysfunctions (validated French tool), quality of life (HAD-scale, MOS-SF-36), and nutritional status are administered by a trained clinical research associate. At T0 and at T6, saliva samples and individual measurement of the salivary flow, without and with salivary glands stimulation, are performed. External thermoluminescent dosimeters are positioned on the skin opposite the salivary glands and at the sternal fork immediately before radioiodine administration and removed 5 days after treatment. From dosimeters, an estimation of the dose received at the salivary glands will be performed using physical and computational phantoms.Genetic and epigenetic analyses will be performed in order to look for potential biomarkers of predisposition to develop salivary dysfunctions after 131I-therapy.Results: 139 patients (71% women, mean age=47.4 (±14.3) years old) were included between September 2020 and April 2021 (45 and 94 patients in 1.1GBq and 3.7GBq groups respectively). The 6-months follow-up is still ongoing, and the 18-months follow-up will start in February 2022. Statistical analyses will study the links between salivary dysfunctions and absorbed doses to the salivary glands, taking into account associated factors. In addition, impacts on the patients' quality of life will be analyzed.Conclusions: To our knowledge, this study is the first to investigate the risk of salivary dysfunctions (using both objective and subjective indicators) in relation to organ (salivary glands) doses, based on individual dosimeter records and dose reconstructions. 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title Salivary Dysfunctions and Conséquences After RadioiodineTreatment for Thyroid Cancer: Protocol for a Self-Controlled Study(START Study)
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