Taste disorders following cancer treatment: report of a case series
Purpose To present the findings of combined oral assessment and gustometry testing of a series of head and neck and hematologic malignancies in patients with self-reported taste change after cytotoxic therapies. Methods Patients with acute myeloid leukemia (AML), multiple myeloma (MM), and head and...
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creator | Epstein, Joel B. de Andrade e Silva, Safira Marques Epstein, Geena L. Leal, Jorge Henrique Santos Barasch, Andrei Smutzer, Gregory |
description | Purpose
To present the findings of combined oral assessment and gustometry testing of a series of head and neck and hematologic malignancies in patients with self-reported taste change after cytotoxic therapies.
Methods
Patients with acute myeloid leukemia (AML), multiple myeloma (MM), and head and neck cancer (HNC) were evaluated for taste function. Chemical gustometry was conducted assessing chemosensory qualities that included sweet, sour, salty, bitter, umami, and spicy. NCI Common Terminology Criteria for Adverse Events (CTCAE) 4.0 and the Scale of Subjective Total Taste Acuity (STTA) were used to describe taste symptoms. Saliva flow rates were measured to determine the presence of hyposalivation. Patients were provided treatment trials for taste dysfunction, including zinc supplements, or medications that included clonazepam, megestrol acetate, and the cannabinoid dronabinol.
Results
According to STTA, hematology cases reported the incidence of grades 2 and 3 taste disturbances as 60% and 40%, respectively. For HNC patients, the incidence of grades 2 and 3 was 44% each. Gustometry tests confirmed dysgeusia in all patients evaluated. In the hematology group, 80% of patients exhibited a decrease in sweet taste perception, and no patients correctly identified umami taste. In the HNC group, most patients could not identify salt taste, 66% of patients reported “no sensation” with spicy taste, bitter taste was reduced in some, and increased or altered in others, while only one patient could identify umami taste. In the hematologic and HNC patient groups, 80% and 66% reported grade 2 dry mouth, respectively, according to CTCAE 4.0. After treatment for taste dysfunction, 71% of all patients in the present study reported improvements in taste function.
Conclusions
Persisting dysgeusia in cancer survivors may be assessed by patient report and taste testing. The taste most affected in our patients was umami. Treatment trials with current interventions for dysgeusia appeared effective and should be considered in cancer survivors. Understanding taste and flavor function during and following cancer treatment is important in developing rational prospective preventive and interventional strategies. |
doi_str_mv | 10.1007/s00520-019-04758-5 |
format | Article |
fullrecord | <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_miscellaneous_2200783232</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A604563289</galeid><sourcerecordid>A604563289</sourcerecordid><originalsourceid>FETCH-LOGICAL-c508t-707f4a6a9a36ec3082533380b44caeae83ba619063af8b2fb5eff5b4f3879d723</originalsourceid><addsrcrecordid>eNp9kUGLFDEQhYMo7uzqH_AgDV689FpJJZ3E2zLoKix4Wc8hna4MvXR3xqQH8d9vxlldFJEcClLfe1TVY-wVh0sOoN8VACWgBW5bkFqZVj1hGy4RW41on7INWMlbiUqdsfNS7gC41ko8Z2cIVmjOccO2t76s1AxjSXmgXJqYpil9H5ddE_wSKDdrJr_OtKzvm0z7lNcmxcbXbqGmUB6pvGDPop8KvXyoF-zrxw-320_tzZfrz9urmzYoMGurQUfpO289dhQQjFCIaKCXMnjyZLD3HbfQoY-mF7FXFKPqZUSj7aAFXrC3J999Tt8OVFY3jyXQNPmF0qE4IepVDAo8om_-Qu_SIS91Oie4tR0HLbpHaucncuMS05p9OJq6qw6k6lAYW6nLf1D1DTSPIS0Ux_r_h0CcBCGnUjJFt8_j7PMPx8Edk3On5FxNzv1Mzqkqev0w8aGfafgt-RVVBfAElNpadpQfV_qP7T3QYaC3</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2199610726</pqid></control><display><type>article</type><title>Taste disorders following cancer treatment: report of a case series</title><source>SpringerLink (Online service)</source><creator>Epstein, Joel B. ; de Andrade e Silva, Safira Marques ; Epstein, Geena L. ; Leal, Jorge Henrique Santos ; Barasch, Andrei ; Smutzer, Gregory</creator><creatorcontrib>Epstein, Joel B. ; de Andrade e Silva, Safira Marques ; Epstein, Geena L. ; Leal, Jorge Henrique Santos ; Barasch, Andrei ; Smutzer, Gregory</creatorcontrib><description>Purpose
To present the findings of combined oral assessment and gustometry testing of a series of head and neck and hematologic malignancies in patients with self-reported taste change after cytotoxic therapies.
Methods
Patients with acute myeloid leukemia (AML), multiple myeloma (MM), and head and neck cancer (HNC) were evaluated for taste function. Chemical gustometry was conducted assessing chemosensory qualities that included sweet, sour, salty, bitter, umami, and spicy. NCI Common Terminology Criteria for Adverse Events (CTCAE) 4.0 and the Scale of Subjective Total Taste Acuity (STTA) were used to describe taste symptoms. Saliva flow rates were measured to determine the presence of hyposalivation. Patients were provided treatment trials for taste dysfunction, including zinc supplements, or medications that included clonazepam, megestrol acetate, and the cannabinoid dronabinol.
Results
According to STTA, hematology cases reported the incidence of grades 2 and 3 taste disturbances as 60% and 40%, respectively. For HNC patients, the incidence of grades 2 and 3 was 44% each. Gustometry tests confirmed dysgeusia in all patients evaluated. In the hematology group, 80% of patients exhibited a decrease in sweet taste perception, and no patients correctly identified umami taste. In the HNC group, most patients could not identify salt taste, 66% of patients reported “no sensation” with spicy taste, bitter taste was reduced in some, and increased or altered in others, while only one patient could identify umami taste. In the hematologic and HNC patient groups, 80% and 66% reported grade 2 dry mouth, respectively, according to CTCAE 4.0. After treatment for taste dysfunction, 71% of all patients in the present study reported improvements in taste function.
Conclusions
Persisting dysgeusia in cancer survivors may be assessed by patient report and taste testing. The taste most affected in our patients was umami. Treatment trials with current interventions for dysgeusia appeared effective and should be considered in cancer survivors. Understanding taste and flavor function during and following cancer treatment is important in developing rational prospective preventive and interventional strategies.</description><identifier>ISSN: 0941-4355</identifier><identifier>EISSN: 1433-7339</identifier><identifier>DOI: 10.1007/s00520-019-04758-5</identifier><identifier>PMID: 30927113</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Blood cancer ; Cancer ; Cancer therapies ; Care and treatment ; Chemotherapy ; Clonazepam ; Complications and side effects ; Cytotoxicity ; Head & neck cancer ; Hematology ; Leukemia ; Medical research ; Medicine ; Medicine & Public Health ; Medicine, Experimental ; Megestrol acetate ; Multiple myeloma ; Nursing ; Nursing Research ; Oncology ; Original Article ; Pain Medicine ; Patient compliance ; Patients ; Radiation therapy ; Rehabilitation Medicine ; Side effects ; Taste ; Taste disorders ; Terminology ; Zinc in the body ; Zoledronic acid</subject><ispartof>Supportive care in cancer, 2019-12, Vol.27 (12), p.4587-4595</ispartof><rights>Springer-Verlag GmbH Germany, part of Springer Nature 2019</rights><rights>COPYRIGHT 2019 Springer</rights><rights>Supportive Care in Cancer is a copyright of Springer, (2019). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c508t-707f4a6a9a36ec3082533380b44caeae83ba619063af8b2fb5eff5b4f3879d723</citedby><cites>FETCH-LOGICAL-c508t-707f4a6a9a36ec3082533380b44caeae83ba619063af8b2fb5eff5b4f3879d723</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00520-019-04758-5$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00520-019-04758-5$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30927113$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Epstein, Joel B.</creatorcontrib><creatorcontrib>de Andrade e Silva, Safira Marques</creatorcontrib><creatorcontrib>Epstein, Geena L.</creatorcontrib><creatorcontrib>Leal, Jorge Henrique Santos</creatorcontrib><creatorcontrib>Barasch, Andrei</creatorcontrib><creatorcontrib>Smutzer, Gregory</creatorcontrib><title>Taste disorders following cancer treatment: report of a case series</title><title>Supportive care in cancer</title><addtitle>Support Care Cancer</addtitle><addtitle>Support Care Cancer</addtitle><description>Purpose
To present the findings of combined oral assessment and gustometry testing of a series of head and neck and hematologic malignancies in patients with self-reported taste change after cytotoxic therapies.
Methods
Patients with acute myeloid leukemia (AML), multiple myeloma (MM), and head and neck cancer (HNC) were evaluated for taste function. Chemical gustometry was conducted assessing chemosensory qualities that included sweet, sour, salty, bitter, umami, and spicy. NCI Common Terminology Criteria for Adverse Events (CTCAE) 4.0 and the Scale of Subjective Total Taste Acuity (STTA) were used to describe taste symptoms. Saliva flow rates were measured to determine the presence of hyposalivation. Patients were provided treatment trials for taste dysfunction, including zinc supplements, or medications that included clonazepam, megestrol acetate, and the cannabinoid dronabinol.
Results
According to STTA, hematology cases reported the incidence of grades 2 and 3 taste disturbances as 60% and 40%, respectively. For HNC patients, the incidence of grades 2 and 3 was 44% each. Gustometry tests confirmed dysgeusia in all patients evaluated. In the hematology group, 80% of patients exhibited a decrease in sweet taste perception, and no patients correctly identified umami taste. In the HNC group, most patients could not identify salt taste, 66% of patients reported “no sensation” with spicy taste, bitter taste was reduced in some, and increased or altered in others, while only one patient could identify umami taste. In the hematologic and HNC patient groups, 80% and 66% reported grade 2 dry mouth, respectively, according to CTCAE 4.0. After treatment for taste dysfunction, 71% of all patients in the present study reported improvements in taste function.
Conclusions
Persisting dysgeusia in cancer survivors may be assessed by patient report and taste testing. The taste most affected in our patients was umami. Treatment trials with current interventions for dysgeusia appeared effective and should be considered in cancer survivors. Understanding taste and flavor function during and following cancer treatment is important in developing rational prospective preventive and interventional strategies.</description><subject>Blood cancer</subject><subject>Cancer</subject><subject>Cancer therapies</subject><subject>Care and treatment</subject><subject>Chemotherapy</subject><subject>Clonazepam</subject><subject>Complications and side effects</subject><subject>Cytotoxicity</subject><subject>Head & neck cancer</subject><subject>Hematology</subject><subject>Leukemia</subject><subject>Medical research</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Medicine, Experimental</subject><subject>Megestrol acetate</subject><subject>Multiple myeloma</subject><subject>Nursing</subject><subject>Nursing Research</subject><subject>Oncology</subject><subject>Original Article</subject><subject>Pain Medicine</subject><subject>Patient compliance</subject><subject>Patients</subject><subject>Radiation therapy</subject><subject>Rehabilitation Medicine</subject><subject>Side effects</subject><subject>Taste</subject><subject>Taste disorders</subject><subject>Terminology</subject><subject>Zinc in the body</subject><subject>Zoledronic acid</subject><issn>0941-4355</issn><issn>1433-7339</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNp9kUGLFDEQhYMo7uzqH_AgDV689FpJJZ3E2zLoKix4Wc8hna4MvXR3xqQH8d9vxlldFJEcClLfe1TVY-wVh0sOoN8VACWgBW5bkFqZVj1hGy4RW41on7INWMlbiUqdsfNS7gC41ko8Z2cIVmjOccO2t76s1AxjSXmgXJqYpil9H5ddE_wSKDdrJr_OtKzvm0z7lNcmxcbXbqGmUB6pvGDPop8KvXyoF-zrxw-320_tzZfrz9urmzYoMGurQUfpO289dhQQjFCIaKCXMnjyZLD3HbfQoY-mF7FXFKPqZUSj7aAFXrC3J999Tt8OVFY3jyXQNPmF0qE4IepVDAo8om_-Qu_SIS91Oie4tR0HLbpHaucncuMS05p9OJq6qw6k6lAYW6nLf1D1DTSPIS0Ux_r_h0CcBCGnUjJFt8_j7PMPx8Edk3On5FxNzv1Mzqkqev0w8aGfafgt-RVVBfAElNpadpQfV_qP7T3QYaC3</recordid><startdate>20191201</startdate><enddate>20191201</enddate><creator>Epstein, Joel B.</creator><creator>de Andrade e Silva, Safira Marques</creator><creator>Epstein, Geena L.</creator><creator>Leal, Jorge Henrique Santos</creator><creator>Barasch, Andrei</creator><creator>Smutzer, Gregory</creator><general>Springer Berlin Heidelberg</general><general>Springer</general><general>Springer Nature B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>0-V</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88J</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ALSLI</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HEHIP</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M2R</scope><scope>M2S</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20191201</creationdate><title>Taste disorders following cancer treatment: report of a case series</title><author>Epstein, Joel B. ; de Andrade e Silva, Safira Marques ; Epstein, Geena L. ; Leal, Jorge Henrique Santos ; Barasch, Andrei ; Smutzer, Gregory</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c508t-707f4a6a9a36ec3082533380b44caeae83ba619063af8b2fb5eff5b4f3879d723</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Blood cancer</topic><topic>Cancer</topic><topic>Cancer therapies</topic><topic>Care and treatment</topic><topic>Chemotherapy</topic><topic>Clonazepam</topic><topic>Complications and side effects</topic><topic>Cytotoxicity</topic><topic>Head & neck cancer</topic><topic>Hematology</topic><topic>Leukemia</topic><topic>Medical research</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Medicine, Experimental</topic><topic>Megestrol acetate</topic><topic>Multiple myeloma</topic><topic>Nursing</topic><topic>Nursing Research</topic><topic>Oncology</topic><topic>Original Article</topic><topic>Pain Medicine</topic><topic>Patient compliance</topic><topic>Patients</topic><topic>Radiation therapy</topic><topic>Rehabilitation Medicine</topic><topic>Side effects</topic><topic>Taste</topic><topic>Taste disorders</topic><topic>Terminology</topic><topic>Zinc in the body</topic><topic>Zoledronic acid</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Epstein, Joel B.</creatorcontrib><creatorcontrib>de Andrade e Silva, Safira Marques</creatorcontrib><creatorcontrib>Epstein, Geena L.</creatorcontrib><creatorcontrib>Leal, Jorge Henrique Santos</creatorcontrib><creatorcontrib>Barasch, Andrei</creatorcontrib><creatorcontrib>Smutzer, Gregory</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Social Sciences Premium Collection【Remote access available】</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Social Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Social Science Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Sociology Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Social Science Database (ProQuest)</collection><collection>Sociology Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Supportive care in cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Epstein, Joel B.</au><au>de Andrade e Silva, Safira Marques</au><au>Epstein, Geena L.</au><au>Leal, Jorge Henrique Santos</au><au>Barasch, Andrei</au><au>Smutzer, Gregory</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Taste disorders following cancer treatment: report of a case series</atitle><jtitle>Supportive care in cancer</jtitle><stitle>Support Care Cancer</stitle><addtitle>Support Care Cancer</addtitle><date>2019-12-01</date><risdate>2019</risdate><volume>27</volume><issue>12</issue><spage>4587</spage><epage>4595</epage><pages>4587-4595</pages><issn>0941-4355</issn><eissn>1433-7339</eissn><abstract>Purpose
To present the findings of combined oral assessment and gustometry testing of a series of head and neck and hematologic malignancies in patients with self-reported taste change after cytotoxic therapies.
Methods
Patients with acute myeloid leukemia (AML), multiple myeloma (MM), and head and neck cancer (HNC) were evaluated for taste function. Chemical gustometry was conducted assessing chemosensory qualities that included sweet, sour, salty, bitter, umami, and spicy. NCI Common Terminology Criteria for Adverse Events (CTCAE) 4.0 and the Scale of Subjective Total Taste Acuity (STTA) were used to describe taste symptoms. Saliva flow rates were measured to determine the presence of hyposalivation. Patients were provided treatment trials for taste dysfunction, including zinc supplements, or medications that included clonazepam, megestrol acetate, and the cannabinoid dronabinol.
Results
According to STTA, hematology cases reported the incidence of grades 2 and 3 taste disturbances as 60% and 40%, respectively. For HNC patients, the incidence of grades 2 and 3 was 44% each. Gustometry tests confirmed dysgeusia in all patients evaluated. In the hematology group, 80% of patients exhibited a decrease in sweet taste perception, and no patients correctly identified umami taste. In the HNC group, most patients could not identify salt taste, 66% of patients reported “no sensation” with spicy taste, bitter taste was reduced in some, and increased or altered in others, while only one patient could identify umami taste. In the hematologic and HNC patient groups, 80% and 66% reported grade 2 dry mouth, respectively, according to CTCAE 4.0. After treatment for taste dysfunction, 71% of all patients in the present study reported improvements in taste function.
Conclusions
Persisting dysgeusia in cancer survivors may be assessed by patient report and taste testing. The taste most affected in our patients was umami. Treatment trials with current interventions for dysgeusia appeared effective and should be considered in cancer survivors. Understanding taste and flavor function during and following cancer treatment is important in developing rational prospective preventive and interventional strategies.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>30927113</pmid><doi>10.1007/s00520-019-04758-5</doi><tpages>9</tpages></addata></record> |
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subjects | Blood cancer Cancer Cancer therapies Care and treatment Chemotherapy Clonazepam Complications and side effects Cytotoxicity Head & neck cancer Hematology Leukemia Medical research Medicine Medicine & Public Health Medicine, Experimental Megestrol acetate Multiple myeloma Nursing Nursing Research Oncology Original Article Pain Medicine Patient compliance Patients Radiation therapy Rehabilitation Medicine Side effects Taste Taste disorders Terminology Zinc in the body Zoledronic acid |
title | Taste disorders following cancer treatment: report of a case series |
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