Comparison of Psychological Quality of Life Between Long-Term Survivors of Childhood Cancer and Their Families
Although treatment outcomes for childhood cancer have improved in recent years, some patients continue to experience physical symptoms and psychological stress several years after the end of treatment. This study aimed to examine the correlation between the quality-of-life (QOL) scores of childhood...
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| Veröffentlicht in: | Journal of adolescent and young adult oncology 2023-06, Vol.12 (3), p.297-302 |
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| container_title | Journal of adolescent and young adult oncology |
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| creator | Shinohara, Yuki Morino, Tappei Shimoura, Kanako Niu, Qian Mukaiyama, Kohei Chen, Changyu Matsumura, Natsuki Shimizu, Hiroki Tabata, Ami Hanai, Akiko Nagai-Tanima, Momoko Ogawa, Masahiro Kato, Toshihiro Tanimukai, Hitoshi Matsuoka, Mari Adachi, Souichi Takita, Junko Tsuboyama, Tadao Aoyama, Tomoki |
| description | Although treatment outcomes for childhood cancer have improved in recent years, some patients continue to experience physical symptoms and psychological stress several years after the end of treatment. This study aimed to examine the correlation between the quality-of-life (QOL) scores of childhood cancer survivors (CCSs) aged 18-39 and (1) their families and (2) the time since the end of treatment.
Measuring the QOL of CCSs attending the long-term follow-up (LTFU) and those of their families. The Short-Form Health Survey (SF-36) was used for CCSs and the Caregiver Quality of Life Index-Cancer (CQOLC) for their families. Spearman's rank correlation analyses were used to examine the relationship between the CCSs' and their families' QOL and the time since the end of treatment.
Twenty-nine CCSs (mean age, 24.2 years; mean the time since the end of treatment, 13.9 years), each paired with one family member, were included. Time since the end of treatment was positively correlated with the CCSs' QOL on the physical component score (
= 0.42,
= 0.03) and negatively correlated with mental health (MH) (
= -0.50,
= 0.01), a subscale of the mental component score (MCS). Furthermore, the CCSs' QOL on the MCS was positively correlated with their families' QOL scores (
= 0.58,
|
| doi_str_mv | 10.1089/jayao.2021.0217 |
| format | Article |
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Measuring the QOL of CCSs attending the long-term follow-up (LTFU) and those of their families. The Short-Form Health Survey (SF-36) was used for CCSs and the Caregiver Quality of Life Index-Cancer (CQOLC) for their families. Spearman's rank correlation analyses were used to examine the relationship between the CCSs' and their families' QOL and the time since the end of treatment.
Twenty-nine CCSs (mean age, 24.2 years; mean the time since the end of treatment, 13.9 years), each paired with one family member, were included. Time since the end of treatment was positively correlated with the CCSs' QOL on the physical component score (
= 0.42,
= 0.03) and negatively correlated with mental health (MH) (
= -0.50,
= 0.01), a subscale of the mental component score (MCS). Furthermore, the CCSs' QOL on the MCS was positively correlated with their families' QOL scores (
= 0.58,
< 0.01).
Psychological stress may persist in CCSs long after treatment, even when physical symptoms improve. Therefore, it is necessary to establish a comprehensive support system for the LTFU of CCSs, including MH care and QOL monitoring for patients and their families.</description><identifier>ISSN: 2156-5333</identifier><identifier>EISSN: 2156-535X</identifier><identifier>DOI: 10.1089/jayao.2021.0217</identifier><identifier>PMID: 35969380</identifier><language>eng</language><publisher>United States: Mary Ann Liebert, Inc</publisher><subject>Adult ; Cancer ; Cancer Survivors ; Child ; Childhood ; Humans ; Neoplasms - psychology ; Quality of life ; Quality of Life - psychology ; Survivors - psychology ; Treatment Outcome ; Young Adult</subject><ispartof>Journal of adolescent and young adult oncology, 2023-06, Vol.12 (3), p.297-302</ispartof><rights>Copyright Mary Ann Liebert, Inc. Jun 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c369t-11861fa289eb06b06a77db625a2ccafc481aa51342004b10a3d6a94d9598abd53</citedby><cites>FETCH-LOGICAL-c369t-11861fa289eb06b06a77db625a2ccafc481aa51342004b10a3d6a94d9598abd53</cites><orcidid>0000-0002-7135-1161 ; 0000-0003-2083-3539</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35969380$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shinohara, Yuki</creatorcontrib><creatorcontrib>Morino, Tappei</creatorcontrib><creatorcontrib>Shimoura, Kanako</creatorcontrib><creatorcontrib>Niu, Qian</creatorcontrib><creatorcontrib>Mukaiyama, Kohei</creatorcontrib><creatorcontrib>Chen, Changyu</creatorcontrib><creatorcontrib>Matsumura, Natsuki</creatorcontrib><creatorcontrib>Shimizu, Hiroki</creatorcontrib><creatorcontrib>Tabata, Ami</creatorcontrib><creatorcontrib>Hanai, Akiko</creatorcontrib><creatorcontrib>Nagai-Tanima, Momoko</creatorcontrib><creatorcontrib>Ogawa, Masahiro</creatorcontrib><creatorcontrib>Kato, Toshihiro</creatorcontrib><creatorcontrib>Tanimukai, Hitoshi</creatorcontrib><creatorcontrib>Matsuoka, Mari</creatorcontrib><creatorcontrib>Adachi, Souichi</creatorcontrib><creatorcontrib>Takita, Junko</creatorcontrib><creatorcontrib>Tsuboyama, Tadao</creatorcontrib><creatorcontrib>Aoyama, Tomoki</creatorcontrib><title>Comparison of Psychological Quality of Life Between Long-Term Survivors of Childhood Cancer and Their Families</title><title>Journal of adolescent and young adult oncology</title><addtitle>J Adolesc Young Adult Oncol</addtitle><description>Although treatment outcomes for childhood cancer have improved in recent years, some patients continue to experience physical symptoms and psychological stress several years after the end of treatment. This study aimed to examine the correlation between the quality-of-life (QOL) scores of childhood cancer survivors (CCSs) aged 18-39 and (1) their families and (2) the time since the end of treatment.
Measuring the QOL of CCSs attending the long-term follow-up (LTFU) and those of their families. The Short-Form Health Survey (SF-36) was used for CCSs and the Caregiver Quality of Life Index-Cancer (CQOLC) for their families. Spearman's rank correlation analyses were used to examine the relationship between the CCSs' and their families' QOL and the time since the end of treatment.
Twenty-nine CCSs (mean age, 24.2 years; mean the time since the end of treatment, 13.9 years), each paired with one family member, were included. Time since the end of treatment was positively correlated with the CCSs' QOL on the physical component score (
= 0.42,
= 0.03) and negatively correlated with mental health (MH) (
= -0.50,
= 0.01), a subscale of the mental component score (MCS). Furthermore, the CCSs' QOL on the MCS was positively correlated with their families' QOL scores (
= 0.58,
< 0.01).
Psychological stress may persist in CCSs long after treatment, even when physical symptoms improve. Therefore, it is necessary to establish a comprehensive support system for the LTFU of CCSs, including MH care and QOL monitoring for patients and their families.</description><subject>Adult</subject><subject>Cancer</subject><subject>Cancer Survivors</subject><subject>Child</subject><subject>Childhood</subject><subject>Humans</subject><subject>Neoplasms - psychology</subject><subject>Quality of life</subject><subject>Quality of Life - psychology</subject><subject>Survivors - psychology</subject><subject>Treatment Outcome</subject><subject>Young Adult</subject><issn>2156-5333</issn><issn>2156-535X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkd9LwzAQx4MoOnTPvknAF18686NNm0ctToWBihN8C9c0dRltM5N1sv_e1ukeDAl3kM99ubsvQueUTCjJ5PUStuAmjDA66V96gEaMJiJKePJ-uM85P0HjEJakPzFhsaDH6IQnUkiekRFqc9eswNvgWuwq_By2euFq92E11Pilg9qut8PHzFYG35r1lzEtnrn2I5ob3-DXzm_sxvkwMPnC1uXCuRLn0GrjMbQlni-M9XgKja2tCWfoqII6mPFvPEVv07t5_hDNnu4f85tZpLmQ64jSTNAKWCZNQUR_IU3LQrAEmNZQ6TijAAnlMeuHKigBXgqQcSkTmUFRJvwUXe10V959diasVWODNnUNrXFdUCztV5HFaTygl__Qpet823enWMYET1lKZU9d7yjtXQjeVGrlbQN-qyhRgxvqxw01uKEGN_qKi1_drmhMuef_ds-_AWVXha0</recordid><startdate>20230601</startdate><enddate>20230601</enddate><creator>Shinohara, Yuki</creator><creator>Morino, Tappei</creator><creator>Shimoura, Kanako</creator><creator>Niu, Qian</creator><creator>Mukaiyama, Kohei</creator><creator>Chen, Changyu</creator><creator>Matsumura, Natsuki</creator><creator>Shimizu, Hiroki</creator><creator>Tabata, Ami</creator><creator>Hanai, Akiko</creator><creator>Nagai-Tanima, Momoko</creator><creator>Ogawa, Masahiro</creator><creator>Kato, Toshihiro</creator><creator>Tanimukai, Hitoshi</creator><creator>Matsuoka, Mari</creator><creator>Adachi, Souichi</creator><creator>Takita, Junko</creator><creator>Tsuboyama, Tadao</creator><creator>Aoyama, Tomoki</creator><general>Mary Ann Liebert, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-7135-1161</orcidid><orcidid>https://orcid.org/0000-0003-2083-3539</orcidid></search><sort><creationdate>20230601</creationdate><title>Comparison of Psychological Quality of Life Between Long-Term Survivors of Childhood Cancer and Their Families</title><author>Shinohara, Yuki ; Morino, Tappei ; Shimoura, Kanako ; Niu, Qian ; Mukaiyama, Kohei ; Chen, Changyu ; Matsumura, Natsuki ; Shimizu, Hiroki ; Tabata, Ami ; Hanai, Akiko ; Nagai-Tanima, Momoko ; Ogawa, Masahiro ; Kato, Toshihiro ; Tanimukai, Hitoshi ; Matsuoka, Mari ; Adachi, Souichi ; Takita, Junko ; Tsuboyama, Tadao ; Aoyama, Tomoki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c369t-11861fa289eb06b06a77db625a2ccafc481aa51342004b10a3d6a94d9598abd53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Adult</topic><topic>Cancer</topic><topic>Cancer Survivors</topic><topic>Child</topic><topic>Childhood</topic><topic>Humans</topic><topic>Neoplasms - psychology</topic><topic>Quality of life</topic><topic>Quality of Life - psychology</topic><topic>Survivors - psychology</topic><topic>Treatment Outcome</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shinohara, Yuki</creatorcontrib><creatorcontrib>Morino, Tappei</creatorcontrib><creatorcontrib>Shimoura, Kanako</creatorcontrib><creatorcontrib>Niu, Qian</creatorcontrib><creatorcontrib>Mukaiyama, Kohei</creatorcontrib><creatorcontrib>Chen, Changyu</creatorcontrib><creatorcontrib>Matsumura, Natsuki</creatorcontrib><creatorcontrib>Shimizu, Hiroki</creatorcontrib><creatorcontrib>Tabata, Ami</creatorcontrib><creatorcontrib>Hanai, Akiko</creatorcontrib><creatorcontrib>Nagai-Tanima, Momoko</creatorcontrib><creatorcontrib>Ogawa, Masahiro</creatorcontrib><creatorcontrib>Kato, Toshihiro</creatorcontrib><creatorcontrib>Tanimukai, Hitoshi</creatorcontrib><creatorcontrib>Matsuoka, Mari</creatorcontrib><creatorcontrib>Adachi, Souichi</creatorcontrib><creatorcontrib>Takita, Junko</creatorcontrib><creatorcontrib>Tsuboyama, Tadao</creatorcontrib><creatorcontrib>Aoyama, Tomoki</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of adolescent and young adult oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shinohara, Yuki</au><au>Morino, Tappei</au><au>Shimoura, Kanako</au><au>Niu, Qian</au><au>Mukaiyama, Kohei</au><au>Chen, Changyu</au><au>Matsumura, Natsuki</au><au>Shimizu, Hiroki</au><au>Tabata, Ami</au><au>Hanai, Akiko</au><au>Nagai-Tanima, Momoko</au><au>Ogawa, Masahiro</au><au>Kato, Toshihiro</au><au>Tanimukai, Hitoshi</au><au>Matsuoka, Mari</au><au>Adachi, Souichi</au><au>Takita, Junko</au><au>Tsuboyama, Tadao</au><au>Aoyama, Tomoki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparison of Psychological Quality of Life Between Long-Term Survivors of Childhood Cancer and Their Families</atitle><jtitle>Journal of adolescent and young adult oncology</jtitle><addtitle>J Adolesc Young Adult Oncol</addtitle><date>2023-06-01</date><risdate>2023</risdate><volume>12</volume><issue>3</issue><spage>297</spage><epage>302</epage><pages>297-302</pages><issn>2156-5333</issn><eissn>2156-535X</eissn><abstract>Although treatment outcomes for childhood cancer have improved in recent years, some patients continue to experience physical symptoms and psychological stress several years after the end of treatment. This study aimed to examine the correlation between the quality-of-life (QOL) scores of childhood cancer survivors (CCSs) aged 18-39 and (1) their families and (2) the time since the end of treatment.
Measuring the QOL of CCSs attending the long-term follow-up (LTFU) and those of their families. The Short-Form Health Survey (SF-36) was used for CCSs and the Caregiver Quality of Life Index-Cancer (CQOLC) for their families. Spearman's rank correlation analyses were used to examine the relationship between the CCSs' and their families' QOL and the time since the end of treatment.
Twenty-nine CCSs (mean age, 24.2 years; mean the time since the end of treatment, 13.9 years), each paired with one family member, were included. Time since the end of treatment was positively correlated with the CCSs' QOL on the physical component score (
= 0.42,
= 0.03) and negatively correlated with mental health (MH) (
= -0.50,
= 0.01), a subscale of the mental component score (MCS). Furthermore, the CCSs' QOL on the MCS was positively correlated with their families' QOL scores (
= 0.58,
< 0.01).
Psychological stress may persist in CCSs long after treatment, even when physical symptoms improve. Therefore, it is necessary to establish a comprehensive support system for the LTFU of CCSs, including MH care and QOL monitoring for patients and their families.</abstract><cop>United States</cop><pub>Mary Ann Liebert, Inc</pub><pmid>35969380</pmid><doi>10.1089/jayao.2021.0217</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0002-7135-1161</orcidid><orcidid>https://orcid.org/0000-0003-2083-3539</orcidid><oa>free_for_read</oa></addata></record> |
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| ispartof | Journal of adolescent and young adult oncology, 2023-06, Vol.12 (3), p.297-302 |
| issn | 2156-5333 2156-535X |
| language | eng |
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| source | MEDLINE; Alma/SFX Local Collection |
| subjects | Adult Cancer Cancer Survivors Child Childhood Humans Neoplasms - psychology Quality of life Quality of Life - psychology Survivors - psychology Treatment Outcome Young Adult |
| title | Comparison of Psychological Quality of Life Between Long-Term Survivors of Childhood Cancer and Their Families |
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