Common analgesics and ovarian cancer survival: the Ovarian cancer Prognosis And Lifestyle (OPAL) Study

Abstract Background Most women with ovarian cancer (OC) are diagnosed with advanced disease. They often experience recurrence after primary treatment, and their subsequent prognosis is poor. Our goal was to evaluate the association between use of nonsteroidal antiinflammatory drugs (NSAIDs), includi...

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Veröffentlicht in:JNCI : Journal of the National Cancer Institute 2023-05, Vol.115 (5), p.570-577
Hauptverfasser: Majidi, Azam, Na, Renhua, Jordan, Susan J, DeFazio, Anna, Obermair, Andreas, Friedlander, Michael, Grant, Peter, Webb, Penelope M
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container_issue 5
container_start_page 570
container_title JNCI : Journal of the National Cancer Institute
container_volume 115
creator Majidi, Azam
Na, Renhua
Jordan, Susan J
DeFazio, Anna
Obermair, Andreas
Friedlander, Michael
Grant, Peter
Webb, Penelope M
description Abstract Background Most women with ovarian cancer (OC) are diagnosed with advanced disease. They often experience recurrence after primary treatment, and their subsequent prognosis is poor. Our goal was to evaluate the association between use of nonsteroidal antiinflammatory drugs (NSAIDs), including regular and low-dose aspirin, and 5-year cancer-specific survival after an OC diagnosis. Methods The Ovarian cancer Prognosis And Lifestyle study is a prospective population-based cohort of 958 Australian women with OC. Information was gathered through self-completed questionnaires. We classified NSAID use during the year prediagnosis and postdiagnosis as none or occasional (
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They often experience recurrence after primary treatment, and their subsequent prognosis is poor. Our goal was to evaluate the association between use of nonsteroidal antiinflammatory drugs (NSAIDs), including regular and low-dose aspirin, and 5-year cancer-specific survival after an OC diagnosis. Methods The Ovarian cancer Prognosis And Lifestyle study is a prospective population-based cohort of 958 Australian women with OC. Information was gathered through self-completed questionnaires. We classified NSAID use during the year prediagnosis and postdiagnosis as none or occasional (&lt;1 d/wk), infrequent (1-3 d/wk), and frequent (≥4 d/wk) use. We measured survival from the start of primary treatment: surgery or neoadjuvant chemotherapy for analyses of prediagnosis use, or 12 months after starting treatment (postdiagnosis use) until the earliest of date of death from OC (other deaths were censored) or last follow-up to 5 years. We used Cox proportional hazards regression to estimate adjusted hazard ratios (HRs) and 95% confidence intervals (CIs) and applied inverse-probability of treatment weighting to minimize confounding. We also calculated restricted mean survival times. Results Compared with nonusers and infrequent users, we observed better survival associated with frequent NSAID use prediagnosis (HR = 0.73, 95% CI = 0.55 to 0.97) or postdiagnosis (HR = 0.65, 95% CI = 0.45 to 0.94). Estimates were similar for aspirin and nonaspirin NSAIDs, new and continuous users and in weighted models. These differences would translate to a 2.5-month increase in mean survival by 5 years postdiagnosis. There was no association with acetaminophen. Conclusions Our findings confirm a previous study suggesting NSAID use might improve OC survival.</description><identifier>ISSN: 0027-8874</identifier><identifier>EISSN: 1460-2105</identifier><identifier>DOI: 10.1093/jnci/djac239</identifier><identifier>PMID: 36744914</identifier><language>eng</language><publisher>United States: Oxford University Press</publisher><subject>Acetaminophen ; Acetaminophen - therapeutic use ; Analgesics ; Analgesics - therapeutic use ; Anti-inflammatory agents ; Anti-Inflammatory Agents, Non-Steroidal - therapeutic use ; Aspirin ; Aspirin - therapeutic use ; Australia - epidemiology ; Cancer ; Chemotherapy ; Confidence intervals ; Female ; Humans ; Medical prognosis ; Nonsteroidal anti-inflammatory drugs ; Ovarian cancer ; Ovarian Neoplasms - drug therapy ; Population studies ; Prognosis ; Proportional Hazards Models ; Prospective Studies ; Risk Factors ; Self completed questionnaires ; Statistical analysis ; Survival</subject><ispartof>JNCI : Journal of the National Cancer Institute, 2023-05, Vol.115 (5), p.570-577</ispartof><rights>The Author(s) 2023. Published by Oxford University Press. 2023</rights><rights>The Author(s) 2023. 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They often experience recurrence after primary treatment, and their subsequent prognosis is poor. Our goal was to evaluate the association between use of nonsteroidal antiinflammatory drugs (NSAIDs), including regular and low-dose aspirin, and 5-year cancer-specific survival after an OC diagnosis. Methods The Ovarian cancer Prognosis And Lifestyle study is a prospective population-based cohort of 958 Australian women with OC. Information was gathered through self-completed questionnaires. We classified NSAID use during the year prediagnosis and postdiagnosis as none or occasional (&lt;1 d/wk), infrequent (1-3 d/wk), and frequent (≥4 d/wk) use. We measured survival from the start of primary treatment: surgery or neoadjuvant chemotherapy for analyses of prediagnosis use, or 12 months after starting treatment (postdiagnosis use) until the earliest of date of death from OC (other deaths were censored) or last follow-up to 5 years. We used Cox proportional hazards regression to estimate adjusted hazard ratios (HRs) and 95% confidence intervals (CIs) and applied inverse-probability of treatment weighting to minimize confounding. We also calculated restricted mean survival times. Results Compared with nonusers and infrequent users, we observed better survival associated with frequent NSAID use prediagnosis (HR = 0.73, 95% CI = 0.55 to 0.97) or postdiagnosis (HR = 0.65, 95% CI = 0.45 to 0.94). Estimates were similar for aspirin and nonaspirin NSAIDs, new and continuous users and in weighted models. These differences would translate to a 2.5-month increase in mean survival by 5 years postdiagnosis. There was no association with acetaminophen. 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Na, Renhua ; Jordan, Susan J ; DeFazio, Anna ; Obermair, Andreas ; Friedlander, Michael ; Grant, Peter ; Webb, Penelope M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c445t-c97ab278756489a0470365b86284706f8265552523fe16b5ef59c7c58653e4973</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Acetaminophen</topic><topic>Acetaminophen - therapeutic use</topic><topic>Analgesics</topic><topic>Analgesics - therapeutic use</topic><topic>Anti-inflammatory agents</topic><topic>Anti-Inflammatory Agents, Non-Steroidal - therapeutic use</topic><topic>Aspirin</topic><topic>Aspirin - therapeutic use</topic><topic>Australia - epidemiology</topic><topic>Cancer</topic><topic>Chemotherapy</topic><topic>Confidence intervals</topic><topic>Female</topic><topic>Humans</topic><topic>Medical prognosis</topic><topic>Nonsteroidal anti-inflammatory drugs</topic><topic>Ovarian cancer</topic><topic>Ovarian Neoplasms - drug therapy</topic><topic>Population studies</topic><topic>Prognosis</topic><topic>Proportional Hazards Models</topic><topic>Prospective Studies</topic><topic>Risk Factors</topic><topic>Self completed questionnaires</topic><topic>Statistical analysis</topic><topic>Survival</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Majidi, Azam</creatorcontrib><creatorcontrib>Na, Renhua</creatorcontrib><creatorcontrib>Jordan, Susan J</creatorcontrib><creatorcontrib>DeFazio, Anna</creatorcontrib><creatorcontrib>Obermair, Andreas</creatorcontrib><creatorcontrib>Friedlander, Michael</creatorcontrib><creatorcontrib>Grant, Peter</creatorcontrib><creatorcontrib>Webb, Penelope M</creatorcontrib><collection>Oxford Journals Open Access Collection</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>JNCI : Journal of the National Cancer Institute</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Majidi, Azam</au><au>Na, Renhua</au><au>Jordan, Susan J</au><au>DeFazio, Anna</au><au>Obermair, Andreas</au><au>Friedlander, Michael</au><au>Grant, Peter</au><au>Webb, Penelope M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Common analgesics and ovarian cancer survival: the Ovarian cancer Prognosis And Lifestyle (OPAL) Study</atitle><jtitle>JNCI : Journal of the National Cancer Institute</jtitle><addtitle>J Natl Cancer Inst</addtitle><date>2023-05-08</date><risdate>2023</risdate><volume>115</volume><issue>5</issue><spage>570</spage><epage>577</epage><pages>570-577</pages><issn>0027-8874</issn><eissn>1460-2105</eissn><abstract>Abstract Background Most women with ovarian cancer (OC) are diagnosed with advanced disease. They often experience recurrence after primary treatment, and their subsequent prognosis is poor. Our goal was to evaluate the association between use of nonsteroidal antiinflammatory drugs (NSAIDs), including regular and low-dose aspirin, and 5-year cancer-specific survival after an OC diagnosis. Methods The Ovarian cancer Prognosis And Lifestyle study is a prospective population-based cohort of 958 Australian women with OC. Information was gathered through self-completed questionnaires. We classified NSAID use during the year prediagnosis and postdiagnosis as none or occasional (&lt;1 d/wk), infrequent (1-3 d/wk), and frequent (≥4 d/wk) use. We measured survival from the start of primary treatment: surgery or neoadjuvant chemotherapy for analyses of prediagnosis use, or 12 months after starting treatment (postdiagnosis use) until the earliest of date of death from OC (other deaths were censored) or last follow-up to 5 years. We used Cox proportional hazards regression to estimate adjusted hazard ratios (HRs) and 95% confidence intervals (CIs) and applied inverse-probability of treatment weighting to minimize confounding. We also calculated restricted mean survival times. Results Compared with nonusers and infrequent users, we observed better survival associated with frequent NSAID use prediagnosis (HR = 0.73, 95% CI = 0.55 to 0.97) or postdiagnosis (HR = 0.65, 95% CI = 0.45 to 0.94). Estimates were similar for aspirin and nonaspirin NSAIDs, new and continuous users and in weighted models. These differences would translate to a 2.5-month increase in mean survival by 5 years postdiagnosis. There was no association with acetaminophen. Conclusions Our findings confirm a previous study suggesting NSAID use might improve OC survival.</abstract><cop>United States</cop><pub>Oxford University Press</pub><pmid>36744914</pmid><doi>10.1093/jnci/djac239</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0003-2815-3060</orcidid><orcidid>https://orcid.org/0000-0002-4566-1414</orcidid><orcidid>https://orcid.org/0000-0003-0057-4744</orcidid><orcidid>https://orcid.org/0000-0003-0733-5930</orcidid><orcidid>https://orcid.org/0000-0003-1350-7508</orcidid><orcidid>https://orcid.org/0000-0002-9830-8462</orcidid><orcidid>https://orcid.org/0000-0003-3090-795X</orcidid><orcidid>https://orcid.org/0000-0003-2199-1117</orcidid><oa>free_for_read</oa></addata></record>
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subjects Acetaminophen
Acetaminophen - therapeutic use
Analgesics
Analgesics - therapeutic use
Anti-inflammatory agents
Anti-Inflammatory Agents, Non-Steroidal - therapeutic use
Aspirin
Aspirin - therapeutic use
Australia - epidemiology
Cancer
Chemotherapy
Confidence intervals
Female
Humans
Medical prognosis
Nonsteroidal anti-inflammatory drugs
Ovarian cancer
Ovarian Neoplasms - drug therapy
Population studies
Prognosis
Proportional Hazards Models
Prospective Studies
Risk Factors
Self completed questionnaires
Statistical analysis
Survival
title Common analgesics and ovarian cancer survival: the Ovarian cancer Prognosis And Lifestyle (OPAL) Study
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