Secondary validation of an ovarian cancer-specific comorbidity index in a US population

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Secondary validation of an ovarian cancer-specific comorbidity index in a US population. / Vranes, Chelsey; Zhao, Hui; Noer, Mette Calundann; Fu, Shuangshuang; Sun, Charlotte C.; Harrison, Ross; Ramirez, Pedro T.; Høgdall, Claus Kim; Giordano, Sharon H.; Meyer, Larissa A.

I: International Journal of Gynecological Cancer, Bind 33, Nr. 5, 2023, s. 749-754.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Vranes, C, Zhao, H, Noer, MC, Fu, S, Sun, CC, Harrison, R, Ramirez, PT, Høgdall, CK, Giordano, SH & Meyer, LA 2023, 'Secondary validation of an ovarian cancer-specific comorbidity index in a US population', International Journal of Gynecological Cancer, bind 33, nr. 5, s. 749-754. https://doi.org/10.1136/ijgc-2022-004100

APA

Vranes, C., Zhao, H., Noer, M. C., Fu, S., Sun, C. C., Harrison, R., Ramirez, P. T., Høgdall, C. K., Giordano, S. H., & Meyer, L. A. (2023). Secondary validation of an ovarian cancer-specific comorbidity index in a US population. International Journal of Gynecological Cancer, 33(5), 749-754. https://doi.org/10.1136/ijgc-2022-004100

Vancouver

Vranes C, Zhao H, Noer MC, Fu S, Sun CC, Harrison R o.a. Secondary validation of an ovarian cancer-specific comorbidity index in a US population. International Journal of Gynecological Cancer. 2023;33(5):749-754. https://doi.org/10.1136/ijgc-2022-004100

Author

Vranes, Chelsey ; Zhao, Hui ; Noer, Mette Calundann ; Fu, Shuangshuang ; Sun, Charlotte C. ; Harrison, Ross ; Ramirez, Pedro T. ; Høgdall, Claus Kim ; Giordano, Sharon H. ; Meyer, Larissa A. / Secondary validation of an ovarian cancer-specific comorbidity index in a US population. I: International Journal of Gynecological Cancer. 2023 ; Bind 33, Nr. 5. s. 749-754.

Bibtex

@article{ae2639d3464848858d0458d919ecb392,
title = "Secondary validation of an ovarian cancer-specific comorbidity index in a US population",
abstract = "Objectives The Ovarian Cancer Comorbidity Index (OCCI) is an age-specific index developed and previously found to be more predictive of overall and cancer-specific survival than the Charlson Comorbidity Index (CCI). The objective was to perform secondary validation of the OCCI in a US population. Methods A cohort of ovarian cancer patients undergoing primary or interval cytoreductive surgery from January 2005 to January 2012 was identified in SEER-Medicare. OCCI scores were calculated with the regression coefficients determined from the original developmental cohort for five comorbidities. Cox regression analyses were used to calculate associations between the OCCI risk groups and 5-year overall survival and 5-year cancer-specific survival in comparison to the CCI. Results A total of 5052 patients were included. Median age was 74 (range 66-82) years. 47% (n=2375) had stage III and 24% (n=1197) had stage IV disease at diagnosis. 67% had a serous histology subtype (n=3403). All patients were categorized as moderate (48.4%) or high risk (51.6%). The prevalence of the five predictive comorbidities were: coronary artery disease 3.7%, hypertension 67.5%, chronic obstructive pulmonary disease 16.7%, diabetes 21.8%, and dementia 1.2%. Controlling for histology, grade, and age-stratification, worse overall survival was associated with both a higher OCCI (hazard ratio (HR) 1.57; 95% confidence interval (CI) 1.46 to 1.69) and CCI (HR 1.96; 95% CI 1.66 to 2.32). Cancer-specific survival was associated with the OCCI (HR 1.33; 95% CI 1.22 to 1.44) but was not associated with the CCI (HR 1.15; 95% CI 0.93 to 1.43). Conclusions This internationally developed comorbidity score for ovarian cancer patients is predictive for both overall and cancer-specific survival in a US population. CCI was not predictive for cancer-specific survival. This score may have research applications when utilizing large administrative datasets.",
keywords = "Ovarian Cancer",
author = "Chelsey Vranes and Hui Zhao and Noer, {Mette Calundann} and Shuangshuang Fu and Sun, {Charlotte C.} and Ross Harrison and Ramirez, {Pedro T.} and H{\o}gdall, {Claus Kim} and Giordano, {Sharon H.} and Meyer, {Larissa A.}",
note = "Publisher Copyright: {\textcopyright} IGCS and ESGO 2023. No commercial re-use. See rights and permissions. Published by BMJ.",
year = "2023",
doi = "10.1136/ijgc-2022-004100",
language = "English",
volume = "33",
pages = "749--754",
journal = "International Journal of Gynecological Cancer",
issn = "1048-891X",
publisher = "Lippincott Williams & Wilkins, Ltd.",
number = "5",

}

RIS

TY - JOUR

T1 - Secondary validation of an ovarian cancer-specific comorbidity index in a US population

AU - Vranes, Chelsey

AU - Zhao, Hui

AU - Noer, Mette Calundann

AU - Fu, Shuangshuang

AU - Sun, Charlotte C.

AU - Harrison, Ross

AU - Ramirez, Pedro T.

AU - Høgdall, Claus Kim

AU - Giordano, Sharon H.

AU - Meyer, Larissa A.

N1 - Publisher Copyright: © IGCS and ESGO 2023. No commercial re-use. See rights and permissions. Published by BMJ.

PY - 2023

Y1 - 2023

N2 - Objectives The Ovarian Cancer Comorbidity Index (OCCI) is an age-specific index developed and previously found to be more predictive of overall and cancer-specific survival than the Charlson Comorbidity Index (CCI). The objective was to perform secondary validation of the OCCI in a US population. Methods A cohort of ovarian cancer patients undergoing primary or interval cytoreductive surgery from January 2005 to January 2012 was identified in SEER-Medicare. OCCI scores were calculated with the regression coefficients determined from the original developmental cohort for five comorbidities. Cox regression analyses were used to calculate associations between the OCCI risk groups and 5-year overall survival and 5-year cancer-specific survival in comparison to the CCI. Results A total of 5052 patients were included. Median age was 74 (range 66-82) years. 47% (n=2375) had stage III and 24% (n=1197) had stage IV disease at diagnosis. 67% had a serous histology subtype (n=3403). All patients were categorized as moderate (48.4%) or high risk (51.6%). The prevalence of the five predictive comorbidities were: coronary artery disease 3.7%, hypertension 67.5%, chronic obstructive pulmonary disease 16.7%, diabetes 21.8%, and dementia 1.2%. Controlling for histology, grade, and age-stratification, worse overall survival was associated with both a higher OCCI (hazard ratio (HR) 1.57; 95% confidence interval (CI) 1.46 to 1.69) and CCI (HR 1.96; 95% CI 1.66 to 2.32). Cancer-specific survival was associated with the OCCI (HR 1.33; 95% CI 1.22 to 1.44) but was not associated with the CCI (HR 1.15; 95% CI 0.93 to 1.43). Conclusions This internationally developed comorbidity score for ovarian cancer patients is predictive for both overall and cancer-specific survival in a US population. CCI was not predictive for cancer-specific survival. This score may have research applications when utilizing large administrative datasets.

AB - Objectives The Ovarian Cancer Comorbidity Index (OCCI) is an age-specific index developed and previously found to be more predictive of overall and cancer-specific survival than the Charlson Comorbidity Index (CCI). The objective was to perform secondary validation of the OCCI in a US population. Methods A cohort of ovarian cancer patients undergoing primary or interval cytoreductive surgery from January 2005 to January 2012 was identified in SEER-Medicare. OCCI scores were calculated with the regression coefficients determined from the original developmental cohort for five comorbidities. Cox regression analyses were used to calculate associations between the OCCI risk groups and 5-year overall survival and 5-year cancer-specific survival in comparison to the CCI. Results A total of 5052 patients were included. Median age was 74 (range 66-82) years. 47% (n=2375) had stage III and 24% (n=1197) had stage IV disease at diagnosis. 67% had a serous histology subtype (n=3403). All patients were categorized as moderate (48.4%) or high risk (51.6%). The prevalence of the five predictive comorbidities were: coronary artery disease 3.7%, hypertension 67.5%, chronic obstructive pulmonary disease 16.7%, diabetes 21.8%, and dementia 1.2%. Controlling for histology, grade, and age-stratification, worse overall survival was associated with both a higher OCCI (hazard ratio (HR) 1.57; 95% confidence interval (CI) 1.46 to 1.69) and CCI (HR 1.96; 95% CI 1.66 to 2.32). Cancer-specific survival was associated with the OCCI (HR 1.33; 95% CI 1.22 to 1.44) but was not associated with the CCI (HR 1.15; 95% CI 0.93 to 1.43). Conclusions This internationally developed comorbidity score for ovarian cancer patients is predictive for both overall and cancer-specific survival in a US population. CCI was not predictive for cancer-specific survival. This score may have research applications when utilizing large administrative datasets.

KW - Ovarian Cancer

U2 - 10.1136/ijgc-2022-004100

DO - 10.1136/ijgc-2022-004100

M3 - Journal article

C2 - 36863760

AN - SCOPUS:85152654779

VL - 33

SP - 749

EP - 754

JO - International Journal of Gynecological Cancer

JF - International Journal of Gynecological Cancer

SN - 1048-891X

IS - 5

ER -

ID: 390243319