Ovarian Cancer and Comorbidity: Is Poor Survival Explained by Choice of Primary Treatment or System Delay?

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Standard

Ovarian Cancer and Comorbidity : Is Poor Survival Explained by Choice of Primary Treatment or System Delay? / Noer, Mette Calundann; Sperling, Cecilie Dyg; Ottesen, Bent; Antonsen, Sofie Leisby; Christensen, Ib Jarle; Høgdall, Claus.

I: International Journal of Gynecological Cancer, Bind 27, Nr. 6, 2017, s. 1123-1133.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Noer, MC, Sperling, CD, Ottesen, B, Antonsen, SL, Christensen, IJ & Høgdall, C 2017, 'Ovarian Cancer and Comorbidity: Is Poor Survival Explained by Choice of Primary Treatment or System Delay?', International Journal of Gynecological Cancer, bind 27, nr. 6, s. 1123-1133. https://doi.org/10.1097/IGC.0000000000001001

APA

Noer, M. C., Sperling, C. D., Ottesen, B., Antonsen, S. L., Christensen, I. J., & Høgdall, C. (2017). Ovarian Cancer and Comorbidity: Is Poor Survival Explained by Choice of Primary Treatment or System Delay? International Journal of Gynecological Cancer, 27(6), 1123-1133. https://doi.org/10.1097/IGC.0000000000001001

Vancouver

Noer MC, Sperling CD, Ottesen B, Antonsen SL, Christensen IJ, Høgdall C. Ovarian Cancer and Comorbidity: Is Poor Survival Explained by Choice of Primary Treatment or System Delay? International Journal of Gynecological Cancer. 2017;27(6):1123-1133. https://doi.org/10.1097/IGC.0000000000001001

Author

Noer, Mette Calundann ; Sperling, Cecilie Dyg ; Ottesen, Bent ; Antonsen, Sofie Leisby ; Christensen, Ib Jarle ; Høgdall, Claus. / Ovarian Cancer and Comorbidity : Is Poor Survival Explained by Choice of Primary Treatment or System Delay?. I: International Journal of Gynecological Cancer. 2017 ; Bind 27, Nr. 6. s. 1123-1133.

Bibtex

@article{f9ca2bc41a1e4cb5af92c6906b8d58e1,
title = "Ovarian Cancer and Comorbidity: Is Poor Survival Explained by Choice of Primary Treatment or System Delay?",
abstract = "OBJECTIVES: Comorbidity influences survival in ovarian cancer, but the causal relations between prognosis and comorbidity are not well characterized. The aim of this study was to investigate the associations between comorbidity, system delay, the choice of primary treatment, and survival in Danish ovarian cancer patients.METHODS: This population-based study was conducted on data from 5317 ovarian cancer patients registered in the Danish Gynecological Cancer Database. Comorbidity was classified according to the Charlson Comorbidity Index and the Ovarian Cancer Comorbidity Index. Pearson χ test and multivariate logistic regression analyses were used to investigate the association between comorbidity and primary outcome measures: primary treatment ({"}primary debulking surgery{"} vs {"}no primary surgery{"}) and system delay (more vs less than required by the National Cancer Patient Pathways [NCPPs]). Cox regression analyses, including hypothesized mediators stepwise, were used to investigate if the impact of comorbidity on overall survival is mediated by the choice of treatment or system delay.RESULTS: A total of 3945 patients (74.2%) underwent primary debulking surgery, whereas 1160 (21.8%) received neoadjuvant chemotherapy. When adjusting for confounders, comorbidity was not significantly associated to the choice of treatment. Surgically treated patients with moderate/severe comorbidity were more often experiencing system delay longer than required by the NCPP. No association between comorbidity and system delay was observed for patients treated with neoadjuvant chemotherapy. Survival analyses demonstrated that system delay longer than NCPP requirement positively impacts survival (hazard ratio, 0.90 [95% confidence interval, 0.82-0.98]), whereas primary treatment modality has no significant impact on survival.CONCLUSIONS: Patients with moderate/severe comorbidity experience often a longer system delay than patients with no or mild comorbidity. Age, stage, and comorbidity are factors influencing the choice of treatment, with stage being the most important factor and comorbidity of lesser importance. The impact of comorbidity on survival does not seem to be mediated by the choice of treatment or system delay.",
keywords = "Adolescent, Adult, Aged, Chemotherapy, Adjuvant, Cohort Studies, Comorbidity, Denmark/epidemiology, Female, Humans, Middle Aged, Models, Statistical, Neoadjuvant Therapy, Neoplasm Staging, Ovarian Neoplasms/drug therapy, Prognosis, Proportional Hazards Models, Time-to-Treatment/statistics & numerical data, Young Adult",
author = "Noer, {Mette Calundann} and Sperling, {Cecilie Dyg} and Bent Ottesen and Antonsen, {Sofie Leisby} and Christensen, {Ib Jarle} and Claus H{\o}gdall",
year = "2017",
doi = "10.1097/IGC.0000000000001001",
language = "English",
volume = "27",
pages = "1123--1133",
journal = "International Journal of Gynecological Cancer",
issn = "1048-891X",
publisher = "Lippincott Williams & Wilkins, Ltd.",
number = "6",

}

RIS

TY - JOUR

T1 - Ovarian Cancer and Comorbidity

T2 - Is Poor Survival Explained by Choice of Primary Treatment or System Delay?

AU - Noer, Mette Calundann

AU - Sperling, Cecilie Dyg

AU - Ottesen, Bent

AU - Antonsen, Sofie Leisby

AU - Christensen, Ib Jarle

AU - Høgdall, Claus

PY - 2017

Y1 - 2017

N2 - OBJECTIVES: Comorbidity influences survival in ovarian cancer, but the causal relations between prognosis and comorbidity are not well characterized. The aim of this study was to investigate the associations between comorbidity, system delay, the choice of primary treatment, and survival in Danish ovarian cancer patients.METHODS: This population-based study was conducted on data from 5317 ovarian cancer patients registered in the Danish Gynecological Cancer Database. Comorbidity was classified according to the Charlson Comorbidity Index and the Ovarian Cancer Comorbidity Index. Pearson χ test and multivariate logistic regression analyses were used to investigate the association between comorbidity and primary outcome measures: primary treatment ("primary debulking surgery" vs "no primary surgery") and system delay (more vs less than required by the National Cancer Patient Pathways [NCPPs]). Cox regression analyses, including hypothesized mediators stepwise, were used to investigate if the impact of comorbidity on overall survival is mediated by the choice of treatment or system delay.RESULTS: A total of 3945 patients (74.2%) underwent primary debulking surgery, whereas 1160 (21.8%) received neoadjuvant chemotherapy. When adjusting for confounders, comorbidity was not significantly associated to the choice of treatment. Surgically treated patients with moderate/severe comorbidity were more often experiencing system delay longer than required by the NCPP. No association between comorbidity and system delay was observed for patients treated with neoadjuvant chemotherapy. Survival analyses demonstrated that system delay longer than NCPP requirement positively impacts survival (hazard ratio, 0.90 [95% confidence interval, 0.82-0.98]), whereas primary treatment modality has no significant impact on survival.CONCLUSIONS: Patients with moderate/severe comorbidity experience often a longer system delay than patients with no or mild comorbidity. Age, stage, and comorbidity are factors influencing the choice of treatment, with stage being the most important factor and comorbidity of lesser importance. The impact of comorbidity on survival does not seem to be mediated by the choice of treatment or system delay.

AB - OBJECTIVES: Comorbidity influences survival in ovarian cancer, but the causal relations between prognosis and comorbidity are not well characterized. The aim of this study was to investigate the associations between comorbidity, system delay, the choice of primary treatment, and survival in Danish ovarian cancer patients.METHODS: This population-based study was conducted on data from 5317 ovarian cancer patients registered in the Danish Gynecological Cancer Database. Comorbidity was classified according to the Charlson Comorbidity Index and the Ovarian Cancer Comorbidity Index. Pearson χ test and multivariate logistic regression analyses were used to investigate the association between comorbidity and primary outcome measures: primary treatment ("primary debulking surgery" vs "no primary surgery") and system delay (more vs less than required by the National Cancer Patient Pathways [NCPPs]). Cox regression analyses, including hypothesized mediators stepwise, were used to investigate if the impact of comorbidity on overall survival is mediated by the choice of treatment or system delay.RESULTS: A total of 3945 patients (74.2%) underwent primary debulking surgery, whereas 1160 (21.8%) received neoadjuvant chemotherapy. When adjusting for confounders, comorbidity was not significantly associated to the choice of treatment. Surgically treated patients with moderate/severe comorbidity were more often experiencing system delay longer than required by the NCPP. No association between comorbidity and system delay was observed for patients treated with neoadjuvant chemotherapy. Survival analyses demonstrated that system delay longer than NCPP requirement positively impacts survival (hazard ratio, 0.90 [95% confidence interval, 0.82-0.98]), whereas primary treatment modality has no significant impact on survival.CONCLUSIONS: Patients with moderate/severe comorbidity experience often a longer system delay than patients with no or mild comorbidity. Age, stage, and comorbidity are factors influencing the choice of treatment, with stage being the most important factor and comorbidity of lesser importance. The impact of comorbidity on survival does not seem to be mediated by the choice of treatment or system delay.

KW - Adolescent

KW - Adult

KW - Aged

KW - Chemotherapy, Adjuvant

KW - Cohort Studies

KW - Comorbidity

KW - Denmark/epidemiology

KW - Female

KW - Humans

KW - Middle Aged

KW - Models, Statistical

KW - Neoadjuvant Therapy

KW - Neoplasm Staging

KW - Ovarian Neoplasms/drug therapy

KW - Prognosis

KW - Proportional Hazards Models

KW - Time-to-Treatment/statistics & numerical data

KW - Young Adult

U2 - 10.1097/IGC.0000000000001001

DO - 10.1097/IGC.0000000000001001

M3 - Journal article

C2 - 28604447

VL - 27

SP - 1123

EP - 1133

JO - International Journal of Gynecological Cancer

JF - International Journal of Gynecological Cancer

SN - 1048-891X

IS - 6

ER -

ID: 195006899