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Nils Skajaa

Cancer Diagnosis and Prognosis After Guillain-Barré Syndrome: A Population-Based Cohort Study

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Cancer Diagnosis and Prognosis After Guillain-Barré Syndrome: A Population-Based Cohort Study. / Girma, Blean; Farkas, Dóra Körmendiné; Laugesen, Kristina et al.
I: Clinical epidemiology, Bind 2022, Nr. 14, 07.2022, s. 871-878.

Publikation: Bidrag til tidsskrift/Konferencebidrag i tidsskrift /Bidrag til avisTidsskriftartikelForskningpeer review

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Girma B, Farkas DK, Laugesen K, Skajaa N, Henderson VW, Boffetta P et al. Cancer Diagnosis and Prognosis After Guillain-Barré Syndrome: A Population-Based Cohort Study. Clinical epidemiology. 2022 jul.;2022(14):871-878. doi: 10.2147/CLEP.S369908

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@article{3a2ef7a6e73e4ad4ae072e0a9f61ad06,
title = "Cancer Diagnosis and Prognosis After Guillain-Barr{\'e} Syndrome: A Population-Based Cohort Study",
abstract = "Introduction: It is unclear whether Guillain-Barr{\'e} syndrome (GBS) can be a marker of a paraneoplastic syndrome. We examined whether GBS is associated with cancer and whether the prognosis of GBS patients with cancer differs from that of other cancer patients.Materials and Methods: We conducted a population-based cohort study of patients diagnosed with GBS between 1978 and 2017 using Danish registry-data. Main outcome measures were cancer incidence and mortality after cancer diagnosis. We calculated absolute risks of a cancer diagnosis, treating death as competing risk, and standardized incidence ratios (SIRs) as measures of relative risk. We matched each GBS cancer patient with up to 10 cancer patients without a GBS diagnosis and examined the six-month survival after cancer diagnosis using Cox regression analysis.Results: We identified 7897 patients (58% male, median age 57 years) with GBS. During a median follow-up of 9.5 years, the one-year risk of cancer was 2.7% (95% confidence interval (CI), 2.4-3.1). The SIR was increased throughout follow-up, but most noticeably during the first year after diagnosis (SIR: 3.35, 2.92-3.83). SIRs were particularly elevated for hematologic cancers (SIR: 8.67, 6.49-11.34), smoking-related cancers (SIR: 3.57, 2.81-4.47), and cancers of neurological origin (SIR: 8.60, 5.01-13.77). Lung cancer was the main contributor to the overall excess risk, which persisted after 36 months of follow-up (SIR: 1.17, 1.09-1.25). The mortality rate ratio comparing patients diagnosed with any cancer within one year of their GBS diagnosis and matched GBS-free cancer cohort members was 1.56 (95% CI, 1.27-1.90).Conclusion: GBS patients had a three-fold increased risk of cancer diagnosis in the first year of follow-up. The absolute cancer risk was almost 3.0%. A GBS diagnosis was an adverse prognostic marker for survival following cancer diagnosis. Clinicians should consider occult cancer in patients hospitalized with GBS.",
keywords = "Guillain–Barr{\'e} syndrome, cancer, cohort, paraneoplastic syndrome, risk, survival",
author = "Blean Girma and Farkas, {D{\'o}ra K{\"o}rmendin{\'e}} and Kristina Laugesen and Nils Skajaa and Henderson, {Victor W} and Paolo Boffetta and S{\o}rensen, {Henrik Toft}",
note = "{\textcopyright} 2022 Girma et al.",
year = "2022",
month = jul,
doi = "10.2147/CLEP.S369908",
language = "English",
volume = "2022",
pages = "871--878",
journal = "Clinical epidemiology",
issn = "1179-1349",
publisher = "Dove Medical Press Ltd.",
number = "14",

}

RIS

TY - JOUR

T1 - Cancer Diagnosis and Prognosis After Guillain-Barré Syndrome

T2 - A Population-Based Cohort Study

AU - Girma, Blean

AU - Farkas, Dóra Körmendiné

AU - Laugesen, Kristina

AU - Skajaa, Nils

AU - Henderson, Victor W

AU - Boffetta, Paolo

AU - Sørensen, Henrik Toft

N1 - © 2022 Girma et al.

PY - 2022/7

Y1 - 2022/7

N2 - Introduction: It is unclear whether Guillain-Barré syndrome (GBS) can be a marker of a paraneoplastic syndrome. We examined whether GBS is associated with cancer and whether the prognosis of GBS patients with cancer differs from that of other cancer patients.Materials and Methods: We conducted a population-based cohort study of patients diagnosed with GBS between 1978 and 2017 using Danish registry-data. Main outcome measures were cancer incidence and mortality after cancer diagnosis. We calculated absolute risks of a cancer diagnosis, treating death as competing risk, and standardized incidence ratios (SIRs) as measures of relative risk. We matched each GBS cancer patient with up to 10 cancer patients without a GBS diagnosis and examined the six-month survival after cancer diagnosis using Cox regression analysis.Results: We identified 7897 patients (58% male, median age 57 years) with GBS. During a median follow-up of 9.5 years, the one-year risk of cancer was 2.7% (95% confidence interval (CI), 2.4-3.1). The SIR was increased throughout follow-up, but most noticeably during the first year after diagnosis (SIR: 3.35, 2.92-3.83). SIRs were particularly elevated for hematologic cancers (SIR: 8.67, 6.49-11.34), smoking-related cancers (SIR: 3.57, 2.81-4.47), and cancers of neurological origin (SIR: 8.60, 5.01-13.77). Lung cancer was the main contributor to the overall excess risk, which persisted after 36 months of follow-up (SIR: 1.17, 1.09-1.25). The mortality rate ratio comparing patients diagnosed with any cancer within one year of their GBS diagnosis and matched GBS-free cancer cohort members was 1.56 (95% CI, 1.27-1.90).Conclusion: GBS patients had a three-fold increased risk of cancer diagnosis in the first year of follow-up. The absolute cancer risk was almost 3.0%. A GBS diagnosis was an adverse prognostic marker for survival following cancer diagnosis. Clinicians should consider occult cancer in patients hospitalized with GBS.

AB - Introduction: It is unclear whether Guillain-Barré syndrome (GBS) can be a marker of a paraneoplastic syndrome. We examined whether GBS is associated with cancer and whether the prognosis of GBS patients with cancer differs from that of other cancer patients.Materials and Methods: We conducted a population-based cohort study of patients diagnosed with GBS between 1978 and 2017 using Danish registry-data. Main outcome measures were cancer incidence and mortality after cancer diagnosis. We calculated absolute risks of a cancer diagnosis, treating death as competing risk, and standardized incidence ratios (SIRs) as measures of relative risk. We matched each GBS cancer patient with up to 10 cancer patients without a GBS diagnosis and examined the six-month survival after cancer diagnosis using Cox regression analysis.Results: We identified 7897 patients (58% male, median age 57 years) with GBS. During a median follow-up of 9.5 years, the one-year risk of cancer was 2.7% (95% confidence interval (CI), 2.4-3.1). The SIR was increased throughout follow-up, but most noticeably during the first year after diagnosis (SIR: 3.35, 2.92-3.83). SIRs were particularly elevated for hematologic cancers (SIR: 8.67, 6.49-11.34), smoking-related cancers (SIR: 3.57, 2.81-4.47), and cancers of neurological origin (SIR: 8.60, 5.01-13.77). Lung cancer was the main contributor to the overall excess risk, which persisted after 36 months of follow-up (SIR: 1.17, 1.09-1.25). The mortality rate ratio comparing patients diagnosed with any cancer within one year of their GBS diagnosis and matched GBS-free cancer cohort members was 1.56 (95% CI, 1.27-1.90).Conclusion: GBS patients had a three-fold increased risk of cancer diagnosis in the first year of follow-up. The absolute cancer risk was almost 3.0%. A GBS diagnosis was an adverse prognostic marker for survival following cancer diagnosis. Clinicians should consider occult cancer in patients hospitalized with GBS.

KW - Guillain–Barré syndrome

KW - cancer

KW - cohort

KW - paraneoplastic syndrome

KW - risk

KW - survival

U2 - 10.2147/CLEP.S369908

DO - 10.2147/CLEP.S369908

M3 - Journal article

C2 - 35898330

VL - 2022

SP - 871

EP - 878

JO - Clinical epidemiology

JF - Clinical epidemiology

SN - 1179-1349

IS - 14

ER -