Recurrence-Free Survival and Disease-Specific Survival in Patients with Pancreatic Neuroendocrine Neoplasms: A Single-Center Retrospective Study of 413 Patients

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Recurrence-Free Survival and Disease-Specific Survival in Patients with Pancreatic Neuroendocrine Neoplasms : A Single-Center Retrospective Study of 413 Patients. / Møller, Stine; Langer, Seppo W; Slott, Cecilie; Krogh, Jesper; Hansen, Carsten Palnæs; Kjaer, Andreas; Holmager, Pernille; Klose, Marianne; Garbyal, Rajendra Singh; Knigge, Ulrich; Andreassen, Mikkel.

In: Cancers, Vol. 16, No. 1, 100, 2023.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Møller, S, Langer, SW, Slott, C, Krogh, J, Hansen, CP, Kjaer, A, Holmager, P, Klose, M, Garbyal, RS, Knigge, U & Andreassen, M 2023, 'Recurrence-Free Survival and Disease-Specific Survival in Patients with Pancreatic Neuroendocrine Neoplasms: A Single-Center Retrospective Study of 413 Patients', Cancers, vol. 16, no. 1, 100. https://doi.org/10.3390/cancers16010100

APA

Møller, S., Langer, S. W., Slott, C., Krogh, J., Hansen, C. P., Kjaer, A., Holmager, P., Klose, M., Garbyal, R. S., Knigge, U., & Andreassen, M. (2023). Recurrence-Free Survival and Disease-Specific Survival in Patients with Pancreatic Neuroendocrine Neoplasms: A Single-Center Retrospective Study of 413 Patients. Cancers, 16(1), [100]. https://doi.org/10.3390/cancers16010100

Vancouver

Møller S, Langer SW, Slott C, Krogh J, Hansen CP, Kjaer A et al. Recurrence-Free Survival and Disease-Specific Survival in Patients with Pancreatic Neuroendocrine Neoplasms: A Single-Center Retrospective Study of 413 Patients. Cancers. 2023;16(1). 100. https://doi.org/10.3390/cancers16010100

Author

Møller, Stine ; Langer, Seppo W ; Slott, Cecilie ; Krogh, Jesper ; Hansen, Carsten Palnæs ; Kjaer, Andreas ; Holmager, Pernille ; Klose, Marianne ; Garbyal, Rajendra Singh ; Knigge, Ulrich ; Andreassen, Mikkel. / Recurrence-Free Survival and Disease-Specific Survival in Patients with Pancreatic Neuroendocrine Neoplasms : A Single-Center Retrospective Study of 413 Patients. In: Cancers. 2023 ; Vol. 16, No. 1.

Bibtex

@article{4802078520f849059a5496683bdc645d,
title = "Recurrence-Free Survival and Disease-Specific Survival in Patients with Pancreatic Neuroendocrine Neoplasms: A Single-Center Retrospective Study of 413 Patients",
abstract = "INTRODUCTION: The prognosis and impact of different prognostic factors in pancreatic neuroendocrine neoplasms (pNEN) remain controversial.AIM: To investigate prognostic factors for recurrence-free survival and disease-specific survival in patients with pNEN, divided into three groups: patients undergoing surveillance (tumor size < 2 cm, group 1), patients followed after curative-intended surgery (group 2), and patients with unresectable disease or residual tumors after resection (group 3).METHOD: A single-center retrospective study including consecutive patients over a 20-year period. Multivariate Cox regression analyses were performed to identify risk factors.RESULTS: 413 patients were included, with a mean (SD) age of 62 ± 14 years. In group 1 (n = 51), median (IQR) follow-up was 29 (21-34) months, and tumor size was 1.0 (0.8-1.4) cm. One progressed and had a tumor resection. In group 2 (n = 165), follow-up 59 (31-102) months, median tumor size 2 (1.2-3.4) cm, median Ki-67 index 5 (3-10)%, the 5-year recurrence rate was 21%. Tumor size ( p < 0.001), Ki-67 index ( p = 0.02), and location in the pancreatic head ( p < 0.001) were independent risk factors. In group 3 (n = 197), follow-up 19 (6-46) months, median tumor size 4.2 (2.6-7.0) cm, Ki-67 index 17 (9-64)%, the median disease-specific survival was 22 (6-75) months-99 in NET G1; 54 in NET G2; 14 in NET G3; and 6 months in neuroendocrine carcinomas (NEC). Age ( p = 0.029), plasma chromogranin A ( p = 0.014), and proliferation, expressed by grade ( p = 0.001) and Ki-67 index ( p < 0.001), were risk factors. CONCLUSION: Growth in pNET < 2 cm requiring surgery was observed in 1/51. Tumor size, Ki-67 index, and location in the head were prognostic factors for disease recurrence, while age, plasma chromogranin A, and proliferation predicted mortality in patients with unresectable disease or residual tumors after resection.",
author = "Stine M{\o}ller and Langer, {Seppo W} and Cecilie Slott and Jesper Krogh and Hansen, {Carsten Paln{\ae}s} and Andreas Kjaer and Pernille Holmager and Marianne Klose and Garbyal, {Rajendra Singh} and Ulrich Knigge and Mikkel Andreassen",
year = "2023",
doi = "10.3390/cancers16010100",
language = "English",
volume = "16",
journal = "Cancers",
issn = "2072-6694",
publisher = "M D P I AG",
number = "1",

}

RIS

TY - JOUR

T1 - Recurrence-Free Survival and Disease-Specific Survival in Patients with Pancreatic Neuroendocrine Neoplasms

T2 - A Single-Center Retrospective Study of 413 Patients

AU - Møller, Stine

AU - Langer, Seppo W

AU - Slott, Cecilie

AU - Krogh, Jesper

AU - Hansen, Carsten Palnæs

AU - Kjaer, Andreas

AU - Holmager, Pernille

AU - Klose, Marianne

AU - Garbyal, Rajendra Singh

AU - Knigge, Ulrich

AU - Andreassen, Mikkel

PY - 2023

Y1 - 2023

N2 - INTRODUCTION: The prognosis and impact of different prognostic factors in pancreatic neuroendocrine neoplasms (pNEN) remain controversial.AIM: To investigate prognostic factors for recurrence-free survival and disease-specific survival in patients with pNEN, divided into three groups: patients undergoing surveillance (tumor size < 2 cm, group 1), patients followed after curative-intended surgery (group 2), and patients with unresectable disease or residual tumors after resection (group 3).METHOD: A single-center retrospective study including consecutive patients over a 20-year period. Multivariate Cox regression analyses were performed to identify risk factors.RESULTS: 413 patients were included, with a mean (SD) age of 62 ± 14 years. In group 1 (n = 51), median (IQR) follow-up was 29 (21-34) months, and tumor size was 1.0 (0.8-1.4) cm. One progressed and had a tumor resection. In group 2 (n = 165), follow-up 59 (31-102) months, median tumor size 2 (1.2-3.4) cm, median Ki-67 index 5 (3-10)%, the 5-year recurrence rate was 21%. Tumor size ( p < 0.001), Ki-67 index ( p = 0.02), and location in the pancreatic head ( p < 0.001) were independent risk factors. In group 3 (n = 197), follow-up 19 (6-46) months, median tumor size 4.2 (2.6-7.0) cm, Ki-67 index 17 (9-64)%, the median disease-specific survival was 22 (6-75) months-99 in NET G1; 54 in NET G2; 14 in NET G3; and 6 months in neuroendocrine carcinomas (NEC). Age ( p = 0.029), plasma chromogranin A ( p = 0.014), and proliferation, expressed by grade ( p = 0.001) and Ki-67 index ( p < 0.001), were risk factors. CONCLUSION: Growth in pNET < 2 cm requiring surgery was observed in 1/51. Tumor size, Ki-67 index, and location in the head were prognostic factors for disease recurrence, while age, plasma chromogranin A, and proliferation predicted mortality in patients with unresectable disease or residual tumors after resection.

AB - INTRODUCTION: The prognosis and impact of different prognostic factors in pancreatic neuroendocrine neoplasms (pNEN) remain controversial.AIM: To investigate prognostic factors for recurrence-free survival and disease-specific survival in patients with pNEN, divided into three groups: patients undergoing surveillance (tumor size < 2 cm, group 1), patients followed after curative-intended surgery (group 2), and patients with unresectable disease or residual tumors after resection (group 3).METHOD: A single-center retrospective study including consecutive patients over a 20-year period. Multivariate Cox regression analyses were performed to identify risk factors.RESULTS: 413 patients were included, with a mean (SD) age of 62 ± 14 years. In group 1 (n = 51), median (IQR) follow-up was 29 (21-34) months, and tumor size was 1.0 (0.8-1.4) cm. One progressed and had a tumor resection. In group 2 (n = 165), follow-up 59 (31-102) months, median tumor size 2 (1.2-3.4) cm, median Ki-67 index 5 (3-10)%, the 5-year recurrence rate was 21%. Tumor size ( p < 0.001), Ki-67 index ( p = 0.02), and location in the pancreatic head ( p < 0.001) were independent risk factors. In group 3 (n = 197), follow-up 19 (6-46) months, median tumor size 4.2 (2.6-7.0) cm, Ki-67 index 17 (9-64)%, the median disease-specific survival was 22 (6-75) months-99 in NET G1; 54 in NET G2; 14 in NET G3; and 6 months in neuroendocrine carcinomas (NEC). Age ( p = 0.029), plasma chromogranin A ( p = 0.014), and proliferation, expressed by grade ( p = 0.001) and Ki-67 index ( p < 0.001), were risk factors. CONCLUSION: Growth in pNET < 2 cm requiring surgery was observed in 1/51. Tumor size, Ki-67 index, and location in the head were prognostic factors for disease recurrence, while age, plasma chromogranin A, and proliferation predicted mortality in patients with unresectable disease or residual tumors after resection.

U2 - 10.3390/cancers16010100

DO - 10.3390/cancers16010100

M3 - Journal article

C2 - 38201527

VL - 16

JO - Cancers

JF - Cancers

SN - 2072-6694

IS - 1

M1 - 100

ER -

ID: 380420035