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Cited 13 time in webofscience Cited 14 time in scopus
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Prognostic factors in patients with metastatic or recurrent pancreatic cancer treated with first-line nab-paclitaxel plus gemcitabine: implication of inflammation-based scores

Authors
Hwang, I[Hwang, Inhwan]Kang, J[Kang, Jihoon]Ip, HNN[Ip, Hei Nga Natalie]Jeong, JH[Jeong, Jae Ho]Kim, KP[Kim, Kyu-pyo]Chang, HM[Chang, Heung-Moon]Yoo, C[Yoo, Changhoon]Ryoo, BY[Ryoo, Baek-Yeol]
Issue Date
Jun-2019
Publisher
SPRINGER
Keywords
Pancreatic cancer; Chemotherapy; nab-paclitaxel; Gemcitabine; Prognostic factor; Neutrophil-lymphocyte ratio; Platelet-lymphocyte ratio; Glasgow prognostic scores
Citation
INVESTIGATIONAL NEW DRUGS, v.37, no.3, pp.584 - 590
Indexed
SCIE
SCOPUS
Journal Title
INVESTIGATIONAL NEW DRUGS
Volume
37
Number
3
Start Page
584
End Page
590
URI
https://scholarworks.bwise.kr/skku/handle/2021.sw.skku/9763
DOI
10.1007/s10637-018-0681-y
ISSN
0167-6997
Abstract
Background Nab-paclitaxel plus gemcitabine (AG) is standard first-line chemotherapy for patients with metastatic pancreatic cancer (mPC). However, prognostic factors for patients with mPC treated with AG, are largely unknown. We retrospectively identified prognostic factors, including inflammation-based prognostic scores, in patients with mPC, and recurrent pancreatic cancer treated with AG as first-line treatment. Method A total of 203 patients with histologically-confirmed recurrent or metastatic pancreatic cancer who were treated with first-line AG in Asan Medical Center, Seoul, Korea, between February 2016 and December 2016 were included in this analysis. As inflammation-based scores, baseline neutrophil-lymphocyte ratio (NLR), platelet-lymphocyte ratio (PLR) and modified Glasgow prognostic scores (mGPS) were tested. Result Median age was 62years and 116 patients (57%) were male. With median follow-up duration of 21.5months, median progression-free survival (PFS) was 7.1 (95% CI 6.2-7.9) months, and overall survival (OS) was 15.1 (95% CI 12.6-17.6) months. In the multivariate analysis, PFS was significantly associated with liver metastasis (HR 1.43), distant lymph node metastasis (HR 1.48), and elevated CA19-9 (HR 1.56). In multivariate analysis for OS, elevated CA19-9 (HR 1.75), liver metastasis (HR 1.76), distant lymph node metastasis (HR 1.41), and high mGPS (mGPS 1 vs.0: HR 1.64) were independent prognostic factors. NLR and PLR were not significantly associated with PFS and OS. Conclusion Among the inflammation based prognostic scores, mGPS was a reliable prognostic indicator that could stratify survival outcomes in patients with recurrent or mPC who received AG as first-line chemotherapy.
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