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Impact of Granulocyte Colony-Stimulating Factor (G-CSF) on the Outcomes of Patients With Metastatic Pancreatic Adenocarcinoma (MPA) During First-Line Treatment With FOLFIRINOX: A Single-Center Retrospective Analysis
by
Fonseca de Jesus, Victor Hugo
, Riechelmann, Rachel P
, Carvalho de Brito, Angelo Borsarelli
in
Adenocarcinoma
/ Adenocarcinoma - drug therapy
/ Antineoplastic Combined Chemotherapy Protocols - therapeutic use
/ Cancer
/ Colony-stimulating factor
/ Disease prevention
/ Granulocyte colony-stimulating factor
/ Granulocyte Colony-Stimulating Factor - therapeutic use
/ Granulocytes
/ Hope In Despair - New Progress in The Diagnosis and Treatment of Pancreatic Cance-Original
/ Humans
/ Leukocytes (granulocytic)
/ Metastases
/ Metastasis
/ Multivariate analysis
/ Neutropenia
/ Neutropenia - drug therapy
/ Neutropenia - etiology
/ Neutropenia - prevention & control
/ Pancreas
/ Pancreatic cancer
/ Pancreatic Neoplasms
/ Pancreatic Neoplasms - drug therapy
/ Pancreatic Neoplasms - etiology
/ Population studies
/ Retrospective Studies
/ Sensitivity analysis
/ Survival
2023
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Impact of Granulocyte Colony-Stimulating Factor (G-CSF) on the Outcomes of Patients With Metastatic Pancreatic Adenocarcinoma (MPA) During First-Line Treatment With FOLFIRINOX: A Single-Center Retrospective Analysis
by
Fonseca de Jesus, Victor Hugo
, Riechelmann, Rachel P
, Carvalho de Brito, Angelo Borsarelli
in
Adenocarcinoma
/ Adenocarcinoma - drug therapy
/ Antineoplastic Combined Chemotherapy Protocols - therapeutic use
/ Cancer
/ Colony-stimulating factor
/ Disease prevention
/ Granulocyte colony-stimulating factor
/ Granulocyte Colony-Stimulating Factor - therapeutic use
/ Granulocytes
/ Hope In Despair - New Progress in The Diagnosis and Treatment of Pancreatic Cance-Original
/ Humans
/ Leukocytes (granulocytic)
/ Metastases
/ Metastasis
/ Multivariate analysis
/ Neutropenia
/ Neutropenia - drug therapy
/ Neutropenia - etiology
/ Neutropenia - prevention & control
/ Pancreas
/ Pancreatic cancer
/ Pancreatic Neoplasms
/ Pancreatic Neoplasms - drug therapy
/ Pancreatic Neoplasms - etiology
/ Population studies
/ Retrospective Studies
/ Sensitivity analysis
/ Survival
2023
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Impact of Granulocyte Colony-Stimulating Factor (G-CSF) on the Outcomes of Patients With Metastatic Pancreatic Adenocarcinoma (MPA) During First-Line Treatment With FOLFIRINOX: A Single-Center Retrospective Analysis
by
Fonseca de Jesus, Victor Hugo
, Riechelmann, Rachel P
, Carvalho de Brito, Angelo Borsarelli
in
Adenocarcinoma
/ Adenocarcinoma - drug therapy
/ Antineoplastic Combined Chemotherapy Protocols - therapeutic use
/ Cancer
/ Colony-stimulating factor
/ Disease prevention
/ Granulocyte colony-stimulating factor
/ Granulocyte Colony-Stimulating Factor - therapeutic use
/ Granulocytes
/ Hope In Despair - New Progress in The Diagnosis and Treatment of Pancreatic Cance-Original
/ Humans
/ Leukocytes (granulocytic)
/ Metastases
/ Metastasis
/ Multivariate analysis
/ Neutropenia
/ Neutropenia - drug therapy
/ Neutropenia - etiology
/ Neutropenia - prevention & control
/ Pancreas
/ Pancreatic cancer
/ Pancreatic Neoplasms
/ Pancreatic Neoplasms - drug therapy
/ Pancreatic Neoplasms - etiology
/ Population studies
/ Retrospective Studies
/ Sensitivity analysis
/ Survival
2023
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Impact of Granulocyte Colony-Stimulating Factor (G-CSF) on the Outcomes of Patients With Metastatic Pancreatic Adenocarcinoma (MPA) During First-Line Treatment With FOLFIRINOX: A Single-Center Retrospective Analysis
Journal Article
Impact of Granulocyte Colony-Stimulating Factor (G-CSF) on the Outcomes of Patients With Metastatic Pancreatic Adenocarcinoma (MPA) During First-Line Treatment With FOLFIRINOX: A Single-Center Retrospective Analysis
2023
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Overview
Introduction
The role of primary prophylaxis (PP) with granulocyte colony-stimulating factor (G-CSF) for patients with metastatic pancreatic adenocarcinoma (MPA) treated with FOLFIRINOX is unknown. We aimed to compare the frequencies of grades 3 or 4 neutropenia (G3/4N) and febrile neutropenia (FN) and survival outcomes according to the use of PP.
Methods
This is a retrospective study. We included patients with pathologically confirmed MPA treated with FOLFIRINOX in first-line. Patients who received primary prophylaxis (PP group) were compared to patients who received secondary or no G-CSF (no-PP group). Overall survival (OS) and progression-free survival (PFS) were evaluated using the standard Cox proportional hazard model. To account for potential biases, we performed sensitivity analyses excluding patients who received secondary prophilaxis and treating G-CSF as a time-dependent covariate in extended Cox proportional hazard models.
Results
The study population consisted of 123 patients. PP was used by 75 patients (61.0%). G3/4 N occurred more frequently among patients without PP (10.7 vs 41.7%; P < .001). There was no difference in the frequency of FN between groups (5.3 vs 8.3%; P = .710). In multivariate analysis, PP was associated with a trend toward improved OS (HR = .66; 95% confidence interval [95% CI] .41 - 1.07; P = .094). In the multivariate model excluding patients with secondary prophylaxis (HR = .54; 95% CI 0.32 - .91; P = .022) and in the time-dependent model (HR = .47; 95% CI 0.28 - .80; P = .005), PP was associated with statistically superior OS.
Conclusions
Despite the reduction in the frequency of G3/4N, the risk of FN among patients treated with FOLFIRINOX without G-CSF is too low to justify its use in a routine basis. However, given the potential of G-CSF to improve survival in this setting, further studies are warranted to assess its role during treatment with FOLFIRINOX for patients with MPA.
Publisher
SAGE Publications,Sage Publications Ltd,SAGE Publishing
Subject
/ Adenocarcinoma - drug therapy
/ Antineoplastic Combined Chemotherapy Protocols - therapeutic use
/ Cancer
/ Granulocyte colony-stimulating factor
/ Granulocyte Colony-Stimulating Factor - therapeutic use
/ Hope In Despair - New Progress in The Diagnosis and Treatment of Pancreatic Cance-Original
/ Humans
/ Neutropenia - prevention & control
/ Pancreas
/ Pancreatic Neoplasms - drug therapy
/ Pancreatic Neoplasms - etiology
/ Survival
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