Early administration of pegfilgrastim for esophageal cancer treated with docetaxel, cisplatin, and fluorouracil: A phase II study.
Adult
Aged
Antineoplastic Combined Chemotherapy Protocols
/ adverse effects
Cisplatin
/ administration & dosage
Docetaxel
/ administration & dosage
Esophageal Neoplasms
/ drug therapy
Female
Filgrastim
/ adverse effects
Fluorouracil
/ administration & dosage
Humans
Male
Middle Aged
Neutropenia
/ prevention & control
Polyethylene Glycols
/ adverse effects
Prospective Studies
cisplatin
docetaxel
esophageal cancer
neoadjuvant chemotherapy
neutropenia
pegfilgrastim
plus 5-fluorouracil therapy
Journal
Cancer science
ISSN: 1349-7006
Titre abrégé: Cancer Sci
Pays: England
ID NLM: 101168776
Informations de publication
Date de publication:
Dec 2019
Dec 2019
Historique:
received:
28
08
2019
revised:
12
10
2019
accepted:
15
10
2019
pubmed:
28
10
2019
medline:
18
12
2019
entrez:
25
10
2019
Statut:
ppublish
Résumé
Preoperative or induction chemotherapy with docetaxel, cisplatin, plus 5-fluorouracil (DCF) is a promising regimen for advanced esophageal cancer. However, the DCF regimen is associated with a high risk of severe neutropenia or febrile neutropenia (FN). However, the current guidelines fail to recommend an optimal dosing schedule of pegfilgrastim along with the DCF regimen to prevent FN. In the present study, we assessed the efficacy and safety of giving pegfilgrastim early on day 3 during DCF therapy for esophageal cancer. In this single-arm phase II study, patients with squamous cell carcinoma of the esophagus were recruited. They were treated with the DCF therapy on days 1-5, with pegfilgrastim given on day 3. Primary endpoint was the occurrence of grade 4 neutropenia. Secondary endpoints included the incidence of FN, grade 3 neutropenia, dose delays/reductions, antitumor effect, and safety. Between July 2016 and December 2018, 23 patients were enrolled. The incidence of grade 4 neutropenia was 8.7% (95% confidence interval 1.1%-28.0%). No patient experienced FN. Of the 19 patients who received two cycles of DCF, one required a dose reduction/treatment delay due to hematological toxicity in the second treatment cycle. No serious adverse events, considered relevant to pegfilgrastim, were observed. This is the first prospective study that showed an efficacious dosing schedule of pegfilgrastim for preventing hematological toxicity during DCF therapy. The results might be generalized to other similar regimens where continuous infusions of 5-fluorouracil are used.
Identifiants
pubmed: 31646714
doi: 10.1111/cas.14218
pmc: PMC6890431
doi:
Substances chimiques
Docetaxel
15H5577CQD
pegfilgrastim
3A58010674
Polyethylene Glycols
3WJQ0SDW1A
Filgrastim
PVI5M0M1GW
Cisplatin
Q20Q21Q62J
Fluorouracil
U3P01618RT
Types de publication
Clinical Trial, Phase II
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
3754-3760Informations de copyright
© 2019 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association.
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