Abstract
Optimal outcome for early breast cancer patients receiving adjuvant chemotherapy requires adequate dose delivery, commonly defined as >85% of planned dose of chemotherapy agents. Outside the clinical trial setting, reports from community oncology centres have demonstrated that a significant proportion of patients fail to receive this dose intensity, with neutropenia being the most commonly cited reason for sub-optimal treatment. Data collected prospectively on 1655 patient treated in a single breast cancer centre demonstrates that patients at risk of sub-optimal dose delivery can be identified by routine assessment of neutropenic events during the first cycle. The uniform administration of secondary G-CSF for all subsequent cycles enables dose delivery ≥85%, which was shown to lead to improved survival outcomes when compared with those patients who received <85%.
Keywords:
Breast cancer; First cycle nadir; G-CSF use; Relative dose intensity.
Copyright © 2014 Elsevier Ltd. All rights reserved.
Publication types
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Evaluation Study
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Research Support, Non-U.S. Gov't
MeSH terms
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Adenocarcinoma / drug therapy*
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Adenocarcinoma / mortality
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Adenocarcinoma / surgery
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Adult
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Aged
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Aged, 80 and over
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Antineoplastic Agents / administration & dosage
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Antineoplastic Combined Chemotherapy Protocols / administration & dosage*
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Antineoplastic Combined Chemotherapy Protocols / adverse effects
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Antineoplastic Combined Chemotherapy Protocols / therapeutic use
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Breast Neoplasms / drug therapy*
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Breast Neoplasms / mortality
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Breast Neoplasms / surgery
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Chemotherapy, Adjuvant
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Dose-Response Relationship, Drug
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Drug Administration Schedule
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Female
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Follow-Up Studies
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Granulocyte Colony-Stimulating Factor / therapeutic use*
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Hematologic Agents / therapeutic use*
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Humans
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Mastectomy*
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Middle Aged
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Neutropenia / chemically induced
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Neutropenia / prevention & control*
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Primary Prevention
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Secondary Prevention
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Survival Analysis
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Treatment Outcome
Substances
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Antineoplastic Agents
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Hematologic Agents
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Granulocyte Colony-Stimulating Factor