Abstract
This phase III study was conducted to evaluate the usefulness of lenograstim as support for ACE (doxorubicin, cyclophosphamide, and etoposide) chemotherapy in previously untreated patients with small-cell lung cancer. Patients were randomized to receive up to six 3-week cycles of either ACE alone (n = 139) or ACE with lenograstim support (150 microg/m2/day subcutaneously, days 4-13, n = 141). Compared with the chemotherapy-alone group, the lenograstim support group was more likely to achieve neutrophil recovery (absolute neutrophil count, > or =1.5 x 10(9) cells/l) by day 14 (95.8-100% vs. 14.3-24.1% across the cycles) and less likely to experience at least one infectious episode (36.7 vs. 54.0%; p = 0.004), chemotherapy delay (51.8 vs. 56.2%; NS), or dose reduction (17.3 vs. 27.7%; p = 0.037). Objective response and event-free and overall survival rates were similar. Lenograstim was well tolerated. Lenograstim may allow the interval between cycles of ACE to be reduced to 2 weeks; such dose intensification may lead to more favorable objective response and survival rates.
Publication types
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Clinical Trial
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Clinical Trial, Phase III
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Comparative Study
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Multicenter Study
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Randomized Controlled Trial
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Research Support, Non-U.S. Gov't
MeSH terms
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Adjuvants, Immunologic / therapeutic use*
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Adult
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Aged
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Antibiotics, Antineoplastic / administration & dosage
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Antineoplastic Agents, Alkylating / administration & dosage
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Antineoplastic Agents, Phytogenic / administration & dosage
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Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
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Carcinoma, Small Cell / drug therapy*
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Cyclophosphamide / administration & dosage
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Doxorubicin / administration & dosage
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Etoposide / administration & dosage
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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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Humans
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Lenograstim
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Leukocyte Count / drug effects
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Lung Neoplasms / drug therapy*
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Male
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Middle Aged
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Neutrophils / drug effects
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Recombinant Proteins / therapeutic use
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Remission Induction
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Survival Rate
Substances
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Adjuvants, Immunologic
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Antibiotics, Antineoplastic
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Antineoplastic Agents, Alkylating
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Antineoplastic Agents, Phytogenic
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Recombinant Proteins
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Granulocyte Colony-Stimulating Factor
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Etoposide
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Lenograstim
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Doxorubicin
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Cyclophosphamide