Abstract
Six hundred eighty assessable patients with measureable stage III M1, non-small-cell lung cancer (NSCLC) were randomized to one of five treatment arms including cisplatin, etoposide (VP-16) +/- methylglyoxal bisguanylhydrazone (MGBG; PVp, PVpM); cisplatin, vinblastine (PVe); or PVe alternating with vinblastine, mitomycin (PVeMi); or fluorouracil, vincristine, mitomycin/cyclophosphamide, doxorubicin, cisplatin (FOMi/CAP). The overall response rate was 20% with 3% complete responses and 17% partial remissions. The duration of these responses was not statistically different by treatment regimen and varied from 2.7 months to 5.0 months. The overall median survival for all patients was 5.3 months and is not different by treatment. Toxicity was greater in PVpM. The similarity of results for response, duration of response, and survival does not establish the superiority of any of these platinum-based regimens for standard clinical usage.
Publication types
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Clinical Trial
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Randomized Controlled Trial
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Adult
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Aged
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Aged, 80 and over
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Antineoplastic Combined Chemotherapy Protocols / adverse effects
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Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
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Carcinoma, Non-Small-Cell Lung / drug therapy*
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Carcinoma, Non-Small-Cell Lung / mortality
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Cisplatin / administration & dosage
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Clinical Protocols
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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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Fluorouracil / administration & dosage
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Humans
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Lung Neoplasms / drug therapy*
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Lung Neoplasms / mortality
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Male
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Middle Aged
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Mitoguazone / administration & dosage
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Mitomycins / administration & dosage
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Peptichemio / administration & dosage
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Survival Rate
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United States
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Vinblastine / administration & dosage
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Vincristine / administration & dosage
Substances
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Mitomycins
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Vincristine
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Vinblastine
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Etoposide
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Doxorubicin
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Cyclophosphamide
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Peptichemio
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Mitoguazone
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Cisplatin
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Fluorouracil