Search Results - "Bizzari, J P"
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Docetaxel in the community setting: An analysis of 377 breast cancer patients treated with docetaxel (Taxotere®) in the UK
Published in Annals of oncology (01-02-1999)“…Background: Given as first- or second-line chemotherapy, docetaxel appears to have great potential in advanced breast cancer. Patients and methods: Three…”
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Activity and unexpected lung toxicity of the sequential administration of two alkylating agents--dacarbazine and fotemustine--in patients with melanoma
Published in European journal of cancer (1990) (1993)“…We report the results and discuss the toxicity of clinical trials based on a single concept: the decrease in O6alkyl DNA alkyltransferase (O6AT) resistance…”
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Multidrug resistance circumvention by a new triazinoaminopiperidine derivative S9788 in vitro: definition of the optimal schedule and comparison with verapamil
Published in British journal of cancer (01-05-1994)“…The current work was undertaken to investigate the importance of exposure sequence and duration in achieving the maximum reversal action of S9788 on…”
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Phase II study of nitrosourea fotemustine as single-drug chemotherapy in poor-prognosis non-small-cell lung cancer
Published in British journal of cancer (01-06-1994)“…A phase II study was designed to evaluate objective response rate and toxicity of fotemustine as single-drug chemotherapy in non-small-cell lung cancer…”
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Effects of a new triazinoaminopiperidine derivative on adriamycin accumulation and retention in cells displaying P-glycoprotein-mediated multidrug resistance
Published in Biochemical pharmacology (03-11-1992)“…A new triazinoaminopiperidine derivative, Servier 9788 (S9788), was investigated for its ability to increase Adriamycin (ADR) accumulation and retention in two…”
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Overview of docetaxel (Taxotere)/cisplatin combination in non-small cell lung cancer
Published in Seminars in oncology (01-06-1999)“…Cisplatin-based chemotherapy is effective in non-small cell lung cancer (NSCLC), although it prolongs survival only modestly. Single-agent docetaxel (Taxotere;…”
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Follow up of soluble IL‐2 receptor level in metastatic malignant melanoma patients treated by chemoimmunotherapy
Published in Clinical and experimental immunology (01-02-1994)“…SUMMARY Immunological parameters following chemoimmunotherapy combination were studied in 31 patients with metastatic malignant melanoina. They received…”
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Combined treatment with dacarbazine, cisplatin, fotemustine and tamoxifen in metastatic malignant melanoma
Published in Melanoma research (01-04-1998)“…The combination of dacarbazine (DTIC), cisplatin (DDP), carmustine and tamoxifen (TAM) has been reported to yield a high rate of response in patients with…”
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Phase I clinical study of the new amino acid-linked nitrosourea, S 10036, administered on a weekly schedule
Published in Cancer research (Chicago, Ill.) (15-12-1987)“…Diethyl-1-[3-(2-chloroethyl)-3-nitrosoureido]ethylphosphonate (S 10036) is a new nitrosourea that has been evaluated in a clinical trial because of its…”
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Interim report of phase II study of new nitrosourea S 10036 in disseminated malignant melanoma
Published in JNCI : Journal of the National Cancer Institute (02-11-1988)“…Thirty-three patients with disseminated malignant melanoma were entered in a phase II study of the new nitrosourea S 10036 using a 100-mg/m2 weekly induction…”
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In vitro chemosensitivity testing of Fotemustine (S 10036), a new antitumor nitrosourea
Published in Cancer chemotherapy and pharmacology (1990)“…Fotemustine (S 10036) is a new anti-tumor nitrosourea characterized by a phosphonoalanine carrier group coupled to the nitrosourea moiety, which potentially…”
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Fotemustine, dacarbazine, vindesine combination chemotherapy in advanced malignant melanoma: a phase II study of 43 patients
Published in Melanoma research (01-12-1995)“…Fotemustine and dacarbazine constitute the most active single chemotherapeutic agents in the treatment of melanoma. In this phase II study we evaluated the…”
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Characterization of the pharmacological antitumor effects of S 12363, a new vinca alkaloid
Published in Anticancer research (01-03-1991)“…S 12363 is a new highly potent vinca alkaloid derivative characterized by the grafting of an a-aminophosphonate, bioisoster of the valine, at the C23 position…”
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The estimation of self-renewal in the clonogenic cells of human solid tumours: A comparison of secondary plating efficiency and colony size
Published in British journal of cancer (01-08-1985)“…The in vitro clonogenicity of 25 human tumours was compared in two simple two layer culture systems, agar/agar and liquid medium/agar. There was a strong…”
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Fotemustine: an overview of its clinical activity in disseminated malignant melanoma
Published in Melanoma research (01-09-1992)“…Fotemustine is a new chloronitrosourea which is active against disseminated malignant melanoma (DMM), and especially against cerebral metastases (CM). This…”
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Fotemustine (S 10036) in the intra-arterial treatment of liver metastasis from malignant melanoma. A phase II Study
Published in American journal of clinical oncology (01-10-1991)“…Fotemustine is a new nitrosourea which has shown some efficacy on disseminated malignant melanoma (DMM) (24.2% response rate (RR) among 153 patients in a Phase…”
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Tamoxifen enhances the cytotoxic effects of the nitrosourea fotemustine. Results on human melanoma cell lines
Published in European journal of cancer (1990) (1993)“…Fotemustine (Fote) is a new amino acid-linked chloroethyl nitrosourea which has been shown to be useful in disseminated malignant melanoma. The aim of the…”
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Sequence-dependent cytotoxic effects of the combination of a new nitrosourea, fotemustine, with 5-fluorouracil plus folinic acid
Published in Cancer chemotherapy and pharmacology (01-01-1991)“…The present study was designed to analyse the cytotoxic effects of the combination of fotemustine with 5-fluorouracil (5-FU) plus folinic acid (FA). Two human…”
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Evaluation of the time-schedule dependency for the cytotoxic activity of the new vinca alkaloid derivative, S 12363 (vinfosiltine)
Published in European journal of cancer (1990) (1993)“…S 12363 is a new vinca alkaloid derivative obtained by appending an optically active alpha-aminophosphonate at the C23 position of 04-deacetyl vinblastine. The…”
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