bms-310705 and Neoplasms

bms-310705 has been researched along with Neoplasms* in 4 studies

Reviews

2 review(s) available for bms-310705 and Neoplasms

ArticleYear
Epothilones and new analogues of the microtubule modulators in taxane-resistant disease.
    Expert opinion on investigational drugs, 2008, Volume: 17, Issue:4

    Microtubule-stabilising agents typified by the epothilone class of drug have demonstrated promising activity in Phase II and III clinical trials.. Data supporting the efficacy of these agents are reviewed and their potential use in taxane-refractory disease assessed.. Preclinical evidence assessing the role of the spindle assembly checkpoint in determining the cellular response to microtubule stabilization are presented together with clinical data documenting the efficacy of non-taxane microtubule modulators.. Evidence suggests that microtubule-stabilising agents prolong activation of the spindle assembly checkpoint which may promote cancer cell death in mitosis or following mitotic exit. A weakened spindle assembly checkpoint is associated with altered sensitivity to agents targeting the microtubule and therefore pathways of drug resistance may be shared by these cytotoxic therapies. Preliminary clinical trial data do suggest modest activity of epothilones in truly taxane-resistant patient cohorts, indicating the potential niche for these agents in a molecularly undefined patient group, potentially implicating the role of P-glycoprotein in the acquisition of taxane-resistant disease. Trial data of these antimitotic agents will be presented together with their potential role in taxane-resistant disease and the implications for future clinical trial design.

    Topics: Animals; Antineoplastic Agents, Phytogenic; Cell Transformation, Neoplastic; Chromosomal Instability; Drug Resistance, Neoplasm; Drugs, Investigational; Epothilones; Gene Expression Regulation, Neoplastic; Humans; Microtubules; Mitosis; Neoplasms; Spindle Apparatus; Taxoids; Tubulin Modulators

2008
Current state of the art of new tubulin inhibitors in the clinic.
    Current clinical pharmacology, 2006, Volume: 1, Issue:1

    For years the microtubule stabilizing agents docetaxel and paclitaxel belong to the most successful clinical chemotherapeutic agents. Several attempts have been made over the years to equal and better these drugs. Both taxanes are associated with the notorious side effect neurotoxicity and are often accompanied with increased drug resistance and cross resistance with other chemotherapeutic agents. In addition their high lipophilicity demands use of co-solvents, which are associated with less favorable side effects such as hypersensitivity. To prevent these disadvantages and improve the clinical application of the taxanes several new agents have entered clinical testing. The agents that are discussed are the drug class of the discodermolides; XAA296A and the epothilones; BMS-247550, BMS-310705, epo906, kos-862 and the agents ABT-751 and D-24851. Here we present an overview of recently performed clinical studies to determine the current state of the art of the tubulin inhibitors which are intended to enlarge and improve the clinical use of the taxanes docetaxel and paclitaxel.

    Topics: Epothilones; Humans; Neoplasms; Tubulin Modulators

2006

Trials

1 trial(s) available for bms-310705 and Neoplasms

ArticleYear
Phase I clinical study of the novel epothilone B analogue BMS-310705 given on a weekly schedule.
    Annals of oncology : official journal of the European Society for Medical Oncology, 2007, Volume: 18, Issue:9

    BMS-310705, a water-soluble semi-synthetic analogue of epothilone B, was selected for clinical development because of its in vivo anti-tumour activity and toxicity profile similar to that of ixabepilone, currently the most extensively evaluated and promising epothilone B analogue. The improved solubility of BMS-310705 allowed a cremophore-free formulation that avoided the need for pre-medication.. Two schedules were tested, one with drug administrations on days (D) 1, 8 and 15 followed by 1-week's rest, the other with administrations on D1 and 8 (D1&8 schedule) followed by 1-week's rest. Treatment was given as a 15-min infusion without pre-medication against hypersensitivity. The plasma pharmacokinetics of BMS-310705 was studied in 30 patients. An accelerated titration design 2B was applied for dose escalations. Twenty-seven patients were accrued in the D1, 8, 15 and 32 in the D1&8 schedule.. The dose was escalated from 5-30 mg/m(2)/week with diarrhoea as dose-limiting toxicity; 15 and 20 mg/m(2) were the recommended doses in the D1, 8, 15 and D1&8 schedule, respectively. Other frequent non-haematological toxicities were neurotoxicity, mainly paraesthesia, asthenia and myalgia. Preliminary results showed linear pharmacokinetics along the range of doses tested with a short half-life. Five objective responses were reported.. Further clinical development of BMS-310705 might be worthwhile in solid tumours where ixabepilone or other epothilones are not indicated.

    Topics: Adult; Aged; Antineoplastic Agents; Diarrhea; Drug Administration Schedule; Epothilones; Female; Humans; Male; Middle Aged; Neoplasms; Nervous System Diseases; Neutropenia; Tubulin Modulators

2007

Other Studies

1 other study(ies) available for bms-310705 and Neoplasms

ArticleYear
From bacteria to antineoplastic: epothilones a successful history.
    Anti-cancer agents in medicinal chemistry, 2013, Volume: 13, Issue:7

    Malignancies are a major cause of morbidity and mortality worldwide. Cancer is a cell disease, characterized by a deviation of the control mechanisms of proliferation and differentiation of cells. Among the treatments available, chemotherapy is often the first choice. Epothilones are a new class of anticancer drugs that act by interacting with cellular microtubules interrupting the proliferation of cancer cells. Many synthetic and semi-synthetic analogues of epothilones have been prepared aiming improvement in effectiveness and tolerability, based on QSAR studies. These analogues have been effective for treatment of tumors resistant to first-line treatments. Six new epothilones are being subjected to clinical trials. Ixabepilone (Ixempra®) was approved by FDA in 2007, patupilone is in phase III clinical trial for ovarian and peritoneum cancer. Sagopilone, desoxiepothilone and KOS-1584 are in phase II clinical trials, for the treatment of recurrent glioblastoma and advanced metastatic breast cancer, metastasic breast cancer and metastatic pulmonary cancer, respectively. Desoxiepothilone reached only phase II trials and BMS-310705 reached phase III/IV trials, but were not approved for clinical use due to adverse effects such as neurotoxicity and severe diarrhea, which were dose-limiting. Furthermore, the low t1/2 (40h) in comparison with other class analogues, does not recommend the clinical use of this derivative. Some other synthetized epothilones presented antineoplastic activity in vitro, but are not yet submitted to clinical studies. Neuropathies and diarrhea are adverse effects presented by some substances of this class of anticancer drugs.

    Topics: Animals; Antineoplastic Agents; Bacteria; Benzothiazoles; Epothilones; History, 20th Century; History, 21st Century; Humans; Neoplasms; Structure-Activity Relationship

2013