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  • 1
    ISSN: 1432-0843
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Carboplatin (Cb) is an active drug in ovarian carcinoma that has fewer visceral side effects than cisplatin (CDDP) but higher myelotoxicity, which makes it difficult to combine at efficient doses with other myelotoxic drugs. In a preliminary study in advanced ovarian carcinoma, Rosso et al. [4] showed the maximum tolerated dose of Cb given in combination with cyclophosphamide (C) and adriamycin (A) to be 200 mg/m2. Since the efficacy of Cb may be dose-dependent, as is that of CDDP, we started a feasibility study of a CACb-300 regimen, that is, using Cb at 300 mg/m2 with lower C and A doses. Our data shows that the CACb-300 combination can safely be given in previously untreated patients for at least six 28-day cycles.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical microbiology & infectious diseases 4 (1985), S. 343-344 
    ISSN: 1435-4373
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract A case of fatal septicemia withSelenomonas sputigena in an immunocompromised patient is reported. The patient had a lung abscess from which the septicemia is believed to have originated. In contrast to the only other case reported in the literature, the isolate from our patient was characterized by very slow and difficult growth.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1569-8041
    Keywords: 5-FU continuous infusion ; metastatic breast carcinoma ; multidrug resistance ; verapamil
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Background:Verapamil (VER), a potent calcium channel blocker, hasbeen found to overcome P-gp-mediated multi-drug resistance (MDR) and toincrease sensitivity to cytotoxic anticancer drugs in refractory myeloma andnon-Hodgkin lymphoma. The value of VER for treating solid tumors is still amatter for debate. Patients and methods:We performed a prospective study in 99patients with anthracycline-resistant metastatic breast carcinoma (MBC), toassess the clinical effect of oral VER given in association with chemotherapy.Instead of retreating patients with anthracycline, we used a partiallynoncross-resistant regimen (VF), combining vindesine (VDS) and 5-fluorouracilgiven as a continuous infusion (5-FU CI). Patients were randomly assigned totwo cohorts. One cohort (47 patients) was treated in 28-day cycles, eachinvolving the administration of VDS (3 mg/m2 i.v. bolus on days 1and 10) and 5-FU CI, (400 mg/m2/day i.v. from day 1 to day 10). Theother cohort (52 patients) received the same VDS and 5-FU treatment and anadditional oral VER treatment (240 mg/day divided in 2 doses), from day 1 today 28 of each cycle. Patients were treated until progression. Results:The treatment was well tolerated and no side effects thatcould be attributed to VER were detected. Patients treated with VER had longeroverall survival (OS) (median OS: 323 vs. 209 days, P = 0.036) anda higher response rate (27% vs. 11%, P = 0.04) thanthose not given VER. Progression-free survival (PFS) was also longer but thedifference was not statistically significant (median PFS: 4.6 and 2.7 monthsfor the VER and non-VER groups respectively, P = 0.6). Conclusions:This clinical trial demonstrates that achemosensitizer, such as VER, can increase the survival of MBC patients withacquired anthracycline resistance.
    Type of Medium: Electronic Resource
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