Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    ISSN: 1432-0584
    Keywords: Acute nonlymphocytic leukemia ; Intensified induction therapy ; Toxicity ; Response
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Sixty patients with ANLL were given intensified remission induction therapy consisting of thioguanine, cytosine arabinoside and daunorubicin (TAD). The mean age of patients was 47.6 years (range 18 to 74 years). Basing on leukemic cell kinetic data time sequencing of drugs was different from the original TAD protocol. Complete remission (CR) was achieved in 43/60 patients (72%) with 10 CR in 15 patients over 60 years of age. Seventy-nine percent of the CR were induced by one cycle vs. thirty percent reported from the original TAD regimen. The major cause of induction failure — in ten of the 60 patients — was thrombocytopenia refractory to platelet transfusions. Persisting leukemia after two induction cycles was documented in only two patients. Median remission duration by life table analysis is 10 months with 17 patients in continuous CR for 1+ to 22+ months.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    ISSN: 1432-0584
    Keywords: Akute nichtlymphoblastische Leukämie ; intensivierte Induktionstherapie ; Toxizität ; prognostische Faktoren ; Acute nonlymphocytic leukemia ; Intensified induction therapy ; Toxicity ; Prognostic factors
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Summary Cytosine arabinoside (ARA-C) and daunorubicin (DNR) (7+3 regimen) produced complete remission (C.R.) in 16 of 31 adult patients with ANLL (regimen A). Addition of vincristine (VCR) and ifosfamide (IF) revealed C.R. in 5 of 11 patients (regimen B). Dosage escalation for ARA-C and DNR and additional thioguanine (T.A.D. regimen) produced C.R. in 5 of 9 patients when ARA-C was given by continuous infusion (regimen D) and in 8 of 10 patients when given by bolus injections (regimen F). Clearance of blasts from the bone marrow by the first course was achieved in 11 of 14 patients by the T.A.D. regimens D and F vs. 15 of 38 patients by regimens A and B (p〈0.05). Time to recovery of neutrophils and platelets after one course of D or F was not prolonged as compared to A and B provided that clearance of bone marrow blasts was adequate. Increased dose of ARA-C by continuous infusion (D) instead of bolus injections (F) induced unacceptable gastrointestinal toxicity. In (only evaluable) regimen A median remission duration was 11.5 (1-31+) months. In patients with adequate blast clearance by the first course median remission duration was 19 (5-31+) months vs. 2.5 (1–6) months in the delayed blast clearance group (p〈0.001). In patients under 60 years of age in regimens D and F 11 of 11 achieved C.R. vs. 18 of 34 in A and B (p〈0.025). In patients receiving chemotherapy at original dosage 12 of 14 in regimens D and F achieved C.R. vs. 13 of 26 in A and B (p〈0.1).
    Notes: Zusammenfassung Cytosin-Arabinosid (ARA-C) und Daunorubicin (DNR) (7+3-Schema) führten bei 16 von 31 erwachsenen Patienten mit ANLL zu einer kompletten Remission (C.R.) (Regime A). Das identische Schema erweitert durch Vincristin (VCR) und Ifosfamid (IF) ergab eine C.R. bei 5 von 11 Patienten (Regime B). Dosissteigerung für ARA-C und DNR sowie Ergänzungen durch Thioguanin (TG) (T.A.D.-Schema) ergab C.R. bei 5 von 9 Patienten, wenn ARA-C kontinuierlich infundiert wurde (Regime D) und bei 8 von 10 Patienten wenn ARA-C als Bolus-Injektionen gegeben wurde (Regime F). Eine adäquate Blastenreduktion im Knochenmark bereits nach dem ersten Kurs zeigten bei den T.A.D.-Schemata D und F 11 von 14 Patienten gegenüber 15/38 bei A und B (p〈0,05). Die Erholungszeit der Neutrophilen und Thrombozyten war nach einem D- oder F-Kurs nicht länger als nach einem A- oder B-Kurs, sofern eine adäquate Blastenreduktion erzielt wurde. Erhöhte Dosis von ARA-C als Dauerinfusion (D) statt Bolusinjektion (F) verursachte inakzeptable gastro-intestinale Nebenwirkungen. Nach dem am längsten verfolgten Regime A betrug die mediane Remissionsdauer 11,5 (1-31+) Monate, und zwar bei Patienten mit adäquater Blastenreduktion durch den ersten Kurs 19 (5-31+) Monate vs. 2,5 (1–6) Monate bei Patienten mit verzögerter Blastenreduktion (p〈0,001). Bei Patienten unter 60 Jahren erreichten 11/11 bei den Regimen D und F eine C.R. gegenüber 18/34 in A und B (p〈0,025). Bei den Patienten ohne Dosisreduktion erreichten 12/14 bei den Regimen D und F und 13/36 bei A und B eine C.R. (p〈0,1).
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 17 (1988), S. 411-414 
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 19 (1990), S. 286-294 
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The electrospray ionization (ESI) and plasma desorption (PD) mass spectra of over 20 peptides and proteins, with molecular weights (Mr) ranging between 1182 and 143000, have been directly compared. Both techniques produced molecular ions for the majority of materials studied; however, neither approach proved to be universally applicable. PD failed for a number of proteins that were successfully analyzed by ESI, including some of very high Mr. On the other hand, ESI failed for proteins that apparently could not acquire a sufficient number of positive charges to allow transmission through the quadrupole mass filter. A non-covalently bound adduct, ribonuclease S, did not survive either method intact and a simple glycoprotein, ribonuclease B, did not yield the expected molecular ion with either approach. The mass measurement accuracy of quadrupole ESI is five to tenfold better than obtained with a commercial time-of-flight PD mass spectrometer. Furthermore, ESI's superior mass resolution (with quadrupole mass spectrometers) will prove to be particularly helpful for the characterization of mixtures of closely related materials. Sensitivity was only compared qualitatively but is highly compound dependent with both techniques. In favorable cases, ESI spectra can be obtained on low femtomolar quantities of proteins while PD typically requires several hundred femtomoles to high picomoles, depending on a number of factors including Mr.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Rapid Communications in Mass Spectrometry 4 (1990), S. 297-299 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: In standard pulsed ion cyclotron resonance mass spectrometry (ICRMS) mass spectra are generated by converting the time domain signal to the frequency or mass domain by fast Fourier transform (FFT). The FFT requires long acquisition times to acquire high resolution mass spectra. In ICRMS, long acquisition times introduce distortions in the peak intensities of the transformed spectrum that lead to errors in ion abundance. We report here the use of linear prediction methods on data sets collected during much shorter acquisition times to determine actual ion abundances more accurately.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...