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  • 1
    ISSN: 1432-2307
    Keywords: Ewing's sarcoma ; Bone ; Histology ; Prognosis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary A retrospective multifactorial analysis on 261 previously untreated patients with Ewing's sarcoma (Es) of bone has been carried out in order to ascertain the prognostic value of several histological variables on survival. Among those cases accepted as Es, 208 (80% of the patients) were considered to be “typical Es”, while 40 (15%) displayed a large cell predominance, being subclassified as “atypical large cell Es”. Furthermore, 13 patients (5%) possessed tumours of endothelial-like appearance. Eleven cases which displayed a mixed histological configuration were finally included within one of the three previous groups according to their predominant histological pattern. After adjustment for therapeutic regimens and initial location of the tumour, only two histological characteristics remain significant; i.e. the presence of necrosis (p=0.002) and, to a lesser degree, the presence of filagree “en damier” pattern (p=0.08), both of which are of poor prognostic value. From this study, it can be assumed that the morphological (and possibly histogenetical) heterogeneity of Es of bone has no prognostic influence on survival.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1569-8041
    Keywords: ABMT ; anaplastic large-cell lymphoma ; children ; relapse ; vinblastine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Purpose:to study response to chemotherapy and the outcome ofchildren treated for a relapsed anaplastic large-cell lymphoma (ALCL) and toevaluate the role of bone marrow transplantation (BMT) in these patients. Patients and methods:Clinical data concerning the 41 relapsesthat occurred in 119 patients with ALCL enrolled in 3 consecutive studiessince 1975 were analysed. First-line treatment consisted of intensivechemotherapy according to the COPAD protocol for the first series of 12patients treated between 1975 and 1989 and to the SFOP (French Society ofPediatric Oncology) HM protocols for the 30 patients treated between 1989 and1997. Twenty-eight patients were treated with CV(B)A (CCNU, vinblastine, ara-Cwith or without bleomycin), and the others with miscellaneous protocols forrecurrent disease. Fifteen patients underwent autologous BMT and 1 allogeneicBMT while in CR2. Results:Thirty-six of forty-one (88%) patients achievedCR2. With a median follow-up of 5 years, 12 patients died, 9 of their diseaseand 29 patients are alive in CR2 (20 patients), CR3 (5 patients), CR4 (2patients), CR5 (1 patient) or CR6 (1 patient). Overall and disease-freesurvival are respectively 69% (53%–82%) and44% (29%–61%) at three years. In univariateanalysis, patients treated with ABMT while in CR2 did not appear to have abetter outcome than the other. Remarkably, a long-lasting remission wasobtained in 8 of 13 patients treated with weekly vinblastine for a relapseincluding 6 relapses occurring after ABMT. Conclusions:Relapsed ALCL are highly chemosensitive but over40% of the patients experience several relapses. Prolonged conventionalchemotherapy based on vinblastine might, in some cases, be as efficient asshort intensive treatment with ABMT.
    Type of Medium: Electronic Resource
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