Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 7 de 7
Filter
Add more filters











Database
Publication year range
1.
Cytotherapy ; 4(2): 177-80, 2002.
Article in English | MEDLINE | ID: mdl-12006213

ABSTRACT

BACKGROUND: Treatment of HD using positively selected stem cells can achieve a durable CR in almost 80% patients, with a median follow-up of 24 months. We have found the use of positive selected CD34+ cells in the treatment of relapsed/progressive HD after high-dose chemotherapy to be a safe procedure with promising results. METHODS: Positively selected (CD34+) stem cells were employed for autografting in the patients with HD after high-dose chemotherapy. RESULTS: Between April 1996 and February 2001, 28 patients with relapsed/progressive HD were autografted with positively selected CD34+ cells at our Institute. All patients are alive and we did not observe any deaths as a result of toxicity. From this group, 22 (78.6%) patients are in durable CR, with a median follow-up of 24 months (range 7-65 months). Six (21.4%) patients relapsed but are now in CR after radiotherapy and mini-allogeneic transplantation (one patient) or radiotherapy (five patients). DISCUSSION: Autologous transplantation with positively selected CD34+ cells in relapsed HD is a safe and effective procedure in the treatment of this disease.


Subject(s)
Antigens, CD34/immunology , Hematopoietic Stem Cell Transplantation , Hematopoietic Stem Cells/immunology , Hodgkin Disease/therapy , Adult , Female , Humans , Male , Middle Aged , Transplantation, Autologous
2.
Anticancer Drugs ; 8(10): 949-57, 1997 Nov.
Article in English | MEDLINE | ID: mdl-9436638

ABSTRACT

Current evidence suggests that epoetin alpha administration is well tolerated and effective in the management of anemia of cancer and cancer chemotherapy. An open-label, multinational, non-comparative study was conducted in 215 cancer patients with anemia secondary to chemotherapy with platinum- or non-platinum-based combinations. Epoetin alpha was administered s.c. (150 IU/kg three times/week) for a planned period of 16 weeks. The response rate of epoetin alpha, defined as an increase in hemoglobin level of 2 g/dl or more from baseline, was 67%. The rate of response was not related to the chemotherapy regimen administered (platinum or non-platinum based). The percentage of patients transfused and the transfusion rate during epoetin alpha treatment were reduced. Transfusional need was eliminated in 64 (75%) of the 85 patients transfused before the study start, after 1 month of therapy. Quality of life, assessed using a visual analog scale, improved markedly in patients who experienced a hematological response. These patients also experienced a statistically significant (p < 0.0001) improvement in mean WHO performance score. These findings indicate that epoetin alpha is a well tolerated and effective agent which increases hemoglobin concentration and reduces transfusion requirements in anemic cancer patients receiving chemotherapy.


Subject(s)
Anemia/chemically induced , Anemia/drug therapy , Antineoplastic Combined Chemotherapy Protocols/adverse effects , Erythropoietin/therapeutic use , Hematinics/therapeutic use , Neoplasms/complications , Adolescent , Adult , Aged , Aged, 80 and over , Anemia/therapy , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Blood Transfusion , Carboplatin/administration & dosage , Cisplatin/administration & dosage , Epoetin Alfa , Erythropoietin/adverse effects , Female , Hematinics/adverse effects , Humans , Male , Middle Aged , Neoplasms/drug therapy , Recombinant Proteins
3.
Chemotherapy ; 38(4): 271-4, 1992.
Article in English | MEDLINE | ID: mdl-1473367

ABSTRACT

58 granulocytopenic patients with confirmed bronchopneumonia were divided retrospectively into two groups for this pilot study: group 1 included neutropenic patients with venous catheters who were treated with ciprofloxacin (CIP; 200-300 mg, i.v. b.i.d.) + vancomycin (VAN; 0.5-1 g, i.v. b.i.d.), and group 2, which included patients without venous catheters treated with ceftazidime (2 g, i.v. t.i.d.) + gentamicin (1 mg/kg, i.v. t.i.d.). Pneumonia was diagnosed clinically and radiologically in all patients; 92.3% in group 1 and 46.8% in group 2 were also microbially confirmed. Mixed infections were present in most patients. 3 of 26 patients (11.5%) in group 1 and 9 of 32 (20.1%) in group 2 did not recover while 88.5% in group 1 and 71.9% in group 2 recovered. CIP + VAN seems to be more effective in treating pneumonia in neutropenic patients, with only 1 patient in the group suffering an adverse effect compared with 5 in group 2.


Subject(s)
Agranulocytosis/complications , Bronchopneumonia/drug therapy , Drug Therapy, Combination/therapeutic use , Adult , Catheterization , Ceftazidime/therapeutic use , Ciprofloxacin/therapeutic use , Gentamicins/therapeutic use , Humans , Middle Aged , Pilot Projects , Vancomycin/therapeutic use
4.
Med Arh ; 43(1): 17-22, 1989.
Article in Croatian | MEDLINE | ID: mdl-2626067

ABSTRACT

The total number of cells, alveolar lymphocytes as well as T lymphocytes is increased in BAL in patients with active sarcoidosis (acute phase and relapse) with disturbed relation T4-T8 subpopulation. T lymphocytes are significantly decreased in peripheral blood of patients with active sarcoidosis, while B lymphocytes are also decreased but without evident significance in relation to normal values.


Subject(s)
Bronchoalveolar Lavage Fluid/cytology , Leukocyte Count , Lung Diseases/immunology , Lymphocytes , Sarcoidosis/immunology , Humans , Lung Diseases/blood , Sarcoidosis/blood
SELECTION OF CITATIONS
SEARCH DETAIL