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1.
Drug Res (Stuttg) ; 63(6): 305-10, 2013 Jun.
Article in English | MEDLINE | ID: mdl-23558603

ABSTRACT

Asthma is an increasing pathology with poor compliance. Achievement of control is possible but under intensive treatment. In this setting, fluticasone/salmeterol association delivered by dry powder inhalers is a valuable and proved option. A prospective, parallel, open-label, phase IV, multicentre non-inferiority study was conducted to determine therapeutic similarity between 2 different inhalers: Generic DPI and Diskus®, which both deliver a fluticasone/salmeterol association (CAS 80474-14-2/CAS 89365-50-4). A 103 uncontrolled asthmatic patients were randomly assigned in 2 groups, Generic (G) and Diskus® (D), and received the association for 18 weeks through the appropriate device. They were evaluated according to Asthma Quality of Life Questionnaire and GINA/NIH guidelines. To demonstrate non-inferiority, the estimation of the Relative Risk between the Global Score Rate per group with its 95% confidence interval was calculated and compared against a non-inferiority margin obtained from a previous study. The Global Score Rate was 82% for G Group and 83% for D Group. The RR was 1.0124 (95% CI: 0.847-1.210). The margin set at 0.832 was not reached by the lower 95% CI (z=-2.097; p=0.018) pointing out non-inferiority. The results have demonstrated non-inferiority between groups. Thus, the 2 products are therapeutically similar.


Subject(s)
Albuterol/analogs & derivatives , Androstadienes/administration & dosage , Anti-Asthmatic Agents/administration & dosage , Asthma/drug therapy , Dry Powder Inhalers , Adult , Albuterol/administration & dosage , Albuterol/adverse effects , Androstadienes/adverse effects , Drug Combinations , Female , Fluticasone-Salmeterol Drug Combination , Humans , Male , Middle Aged
2.
Med Pediatr Oncol ; 34(5): 338-42, 2000 May.
Article in English | MEDLINE | ID: mdl-10797355

ABSTRACT

BACKGROUND: Desmoplastic small round cell tumour (DSRCT) is a rare highly aggressive neoplasm, and clinical studies are scarce. PROCEDURE: We report six cases of children and adolescents (median age 14 years, range 6.9-17.5) with DSRCT (5 abdominal, 1 paratesticular) registered by the Italian Cooperative Group (ICG) for soft tissue sarcoma over a 9-year period. Patients received a multidisciplinary treatment, including aggressive initial or delayed surgery and radiotherapy. Chemotherapy regimen was based on the use of ifosfamide, vincristine, dactinomycin, and a few doses of antharacyclines (doxorubicin or epirubicin). RESULTS: Complete surgical resection was possible only for the paratesticular tumour. Among the patients with abdominal lesions, macroscopically radical excision was possible in only one case. All patients received multidrug chemotherapy, and tumour reduction was obtained in the 4 evaluable patients. No relapses were evident in the irradiated fields in the 4 patients who received radiotherapy. Two patients remained progression-free 22 and 63 months after diagnosis, one is in third complete remission, whereas three died 10-25 months after diagnosis. CONCLUSIONS: DSRCT is a chemosensitive tumour, but survival rates remain disappointing despite aggressive multimodality therapy. Our results support surgical tumour removal and radiotherapy to achieve local control. Our experience and a review of the literature suggest that patients with localised abdominal tumours or a paratesticular primary may have a better prognosis.


Subject(s)
Sarcoma, Small Cell/surgery , Abdominal Neoplasms/drug therapy , Abdominal Neoplasms/radiotherapy , Abdominal Neoplasms/surgery , Adolescent , Antibiotics, Antineoplastic/administration & dosage , Antineoplastic Agents, Alkylating/administration & dosage , Antineoplastic Agents, Phytogenic/administration & dosage , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Child , Combined Modality Therapy , Dactinomycin/administration & dosage , Disease-Free Survival , Humans , Ifosfamide/administration & dosage , Male , Neoplasm Recurrence, Local , Prognosis , Remission Induction , Salvage Therapy , Sarcoma, Small Cell/drug therapy , Sarcoma, Small Cell/radiotherapy , Sarcoma, Small Cell/secondary , Survival Rate , Testicular Neoplasms/drug therapy , Testicular Neoplasms/radiotherapy , Testicular Neoplasms/surgery , Vincristine/administration & dosage
3.
J Surg Oncol ; 71(4): 269-72, 1999 Aug.
Article in English | MEDLINE | ID: mdl-10440769

ABSTRACT

Desmoplastic small round cell tumor (DSRCT) is a rare neoplasm mainly affecting young males and typically located in the abdomen. Prognosis is generally very poor. We report a rare case of paratesticular DSRCT in a 17-year-old boy, presenting with an isolated left scrotal mass. The patient had an excellent outcome after complete surgical resection of the tumor and adjuvant multi-agent chemotherapy. DSRCT should be included in the differential diagnosis of small round cell tumors of the paratesticular region in adolescents and young adults. Tumor resection and chemotherapy may be beneficial for these patients. Our experience and a review of the literature suggest that DSRCT located in the paratesticular region may have a better prognosis than its more frequent abdominal counterpart.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Carcinoma, Small Cell/surgery , Genital Neoplasms, Male/surgery , Scrotum , Adolescent , Carcinoma, Small Cell/drug therapy , Combined Modality Therapy , Dactinomycin/administration & dosage , Genital Neoplasms, Male/drug therapy , Humans , Ifosfamide/administration & dosage , Male , Urologic Surgical Procedures, Male/methods , Vincristine/administration & dosage
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