Not provided
| ID | Type | Description | Link |
|---|---|---|---|
| 2006-006482-16 |
Not provided
Not provided
Not provided
Difficulties of enrollment
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Class |
|---|---|
| Centro di Riferimento per l'Epidemiologia e la Prev. Oncologica Piemonte | OTHER |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
This is a prospective, randomized multicenter phase III clinical trial designed to evaluate the safety and activity of comparison between Erythropoietin and Erythropoietin Associated to Differentiating Therapy With Acid 13-Cis-Retinoic and Dihydroxyvitamin D3 in Myelodysplastic Syndromes Without Excess of Blasts
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Infusion A: rEPO | Experimental | rEPO for 4 mounths consequently |
|
| Infusion B combined r-EPO | Experimental | rEPO in association with acid 13-cis-retinoic acid and Dihydroxyvitamin D3 for 4 mounths consequently |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| infusion A: rEPO | Drug | rEPO 40.000 unit/week for 4 mounths, then patients who have obtained an erythroid response, will continue for another 4 months with therapy rEPO. Patients who have not obtained an erythroid response, will increase the dose rEPO to 80,000 units per week for an additional 4 months. |
| Measure | Description | Time Frame |
|---|---|---|
| study of comparison between standard theraphy rEPO (40.000unit/week) and association therapy between rEPO (40.000unit/week)plus Acid 13-Cis-Retinoic and Dihydroxyvitamin D3 | After 8 months |
| Measure | Description | Time Frame |
|---|---|---|
| TO evaluate if,the patients without eritroyd response at the end of the 4° month of therapy, the increase of dose of rEPO to 80.000 U / week allows to get an increase of valued response at the end of the 8° month. | 8 months | |
| To evaluate if there is a difference of duration in the eritroyd response with standard therapy rEPO in comparison with association therapy rEPO plus Acid 13-Cis-Retinoic and Dihydroxyvitamin D3. |
Not provided
Inclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Affiliation | Role |
|---|---|---|
| Dario Ferrero, MD | University of Torino - Ospedale San Giovanni Battista | Study Director |
| Alessandro Levis, MD | Ospedale SS. Antonio, Biagio e Cesare Arrigo | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Ospedale SS. Antonio, Biagio e Cesare Arrigo | Alessandria | Italy | ||||
| Ospedale degli Infermi |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
|
| B Infusion rEPO combined with vitamins pills | Drug | rEPO 40.000 unit/week plus acid 13 cis-retinoic (20 mg/die) plus Dihydroxyvitamin D3 (1 μg os/die), for 4 mounths. Patients who have obtained an erythroid response will continue for another 4 months with the same therapy. Patients who have not obtained an erythroid will increase the dose of rEPO to 80,000 units per week for additional 4 months.Patients also will continue with the same doses of acid 13-cis-retinoic acid and Dihydroxyvitamin D3 |
|
| 20 mounths |
| To evaluate the existing relationships among eritroyd response and clinical-biological parameters at baseline of anemia, subclass of MDS, silky dosing of the EPO etc. | 20 mounths |
| To evaluate the quality of life improvement due to therapy. | 8 mounths |
| To evaluate the percentage of leukemic progression. | 20 mounths |
| Biella |
| Italy |
| Spedali civili | Brescia | Italy |
| Ospedale Santo Spirito | Casale (AL) | Italy |
| Ospedale Maggiore | Chieri (TO) | Italy |
| Policlinico dell'Annunziata | Cosenza | Italy |
| Ospedale Santa Croce e Carle | Cuneo | Italy |
| Ospedale Santa Croce | Fano (PU) | Italy |
| Ospedale San Martino | Genova | Italy |
| Ospedale civile | Ivrea (TO) | Italy |
| Ospedale San Gerardo | Monza (MI) | Italy |
| Ospedale Maggiore della Carità | Novara | Italy |
| Ospedale Civile | Ovada (AL) | Italy |
| Istituto clinico Humanitas | Rozzano (MI) | Italy |
| Ospedale San Giovanni Battista Molinette | Torino | Italy |
| Ospedale Cardinale Panico | Tricase (LE) | Italy |
| Ospedale Sant'Andrea | Vercelli | Italy |
| Ospedale San Bortolo | Vicenza | Italy |
| ID | Term |
|---|---|
| D009190 | Myelodysplastic Syndromes |
| ID | Term |
|---|---|
| D001855 | Bone Marrow Diseases |
| D006402 | Hematologic Diseases |
| D006425 | Hemic and Lymphatic Diseases |
Not provided
Not provided