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Objectives
This is an observational study aimed at updating the overall survival (OS), the progression free survival (PFS) to accelerated-blastic (AB) phase and the complete cytogenetic response (CCgR) duration of the CML patients who between 1986 and 2001 were treated with an IFN based therapy (either alone or in combination) and who obtained a CCgR. It also aims at analysing the clinical and biological features of this selected cohort of patients with persisting CCgR after treatment with IFN.
Study design This study is an observational retrospective multicenter study.
Assessment and Follow-up Patients' demographic data and retrospective collection of CML cytogenetic and molecular data will be reported in the "Assessment and Follow-up FORM".
In this FORM the events related to therapy, disease and survival will also be reported.
Duration of the study:
The recruitment period is estimated in approximately 2 years.
Study rational
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| CML and interpheron alpha | Adult Ph+CML pts in CCgR after IFN alpha. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Interpheron alpha | Drug | Long term outcom after interferon alpha discontinuation or not |
|
| Measure | Description | Time Frame |
|---|---|---|
| Progression Free Survival | One primary outcome measure is the PFS of the CML patients who between 1986 and 2001 were treated with IFN based therapy (either alone or in combination) and who obtained the CCgR. | From date of enrollment until the date of first documented progression, assessed up to 240 months |
| Duration of Complete Cytogenetic Response (CCgR) | One primary outcome measure is the duration of CCgR of the CML patients who between 1986 and 2001 were treated with IFN based therapy (either alone or in combination) and who obtained the CCgR. | From date of enrollment until the date of first documented loss of CCgR, assessed up to 240 months |
| Overall Survival | OS will be calculated from the date of diagnosis until date of death (whatever the cause). Patients still alive will be censored at the moment of last follow-up. | From date of enrollment until the date of first documented death from any cause, assessed up to 240 months |
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Inclusion criteria
Exclusion Criteria:
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Adult (>18 years old) patients with CP Ph+/BCR-ABL CML and with CCgR after therapy including IFN alpha.
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| Name | Affiliation | Role |
|---|---|---|
| Domenico Russo | Università degli Studi di Brescia | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Chair of hematology | Brescia | 25123 | Italy |
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| ID | Term |
|---|---|
| D015464 | Leukemia, Myelogenous, Chronic, BCR-ABL Positive |
| ID | Term |
|---|---|
| D007951 | Leukemia, Myeloid |
| D007938 | Leukemia |
| D009370 | Neoplasms by Histologic Type |
| D009369 | Neoplasms |
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| D009196 |
| Myeloproliferative Disorders |
| D001855 | Bone Marrow Diseases |
| D006402 | Hematologic Diseases |
| D006425 | Hemic and Lymphatic Diseases |
| D002908 | Chronic Disease |
| D020969 | Disease Attributes |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |