T-Cell Project: Prospective Collection of Data in Patients With Peripheral T-Cell Lymphoma
The designed study follows up the retrospective previous one by the International T-cell Non-Hodgkin's Lymphoma Study Group (International Peripheral T-Cell Lymphoma Project).
It is designed as a prospective collection of information potentially useful to predict the prognosis of newly diagnosed patients with the more frequent subtypes of Peripheral T-cell lymphoma (Peripheral T-cell lymphoma unspecified and Angioimmunoblastic T-cell lymphoma) and to better define clinical characteristics and outcome of the more uncommon subtypes
Lymphoma, T-Cell, Peripheral
|Study Design:||Observational Model: Cohort
Time Perspective: Prospective
|Official Title:||Prospective Collection of Data in Patients With Peripheral T-Cell Lymphoma: PTCL,NOS;AITL; Extranodal NK/T-cell;Enteropathy-type T-cell; Hepatosplenic γ-δ T-cell; Subcutaneous Panniculitis-like T-cell; ALCL,T/Null Cell,Primary Systemic Type. From the International T-Cell Lymphoma Project.|
- Overall Survival (OS) [ Time Frame: 5 years ] [ Designated as safety issue: No ]
- Event Free Survival (EFS) [ Time Frame: 5 years ] [ Designated as safety issue: No ]
- Remission rate with initial therapy [ Time Frame: End of front-line therapy ] [ Designated as safety issue: No ]
- Progression Free Survival (PFS) [ Time Frame: 5-years ] [ Designated as safety issue: No ]
Biospecimen Retention: Samples Without DNA
Formalin-fixed tissue for central diagnostic pathology review
|Study Start Date:||September 2006|
|Estimated Study Completion Date:||December 2016|
|Estimated Primary Completion Date:||June 2016 (Final data collection date for primary outcome measure)|
Peripheral T-cell lymphomas (PTCLs) comprise a heterogeneous group of neoplasms that are derived from post-thymic lymphoid cells at different stages of differentiation with different morphological patterns, phenotypes, and clinical presentations. PTCLs are highly diverse, reflecting the diverse cells from which they can originate. Peripheral T-Cell Lymphomas account for 5-10% of all lymphoproliferative disorders in the Western hemisphere, with an overall incidence of 0.5-2 per 100,000 per year, and have a striking epidemiological distribution, with higher incidence in Asia.
The clinical features of PTCLs are extremely heterogeneous. PTCLs express even more clinical diversity than B-cell NHLs, and there is a close, though not absolute, relationship between some unusual clinical features and certain histological subtypes. Despite efforts to transferring to patients with T-cell lymphomas the most recent advances in the treatment of other subtypes of B-cell lymphomas, the prognosis of patients with PTCL is still poor an, unfortunately, the optimal therapy for PTCL is still unknown. The complete response rate is rather low, ranging from 40% to 50% with a median Relapse Free Survival (RFS) of 2-3 years. As a consequence of the aggressiveness of the disease and of the low efficacy of available salvage treatments, Overall Survival (OS) is also short and the long-term survival rate is lower than 10% in many series.
To better define the clinical outcome of PTCL-u, the Intergruppo Italiano Linfomi (IIL) performed a large study on 385 patients diagnosed and treated in the 1990s and defined a prognostic model specifically devised for patients with this uncommon disease (Gallamini, A. et al Blood, 2004. 103(7): p. 2474-9). In addition to defining a prognostic model specifically devised for PTCL-u, the IIL study confirms the relevance of research on series of clearly defined cases in order to the development of rationally designed and potentially more-efficacious treatment modalities. More recently, the role of biological features of the disease is emerging as an important issue not only for understanding its pathogenesis but also for prognosis and for addressing specific biologic targets altered in the neoplasia. Significant progress in the prognosis of PTCL can be expected from the novel, sophisticated, and powerful technologies of genomics and proteomics, which will allow more reliable subtyping of PTCL into distinct clinical groups characterized by different patterns of survival, as already demonstrated for some B-NHLs.
One common limitation of existing studies on prognosis of PTCL is their retrospective nature. Currently available data are based on analysis performed on series collected over a long period of time. This aspect is very important as it may introduce relevant biases in the collected series. First classification systems have changed dramatically over time and cases may have been defined in differently based on diagnosis year. Second some clinical or laboratory data which now are considered as prognostic relevant may have not been determined in older series of patients. Third in a retrospective analysis there is no guarantee that collected series are based on real consecutive cases. These are the reasons why we thought it would be useful to start a new study based on the prospective registration in a short period of time of patients with diagnosis of Peripheral T-cell lymphoma for whom it would be possible collect an exhaustive set of clinical data and biological information.
Please refer to this study by its ClinicalTrials.gov identifier: NCT01142674
|Contact: Monica Bellei, MSc, PhD||+39 059 422 firstname.lastname@example.org|
|Contact: Emanuela A. Pesce, MSc,PhD||+39 059 422 email@example.com|
Show 76 Study Locations
|Study Chair:||Massimo Federico, MD||Dip. Medicina Diagnostica - Università di Modena e Reggio Emilia, , Modena, IT|
|Study Chair:||Julie M. Vose, MD||Nebraska Medical Center, Omaha, NE, USA|
|Study Chair:||Raymond Liang, MD||Queen Mary Hospital - University of Hong Kong, Hong Kong, HK|
|Study Chair:||Emanuele Zucca, MD||IOSI/Oncology Institute of Southern Switzerland, Ospedale S. Giovanni - Bellinzona, CH|
|Study Chair:||Joseph M Connors, MD||British Columbia Cancer Agency, Vancouver, CA|
|Study Chair:||Steven M. Horwitz, MD||Memorial Sloan Kettering Cancer Center|
|Study Chair:||Francine M. Foss, MD||Yale Cancer Center, New Haven, CT, USA|
|Study Chair:||Pier Luigi Zinzani, MD||Istituto di Ematologia e Oncologia Medica "L. e A. Seragnoli", Policlinico Sant'Orsola, Bologna, IT|
|Study Chair:||Silvia Montoto, MD||St. Bartholomew Hospital, London, UK|
|Study Chair:||Aaron Polliack, MD||Sourasky Medical Center, Tel Aviv, IL|
|Study Chair:||Stefano A. Pileri, MD||Istituto di Ematologia e Oncologia Medica "L. e A. Seragnoli", Policlinico Sant'Orsola, Bologna, IT|
|Study Chair:||Dennis D. Weisenburger, MD||Nebraska Medical Center, Omaha, NE, USA|
|Study Chair:||Thomas Ruediger, MD||Universitat Wurzburg, Wurzburg, DE|
|Study Chair:||Young H. Ko, MD||Samsung Medical Center, Seoul, KR|