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1. The International Prognostic Index predicts outcome in aggressive adult T-cell leukemia/lymphoma: analysis of 126 patients from the International Peripheral T-Cell Lymphoma Project

Author

Suzumiya J, Ohshima K, Tamura K, Karube K, Uike N, Tobinai K, Gascoyne RD, Vose JM, Armitage JO, Weisenburger DD, for the International Peripheral T. Cell Lymphoma Project [Savage K, Connors J, Gascoyne R, Chhanabhai M, Wilson W, Jaffe E, Armitage J, Vose J, Weisenburger D, Anderson J, Ullrich F, Bast M, Hochberg E, Harris N, Levine A, Nathwani B, Miller T, Rimsza L, Montserrat E, Lopez Guillermo A, Campo E, Cuadros M, Alvarez Ferreira J, Martinez Delgado B, Holte H, Delabie J, Rüdiger T, Müller Hermelink K, Reimer P, Adam P, Wilhelm M, Schmitz N, Nerl C, MacLennan KA, Federico M, Bellei M, Coiffier B, Berger F, Tanin I, Wannakrairot P, Au W, Liang R, Loong F, Rajan S, Sng I, Matsuno Y, Morishima Y, Nakamura S, Seto M, Tanimoto M, Yoshino T, Kim WS, Ko Y.H. ], ZINZANI, PIER LUIGI, PILERI, STEFANO, Suzumiya J, Ohshima K, Tamura K, Karube K, Uike N, Tobinai K, Gascoyne RD, Vose JM, Armitage JO, Weisenburger DD and for the International Peripheral T-Cell Lymphoma Project [Savage K, Connors J, Gascoyne R, Chhanabhai M, Wilson W, Jaffe E, Armitage J, Vose J, Weisenburger D, Anderson J, Ullrich F, Bast M, Hochberg E, Harris N, Levine A, Nathwani B, Miller T, Rimsza L, Montserrat E, Lopez-Guillermo A, Campo E, Cuadros M, Alvarez Ferreira J, Martinez Delgado B, Holte H, Delabie J, Rüdiger T, Müller-Hermelink K, Reimer P, Adam P, Wilhelm M, Schmitz N, Nerl C, MacLennan KA, Zinzani PL, Pileri S, Federico M, Bellei M, Coiffier B, Berger F, Tanin I, Wannakrairot P, Au W, Liang R, Loong F, Rajan S, Sng I, Matsuno Y, Morishima Y, Nakamura S, Seto M, Tanimoto M, Yoshino T, Kim WS, and Ko YH.]

Subjects
Oncology, Adult, Male, medicine.medical_specialty, INTERNATIONAL, Adult T-cell leukemia/lymphoma, International Prognostic Index, T-cell, immune system diseases, Internal medicine, hemic and lymphatic diseases, medicine, LYMPHOMA, Humans, Leukemia-Lymphoma, Adult T-Cell, Aged, Aged, 80 and over, Univariate analysis, business.industry, prognostic index, leukemia, Combination chemotherapy, Hematology, Middle Aged, medicine.disease, Prognosis, Peripheral T-cell Lymphoma, Peripheral T-cell lymphoma, Lymphoma, Leukemia, B symptoms, ATL, Immunology, Female, medicine.symptom, business
Abstract

Background: The International Peripheral T-cell Lymphoma Project was organized to better understand the T-cell and natural killer (NK) cell lymphomas, and our task is to present the clinicopathologic correlations and therapeutic results for adult T-cell leukemia/lymphoma (ATL). Patients and methods: Among 1153 patients with T-cell or NK cell lymphomas, 126 patients (9.6%) with ATL were represented in this project. All were categorized as aggressive ATL, i.e. acute or lymphoma type, and 87% fell into the lymphoma type. Results: The median age was 62 years and the male to female ratio was 1.2 : 1. Significant prognostic factors for overall survival (OS) by univariate analysis were the presence of B symptoms (P = 0.018), platelet count

Published
2009

2. International peripheral T-cell and natural killer/T-cell lymphoma study: pathology findings and clinical outcomes

Author

Savage K, Connors J, Gascoyne R, Chhanabhai M, Wilson W, Jaffe E, Armitage J, Vose J, Weisenburger D, Anderson J, Ullrich F, Bast M, Hochberg E, Harris N, Levine A, Nathwani B, Miller T, Rimsza L, Montserrat E, Lopez Guillermo A, Campo E, Cuadros M, Alvarez Ferreira J, Martinez Delgado B, Holte H, Delabie J, Rüdiger T, Müller Hermelink K, Reimer P, Adam P, Wilhelm M, Schmitz N, Nerl C, Lister A, Norton A, MacLennan KA, Federico M, Bellei M, Coiffier B, Berger F, Tanin I, Wannakrairot P, Au W, Liang R, Loong F, Rajan S, Sng I, Tobinai K, Matsuno Y, Morishima Y, Nakamura S, Seto M, Tanimoto M, Yoshino T, Suzumiya J, Ohshima K, Kim WS, Ko Y.H., ZINZANI, PIER LUIGI, PILERI, STEFANO, Savage K, Connors J, Gascoyne R, Chhanabhai M, Wilson W, Jaffe E, Armitage J, Vose J, Weisenburger D, Anderson J, Ullrich F, Bast M, Hochberg E, Harris N, Levine A, Nathwani B, Miller T, Rimsza L, Montserrat E, Lopez-Guillermo A, Campo E, Cuadros M, Alvarez Ferreira J, Martinez Delgado B, Holte H, Delabie J, Rüdiger T, Müller-Hermelink K, Reimer P, Adam P, Wilhelm M, Schmitz N, Nerl C, Lister A, Norton A, MacLennan KA, Zinzani PL, Pileri S, Federico M, Bellei M, Coiffier B, Berger F, Tanin I, Wannakrairot P, Au W, Liang R, Loong F, Rajan S, Sng I, Tobinai K, Matsuno Y, Morishima Y, Nakamura S, Seto M, Tanimoto M, Yoshino T, Suzumiya J, Ohshima K, Kim WS, and Ko YH.

Subjects
Adult, Male, Cancer Research, Pathology, medicine.medical_specialty, Angioimmunoblastic T-cell lymphoma, Hepatosplenic T-cell lymphoma, Biopsy, T-Lymphocytes, Peripheral T-cell lymphoma not otherwise specified, Lymphoma, T-Cell, Immunophenotyping, Cohort Studies, immune system diseases, hemic and lymphatic diseases, medicine, Mogamulizumab, LYMPHOMA, Humans, Aged, Models, Genetic, business.industry, Pralatrexate, Middle Aged, medicine.disease, Prognosis, Peripheral T-cell lymphoma, Lymphoma, Killer Cells, Natural, T-Cell Non-Hodgkin Lymphoma, Treatment Outcome, Oncology, Female, business, medicine.drug
Abstract

Purpose Peripheral T-cell lymphoma (PTCL) and natural killer/T-cell lymphoma (NKTCL) are rare and heterogeneous forms of non-Hodgkin's lymphoma (NHL) that, in general, are associated with a poor clinical outcome. Patients and Methods A cohort of 1,314 cases of PTCL and NKTCL was organized from 22 centers worldwide, consisting of patients with previously untreated PTCL or NKTCL who were diagnosed between 1990 and 2002. Tissue biopsies, immunophenotypic markers, molecular genetic studies, and clinical information from consecutive patients at each site were reviewed by panels of four expert hematopathologists and classified according to the WHO classification. Results A diagnosis of PTCL or NKTCL was confirmed in 1,153 (87.8%) of the cases. The most common subtypes were PTCL not otherwise specified (NOS; 25.9%), angioimmunoblastic type (18.5%), NKTCL (10.4%), and adult T-cell leukemia/lymphoma (ATLL; 9.6%). Misclassification occurred in 10.4% of the cases including Hodgkin's lymphoma (3%), B-cell lymphoma (1.4%), unclassifiable lymphoma (2.8%), or a diagnosis other than lymphoma (2.3%). We found marked variation in the frequency of the various subtypes by geographic region. The use of an anthracycline-containing regimen was not associated with an improved outcome in PTCL-NOS or angioimmunoblastic type, but was associated with an improved outcome in anaplastic large-cell lymphoma, ALK positive. Conclusion The WHO classification is useful for defining subtypes of PTCL and NKTCL. However, expert hematopathology review is important for accurate diagnosis. The clinical outcome for patients with most of these lymphoma subtypes is poor with standard therapies, and novel agents and new modalities are needed to improve survival.

Published
2008

3. Fatal Interstitial Pneumonia Due to Cytomegalovirus Following Cyclophosphamide Treatment in a Patient with Systemic Lupus Erythematosus: LETTER TO THE EDITOR

Author

L. A Pérez de Llano, Carlos Garcia-Porrua, M. A. González-Gay, and Alvarez-Ferreira J

Subjects
medicine.medical_specialty, Letter to the editor, business.industry, Immunology, Congenital cytomegalovirus infection, General Medicine, medicine.disease, Dermatology, Rheumatology, Cyclophosphamide treatment, immune system diseases, Internal medicine, Immunology and Allergy, Medicine, Interstitial pneumonia, skin and connective tissue diseases, business, Anti-SSA/Ro autoantibodies
Abstract

(1998). Fatal Interstitial Pneumonia Due to Cytomegalovirus Following Cyclophosphamide Treatment in a Patient with Systemic Lupus Erythematosus: LETTER TO THE EDITOR. Scandinavian Journal of Rheumatology: Vol. 27, No. 6, pp. 465-466.

Published
1998
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