Literature DB >> 2474057

LNH-84 regimen: a multicenter study of intensive chemotherapy in 737 patients with aggressive malignant lymphoma.

B Coiffier1, C Gisselbrecht, R Herbrecht, H Tilly, A Bosly, N Brousse.   

Abstract

From July 1984 to September 1987, 737 patients with aggressive malignant lymphoma (ML) were treated by an intensive regimen (LNH-84) comprising three or four courses of doxorubicin, 75 mg/m2; cyclophosphamide, 1,200 mg/m2; vindesine, 2 mg/m2 x 2; bleomycin, 10 mg x 2; and prednisolone, 60 mg/m2 x 5 (ACVB), consolidation with high-dose methotrexate, ifosfamide, etoposide, asparaginase, and cytarabine, and a randomized late intensification with two courses of cytarabine, cyclophosphamide, teniposide, bleomycin, and prednisone (AraCVmB). Four hundred forty-two patients had intermediate-grade ML, 221 highgrade ML, and 74 unclassified ML. Most of the patients had advanced disease: stage IIE (23%), III (13%), or IV (47%); 38% disseminated nodes; 38% two or more extranodal sites; and 41% a tumoral mass greater than 10 cm. Five hundred fifty-three patients (75%) went into complete remission (CR), 63 (9%) into partial remission, 62 (8%) failed to respond, and 59 (8%) died during ACVB courses, 17 of them from progression of the disease. With a median follow-up of 23 months, the estimated 2-year overall survival time to failure (TTF), and time to relapse (TTR) survival are 67%, 56%, and 67%, respectively. Patients receiving a late intensification had the same relapse rate as the other patients. A persistent fibronecrotic mass was found in 150 patients (20%) and did not influence the relapse rate. Toxicity was mainly neutropenia and infection during the ACVB courses, with 40 patients (5%) dying from septic complications while responding to treatment. Fifty-three percent of the patients had a neutropenia less than 0.500 x 10(9)/L, 58% fever (6% grade 4), and 49% a documented infection (8% grade 4). These results obtained with the LNH-84 regimen demonstrate that this therapeutic scheme is an effective treatment for aggressive ML.

Entities:  

Mesh:

Substances:

Year:  1989        PMID: 2474057     DOI: 10.1200/JCO.1989.7.8.1018

Source DB:  PubMed          Journal:  J Clin Oncol        ISSN: 0732-183X            Impact factor:   44.544


  23 in total

Review 1.  Assessment of response to therapy using conventional imaging.

Authors:  Sheila C Rankin
Journal:  Eur J Nucl Med Mol Imaging       Date:  2003-03-27       Impact factor: 9.236

2.  Phase II study of cyclophosphamide, doxorubicin, vincristine, prednisolone (CHOP) therapy for newly diagnosed patients with low- and low-intermediate risk, aggressive non-Hodgkin's lymphoma: final results of the Japan Clinical Oncology Group Study, JCOG9508.

Authors:  Yoshitoyo Kagami; Kuniaki Itoh; Kensei Tobinai; Haruhiko Fukuda; Kiyoshi Mukai; Takaaki Chou; Chikara Mikuni; Tomohiro Kinoshita; Noriyasu Fukushima; Yoshio Kiyama; Takayo Suzuki; Tsuneo Sasaki; Yuko Watanabe; Kunihiro Tsukasaki; Tomomitsu Hotta; Masanori Shimoyama; Michinori Ogura
Journal:  Int J Hematol       Date:  2012-06-03       Impact factor: 2.490

3.  The BFM-protocol for HIV-negative Burkitt's lymphomas and L3 ALL in adult patients: a high chance for cure.

Authors:  H W Pees; H Radtke; J Schwamborn; N Graf
Journal:  Ann Hematol       Date:  1992-11       Impact factor: 3.673

4.  Intensive chemotherapy in the treatment of aggressive diffuse large B-cell lymphoma: malignant lymphoma.

Authors:  Agustin Avilés; M Jesús Nambo; Natividad Neri; Alejandra Talavera; Claudia Castañeda; Edgar Murillo; Sergio Cleto; Judith Huerta-Guzmán
Journal:  Med Oncol       Date:  2004       Impact factor: 3.064

5.  VP-16, ifosfamide, and methotrexate combination chemotherapy for aggressive non-Hodgkin's lymphomas after failure of the LNH 84 regimen.

Authors:  R Herbrecht; J J Garcia; J P Bergerat; P Dufour; B Duclos; F Oberling
Journal:  Cancer Chemother Pharmacol       Date:  1989       Impact factor: 3.333

6.  Long-term outcome of mesna, ifosfamide, mitoxantrone, etoposide (MINE) regimen as a consolidation in patients with aggressive non-Hodgkin lymphoma responding to CHOP.

Authors:  Dilek Dincol; Abdullah Buyukcelik; Mutlu Dogan; Hakan Akbulut; Mustafa Samur; Ahmet Demirkazik; Filiz Cay Senler; Handan Onur; Fikri Icli
Journal:  Med Oncol       Date:  2009-09-29       Impact factor: 3.064

Review 7.  Malignant tumours in patients with HIV infection.

Authors:  U Tirelli; S Franceschi; A Carbone
Journal:  BMJ       Date:  1994-04-30

8.  Clinical, biologic, and pathologic features in 157 patients with angioimmunoblastic T-cell lymphoma treated within the Groupe d'Etude des Lymphomes de l'Adulte (GELA) trials.

Authors:  Nathalie Mourad; Nicolas Mounier; Josette Brière; Emmanuel Raffoux; Alain Delmer; Alfred Feller; Chris J L M Meijer; Jean-François Emile; Réda Bouabdallah; André Bosly; Jacques Diebold; Corinne Haioun; Bertrand Coiffier; Christian Gisselbrecht; Philippe Gaulard
Journal:  Blood       Date:  2008-02-21       Impact factor: 22.113

9.  Long-term outcome of follicular low-grade lymphoma. A report of 91 patients.

Authors:  P Morel; B Dupriez; I Plantier-Colcher; B Gosselin; C Declercq; J P Pollet; F Bauters
Journal:  Ann Hematol       Date:  1993-06       Impact factor: 3.673

10.  Virus reactivation in high-risk non-Hodgkin's lymphoma patients after autologous CD34+ -selected peripheral blood progenitor cell transplantation.

Authors:  Peng-Chan Lin; Ming-Yang Lee; Jen-Tsun Lin; Liang-Tsai Hsiao; Po-Min Chen; Tzeon-Jye Chiou
Journal:  Int J Hematol       Date:  2008-05       Impact factor: 2.490

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.