PERIPHERAL T-CELL LYMPHOMAS RESPOND WELL TO VINCRISTINE, ADRIAMYCIN, CYCLOPHOSPHAMIDE, PREDNISONE AND ETOPOSIDE (VACPE) AND HAVE A SIMILAR OUTCOME AS HIGH-GRADE B-CELL LYMPHOMAS

Citation
T. Karakas et al., PERIPHERAL T-CELL LYMPHOMAS RESPOND WELL TO VINCRISTINE, ADRIAMYCIN, CYCLOPHOSPHAMIDE, PREDNISONE AND ETOPOSIDE (VACPE) AND HAVE A SIMILAR OUTCOME AS HIGH-GRADE B-CELL LYMPHOMAS, Leukemia & lymphoma, 24(1-2), 1996, pp. 121-129
Citations number
40
Categorie Soggetti
Hematology
Journal title
ISSN journal
10428194
Volume
24
Issue
1-2
Year of publication
1996
Pages
121 - 129
Database
ISI
SICI code
1042-8194(1996)24:1-2<121:PTLRWT>2.0.ZU;2-#
Abstract
Peripheral T-cell lymphomas (PTCL) represent a heterogeneous group of T-cell malignancies including subentities with favourable (large cell anaplastic) or unfavourable (pleomorphic) prognosis. The clinical outc ome of PTCL has been controversially discussed, but a worse prognosis than high-grade B-cell Non-Hodgkin's lymphomas (NHL) has been postulat ed by most authors. In this report we summarize the results of a prosp ective comparative study investigating the therapy outcome of 27 patie nts (pts) with PTCL and 55 pts. with high grade B-cell NHL and give an overview of therapy studies in PTCL. The histological subtypes were 1 4 pleomorphic, 8 large-cell anaplastic (Ki-1+), 2 angioimmunoblastic ( AILD) and 3 other PTCL. In three patients the PTCL was associated with non-tropical sprue (11%). Nineteen patients presented with an advance d stage of disease (stage III and IV, 70%), 17 (63%) pts. had B-sympto ms. The patients were treated with vincristine 2 mg d1, adriamycin 25 mg/m(2) d1-3, cyclophosphamide 800 mg/m(2) d1, prednisone 60 mg/m(2) d 1-7 and etoposide 120 mg/m(2) d1-3 (VACPE). In 77% of pts. with PTCL a nd 84% of patients with high-grade B-cell NHL a complete remission (CR ) was achieved. 75% of the complete responders with PTCL and 70% with B-NHL are still in ongoing CR. The subgroup of large-cell anaplastic a ttained a CR in 88%. The median observation time is 44 months (1+-77+) . The probability of 1-, 3- and 5-year overall and disease-free surviv al for the T-cell group were 76%, 54%, 48% and 76%, 62%, 62%, respecti vely according to Kaplan-Meier. There was no significant difference re garding the remission rate, the overall-, event-free or disease-free s urvival compared to high-grade B-cell lymphomas. In conclusion, the VA CPE regimen is an effective and feasible regimen in the management of PTCL achieving complete remissions in a large proportion of patients.