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Santini et al. 193<br />

to evaluate the effectiveness of aggressive therapy in improving outcome. One<br />

hundred twenty-four patients between the ages of 15 <strong>and</strong> 60 years were included<br />

in the trial. Diagnosis had confirmed diffuse intermediate- to high-grade non-<br />

Hodgkin's lymphoma (Working Formulation groups F, G, H, <strong>and</strong> K) in stages II<br />

bulky (>10 cm), III, or IV. All patients were r<strong>and</strong>omized at diagnosis. Sixty-one<br />

patients were assessed to receive etoposide, doxorubicin, cyclophosphamide,<br />

vincristine, prednisone, bleomycin (VACOP-B) for 12 weeks <strong>and</strong> dexamethasone,<br />

cytarabin, cisplatin (DHAP) as salvage regimen (arm A), while 63<br />

patients were to receive VACOP-B for 12 weeks plus high-dose therapy (HDT)<br />

<strong>and</strong> <strong>autologous</strong> bone <strong>marrow</strong> <strong>transplantation</strong> (arm B). There was no significant<br />

difference in the frequency of complete remission (CR) between the two groups:<br />

75% for the VACOP-B plus DHAP regimen group <strong>and</strong> 73% for the VACOP-B<br />

plus autoBMT group. With a median follow-up observation time of 37 months<br />

(range 10-72 months), the 6-year survival probability was 64% in arm A <strong>and</strong><br />

65% in arm B. There was no difference in the 6-year disease-free survival (DFS)<br />

<strong>and</strong> progression-free survival (PFS) probability of the two groups. DFS was 57%<br />

with conventional chemotherapy <strong>and</strong> 80% with autoBMT (P=0.1). PFS was 47<br />

<strong>and</strong> 60%, respectively (P=0A). Results of patients categorized according to the<br />

International Index as being at risk were analyzed. This showed a statistical<br />

improvement in terms of DFS (P=0.0l) <strong>and</strong> a favorable trend in terms of PFS<br />

(/>=0.08) for intermediate-/high- plus high-risk group patients receiving<br />

autoBMT compared with patients categorized in the same groups who were<br />

treated with conventional chemotherapy. In this study, conventional<br />

chemotherapy followed by HDT <strong>and</strong> autoBMT as front-line therapy seems to be<br />

no more successful than conventional treatment in terms of overall results.<br />

However, our study suggests that HDT plus ABMT should be proposed for<br />

higher-risk group patients at diagnosis.<br />

INTRODUCTION<br />

HDT with ABMT represents an efficient approach (30-40% cure rate) for those<br />

aggressive non-Hodgkin's lymphoma (NHL) patients who have "chemosensitive<br />

relapse" after the failure of conventional chemotherapy. 1<br />

" 4<br />

Its true role in the<br />

treatment of patients in first partial remission (PR) after front-line therapy is still<br />

uncertain. 5,6<br />

Haioun et al., in a r<strong>and</strong>omized trial, demonstrated no difference in<br />

terms of overall survival <strong>and</strong> DFS between patients in CR receiving conventional<br />

therapy or HDT plus autoBMT. 7<br />

This contrasts with previous reports of nonr<strong>and</strong>omized<br />

trials. 8,9<br />

In a retrospective analysis, the same authors suggested a survival<br />

benefit for intermediate-/high- <strong>and</strong> high-risk patients (as defined by the<br />

International Index 10<br />

) treated with HDT <strong>and</strong> autoBMT. 11<br />

A different approach<br />

using sequential chemotherapeutic agents given at full dosage (high-dose

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