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170 Chapter 4: Lymphoma<br />

Local or locoregional relapse was defined as a relapse occurring in a lymph<br />

node region or extranodal site that had been previously involved or in an<br />

immediately contiguous site. Distant relapse was defined as relapse occurring at<br />

sites other than local or locoregional sites. Patients who relapsed synchronously at<br />

local <strong>and</strong> distant sites were identified separately from the other two categories.<br />

Treatment at relapse. None of the patients relapsing after autoSCT were treated<br />

with curative intent. Therapy was determined by patient <strong>and</strong> physician preference.<br />

Localized relapses at previously unirradiated sites were treated with involved-field<br />

radiotherapy (nine patients). Some patients with disseminated disease at relapse<br />

declined further therapy (n=9). The remaining patients were treated with corticos­<br />

teroids alone, single-agent—or low dose combination—chemotherapy, or a<br />

combination of these.<br />

Group B<br />

The lymphoma registry of the EBMT was searched, <strong>and</strong> patients undergoing<br />

high-dose therapy <strong>and</strong> autoSCT for NHL were identified. In addition, a small number<br />

of patients undergoing allogeneic bone <strong>marrow</strong> <strong>transplantation</strong> were included in this<br />

analysis. Of the total of 11,883 patients, 3454 patients who had relapsed after SCT<br />

were identified. Of these, data concerning sites of relapse were available for 1339. An<br />

initial comparison of these 1339 patients with those on whom relapse sites were not<br />

available showed no difference in the distribution of major demographic or<br />

prognostic features. The characteristics of these patients are shown in Table 2.<br />

High-dose therapy <strong>and</strong> <strong>transplantation</strong> procedures. Chemotherapy-only highdose<br />

regimens were used in 749 patients, <strong>and</strong> chemotherapy plus TBI-containing<br />

regimens were used in 590. The precise regimens varied according to the active<br />

protocols of the participating institutions. The source of <strong>autologous</strong> hematopoietic<br />

stem cells was bone <strong>marrow</strong> in 753, peripheral <strong>blood</strong> in 420, <strong>and</strong> both in 61. In<br />

addition, 105 patients receiving allogeneic stem cells from HLA-identical sibling<br />

donors were identified.<br />

Positive stem cell selection was used in 16 patients. Purging of stem cell<br />

products was performed in 87 patients, using 4-hydroperoxycyclophosphamide<br />

(4HC) in 30 <strong>and</strong> antibody-based methods in 57.<br />

All patients underwent high-dose therapy in registered transplant centers.<br />

Supportive measures including antibiotic <strong>and</strong> <strong>blood</strong> product support were given<br />

according to the active protocols of the centers, as were hematopoietic growth factors.<br />

Definition of relapse/progression <strong>and</strong> relapse sites. The definition of relapse or<br />

progressive disease was the same as for group A. The definition of relapse sites was<br />

also the same, except that group B patients with synchronous relapses at local <strong>and</strong><br />

distant sites were included in the distant relapse category. Insufficient data on<br />

treatment after relapse were available to allow analysis of its effectiveness.

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