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Crouse, 1992).<br />

In the present report we update the clinical outcome of 65 patients with non-<br />

Hodgkin's lymphoma 20 of whom received autologous peripheral blood derived<br />

stem cell transplantation (PSCT) largely because their marrow was histologically<br />

and culture positive for lymphoma and 45 who received autologous<br />

bone marrow transplantation (ABMT). The ABMT patients received histologically<br />

negative marrows, however in 17 instances these marrows were culture<br />

positive for lymphoma. In addition, we present the outcome for 29 patients with<br />

breast cancer or other gynecological epithelial tumors whose marrow was histologically<br />

and/or culture positive for tumor cells and therefore, with the exception<br />

of one patient who died before transplant, they underwent PSCT. Culture<br />

studies evaluated retrospectively showed that 6 patients had apheresis harvests<br />

that grew abnormal, suspected epithelial tumor cells, 23 did not. The results<br />

overall demonstrate that imnimal contamination of hematopoietic harvests is an<br />

important determinant of outcome of high dose therapy and hematopoietic cell<br />

transplantation.<br />

MATERIALS AND METHODS<br />

<strong>Bone</strong> marrow and/or peripheral blood stem cell harvests obtained by<br />

leukapheresis were examined histologically or cytologically, respectively, for the<br />

presence of tumor cells. Aliquots of these harvests were then placed into culture<br />

as described previously for non-Hodgkin's lymphoma patient samples (Sharp et<br />

al., 1991; Sharp et al., 1992) or breast cancer patient harvests (Sharp and Crouse,<br />

1992) and aliquots obtained at various times subsequently and evaluated for the<br />

presence of tumor cells as described previously.<br />

The frequency of tumor cell detection from both histologically and cytologically<br />

positive and negative harvests was noted. In addition clinical outcome in<br />

terms of whether or not patients achieved a complete remission (CR) when restaged<br />

at 100 days was noted and for those patients receiving a CR at 100 days,<br />

the time to subsequent disease progression was recorded. These data were then<br />

analyzed to determine the influence of tumor cells detected histologically or cytologically<br />

or by culture techniques, or both, on clinical outcome.<br />

All of the protocols employed were approved by the University of Nebraska<br />

Institutional Review Board and patients voluntarily signed informed consent for<br />

these studies.<br />

RESULTS AND DISCUSSION<br />

Non-Hodgkin's Lymphoma: A total of 65 patients have now been followed<br />

for a median of 3 years with actuarial follow-up predicted to 5 years. Of these 65<br />

patients 45 who had histologically negative marrows underwent ABMT. However<br />

17 of these patients had culture positive marrows, 27 culture negative marrows<br />

and one was unevaluable. The remaining 20 patients had either histologically<br />

positive (19) or hypocellular (1) marrows and underwent PSCT. Two had<br />

tumor culture and/or molecular biology positive apheresis harvests, 18 were<br />

negative.<br />

All grades of lymphoma were included since our experience suggests that<br />

primary refractory or relapsed low grade lymphoma patients have a poor outcome<br />

similar to the same categories of intermediate and high grade lymphoma<br />

224 SIXTH INTERNATIONAL SYMPOSIUM ON AUTOLOGOUS BONE MARROW TRANSPLANTATION

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