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Autologous Bone Marrow Transplantation - Blog Science Connections

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324 Proposed International Adult Lymphoma Study<br />

show in Figure 11 the survival curves of the MIME patients according to their<br />

histological subtype. These curves are almost identical to those from<br />

previous experience with 1MVP-16-213 (ifosfamide, methotrexate, etoposide)<br />

and AIVP-16-213 (doxorubicin, ifosfamide, etoposide) for both the aggressive<br />

and the indolent disease types.<br />

We used MIME to treat diffuse large cell lymphoma in patients less than<br />

60 years of age who had no bone marrow involvement: 52 patients have been<br />

treated who meet these criteria. Twenty-two achieved a CR (42%), 13<br />

achieved a PR (overall response rate, 67%), and 17 did not respond. There are<br />

three long-term survivors at 46+, 26+, and 12+ months. The median survival<br />

of this group is 40 weeks (Fig 11).<br />

The toxicity for patients on MIME was acceptable in most instances.<br />

However, despite good results—the best ever reported in relapse of non-<br />

Hodgkin's lymphoma—and low toxicity, mitoguazone and ifosfamide, which<br />

were available for this study, are no longer available for use in the United<br />

States. Furthermore, since the completion of the MIME studies, many<br />

patients now receive etoposide as primary therapy. A program with<br />

nonexperimental drugs, possibly drugs non-cross-resistant to primary therapy<br />

having response rates equal to those associated with MIME would be<br />

desirable for reinduction therapy.<br />

DHAP Results<br />

Previous experience with either cisplatin or high-dose cytarabine shows<br />

response rates of approximately 20%, practically all of the patients being in PR<br />

Figure 11. Survival of patients treated with the MIME (mitoguazone, ifosfamide, methotrexate,<br />

etoposide) salvage regimen according to histological subtype compared with that<br />

of controls treated with other ifosfamide-etoposide combination regimens.

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