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Autologous Bone Marrow Transplantation - Blog Science Connections

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Panel Discussion: Session IIA 239<br />

DR. VRIESENDORP: Dr. Jagannath, I was wondering, when you looked at<br />

your factors, which predicted the outcome of transplantation in Hodgkin's<br />

disease, whether you looked at the effect of bulky disease? The reason I ask is<br />

because we've looked at our patients with Hodgkin's disease and, like you, we<br />

haven't found that their initial response to chemotherapy predicted for<br />

response if you took into account bulky disease. We've done 10 patients now<br />

without bulky disease and of the 10, 7 are alive and disease free. Median<br />

follow-up was around 1 year. Our results of non-Hodgkin's disease are similar.<br />

DR. JAGANNATH: Yes, tumor burden at the time of transplantation is one of<br />

the factors looked into. These patients who are treated with CBV and tumor<br />

burden are of importance. The tumor burden definition is a bit complicated.<br />

Any patient who had more than a 5-cm tumor bulk on any one side or a patient<br />

who had extensive abdominal disease (i.e., simultaneous involvement of paraaortic<br />

and pelvic disease or any involvement of mediastinum, even if not huge)<br />

was prone to have a poor prognosis by this treatment, which was very<br />

significant. Patients with mediastinal involvement, whatever size at the time of<br />

transplant, had prior radiation therapy to the mediastinum, therefore, patients<br />

who had mediastinum disease have a somewhat poorer prognosis.<br />

DR. J. CAHN: Did you find any difference in terms of response rate in<br />

patients who had relapsed in previously irradiated fields?<br />

DR. JAGANNATH: Involved-field relapses are not significant.<br />

DR. WOLFF: Hodgkin's disease is a notoriously indolent disease in which<br />

patients can remain alive for prolonged periods of time with active illness, and 1<br />

think that to critically evaluate the effect of a regimen, you have to look at<br />

event-free survival and not just the overall survival.<br />

DR. HAGEMEISTER: Steve (Dr. Wolff), you can estimate that about 70% of<br />

the complete responders, which were about half the patients, stay well. So you<br />

can anticipate it's going to be about 30%.<br />

DR. D. HEARD: I may have missed these comments earlier, but I just<br />

wanted to say something about peripheral blood stem cells in Hodgkin's<br />

disease. We have now done a couple of patients and clearly, the marrow<br />

involvement by Hodgkin's disease should not be a contraindication of going<br />

ahead and doing these patients. Repeated leukaphereses and storage of<br />

peripheral blood stem cells certainly lead to rapid engraftment following the<br />

CBV therapy. As a matter of fact, patients reconstituted with peripheral stem<br />

cells leave the hospital generally around 3V£ weeks, when the average time of<br />

hospitalization for the marrow patients has been closer to 5 weeks.<br />

DR. ARMITAGE: That also has been our experience, a much more rapid<br />

recovery.<br />

DR. T. PHILIP: Dr. Carella, can you comment on the toxicity of CBV1<br />

versus CBV2 and, specifically, about toxic deaths in both of your protocols?

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