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Transplant

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Now, does it benefit every patient with myeloma?  No.  But I think that the way I visualize the use of transplant is that it is not the single one treatment that we say yes or no to.  It is one of the tools that we use to treat myeloma and keep myeloma under control over the life of the course of a given disease.  So to say to somebody be who is young and fit, I don’t believe in transplant so I’m not going to bring it up with you is like saying I’m going to build a house and I’m not--I’m going to do it without a hammer.  You need different tools to build that house, and you need different options to control the disease over time, and I think transplant is one of them.

The one negative thing I would say about transplant is that there was a presentation from one large randomized study that looked at tandem autologous transplant versus an autologous followed by what’s called a mini or nonmyeloablative allo transplant where the second transplant is given from stem cells from a donor like a brother or a sister.  And in that study the tandem autologous transplant did as well as the other arm with less side effect, which I think really says that we should still consider allogeneic transplant or stem cells from another donor as still being experimental.  And I think some people, and I’d be interested to hear what Dr. Lonial thinks, some people may say even that that approach shouldn’t be considered even in a clinical trial.

You’ve heard about all the great stuff that’s happening, all the new drugs that are being developed, how the survival of patients with myeloma has increased markedly over the last five to 10 years, and so I think that if you break down patients into three categories, standard risk, high risk and then somewhere am the middle, where we’re not exactly sure where they fit, if you take the standard or good risk patients I think that their median survival is over eight years.  If you look at the high-risk patients where we’ve not done as well with the new drugs as we would like to do, in both of those patient subsets in the trial that Dr. Orlowski referred to there was no benefit for an allo transplant. 

And so I would argue that for the standard or good risk patients the risk is much, much higher in those patients without significant benefit.  And in the high-risk patients, while the benefit--potential benefit may be high the time for that maneuver to really work was simply not there because the disease grows too fast.  And so for both of those I would say I don’t think allografting offers much of an advantage for them.  It’s the people in the middle that I think we’re debating about oftentimes and again I think you really--the burden is on the trials to show the benefit rather than saying we should keep doing it.

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