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autologous blood and marrow transplantation - Blog Science ...

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730 Chapter 16: Summaries<br />

Table 1. Continued from previous page<br />

Barrier Strategies<br />

9) Competition with<br />

community physicians:<br />

will we see enough<br />

patients to do<br />

our research?<br />

10) High cost of research:<br />

will the care of our<br />

patients be reimbursed?<br />

» Explore new strategies<br />

1<br />

Treat high risk patients<br />

• Extend indications or HDRx options<br />

' Reduce research costs: shorten hospital stays<br />

<strong>blood</strong> or <strong>marrow</strong> transplants. Although the table is long <strong>and</strong> appears to be<br />

complicated, it should be easy to follow. Further, although hoped to be nearly<br />

complete, it cannot be counted on to be comprehensive, exhaustive, or all-<br />

inclusive. Columns 1-3 present barriers to success, potential (but not all possible)<br />

strategies to overcome the barriers, <strong>and</strong> a limited number of examples pursuing<br />

specific strategies.<br />

Each solid tumor session abstract usually recognized one (but sometimes more<br />

than one) barrier to success <strong>and</strong> presented data exploring one of the methods to<br />

pursue a potential strategy to overcome the barrier. The fourth column lists the last<br />

name of the first author of each abstract on the same line as the strategy that the<br />

abstract's authors were pursuing or the strategy about which the presenter made his<br />

or her most salient comments. Although many strategies appear to remain<br />

unexplored, it should be remembered that the symposium had only a limited<br />

number of invited investigators to discuss their work.<br />

THEMATIC AREAS FOR CONSIDERATION<br />

During the course of listening to the oral presentations in both scientific sessions,<br />

the author recognized four major questions that had been discussed but remained<br />

unresolved, predominantly because of limitation of time. Table 2 is the author's<br />

attempt to crystallize these questions <strong>and</strong> formulate concise, logical answers that<br />

pertain to the circumstances which represent the current state-of-the-art.<br />

Tables 3 <strong>and</strong> 4 are necessary to complete the author's response to the fourth<br />

question: "Should just phase III trials be done?" Table 3 presents the meanings of<br />

phase I, phase II, <strong>and</strong> phase III trials for high-dose therapy <strong>and</strong> hematopoietic<br />

progenitor cell transplant. Table 4 presents the author's recommendation of what<br />

type of study to do under what set of conditions. Consideration of 7) issues about<br />

the ease of doing the study (number of patients needed, expected accrual rate of

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