Clinical Oncology News - Randomized Phase II trials: A Pragmatic Way To Inform Clinical Practice
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Consider, for example,
the recent report on the biological activity of single-agent,
nanoparticle albumin-bound paclitaxel in the second-line treatment of
epithelial ovarian cancer.1 This
nonrandomized study, conducted by the Gynecologic Oncology Group,
revealed an objective response rate of 23%, similar to that previously
reported with the far less expensive generic paclitaxel.2,3
But is it possible that this agent is actually superior to
paclitaxel in that treatment with nanoparticle albumin-bound paclitaxel
achieves a similar degree of objective clinical benefit (e.g., degree of
tumor shrinkage and delay in time to progression) but with a measurably
more favorable toxicity profile that includes a substantially reduced
risk for peripheral neuropathy?
Unfortunately, in the complete absence of data from a randomized
trial, the answer to this specific question will simply be unknown
because any suggested “superior” outcomes may solely reflect the
inadvertent selection bias resulting from the favorable baseline
clinical features inherent in all nonrandomized studies........
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