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<IndexPatientGuideline ID="x23007" Name="Guideline Statement 28" IsComponent="true" Changed="20260512T14:50:26" Created="20260506T17:30:09" Published="20260512T10:50:44" SiteBaseUrl="https://www.auanet.org" Locale="" XPowerPath="/Home/Guidelines &amp; Quality/Guidelines/Clinical Guidelines/Advanced Prostate Cancer/Page Elements/Metastatic Castration-Resistant Prostate Cancer/Treatment/Guideline Statement 28">
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  <Header type="string" UID="faf9fd2842b549d09e761cd943c2be20" label="Header" readonly="false" hidden="false" required="false" indexable="false" CIID="">Guideline Statement 28</Header>
  <BodyCopy type="xhtml" UID="41a2d8598c364193bbfe9ad86d7bcd3c" label="Body Copy" readonly="false" hidden="false" required="false" indexable="false" Height="" CIID="">&lt;p&gt;&lt;strong&gt; &lt;/strong&gt;&lt;strong&gt;In mCRPC patients with disease progression following treatment with an ARPI, clinicians should offer docetaxel.&amp;nbsp;&lt;em&gt;(Strong Recommendation; Evidence Level: Grade B)&lt;/em&gt;&lt;/strong&gt;&lt;/p&gt;</BodyCopy>
  <DiscussionLinkName type="string" UID="b364402056154f78b38cd8d663eaf3ba" label="Discussion Link Name" readonly="false" hidden="false" required="false" indexable="false" CIID="">Discussion</DiscussionLinkName>
  <DiscussionTitle type="string" UID="ceedafe4ad314b5d8d3225bc0083b81c" label="Discussion Title" readonly="false" hidden="false" required="false" indexable="false" CIID="">Discussion</DiscussionTitle>
  <DiscussionBody type="xhtml" UID="9bbbac02721d4eefba59c63ee7ff9007" label="Discussion Body" readonly="false" hidden="false" required="false" indexable="false" Height="" CIID="">&lt;p&gt;Docetaxel (typically in combination with 10 mg of prednisone/day) is an effective option in both mCRPC and mHSPC and should be considered as standard first-line chemotherapy in the setting of mCRPC based on a randomized, multicenter, active-controlled trial (TAX 327),&lt;sup&gt;22&lt;/sup&gt; which demonstrated a statistically significant OS advantage over mitoxantrone, with a median survival of 18.9 months versus 16.5 months (HR=0.761; 95% CI: 0.619 to 0.936). The palliative data from this study is compelling demonstrating significant pain reduction and improvement in QOL.&lt;sup&gt;124&lt;/sup&gt;&lt;/p&gt;</DiscussionBody>
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