Date:         Wed, 21 May 2008 11:25:09 -0700
Reply-To:     Al <ali6058@GMAIL.COM>
Sender:       "SAS(r) Discussion" <SAS-L@LISTSERV.UGA.EDU>
From:         Al <ali6058@GMAIL.COM>
Organization: http://groups.google.com
Subject:      Phase 1 (Oncology)
Comments: To: sas-l@uga.edu
Content-Type: text/plain; charset=ISO-8859-1

Hi
                  I am woking on Phase1(oncology) and i have few
questions
   1.Is it the SAS Programmer who decide Maximum Tolerable Dose(MTD)
and Dose Limiting Toxicity by
      using the SAS reports?

   2.For example if a Patient gets say dose 5.0 (day1 day2 and day3)
on visit1 and  dose 6.0 (day1 , day2 and day3) on visit2 and
     again dose 5.0(day1 day2 and day3 ) on visit3
    which category of doses(5 or 6) this  patient fall under if i were
to code a demog table by dose

   If any one of you has worked on phase 1 dose escalation
protcols.Please provide me some insights

   Thanks in advance