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Here's news and info about three primary blood cancers, Lymphoma, Myeloma and Leukemia with a decided patient's perspective.  I hope this helps whether you're newly diagnosed or veteran survivor.  

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Education Network to Advance Clinical Trials

 

It's no secret that I'm a big advocate encouraging cancer patients to seriously consider Clinical Trials as a safe and effective treatment option for cancer, particular incurable blood cancers. There is much evidence that supports the theory that many of the emerging targeting biologic and small molecule agents can be safer than many conventional chemotherapies including alkylating agents and nucleoside analogs.  There are far too many myths and misconceptions surrounding Clinical Trials.  Accordingly, there is an urgent need to educate physicians, patients and caregivers about the current state of the art.   I'm working with the Education Network to Advance Cancer Clinical Trials as a webcast speaker.  Check out www.enaact.org for more info.  

Comments

From Has | On January 02, 2014 @05:36 am
Many thanks for those thtouhgs, Kerstin, that's very interesting.I think the validity of my assertion that anyone else using the dataset would know exactly what the data mean depends on the purpose for which someone else wants the raw data.You make a good point that if it's to get raw data from several studies for cross-study analyses, then the wiggle room inherent in SDTM is going to make life tricky, particularly if studies have come from different companies. For those cross-study analyses, I think you are right to pick me up on my assertion that the problems are largely solved. Having read your links, I agree that I was being a bit over optimistic there.It will be interesting to see if the CDISC SHARE initiative can help standardise things. I have to say I'm skeptical about the prospect of having any standard that's sufficiently flexible to be useful in the huge variety of different study designs that are always going to exist, and yet eliminates the wiggle room , but I'll watch developments with interest.However, if data recipients are receiving raw data only for the purposes of re-analysing a single study, then I think I stand by my assertion. Certainly it's been my own experience that if I'm receiving SDTM data from someone else, then provided they have done a good job of completing their define.xml document (and of course that's not always true!), I have no problem figuring out what the data mean and doing whatever analyses are needed. I don't think I saw anything in the documents you provided that convinces me otherwise, unless you think I've missed something important?

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