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by ejstronge
4115 days ago
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> The drugs being tested are all already approved, so safety would not be really a concern I think the problem is that Notable Labs would be testing combinations of FDA-approved drugs: Step 2: We use lab robotics to apply thousands of combinations of FDA-approved drugs...
> After some time to collect the data, you could fairly easily compare outcomes of patients who undergo this test versus those who do notUntil then, this won't be broadly available. I do think such a comparison would be interesting. I guess you'd need to compare the expected benefit of using the Notable Labs-suggested combination to using the standard of care. You'd need to have cells from patients who did not use the Notable Labs-suggestion. This requirement could turn an 'easy comparison' into a lengthy clinical trial. |
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Yes we'll be testing combinations, as this brain cancer has not responded historically to single agent therapy for decades.
With combinations of existing drugs it is possible to affect multiple driver pathways in the tumor at once. Similar to the dramatic improvement of AIDS therapy and infectious disease treatment with cocktails, tumors could respond much differently to combinations instead of a "one at a time approach" that has resulted in very small survival gains in this disease.
Please see this paper for more detail on the scientific approach to mutli-agent combinations to target many pathways at once. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4226667/
Patients have been taking the CUSP-9 protocol without any serious adverse affects on a compassionate use basis. This has now moved into a prospective clinical trial for recurrent glioblastoma patients in Germany http://www.anticancerfund.org/projects/cusp9-a-combination-o...
Personalized medicine services like this could allow clinicians to move beyond traditional randomized controlled trials. Commercial services such as Foundation Medicine provide test results to oncologists who then use their discretion to treat the patient outside of a clinical trial with scientific rationale based on the test itself as opposed to a standard of care.
In a severe disease like Glioblastoma where average survival is 15 months, if the majority of patients using a system like Notable Labs live substantially longer, is a control arm necessary? The HAART cocktail for AIDS treatment never went through a phase 3 trial, so there is precedent in high need diseases.
I also would like provide a link to a recent documentary that highlights the combination approach in brain cancer by telling the story of a 20 year survivor of Glioblastoma, Ben Williams. Other patients who safely used combinations of existing drugs are featured as well. http://www.survivingterminalcancer.com/