Hypothesis
Does sorafenib increase the survival in cancer patient with hepatocellular carcinoma?
Sorafenib- oral multikinase inhibitor of vascular endothelial growth factor receptor, inhibits tumor cell proliferation
Methods
Study population- patients with advanced hepatocellular carcinoma
None of these people received previous systemic chemotherapy
Used child pugh classification??? Why not MELD score?? This is a definite drawback.
Study design
Multi center, randomized double blind, placebo controlled
Phase 3 trial
400 mg daily sorfenib
Placebo
Designed by Bayer- scary
Primary outcome
Symptomatic progression
Decrease in 4 or more points from the baseline score on patients response
Death
Secondary outcome
Time to radiologic progression
Statistical analysis
Intention to treat analysis- analysis is based on the intention to treat in the beginning
This is to avoid the cross over and drop out effects.
Every one who begins he treatment considered as a part of the trial
Patients
902 patients’ screened
602 met the eligibility criteria
Overall survival
143 vs 178 in the sorafenidb vs placebo
Total of 321 died
Survival 44% vs 33% sorafenib vs placebo
31% relative risk reduction
Overall survival by cox proportional hazard significant
Radiologic progression was lower in sorafenib group
Discussion
Bottom line. You don’t have any choice. Take it.
FDA is dragging the foot in approving the cancer drugs, people are fed up
Not a great trial.
Some benefit is definitely there.
Introduction did not do justice this to article. Authors did a poor job in introduction, Not much information about the previous studies.
Well planned study. Patient population was selected from 8 different countries and impressive number of 4162 patients. Lot of ineligibility criteria about he previous statin use. A creatinine level of 2.0 is a cut off, why? Every one knows renal insufficiency people are at high risk
Pravastatin 40mg daily vs atorvastatin 80mg daily
Non-inferiority trial
10 day course of Gatifloxacin was also mentioned given to the patients. If you are mentioning in the trial, please tell us why?
When will the authors report this?
Average follow up time 2 years. Not good. 5 years may be better.
Statistical analysis - Looked at the sample size for 87% power, Please mention which software packet was used for analysis. This is not acceptable.
Primary endpoint-
Pravastatin group was 26.3%
Atorvostatin was 22.4%
Again primary end point was death
So clearly statistically significant benefit is here.
One other finding is clearly in favor is the reduction of C reactive protien
base line was 12.1
Pravastatin group it was 2.1
Atorvostatin group it was 1.3
but the dose difference is very significant. Pravastatin 40 vs Atorvostatin 80 mg
Now let us look at the HDL level
Pravastatin increased HDL by 8.1%
Atorastatin only 6.5%
P value is .001
Main points
Lower LDL goal is better.
Reduction of CRP is achieved by any statin.
Is there any benefit in increasing the HDL by drug therpay?- Probably not in this tudy group
All praises for this powerful software.
Future is R according to NYT.
SAS are they worried?
They should be worried.
Some guy at SAS compared to R with an aircraft engine wihtout any guarantee.
he was stupid enough to say that o NY times correspondent.
Suppose we wished to find the standard deviation of the set of the numbers 4 and 8.
Step 1: find the arithmetic mean (or average) of 4 and 8,
Step 2: find the deviation of each number from the mean,
Step 3: square each of the deviations (amplifying larger deviations and making negative values positive),
Step 4: sum the obtained squares (as a first step to obtaining an average),
Step 5: divide the sum by the number of values, which here is 2 (giving an average),
Step 6: take the non-negative square root of the quotient (converting squared units back to regular units),
So, the standard deviation is 2.