Thursday, April 21, 2016

A cancer lesson from Niccolò Machiavelli






“The Prince”, 1513:

"… men ought either to be well treated or crushed, because they can avenge themselves of lighter injuries, of more serious ones they cannot; therefore the injury that is to be done to a man ought to be of such a kind that one does not stand in fear of revenge."

Ch. 3; Variant translation:

"Never do any enemy a small injury for they are like a snake which is half beaten and it will strike back the first chance it gets".

And this is my paraphrase of Machiavelli's thought when applied to cancer treatment:


"Never do a cancer a small injury for it is like a snake which is half beaten and it will strike back the first chance it gets".

This means that we should carefully design the first strike against cancer

The first strike should aim at multiple cancer targets, thus not leaving a chance for cancer to come back. Multiple targets require multiple drugs and multiple treatment conditions, all combined in one regimen that does not give the cancer cells time to evolve, adjust and thrive again. This approach is the approach of combination therapies.

The requirement for combination therapies is well explained in the documentary Surviving Terminal Cancer that I mentioned earlier this month.

Why can cancer strike back if we do not obliterate it with the first attempt? Why are monotherapies or even current combined therapies of 2-3 drugs unsuccessful? There are several considerations that address these questions:

1. Each cancer patient has a different mutation profile; therefore, the treatment regimen of each patient must be tailored according to the mutation profile.

2. All druggable targets (based upon the cancer mutation profiles) should be simultaneously "hit" from the very first round of treatment so that the cancer does not have time to evolve (i.e., to acquire additional mutations or favor smaller, already existent subsets of cells with differential mutation profile).

3. The mutation profile CANNOT be the only criterion for selection of the multi-drug regimens: it has been shown over and over again that when we target proven mutations, several survival pathways are activated. These survival pathways may not be even supported by mutations, and yet, they are activated and allow the cancer cells to survive the "assault" of the targeted drugs. Therefore, each anti-cancer regimen should include an anti-survival signaling cocktail of drugs. 


4. Drug regimens need to be accompanied by additional treatment conditions. The majority of cancers are glycolitic, and ketogenic diet and intermittent fasting have been shown to counteract neoplastic development that relies on glycolysis. The two dietary patterns could be combined in 16/8 regimen, where ketogenic diet is consumed in a window of up to 8 hours a day, followed by a 16-hour fasting period.  The application of 3-bromopyruvate, a hexokinase 2 inhibitor, might be synergistic with the ketogenic diet/intermittent fasting regimen.

5. One very strong differentiation factor between neoplastic and normal cells is the relatively higher sensitivity of the cancer cells to fever/higher body temperature. The first cells to die at high body temperatures corresponding to fever are the cancer cells. This differential sensitivity is the foundation of the anti-cancer effect of Coley's toxins as mentioned in my early post 

Can anyone imagine an anti-cancer treatment protocol that combines multiple drugs based upon cancer mutation profiles, an anti-survival signaling cocktail of inhibitors, hyperthermia (high body temperature) and a dietary regimen of ketogenic diet/intermittent fasting?  Under current legislation rules this is an absurd idea.  No oncologist will risk his/her license to oblige a cancer patient. We need legislation that supports these drastically new approaches to combination therapies.  Such legislation will allow oncologists to follow on patients who select to administer novel combination approaches to treat their terminal cancer.  The choice for cure should be given to these cancer patients. Today, we endlessly talk about the "empowered" patient, and yet, our legislation has taken this power away from the most vulnerable - the terminal cancer patients.

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