To some degree you are correct, but you are conflating processes that occur at different scales.
And important part of a functional immune system is checkpointing and surveillance of cells. Cells with errors in transcription in theory are flagged for destruction. Cell surface signaling is another way that the immune system jumps in to attack abnormal cells. This process is happening continuously, so in a technical sense if you wish to define cancer at the level of a single cell with proliferative potential, then sure, cancer is popping up all the time. As a result it is also why immunosuppressives carry warnings about increased risk of cancer, because they are downregulating a critical safeguard.
Cancer detection is still predominantly at the level of macroscopic disease, at which point it has far surpassed the point of failure on a cellular level. While a rise in cancer diagnoses are to be expected with improved screening, a hypothetical situation where cancers are coming and going does not occur at a clinically detectable level.
That said, you seem to imply that detected cancer does not resolve without modern medicinal treatment? Small sample, but I personally know one case where it did.
Also, do you believe that ongoing stress (after receiving what is widely considered a death sentence or one way road to constant treatment) has no influence the outcome?
Not GP. Clinico-laboratory detected cancer will never resolve without treatment and will lead to death, fast or slow. I do not understand the second point. Anticancer treatment is very stressful and damaging in many ways (middle ages' level of technology...) but care is taken that its side effects are less than the desired ones
> It’s an unexpected question that has stirred the world of cancer treatment in recent years, most notably now with prostate cancer. A growing number of doctors are advocating what might seem like an unusual position: That low-grade prostate cancers that grow very slowly or not at all shouldn’t be called cancer or carcinoma.
> The reason, they say, is that those words scare men, their families and sometimes even their doctors into seeking more aggressive treatment than patients need—leaving men with debilitating side effects—rather than pursuing a carefully monitored wait-and-see approach.
This is not cancer resolution. This is 'You die from another cause before you die from the cancer' (I cannot remove the 'lead to death' from my answer above)
For the patient it is the same, for the doctor (definition, surveys) it is different
If the cancer doesn’t grow or goes into spontaneous remission (which you claimed doesn’t happen yet is documented to happen, with a frequency that we do not have the data to determine, and for reasons we do not have the data to determine—with the implication that we cannot reliably causally connect it to treatment) then claiming “it leads to death anyway but something else gets you first” is not even logically true (let alone the fact that you would have no way to prove it, or that it would have no practical implications except perhaps creating undue agitation, contributing to inflammation and so on). It would lead to death the same way breathing, drinking water, or living leads to death.
> For the patient it is the same, for the doctor (definition, surveys) it is different
The whole point of the article is that it is different for the patient, leading to worse outcomes if the patient recognizes cancer as cancer.
I think the problem is that this conversation is lacking in precision of language. Amongst doctors the word cancer carries minimal value. Describing a mass as (in simple terms) a locally invasive carcinoma or an encapsulated adenoma gives a much better idea of expectations and a basis for factual claims. In fact the entire point of a histopath report is to give descriptive language that sufficiently grounds the findings in a usable level of detail for treatment/prognosis/etc.
Saying "cancers are X" will just invite anecdotal comments that refer to completely dissimilar processes.
I do have one example
Similar to yours - really advanced liver cancer resolved by itself (of course the patient thought it was his vegan diet). But this is probably one of a thousand liver cancers I’ve seen so it’s rare on a macroscopic level. There’s also the abscopal effect.
And important part of a functional immune system is checkpointing and surveillance of cells. Cells with errors in transcription in theory are flagged for destruction. Cell surface signaling is another way that the immune system jumps in to attack abnormal cells. This process is happening continuously, so in a technical sense if you wish to define cancer at the level of a single cell with proliferative potential, then sure, cancer is popping up all the time. As a result it is also why immunosuppressives carry warnings about increased risk of cancer, because they are downregulating a critical safeguard.
Cancer detection is still predominantly at the level of macroscopic disease, at which point it has far surpassed the point of failure on a cellular level. While a rise in cancer diagnoses are to be expected with improved screening, a hypothetical situation where cancers are coming and going does not occur at a clinically detectable level.