| ▲ | New iron nanomaterial wipes out cancer cells without harming healthy tissue(sciencedaily.com) |
| 161 points by gradus_ad 6 hours ago | 47 comments |
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| ▲ | quantummagic an hour ago | parent | next [-] |
| Hope this makes it to people soon. Have a family friend who was diagnosed with cancer a few days ago. It was here in Canada, so they offered her assisted suicide, literally within 30 seconds after telling her she had cancer. She didn't even really process the diagnosis before they were offering to help her die. They didn't offer to try any experimental medicine. |
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| ▲ | xbar 3 hours ago | parent | prev | next [-] |
| I lost my brother yesterday to cancer. I hope one day this can save lives. Go Beavs. |
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| ▲ | RomanPushkin 3 hours ago | parent | prev | next [-] |
| Experiencing cancer in my family I can tell for sure all of that buzz is quite exciting, but in the last 5 years there haven't been breakthroughs that would significantly improve outcomes for an average patient. |
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| ▲ | slapshot 2 hours ago | parent | next [-] | | There have been massive improvements in treatments in the last 5 years. Sure, cancer is far from being "cured" - but survival today is far better than 5 years ago for many forms. Among many others: - CAR T therapy going from lab to oncology suite (first launch 2017, but use rapidly growing) - Approval of Keytruda and similar for many additional forms of cancer (see the 2021-2026 milestones here: https://www.drugs.com/history/keytruda.html ) - Liquid biopsy going from lab to PCP's office - starting with Grail Galleri and moving from there (yes, the NIH results were weak, but the idea of a liquid biopsy at all would be laughed off 10 years ago) - Move of Atezolizumab and Tecentriq from infusion (hour) to injection (minutes) to increase availability - Lower dose CT scanning for lung cancer, including for non-smokers And a long line of immunotherapies that are making the leap from lab to chair right now. The last 5 years have probably been the most exciting in cancer research since the launch of the monoclonal antibodies in the early 2010s. There is still incredibly far to go, but the trend is in the right direction: https://employercoverage.substack.com/p/decline-in-cancer-mo... | | |
| ▲ | parineum an hour ago | parent | next [-] | | I've heard that the improvements in cancer survival are mostly a statistical trick centered around earlier detection. That people aren't actually living longer with cancer, they're living longer while we know they have cancer. Is there any truth to that? | | |
| ▲ | greygoo222 18 minutes ago | parent | next [-] | | Short answer, no. Long answer, it's a variable you need to consider when doing data analysis, and it depends on what exactly you're talking about, but it's absolutely not true for improvements in cancer survival general. One alternative method is to look at per-capita death rates, for example: Reduction in US and UK childhood cancer death since 2000
https://ourworldindata.org/grapher/cancer-death-rates-in-chi... Reduction in several countries' age-standardized breast cancer death since 2000
(Why did it increase in South Africa? I'm not sure, maybe socioeconomic factors)
https://ourworldindata.org/grapher/breast-cancer-death-rate-... Reduction in global age-standardized cancer death rate since 2000
(Scroll down to second graph. Since the population is getting older, age-standardization makes a fairer comparison)
https://ourworldindata.org/grapher/cancer-death-rates 2000 is an arbitrary year I picked for clear visual changes without needing to haggle over statistics. If you want to feel optimistic, switch the childhood cancer death graph to 1960-now. This method has different possible failure points. It could be that less people are getting cancer, or that people who would get cancer are dying of other causes, or reporting of cause of death has changed, though this is very unlikely for some figures, such as leukemia death rates for children in the US. Statistics is hard. Overall though, the evidence is very good that cancer survival has improved a lot due to better treatments since 2000. If you have a more specific claim you're dubious about, I'd be willing to look into it for you. I'm very enthusiastic about this topic. | | |
| ▲ | parineum 5 minutes ago | parent [-] | | I'm not exactly dubious about anything really, it was just something plausible I had heard a while ago and, while I don't recall where I heard it, I must have given it some credence for it to stick with me. |
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| ▲ | dsjoerg 39 minutes ago | parent | prev [-] | | Cool question. What form would an answer take? We need some detection benchmark data thats invariant over the period of interest. I hope the data exists but I would be surprised. Another way to come at it would be mortality data. But that has a bunch of its own problems. Everything is changing at once, it makes this kind of science so hard. |
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| ▲ | baxtr an hour ago | parent | prev | next [-] | | You seem to be knowledgeable on this topic. What’s your prediction for the next five years? | | | |
| ▲ | greygoo222 40 minutes ago | parent | prev [-] | | mRNA cancer vaccines are the most exciting new treatment about to hit the clinic. Moderna's Phase 2b intismeran autogene randomized trial found a 49% (!!!) reduction in the risk recurrence or death for patients with high risk melanoma already on standard treatment. Several Phase 3 trials are underway. mRNA vaccines have the potential to work for a wide variety of tumors. (95% confidence interval is 0.294-0.887, wide but not too wide, n=157, to be expected for phase 2). How they work is also completely fucking insane. Intismeran autogene is personalized for every patient via sequencing their tumor DNA. That's sci-fi shit. If you're not impressed by that, you should be. Fast and scalable DNA sequencing, neoantigen identification, RNA synthesis, none of this is easy and all of it relies on recent innovations across multiple fields. The first proofs of concept for personalized vaccines like this date back to 2017[1] or 2015[2]. The process for designing the vaccines requires a machine learning algorithm first published in 2020[3]. Details of the algorithm aren't available, but it validated against data published in 2019[4], and there have been many recent advancements in algorithms and datasets for biotech ML that it likely relied on. As you might already know, mRNA vaccines were first tested in humans around the 2010s[5]. [1] https://www.nature.com/articles/nature22991
[2] https://pubmed.ncbi.nlm.nih.gov/25837513/
[3] https://aacrjournals.org/cancerres/article/80/16_Supplement/...
[4] https://pmc.ncbi.nlm.nih.gov/articles/PMC7138461/
[5] https://pubmed.ncbi.nlm.nih.gov/26082837/ |
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| ▲ | ImageXav 2 hours ago | parent | prev | next [-] | | It may feel that way due to the iterative nature of medical improvements, but over the past few decades there has been a consistent reduction in cancer mortality rates across most types of cancer [0]. Treatments really are getting better and more targeted. Immunotherapy has made huge breakthroughs. Combination treatments allow for significantly improved lifespans and better quality of life during treatments. There are a few cancers that remain hard to treat, but I have a lot of confidence that in the coming decades we will make strides in attacking them. That being said, I'm very sorry to hear about the pain you and your family must be going through. I've had a few close loved ones undergo cancer treatment and it was tough. [0] https://acsjournals.onlinelibrary.wiley.com/doi/10.3322/caac... | |
| ▲ | Retric 2 hours ago | parent | prev [-] | | Major breakthroughs of the kind you’re talking about are extremely uncommon. Instead it’s lots of little gains that keep adding up because cancer isn’t adapting overall people still get the same mutations they got 10,000 years ago. So average person with cancer does better when any individuals cancer treatment improves and it keeps compounding over time. This doesn’t mean everyone with cancer gets a slight improvement, often it’s specific types or stages that improve without impacting others. Where general progress comes from is it’s not the same improvements year after year. | | |
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| ▲ | msie 5 hours ago | parent | prev | next [-] |
| They should give it to some people with fatal stages of cancer. |
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| ▲ | gimmeThaBeet 4 hours ago | parent [-] | | I agree, or at least I would stress that people should be allowed to consent to that.
I don't know what the prevailing medical ethics of doing that kind of thing in consenting patients
in that state, but my uninformed intuition is I would disagree with it. Though one thing that I might think researchers might not want is people may be too sick to recover even if their cancer disappeared tomorrow. | | |
| ▲ | greygoo222 3 hours ago | parent | next [-] | | Both patient participation in clinical trials and compassionate use of experimental treatments are fairly common for cancer patients, with various accessibility barriers. (One issue with the latter, for example, is that the incentives aren't lined up for companies to provide unapproved drugs to dying patients, you're way more likely to get a horrible complication that leads to bad press than a miraculous recovery). Here's an insightful blog series about Jake Seliger's experience participating in clinical trials. He was a regular HackerNews user who passed away in 2024: https://bessstillman.substack.com/p/please-be-dying-but-not-... | | |
| ▲ | amelius an hour ago | parent [-] | | What is the success rate of a clinical trial? Just to see things in perspective. | | |
| ▲ | throwup238 an hour ago | parent [-] | | It's around 10-15% for the whole drug I-III flow (13.8% according to [1]), but that varies dramatically based on therapeutic area. On the order of a third of infectious disease vaccines might be approved but only maybe 5% of oncology therapies because the latter often have a different standard for approval so it's cheaper to run trials. [1] https://pmc.ncbi.nlm.nih.gov/articles/PMC6409418/ | | |
| ▲ | amelius 24 minutes ago | parent [-] | | That's interesting, but I was talking about the success rate of someone with a terminal illness going the clinical trial route. Sorry, I now see that my question was not so precise. | | |
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| ▲ | tyre 3 hours ago | parent | prev | next [-] | | In the US, the FDA has a Compassionate Use exemption to clinical trials for exactly this circumstance! There must be informed consent, no reasonable alternatives (which, in cases we deem terminal, is often the case), and some evidence pointing to the treatment possibly being helpful. It's an excellent ethical program that gives patients a choice and advances science. | | |
| ▲ | throwup238 3 hours ago | parent [-] | | In my experience most legitimate biotech companies working on promising drugs and therapies don’t want to touch the exemption with a 30 foot pole. Since they raise most of their money from the public to fund clinical trials, a single bad reaction could generate enough bad PR to derail fundraising and kill the drug. Sticking to clinical trials allows them to control that blast radius so even though the FDA approves >95% of applications, in practice very few drugs are available that way. The biggest exception is oncology. Since everyone knows that chemotherapy is hell, cancer drugs tend to get a pass and pre-approval companies are (slightly) more willing to work with compassionate use exemptions. |
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| ▲ | contingencies 2 hours ago | parent | prev [-] | | Both of my parents have benefited from access to early medical trials. One is currently very late stage IV cancer. Access to trials is usually proxied through respected doctors/oncologists affiliated with major hospitals rather than offered broadly. I assume for reasons of experimental protocol and integrity the overseeing doctors are typically not the same as the conceiving research team. |
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| ▲ | fnord77 an hour ago | parent | prev | next [-] |
| Command-F "mice" yup. every time |
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| ▲ | mcc1ane 5 hours ago | parent | prev | next [-] |
| in mice? |
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| ▲ | jbotz 5 hours ago | parent | next [-] | | Yes, in mice, but human cancer cells: "When we systemically administered our nanoagent in mice bearing human breast cancer cells, it efficiently accumulated in tumors, robustly generated reactive oxygen species and completely eradicated the cancer without adverse effects ..." So it kills human cancer and doesn't harm the mouse in the process. | | |
| ▲ | greygoo222 3 hours ago | parent | next [-] | | Xenografted human tumors in mice != human cancer. The support structure of the tumor (tumor microenvironment) differs between model mice and humans, cells derived from human cancer that can be cultivated in a lab and xenografted differ from typical human cancer cells, and xenografting requires immunodeficient mice, just to name a few factors that affect treatment response. Mice models of cancer are useful, but you should never be too surprised when something that works in mice doesn't work in the clinic, xenografting or no. Cancer is complicated. | |
| ▲ | yyyk 2 hours ago | parent | prev [-] | | Doesn't harm the mouse. But would it harm the normal human cells? |
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| ▲ | YarickR2 5 hours ago | parent | prev [-] | | Human breast cancer, in mice. |
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| ▲ | esafak 4 hours ago | parent | prev | next [-] |
| If it worked, how much might it roughly cost per treatment, at scale? |
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| ▲ | abeppu 3 hours ago | parent | next [-] | | Actually, when in the lifecycle of developing a treatment does anyone have a real idea of what cost will be? Can anyone know this yet? In terms of where _prices_ are set, that negotiation is a function of efficacy relative to other things in the market right? If it ends up treating cancers that each already have a reasonably effective treatment, maybe the pricing isn't that high -- but if it is effective in cases where currently there are no options, the price should be high? But for something that potentially works against a range of cancers, should we expect to see a sequence of more specific trials (i.e. one phase 1 for basic safety, a bunch of phase 2s for efficacy on specific cancer types, a sequence of phase 3s in descending order of estimated market value? And in 10 years, Alice and Bob with different cancers will pay radically different amounts for almost exactly the same treatment but with small variations in some aspect of the formulation so they can be treated as distinct products? | |
| ▲ | alansaber 3 hours ago | parent | prev | next [-] | | As far as nanomaterial assembly goes MOF syntheis is pretty scalable | |
| ▲ | stevekemp 3 hours ago | parent | prev [-] | | Does the cost matter? Many countries subsidize healthcare, so there's either no charge or a token payment which doesn't even pretend to cover the cost of treatment. Other countries use insurance, so once again the end cost is essentially irrelevant. | | |
| ▲ | skeletal88 an hour ago | parent | next [-] | | The cost absolutely matters. If something costs tens of thousands of € per month for a long time then it will either not be approved or will be used very rarely. The cost is not irrelevant because the insurance does not have infinite money. They need to decide which cures, medicines, operations they fund. They can spend 1000€ to cure 100 people of something or to spend 100k to maybe cure someone with an experimental treatment. This is one of the issues with the modern cancer cures, thst they are very specific to the cancer, the patient, need one off lab work for each patient and this makes them very expensive and not affordable to many. Despite having public healthcare the managers of it still need to decide what to spend their limited funds on. | |
| ▲ | Groxx 3 hours ago | parent | prev | next [-] | | Yes? Countries that subsidize healthcare don't calculate infinite value per person. | |
| ▲ | nickjj 2 hours ago | parent | prev | next [-] | | > Other countries use insurance, so once again the end cost is essentially irrelevant. I think it matters because oftentimes insurance companies won't cover treatments if a cheaper form of treatment exists. It doesn't matter if the old treatment is less effective or a much worse outcome for a patient. This is especially true for "new" treatments. | |
| ▲ | esafak 3 hours ago | parent | prev [-] | | Of course it does. Countries have budgets. Expensive drugs aren't doled out like candy; they require screening, waits, connections, and even bribes. |
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| ▲ | dyauspitr 5 hours ago | parent | prev [-] |
| Anything that doesn’t genetically target cancer cells is just not the solution long term. Any progress is good though. |
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| ▲ | lightedman 5 hours ago | parent [-] | | Literally reactive oxygen species targets cancer cell DNA. We are taking advantage of the unique chemical environment of the inside of a cancer cell and using it to generate oxygen in a double-whammy to destroy itself. This is perhaps the best targeted method devised as it seems to collect basically entirely in tumors. Chemo and Radio therapy just aren't that targeted. |
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