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Trial results for new lung cancer drug are 'off the charts'

202 pointsby charlieirish12 months ago

10 comments

dannykwells12 months ago
Note that this drug is not new - it is fully approved for ALK+ NSCLC and has been since 2015.<p>It&#x27;s not clear why these data are just coming out now or what is different from the original trials run in this setting.<p><a href="https:&#x2F;&#x2F;en.wikipedia.org&#x2F;wiki&#x2F;Lorlatinib" rel="nofollow">https:&#x2F;&#x2F;en.wikipedia.org&#x2F;wiki&#x2F;Lorlatinib</a>
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BenFranklin10012 months ago
Not mentioned by the Guardian, but Lorlatinib was developed by Pfizer.<p><a href="https:&#x2F;&#x2F;www.nbcnews.com&#x2F;health&#x2F;cancer&#x2F;lung-cancer-treatment-pfizers-lorbrena-extends-life-non-small-cell-lun-rcna154798" rel="nofollow">https:&#x2F;&#x2F;www.nbcnews.com&#x2F;health&#x2F;cancer&#x2F;lung-cancer-treatment-...</a>
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hnpolicestate12 months ago
Still no progress with small cell lung cancer?<p>It killed my 43 year old aunt in less than two months back in 2002. Smoker though.
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noncoml12 months ago
Lung cancer is not the death penalty that it use to be if you are “lucky” to have one of the mutations that this, and other similar drugs, target.
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adamredwoods12 months ago
Tyrosine kinase, when mutated, causes uncontrolled cell growth.<p>TKIs: Crizotinib (1st gen), alectinib.<p>&gt;&gt; Lorlatinib is a third-generation, highly potent, macrocyclic ALK&#x2F;ROS1 TKI that competitively binds to the adenosine triphosphate‐binding pocket, blocking ALK‐dependent oncogenic signaling. The advantage of Lorlatinib is high penetration of the blood-brain barrier by decreasing p‐glycoprotein‐1‐mediated efflux. Besides, it has broad‐spectrum activity against most known resistance mutations that develop during treatment with first and second‐generation ALK TKIs, including ALK G1202R mutation. The introduction of Lorlatinib to salvage these patients has shown the potential to add life. This has been shown in a global phase II study and other real-world studies, however, data is scant from LMIC. The most common toxicities were peripheral edema (9–48%), hyperlipidemia (47–94%), weight gain (3–25%), peripheral neuropathy (30%), fatigue (15–30%) and cognitive effect (6–18%) in earlier studies. The treatment discontinuation rate varied from 3–14% due to toxicity.<p><a href="https:&#x2F;&#x2F;www.nature.com&#x2F;articles&#x2F;s44276-024-00055-9" rel="nofollow">https:&#x2F;&#x2F;www.nature.com&#x2F;articles&#x2F;s44276-024-00055-9</a><p><a href="https:&#x2F;&#x2F;en.wikipedia.org&#x2F;wiki&#x2F;Lorlatinib" rel="nofollow">https:&#x2F;&#x2F;en.wikipedia.org&#x2F;wiki&#x2F;Lorlatinib</a><p><a href="https:&#x2F;&#x2F;en.wikipedia.org&#x2F;wiki&#x2F;Tyrosine_kinase" rel="nofollow">https:&#x2F;&#x2F;en.wikipedia.org&#x2F;wiki&#x2F;Tyrosine_kinase</a>
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zzzeek12 months ago
Why do all the new cancer drugs coming out end in the letter &quot;B&quot;?
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dontreact12 months ago
Another good reason more people should get screened for lung cancer. If you can find it early, you can maybe halt the progression with this drug!
noobermin12 months ago
Just a comment, these drugs are very expensive. Especially as these aren&#x27;t one time treatments but are taken daily, costing patients 1000s a month.
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nemo44x12 months ago
Too bad cancer is the least of your concerns if you smoke. The COPD and numerous related illnesses are as bad if not worse.<p>Hopefully this drug helps anyone with lung cancer.
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benmarten12 months ago
RCT? Doesn’t look like it…
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