The leading side effect of EGFR inhibitors, both the oral tyrosine kinase inhibitors (such as tarceva (erlotinib)) and the IV monoclonal antibodies (such as erbitux (cetuximab)), is rash, dryness, and other skin side effects. While a rash sounds modest to many people compared to many of the leading problems with chemo, many of the members here can attest that while an EGFR rash can range be as mild as a pimple or two, it can also be itchy, painful, and be as severe as a skin rash covering large amounts of the body, sometimes with open lesions. And for some patients, the skin side effects can require dose reductions or even lead patients to discontinue their EGFR inhibitor, even if it might help against their lung cancer.
As described in a press release last week, Hana Biosciences, based in South San Francisco, has initiated a study of topical menadione, a precursor to forms of vitamin K that also activates EGFR. This topical medication is being studied in the setting of both a prophylactic treatment and as a treatment for skin side effects that emerge on treatment. This research is being led by Dr. Mario Lacouture at Northwestern, who I’d consider to be the leading expert in EGFR rash treatment right now.
There have been several posts and forum threads on managing the rash, but it’s very encouraging to see that not only is more attention being paid to this problem, there are actually trials being run, even with new agents, that are trying to reduce a side effect that can significantly worsen the quality of life for patients on EGFR inhibitors, sometimes even keeping them from getting the drug, or perhaps a dose that could be managed chronically if the rash was controlled more effectively.
posted by Dr. West @ 9:18 pm link to this post





April 13th, 2008 at 11:10 pm
This is a VERY worthwhile project. With most chemos, treatment is planned for a specific period of time, and even if the side effects are quite bothersome, we can put up with a lot when there’s light at the end of the proverbial tunnel. But with drugs like Tarceva, the period of treatment is open ended — we hope it will be for a long time, but if a person is miserable with no end in sight, the question can become “is it worth it?” What a shame when that happens. Aloha,
Ned
April 14th, 2008 at 8:23 am
Hi Dr. West, I have been using Tarceva since March 19. I developed bad acne at about day eight. The protocol I am on has discontinuous use of Tarceva (take 200 mg/day days 2 through 16 of 21 day cycle). The rash is very mild now but maybe builing again. I hope to find it manageable because symptomatically it appears to be helping with my bone mets in my left leg.
Another issue I have read about and I am struggling with is drowsiness. I sit and read or watch TV and keep dropping off. I really hope this will improve as it affects my QOL.