Dear Smokey234: Most of the data using dose dense therapy has been on
womenWomen's way with high risk disease. Based on your nodal status and HER2 status, your risk may not be considered "high" from the point of view of
systemicSystemic lupus erythematosus
Systemic lupus erythematosus rash on the face disease. From our perspective, neulasta is a safe medication. We have not had any serious problems using it. In the setting of a clinical trial, anything bad that happens to a person must be reported, regardless of whether it is thought to be due to the medication or not. If, in fact, this story is true, it may be that the person suffered some type of event and coincidentally was taking neulasta. Growth factors (neupogen or neulasta) are given during dose dense therapy for prophylaxis as part of the protocol. The theory is that part of dose dense therapy means keeping on schedule. If we wait to see if the counts drop before using growth factors, we may delay therapy such that the benefit of dose dense therapy is not obtained. Of course, in lower risk women, we do not know whether there is an advantage to using dose dense therapy at this time.
Finally, you mention that LCIS remains in the breast. This does not mean clean margins. If there is LCIS in the breast, most would recommend additional intervention for local control; either reexcision of the lump, mastectomy, or, in some cases, radiation therapy may be acceptable. Radiation would be recommended in any case if a lumpectomy were performed.