Dear Belleview Teacher: 50 years ago the "cut" was a total mastectomy, which included removing the breast and part of the muscles of the chest wall, leaving a concave area on the person's chest. Today, in many cases a lumpectomy + radiation can be done with better survival rates. Even if a lumpectomy is not feasible, a mastectomy now, though still removing a body part, is not nearly as disfiguring nor does it affect function the way the old surgery did. In terms of progress in "poison," 50 years ago, we had a handful of drugs that we gave in large doses that caused significant toxicity for which we had no real rememdies. Today, several generations of "poison" later, we now give drugs that specifically have an improved survival rate and with the new medications for nausea and other side effects, most people tolerate treatments reasonably well, though we realize it is not a walk in the park. Also, treatments can be given outpatient so that people can recover, if needed, in their own homes. 50 years ago, the mortality rate was quite high. To give you some statistics, although the incidence of breast cancer is higher, the mortality rate is lower. For example, as recently as 1991, deaths from breast cancer were 25 percent. In 2003, only 12 years later, deaths from breast cancer are down to 18 percent. This seven percent improvement can be attributed entirely to research on early detection (including mammotome, MRI, mammogram, ductal lavage, and ductoscopy, to name a few), research on surgery (lumpectomy, modified radical mastectomy, and now nipple sparing surgery research is underway), research on radiation therapy (including ways to reduce toxicity to the opposite breast and some new research on implanted radiotherapy - brachytherapy), and research on chemotherapy (including the drugs like paclitaxel[taxol] and trastuzumab[herceptin], new and improved schedules that have improved survival, and growth factors such as filgastrim[neupogen] and the longer acting peg-filgastrim[ neulasta] that have practically eliminated death from overwhelming infection due to low white blood cell counts from chemotherapy, not to mention better antinausea medications and venous access devices such as port-o-caths that allow medication to be given when venous access is a problem). In terms of the "clone" issue, a better way to explain this might be to refer to this as targeted therapy. Herceptin is a newer drug that targets the HER2neu antibody that is expressed on the surfaces of some breast cancer cells. This technology (including the identification of this antibody and the ability to test for this) is less than 10 years old. And...let's not forget that there are three new medications to address positive estrogen receptor status on tumors that have shown increased disease free survival in postmenopausal women (research is underway in premenopausal women). These drugs are called aromatase inhibitors and have better toxicity profiles than the already well tolerated tamoxifen. One of the most recent studies to be published is a direct result of the Human Genome Project in which a blood test has been identified that looks to determine risk of recurrence by identifying circulating tumor cells. This, as the research moves forward, will help doctors identify which patients require more aggressive therapy. So, while your friends may have a point if the topic is oversimplified to "cut" and "poison," I would argue that research has improved both the quality and quantity of many lives. If your friends think research dollars don't matter, tell them to look at you. You are "living" evidence that they do, indeed, matter.