Targeted Cancer Therapy
A privately practicing hematologist and oncologist in Salem, Oregon, Natasha Tiffany, MD, also serves as oncology medical director at Salem Hospital and affiliate assistant professor at the Oregon Health and Science University School of Medicine. Natasha Tiffany, MD, draws on an in-depth knowledge of targeted therapies and other advancements in cancer care.
Targeted therapies for cancer are individualized cancer treatment options that work by identifying the molecular processes that speed tumor growth. Unlike traditional chemotherapies, which kill both cancerous and noncancerous cells, targeted therapies focus particularly on a particular process. Some are laboratory-produced antibodies that act on a particular cell target, while others are synthetic small-molecule chemicals.
Many targeted therapies block the chemical signals that tell cancer cells to grow. Others induce apoptosis, or cell death, by interrupting the breakdown of proteins that facilitate this process. Still others prevent the development of new blood vessels which, if left to grow uninterrupted, provide tumors with the nutrients that allow them to grow uncontrollably.
Within these general categories of targeted therapies exist a number of specific drugs. EGFR inhibitors, for example, block the growth of lung and colorectal cancers as well as some other tumors, while BRAF inhibitors target certain melanomas. Only an oncologist with experience in targeted cancer treatment can determine if such a therapy would be appropriate and, if so, which would provide the patient with the best chance of success.
sickle cell disease
Natasha Tiffany, MD, is a board-certified hematologist and medical oncologist with experience in a hospital setting. Since 2004, Natasha Tiffany, MD, has been providing care at her private practice for patients diagnosed with such serious conditions as sickle cell disease.
Sickle cell disease involves disorders of hemoglobin in the blood. People with the disease have inherited two abnormal hemoglobin genes, one from each parent, and at least one of the genes causes the body to make hemoglobin S, the defective form of hemoglobin in red blood cells.
Instead of the normal disc shape, these red blood cells are shaped like a sickle (hence the name) and are inflexible and tend to stick to blood vessel walls, obstructing the flow of blood. This deprives tissues of oxygen, leading to sudden attacks of pain, called pain crises. A lifelong illness, sickle cell disease requires the patient to remain under an oncology doctor’s care.
The disease mainly affects those of African descent. In the United States, approximately 1 in 365 black children are born with the disease, and around 100,000 Americans live with sickle cell disease today.
A triple board-certified physician specializing in hematology and oncology, Natasha Tiffany, MD, serves as a partner and practicing physician at Hematology Oncology of Salem in Salem, Oregon. Natasha Tiffany, MD, and the medical staff at Hematology Oncology of Salem utilize the latest cancer treatments, therapies, and medications, including aromatase inhibitors.
Aromatase inhibitors are a newer class of drugs that are often used to treat breast cancer or prevent its recurrence following surgery in postmenopausal women. Drugs in this class, which include letrozole, anastrozole, and exemestane, work by inhibiting the action of aromatase, the enzyme responsible for converting androgen into estrogen. These drugs are particularly effective in treating estrogen receptor-positive (ER+) breast cancers because they reduce the amount of available estrogen, which these types of cancers need to grow.
Either used alone or in combination with other drugs, aromatase inhibitors have been shown to be an effective treatment for both early and metastatic or recurring ER+ breast cancer. These drugs are also often prescribed off-label to treat conditions such as infertility and endometriosis. While they tend to be milder than other cancer drugs, the most common side effects of aromatase inhibitors include joint pain or stiffness, hot flashes, and bone thinning.
Cancer treatments are rapidly evolving. Traditional chemotherapy targets rapidly replicating cells. This kills the cancer cells, but can also lead to side effects such as hair loss, nausea and vomiting because the hair cells and the cells lining the gastrointestinal tract also divide quickly.
In recent years, scientists have been designing targeted treatments that are designed to block pathways needed for cancer cells to replicate and survive. Many cancer cells have genetic mutations in them that drive tumor growth. If we can identify a driving mutation in a tumor, we can design treatments that shut down the pathway it uses to promote cell division and survival. This targeted approach often has fewer side effects than traditional chemotherapy.
This personalized cancer therapy is very promising. We are committed to providing our patients the most up to date and cutting edge treatments available. We may talk to you about doing genetic testing of your tumor to see if you might benefit from targeted therapy.
Currently, many of the targeted treatments are available only through clinical trials, but some are already available as standard of care. We can help you find the best treatment options for you. If you have questions about personalized cancer treatments, please talk to your oncologist.
Natasha Tiffany, MD, administers innovative cancer treatments, such as targeted therapy, through Hematology Oncology of Salem, LLP, in Salem, Oregon. In preparation for her career, she underwent fellowship training in modern cancer care through Oregon Health and Science University. Before deciding whether to pursue targeted cancer therapy, patients ought to consult with an experienced professional like Natasha Tiffany, MD.
A relatively new treatment method, targeted therapy encompasses those medications that hone in on and influence specific molecules that regulate the growth and overall survival of cancer cells. Such methods are distinct from traditional chemotherapy, which does damage to both healthy and malignant cells. Currently, there is a range of targeted therapies available, including those that rely on hormones to treat hormone-sensitive growths and those that trigger controlled cell death in tumors.
For an oncologist to consider targeted therapy as a possible option, the patient in question needs to have a cancer that matches the available therapies. This may require that patients undergo genetic testing to see if their tumor cells actually have the necessary molecules for the therapy to target.
A cum laude graduate of Oregon Health and Science University, Natasha Tiffany, M.D., practices with Hematology Oncology of Salem. She has a professional interest in breast cancer therapy and prescribes aromatase inhibitors such as anastrozole and letrozole in treating certain patients. A newer type of medication, aromatase inhibitors are used by postmenopausal women to halt harmful estrogen production by the aromatase enzyme.
Without the inhibitor, aromatase turns androgen into small amounts of estrogen, which in turn stimulates the growth of breast cancer cells that are hormone-receptor-positive. This treatment approach is distinct from drugs such as raloxifene and tamoxifen, which work by blocking the estrogen receptors. Several studies have compared aromatase inhibitors and tamoxifen. Breastcancer.org notes that aromatase inhibitors typically are recommended as the best hormonal treatment to begin with, particularly among early-stage breast cancer patients who have undergone surgery (and in some cases radiation therapy and chemotherapy). The reason is that aromatase inhibitors appear to have fewer serious side effects, and more benefits overall, than their tamoxifen counterparts.
Natasha Tiffany, M.D., of Hematology Oncology of Salem, LLP, possesses 15 years of post-doctoral training and professional experience. Board-certified in internal medicine, medical oncology, and hematology, Dr. Tiffany became a physician partner at Hematology Oncology of Salem, in Salem, OR, in 2005. She holds a medical degree from Oregon Health & Science University.
Used in breast cancer related hormone therapy for pre- and post-menopausal patients, the anti-estrogen drug tamoxifen works by blocking the estrogen receptors found on breast cancer cells, thus preventing estrogen from binding to the cells and stimulating their growth. Taken daily in tablet or liquid form, tamoxifen decreases the recurrence of early stage breast cancer and treats metastatic breast cancer. Additionally, tamoxifen is effective in reducing the incidence of breast cancer in high-risk patients.
Women and men using tamoxifen may experience common, occasional, and rare side effects. About 10 in every 100 patients on tamoxifen report at least one common side effect, such as hot flushes and sweats, fatigue, and irregular periods. Occasional side effects include vaginal discharge, vaginal dryness, weight gain, headaches, and depression. Lastly, rare adverse effects include skin rashes, uterine cancer, blood clots and stroke. The risk of uterine cancer and stroke are greatest in post-menopausal women. Women taking tamoxifen who have not had a hysterectomy need to report any unusual vaginal bleeding, and require yearly pelvic exams.