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 Tuesday, August 20, 2019 - 04:05 pm
Cancer Research & News

Learning the difference between chemotherapy, immunotherapy and targeted therapy

Until the 1960s, surgery and radiation were the mainstays of cancer treatment; drugs were not seen as a “cure” for cancer. 
With the exception of hormone therapy for men with prostate cancer in the late 1930s, drug therapies, at best, offered brief, 
incomplete remission. Then, the National Cancer Act of 1937 provided support for cancer research, setting up the National 
Cancer Institute (NCI), and doctors and researchers began to pay more attention to using chemical agents and drugs against 
cancer. The first breakthroughs came in the 1960s and early 1970s, when chemotherapies successfully treated adults with 
advanced Hodgkin lymphoma and children with leukemia. Today, more than 500 drugs are approved in the U.S. to treat cancer. 
Most of these fall into three main categories — chemotherapy, immunotherapy and targeted therapy — and work against cancer 
in different ways.
Chemotherapy Attacks Cancer Cells

Chemotherapy drugs kill cancer cells by stopping them from growing and multiplying. If the cells can’t grow and multiply, 
they usually die. Some chemotherapy drugs work during a specific stage of the cell cycle. One of the reasons chemotherapy 
is given in treatment cycles is to deliver drugs when they will be the most effective. Treatment periods are often 
alternated with rest periods to allow your body time to get stronger before the next round or “cycle” of chemotherapy.

Chemotherapy drugs attack cells that grow and replicate quickly, like most cancer cells. The bad news is that some normal 
cells (such as blood cells and cells in the hair follicles and lining of the digestive tract) also replicate quickly and
 are attacked. The effect on these normal cells cause many of the side effects commonly associated with chemotherapy — 
 hair loss, nausea, vomiting, diarrhea, and low blood-cell counts that lead to increased infection risk, fatigue and 
 bleeding. The good news is that the healthy cells usually repair themselves after chemotherapy has ended.
Examples of Chemotherapy

    Alkylating agents:  busulfan, procarbazine, carmustine, carboplatin, and cisplatin
    Plant Alkaloids: vincristine, paclitaxel, docetaxel, etoposide, and irinotecan
    Antitumor antibodies: doxorubicin, idarubicin, mitomycin, and bleomycin
    Antimetabolites: methotrexate (MTX), gemcitabine, cytarabine, 5-fluorouracil (5-FU), and capecitabine
    Topoisomerase inhibitors: irinotecan, topotecan, and amsacrine
    Miscellaneous: hydroxyurea, mitotane, estramustine, bexarotene, and tretinoin (ATRA)

Side effects will depend on your health before treatment, your type of cancer, and the type and dose of the drugs. 
Chemotherapy can cause nausea, diarrhea, fatigue, increased risk for bleeding and infection, hair thinning or loss,
 mouth sores, constipation, taste changes, loss of appetite, and nerve and skin problems.
Immunotherapy Mounts Your Defenses

Your immune system involves the many organs and tissues of the lymphatic system and several types of white blood 
cells. Normally, your immune system attacks foreign invaders — including abnormal cells — but cancer cells are sneaky 
and can “hide” from the immune system, avoiding detection.

Immunotherapy (also called biotherapy) uses drugs that go after the ability of cancer cells to hide from your immune 
system. Some immunotherapy drugs mark the cancer cells, allowing the immune system to find and destroy them. Other 
immunotherapies boost your immune system to work better against cancer.
Types of Immunotherapies

    Checkpoint inhibitors don’t target the tumor directly but interfere with the ability of cancer cells to avoid 
    an attack by the immune system by releasing the “brakes” that keep T-cells (a type of white blood cell) from 
    killing the cancer cells. Examples include Keytruda® (pembrolizumab) and Opdivo® (nivolumab).
    Adoptive cell therapy aims to boost the natural ability of your T-cells to fight cancer. We take T-cells from
     your tumor and test them. The T-cells most active against your cancer are grown in a laboratory and multiplied 
     in large numbers, a process that takes two to eight weeks. During this time, you may have chemotherapy and/or 
     radiation therapy to reduce the number of immune cells in your body. After these treatments, the multitudes
      of laboratory-grown T-cells are given back to you through an intravenous (IV) line to attack the cancer 
      cells. Examples include Kymriah® (tisagenlecleucel) and Yescarta™ (axicabtagene ciloleucel).
    Monoclonal antibodies are immune system proteins made in a laboratory and designed to attach to specific 
    targets found on cancer cells. Some monoclonal antibodies mark cancer cells so the immune system can detect
     and attack them. (Other monoclonal antibodies work differently and are considered targeted therapy.) 
     Examples include Erbitux® (cetuximab) and Herceptin® (trastuzumab).
    Treatment vaccines work against cancer by boosting your immune system’s response to cancer cells. 
    Treatment vaccines are different from the vaccines that help prevent disease. An example is 
    Provenge® (sipuleucel-T).

Side effects may include skin reactions or problems, flu-like symptoms (aches, fever), diarrhea, 
fatigue, risk of infection, and inflammation.
Targeted Therapy Blocks Cancer Growth

This class of drugs works by interfering with certain molecules or “targets” that are key to the 
cancer cells’ ability to grow and spread. Where chemotherapy drugs aim to kill cancer cells directly, 
targeted therapies focus on blocking the cancer cells’ growth, with less harm to normal cells.

Most targeted therapies are either monoclonal antibodies, which attach to proteins on the outside 
of the cancer cell, or small molecules, which target specific proteins inside the cancer cells. 
Researchers continually look for new “targets” for these therapies, including:

    abnormalities in the chromosomes of the cancer cells that are not present in normal cells
    cancer cells that make proteins that instruct the cancer to progress
    specific proteins that are present in cancer cells but not in normal cells, or are found in 
    higher amounts in cancer cells than in normal cells.

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Types of Targeted Therapies

    Hormone therapies slow or stop the growth of cancers that need those hormones to grow. Examples 
    include Arimidex® (anastrozole) and Lupron® (leuprolide).
    Angiogenesis inhibitors stop the tumor from growing the new blood vessels it needs for continued 
    growth. Examples include Avastin® (bevacizumab) and Zaltrap® (ziv-aflibercept).
    Signal transduction inhibitors block signals from one molecule to another inside a cell, such as 
    the signal for the cell to grow and divide. Examples include Herceptin® (trastuzumab) and Gleevac®
     (imatinib).
    Apoptosis inducers make cancer cells vulnerable to the normal cell process called apoptosis, which
     directs old cells to die. Examples include Velcade® (bortezomib) and Lynparza™ (olaparib).

Targeted therapies do have some limitations. The cancer can become resistant and the drugs no longer
 have the desired effect. To get around this — or delay it as long as possible — targeted therapies 
 are often given in combinations. Side effects of targeted therapies include diarrhea, high blood 
 pressure, skin rashes and problems with liver function, wound healing and blood clotting.

Drug therapies are part of the treatment plan for many patients to cure cancer, keep the cancer in 
check, relieve symptoms and improve the quality of life. If you have questions, please talk to your 
oncologist or your clinical pharmacist.




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