In the therapy of neoplastic infections with cytotoxic drugs, there is little basis for the selective killing of the abnormal
cells as opposed to the healthy cells in the body. There are only a few known differences in receptors and metabolism that
are suitable drug targets at the present time. Instead, the major difference between neoplastic cells and healthy cells is
in the rate and timing of cell growth, as neoplastic cells exhibit excessive, uncoordinated growth. Therefore, most anticancer
drug therapies target all rapidly growing cell populations. Some phase of DNA synthesis and mitosis may be specifically targeted
by cytotoxic therapy, or a critical step in the metabolism of rapidly dividing neoplastic cells may be targeted. Because these
targets are minimally selective for neoplastic cells, many normal cells in the body will also be killed or damaged by cytotoxic
drugs. The rapidly growing, renewing populations of cells are most susceptible to toxicity, and include: gametes, blood stem
cells, epidermis, and gastrointestinal epithelium. Ironically, whereas the use of the cytotoxic anticancer drugs are intended
to kill cancer cells, an important potential side effect of their administration is the generation of new populations of cancerous
cells, as a result of damage to DNA that does not result in cell death. Reproductive toxicity can be considered an extension
of the pharmacological effects of toxicity to rapidly dividing cells, as the healthy gametes and embryo also undergo rapid
cell division. Due to these concerns, it is most prudent for women who are pregnant or attempting to become pregnant to avoid
unnecessary contact with cytotoxic agents, especially during the first trimester of pregnancy when the developing embryo is
particularly susceptible to teratogens.
Preparation of Cytotoxic Drugs: The likelihood of drug exposure must be taken into account when considering the safety of personnel who will handle cytotoxic
drugs and patients during or after drug administrations. Although the cytotoxic agents are used therapeutically, and most
chemotherapy protocols are well-tolerated by veterinary patients, the cumulative toxicity to personnel that arises from repeated
contact with these drugs can cause health problems in the nursing staff that are beyond those expected in the patient. The
main routes of personnel exposure to cytotoxic drugs are by aerosolization or by absorption through skin. Both types of exposure
can occur when preparing drugs for administration. The act of withdrawing cytotoxic drug from the vial into a syringe is generally
the step that presents personnel with the greatest potential for exposure to a high concentration of drug. Ideally, personnel
are protected from drug exposure and patients are protected from contamination of the product by the use of a Class 11, Type
B or C laminar flow biosafety cabinet during drug preparation. Class 11 biosafety cabinets provides HEPA filtration of incoming
air, a feature that is designed to protect the product and personnel from large particulates, such as bacteria and viruses.
However, many biosafety cabinets, or laminar flow hoods, are Class 11, Type A hoods, which are usually set up to exhaust HEPA
filtered air back into the room. As HEPA filters cannot efficiently filter small, volatile compounds, most Type A hoods are
not appropriate for preparation of cytotoxic drugs. In contrast, the Class 11, Type B2 biosafety cabinet vents all exhausted
air to the atmosphere, protecting personnel from exposure to volatile chemicals, and is therefore preferred over the Class
11, Type A biosafety cabinet. However, the NIH Division of Occupational Health and Safety (DOHS) permits the use of a Class
11, Type A biosafety cabinet that is equipped with a canopy that exhausts air from the cabinet to the outside. For the practitioner,
the need for protection of personnel during preparation of cytotoxic drugs presents the most significant obstacle to the safe
provision of chemotherapy, as most practices are not equipped with the appropriate biosafety cabinet. For the practitioner
without a Class 11, Type B2 biosafety cabinet, some suggested means of preparing cytotoxic drugs for administration include
having a pharmacy or hospital prepare doses of cytotoxic drugs, or using personal protective equipment and a dedicated clean
room to prepare drug doses. There are obvious advantages to using a pharmacy or hospital to dispense the cytotoxic dose. Many
pharmacies have appropriate biosafety cabinets in order to meet regulations concerning both the handling of cytotoxic agents
and the compounding of injectable drugs. Several veterinary compounding pharmacies now advertise this service. In addition,
human hospitals and outpatient cancer clinics may regularly dispense cytotoxic medications for human patients and may be willing
to prepare drug doses for veterinary patients as well.
If a veterinary practice decides to prepare doses of cytotoxic drugs on the premises without an appropriate biosafety cabinet,
then the personnel should be aware that they are stepping outside of accepted protocols for personnel safety. If a product
is dispensed at such a practice, then a respirator mask must be used in lieu of a biosafety cabinet, and the preparation of
cytotoxic drugs should be rare, rather than routine. Current National Institute of Occupational Safety and Health (NIOSH)
recommendations are for the use of a powered, air-purifying respirator with a high-efficiency filter. It should be noted that
surgical masks are not appropriate, as they cannot filter volatile chemicals and can even trap cyototoxic drugs in close proximity
to inspired air. If a biosafety cabinet is not available, then a modified cleanroom should be used. The area should be free
of distractions, extraneous personnel, clutter, and food or drink. A plastic-backed, absorbent liner should be placed on a
solid surface table and all necessary supplies collected. The recommendations stated below regarding the use of personal protective
equipment should be followed, with the addition of a suitable respirator.
Before preparing drugs, personnel should don a polyethylene gown with cuffed sleeves and eye protection. Double layers of
patient examination gloves may be worn, with one glove under the gown cuff and the second pair over the cuff of the gown.
Two layers of gloves are worn because some drugs can quickly penetrate the latex glove, and because the second layer affords
some protection in case of a manufacturing defect. Powder-free gloves are necessary as cytotoxic drugs can adsorb to powder
and then be dispersed throughout the room. Chemotherapy gloves are sold specifically as a single layer for chemotherapy use,
are thicker and longer than exam gloves (minimal thickness of 0.10 mm, minimal length of 270 mm), and have been tested for
their permeation to common cytotoxic agents. Such testing indicates that nitrile gloves are at least as effective as latex
gloves in slowing permeation of cytotoxic drugs through the gloves. Hands are washed before and after applying gloves, and
gloves are changed immediately when contaminated, or at least hourly.
The work surface should be protected with a plastic-backed, absorbent liner. When preparing a dose of a cytotoxic drug from
a vial, personnel should make every attempt to avoid aerosolization of the product, even when working in an appropriate biosafety
cabinet. A luer-lock syringe should be selected that is of sufficient volume that it will never be more than 1/2-2/3 full.
A chemotherapy pin is used to help prevent the contents of the drug vial from becoming pressurized. In addition, if a diluent
must be added, a careful adjustment of pressure can made by aspirating air into the syringe containing diluent before adding
a small amount of diluent to the vial, followed by aspirating air into the syringe, etc. A newer product, PhaSeal®, offers
an improvement on the traditional use of the chemotherapy dispensing pin and the pumping technique. This system is completely
closed, providing a double-membraned, sealed line of connection from the drug vial to the syringe and the IV line.
Many injectable cytotoxic drugs are vesicants, and can cause severe tissue necrosis if extravasated. Therefore, personnel
should be very cognizant of the drug that may be present on the needle. For that reason, infusion lines should be used and
needles should not be capped, or a one-handed technique should be used. The infusion line may be prefilled with an appropriate
priming solution, such as normal saline solution, prior to preparation of the cytotoxic drug dose. Heparinized solution generally
should not contact the cytotoxic agent as precipitation of some drugs can occur. The syringe containing the drug dose can
then be attached to the infusion line, without the use of an injection cap, which would again necessitate the use of a needle.
Any contamination of the outer syringe surfaces can be cleaned with 70% isopropyl alcohol on a gauze sponge. When oral cytotoxic
therapy is to be used, similar precautions should be followed when handling this medication. Pills should never be split or
crushed, to prevent airborne exposure to drug. Once the dose has been prepared, it may be placed in a bag that will protect
against spills, such as a ziplock bag, and labeled with the date, dose, patient's name, and responsible personnel's initials.
Some cytotoxic drugs (e.g., cisplatin and 5-fluorouracil) are light sensitive and should be stored in amber bags. Other drugs
may be thermally labile and should be placed with a cold pack if they will not be immediately used.