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chemotherapy
medications used to destroy or prevent growth of cancer (rapidly dividing) cells, interferes with the ability to divide/duplicate
cell cycle specific
antimetabolites
plant alkaloids
cell cycle nonspecific
alkylating agents
nitrosoureas
anti-tumor antibiotics
topoisomerase I inhibitor
biologic response modifiers
asparaginase
heavy metals
hormonal agents
antimetabolites
cell cycle specific chemo- interfere with DNA/RNA in S phase
5FU
6MP
Gemcitabine
cytarabine
fludarabine
MTX
Numbers, -abines, MTX
plant derivatives
cell cycle specific chemo- from natural products that blocks ability to divide by stopping enzyme from making reproduction proteins
4 classes:
Vinca Alkaloids
Epipodophyllotoxins
Taxanes
Camptothecin
Vinca Alkaloids
plant derivative, cell cycle specific chemo- in M phase, major side effect peripheral neuropathy
VCR
Vinblastine
Vindesine
Vinorelbine
Epipodophyllotoxins
plant derivative, cell cycle specific chemo- in S and G2 phase cause DNA strand breaks
Etoposide
Teniposide
Taxanes
plant derivative, cell cycle specific chemo- in M phase, inhibits mitosis
paciltaxel
docetaxel
camptothecins
plant derivative, cell cycle specific chemo- in G2 and M phase binds to topoisomerase I and cause damage
camptotecin
topotecan
irinotecan
alkylating agents
nonspecific chemo, damages DNA and works on all cycles, increases risk of leukemias 5-10 years after treatment
Carboplatin
Cisplatin
cyclophosphamide
Ifosfamide
Melphalan
Procarbazine
Temozolomide
Thiotepa
-in, -ine, -ide, thiotepa, melphalan
nitrosoureas
nonspecific chemo, subset of alkylating agents, slow enzymes that repair DNA
Carmustine
Lomustine
antibiotics
nonspecific chemo, made from microorganisms, break or bind DNA
Bleomycin
Dactinomycin
Daunorubicin
Mitomycin
Doxarubicin
Mitoxantrone
-cin, mitoxantrone
hormones
nonspecific chemo, enters and modifies transcription, can also be used to prevent nausea/vomiting and allergic reactions
dexmethasone
prednisone
miscellaneous agents
nonspecific chemo, does not fit into category
enzymes (PEG)
Hydroxyurea
Procarbazine
biotherapy
nonspecific, function as antineoplastics
monoclonal antibodies
cytokines
tyrosine kinase inhibitors
vaccines
gene therapy
retinoids
hematopoietic growth factors
monoclonal antibodies
nonspecific biotherapy, lab produced molecules that act as antibiotics and attack cells- seek out proteins on cancer cells
Rituximab
Alemtuzumab
Bevacizumab
Cytokines
nonspecific biotherapy, signals immune system to do its job
Interferons
Interleukins
tyrosine kinase inhibitors
nonspecific biotherapy, block enzyme (TK) which stops cancer cells from dividing, targeted therapy/less side effects
Imatinib
vaccines
nonspecific biotherapy, can be used to treat/prevent cancer
Gardasil: HPV
Hep B: liver cancer
immunotherapy: treat by boosting immune system
gene therapy
nonspecific biotherapy, designed to target specific genes and proteins involved in growth and survival of cancer cells
retinoids
nonspecific biotherapy, facilitate differentiation and suppress proliferation of cancer cells, well tolerated antitumor activity
All-trans retinoic acid (ATRA)
Isotretinoin
colony stim factors
responsible for maturation of blood cells, shortens length of myelosuppression
Epoetin/Darepoetin: RBC production
oprelvekin: plt production
sargramostim: granulocyte production
filgrastim: neutrophil production
pegfilgrastim: WBC production
vesicants
medications that can cause significant tissue injury
SLAPP: Stop, leave needle, aspirate, pull needle, provider notify
Give antidotes
Ex:
Dactinomycin, Daunorubicin, Doxorubicin, Idarubicin, plant alkaloids
radiation
can be used alone for treatment of cancer or in combination with chemotherapy, destroys rapidly dividing cells
side effects: fatigue, myelosuppression, skin changes (hair loss, burn, desquamation), radiation recall (burns- cool cloths)
late: dose >10gy effects on growth, >30 cause vasculopathies in large brain vessels
external beam radiation
most common form of radiation, high energy beams delivered to tumor
proton: directly the tumors, minimize damage to surrounding tissue
conformal: delivers different amounts to different parts of tumor
image guided: scans/XRs to ensure position
stereotactic: give in different directions
internal beam radiation (brachytherapy)
type of radiation where radioactive seeds are implanted in body to continuous attack cancer cells
surgery
cancer treatment focused on removing tumor
biopsy
primary- complete resection
debulking- partial resection
second look- exploratory/further debulk
HSCT (hemopoietic stem cell transplant)
immature cells that give rise to other blood cells, replaces diseased cells with non-cancerous stem cells
syngeneic- from identical twin
allogenic- donor, preferred match sib
auto- self, harvested and preserved
HLA typing (human leukocyte antigen)
used in BMTs to match patients and donors, they are proteins on cell surfaces- major histocompatibility complex that identifies self from non-self
more match= less risk GVHD
harvest
marrow- process of removing stem cells from donor’s iliac crest
peripheral stem cell- collected through apheresis
donor
to give cells:
screening history (meds/illness/zika/exclude)
high risk= tattoos, piercings, IV drug use
HLA typing
Dental & Psych Eval
recipient
to receive cells:
screening/exam/HLA
organ function/scans
urine collection/sperm or egg bank/harvest
central line
lodging post transplant
matched related
type of Allo BMT
pros: rapid hematopoiretic and immunological reconstitution, less incidence of infection & GVHD
cons: only 30% patient have this (sib)
mismatch related
type of Allo BMT
pros: healthy source of cells, easy donor access and availability
cons: increased risk GVHD and graft failure
MUD
type of Allo BMT
pros: viable alternative for 75% pts
cons: GVHD, locate donor, infection, graft failure, death
cord
type of Allo BMT
pros: decreased incidence of GVHD
cons: limited cells, once transplanted- no more cells can be harvested, increased engraftment time
auto
type of BMT:
pros: faster recovery of cells, no GVHD risk
cons: no graft vs leukemia risk (increased relapse risk), risk of tumor contamination
syngeneic
type of BMT:
pros: GVHD not a risk, no cancer in transplanted cells (best option)
cons: risk of graft vs leukemia effect
conditioning
prep for BMT, includes:
eradicating tumor cells
immunosuppress pt to reduce rejection risk
reduce risk of GVHD
prepares marrow space for healthy cells
1-2 weeks: chemo, radiation, combo
HSCT complications
early: mucositis, sepsis, hemorrhagic cystitis, VOD
good oral cares, nutrition education, anti-infective prophylaxis
intermediate/late: infection, graft failure, GVHD, pulmonary effects, endocrine dysfunction, secondary cancers, relapse
sepsis
HSCT complication:
risk factors include neutropenia, barrier breakdown, depressed B and T cell function, not in remission at time of transplant
tx: early recognition, VS, cultures and antibiotics in an hour of fever, IV fluids, oxygen
hemorrhagic cystitis
HSCT complication:
diagnosis confirmed by hematuria and symptoms of cystitis
early onset: due to conditioning tx
late onset: typically due to viral (BK)
tx: hyperhydration, analgesia, platelets, catherization and irrigation, cystoscopy
VOD (veno-occlusive disease or sinusoidal obstruction syndrome)
HSCT complication:
early, rare but significant, caused by backflow of liver sinusoid glands due to inflammation
tx: prophy- defibrotide, monitoring labs and abdominal distension
GVHD (graft vs host disease)
HSCT complication:
immune response where the donor graft recognizes recipient antigens as foreign and cause inflammatory response, higher risk for HLA disparity
affects skin/GI/liver and lungs
dx clinically (rash, cramping/diarrhea, high bili) or bx (skin/GI tract)
tx aimed at immunosuppression
GVHD grading
1: skin involvement alone
2: skin involvement, gut or liver involvement
3: stage 3 involvement of any organ system (generalized erythroderma, bili greater than 6,1, diarrhea)
4: stage 4 involvement of any organ system ( generalized erythroderma with bullous formation, bili >15, diarrhea and ileus/pain)
HSCT discharge
pt must be/have:
ANC >500
afebrile
off IV antibiotics
oral meds and intake
family manage lines
complications resolved
follow up adherence
irradiated
blood product treatment that helps autoimmunization
leukocyte reduced
blood product treatment indicated for patients receiving chemo, helps prevent CMV (negative- can cause infection and death in immunosuppressed pts) and autoimmunization
platelets
blood product that helps with clotting, normal value is >100, given when <10
prophylactically in brain tumors or invasive surgery (>50)
FFP (fresh frozen plasma)
blood product when RBCs removed from whole blood, contains proteins and coag factors (replace in DIC or liver failure)
albumin
blood product used to treat patients with hypovolemia and hypoproteinemia
use cautiously with patients susceptible to fluid overload
cryoprecipitate
blood product prepared by thawing FFP, replaces fibrinogen and clotting factor deficiencies
contains factor VIII and XIII, fibrinogen, and von willebrand
thrombosis
blocking of blood vessel by a particle that has broken from blood clot at site of formation
risks: obesity, immobility, autoimmune disorders, dehydration, malignancies, surgery, ARA-C
clotting factors
tx clotting deficiencies (8&9), cross match not required, used for bleed or prophylaxis
apheresis
nonsurgical treatment where component of blood (plasma or RBCs) is removed or replaced, usually monthly exchanges
indicated for stoke, severe SCD
iron chelation therapy: deferasirox- exjade or jadenu
phlebotomy
used to treat iron overload from sickle cell disease, polycythemia, and transplant
removal of % of blood and replace with NS or non-sickled blood
hydroxyurea
antimetabolite chemo, can be used in SCD to reduce frequency of pain crisis and need for blood transfusions, myelosuppression common
heparin
treatment for thrombosis: inactivates thrombin and factor Xa, SQ or IV
easily reversed
sx: bleeding, HIT
LMWH (low molecular weight heparin)
treatment for thrombosis: inhibits factor Xa, q12 hour SQ, more predictable than heparin
warfarin (coumadin)
treatment for thrombosis: inhibits synthesis of vit k clotting factors, watch PT and INR (2-3), frequent monitoring
encourage consistent amounts of vit k foods to not affect dosing
phase I
part of clinical trial:
determines safety or maximum tolerated dose of drug/agent
phase II
part of clinical trial:
determines efficacy of new agent/treatment in treating specific types of cancer
phase III
part of clinical trial:
determines the overall response, survival, and QOL with new treatment plan- is new treatment the same or better than current treatment plan
phase IV
part of clinical trial:
determines long term safety and efficacy of treatment, after approval for use- decrease side effects
informed consent
recommendation of treatment performed in lay terms, alternative options offered, benefits and burdens explained, research purpose and compensation
decision maker must be able to: understand information, weigh it out in current situation, and communicate their choice