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Carcinogenesis
The process by which normal cells transform into cancer cells involving stages of initiation, promotion, conversion, and progression.
Initiation
The first step of carcinogenesis where a normal cell undergoes a permanent genetic mutation caused by carcinogens like chemicals, radiation, or viruses.
Promotion
A reversible stage where initiated cells are stimulated to proliferate by promoters such as hormones or inflammation.
Conversion
Also called transformation, this is the stage when proliferating cells acquire malignant characteristics and become cancerous.
Progression
The stage where malignant cells undergo further genetic changes, gaining abilities like rapid growth, invasiveness, and metastatic potential.
Angiogenesis
The process by which cancer cells stimulate the formation of new blood vessels to supply nutrients and oxygen for tumor growth.
Apoptosis
Programmed cell death, a normal mechanism that cancer cells evade to survive despite genetic abnormalities.
TNM Staging
A system used to describe how advanced cancer is, where T is Tumor (size/growth), N is Nodes (spread to lymph nodes), and M is Metastasis (spread to distant parts).
T2 N1 M0
A breast cancer staging example where the tumor is between 2−5cm, cancer has spread to nearby lymph nodes, and no distant metastasis is found.
Palliation
A treatment goal focused on relieving symptoms and improving quality of life without necessarily curing the disease.
Cell-cycle phase-specific agents
Chemotherapy drugs that target a particular phase of the cell cycle (S phase or M phase) and are usually given more frequently or by continuous infusion.
Cell-cycle phase-nonspecific agents
Chemotherapy drugs that kill cells regardless of their cycle phase and are typically given less frequently.
Small-molecule inhibitors
Targeted therapies, such as tyrosine kinase inhibitors, that inhibit enzymes involved in intracellular signaling pathways dysregulated in cancer.
Monoclonal antibodies
Large proteins like trastuzumab or rituximab designed to recognize specific antigens on cancer cells or immune cells to block growth signals or deliver toxins.
Immune checkpoint inhibitors
A type of immunotherapy that blocks proteins like PD-1 or CTLA-4 that prevent immune cells from attacking cancer.
CAR T-cell therapy
A treatment where a patient's T cells are genetically engineered to recognize and kill cancer cells.
Body Surface Area (BSA)
A dosing method for traditional cytotoxic chemotherapy used to estimate heart function, blood flow, and drug distribution/clearing.
P-glycoprotein
A mechanism of drug resistance where cancer cells pump drugs out of the cell.
Dose intensity
The total amount of drug given over time, determined by dose size, frequency, and total duration.
Dose density
The strategy of giving the same dose more frequently to kill more cancer cells by not allowing them time to regrow.
Prognostic biomarkers
Molecular markers that provide information about the likely course of the disease.
Predictive biomarkers
Molecular markers, such as HER2 overexpression or EGFR mutations, that indicate if a specific treatment is likely to be effective.
USP Chapter 800
Standards for handling hazardous drugs, including the use of ISO Class 5 biological safety cabinets and specific PPE for intravenous chemotherapy preparation.
Vesicants
Anticancer agents like Vincristine, Vinblastine, and Anthracyclines that can cause tissue damage and are preferred for administration via central lines.
Cure
eliminate cancer completely
Control
manage cancer as a chronic condition
Surgery
removal of tumor masses
Radiation Therapy
use of ionizing radiation to destroy cancer cells
Systemic anticancer agents
Chemotherapy
Targeted therapy
Immunotherapy
Cytokines
boost immune system activity (interleukins, interferons).
Therapeutic vaccines
stimulate immune responses against tumor antigens.
Lung Cancer
Osimertinib,
Cisplatin,
Pemetrexed,
Erlotinib
Breast Cancer
Trastuzumab,
Tamoxifen,
Paclitaxel
Colorectal Cancer
Oxaliplatin,
Bevacizumab,
5-FU
Prostate Cancer
Leuprolide,
Bicalutamide,
Abiraterone
Flat (fixed) dosing
Makes dosing easier and more convenient
For oral targeted therapies and some immunotherapies
Tumor burden and cancer cell diversity
refers to the size or extent of cancer in the body. Larger tumors are often harder to treat because they contain more cancer cells with different genetic mutations.
Drug resistance
Resistance can be inherited (present from the beginning) or acquired (developed during treatment)
High-dose chemo + stem cell transplant
may increase effectiveness but also increases risk of serious side effects.
Supportive treatments
like colony-stimulating factors (CSFs) help maintain dose intensity by preventing complications like neutropenia.
Prognostic
tell us about the likely course of disease
Predictive
tell us if a treatment is likely to work
Genetic differences
can lead to toxicity or treatment failure
Comorbidities
may limit treatment choices
Doxorubicin
protect from light during storage and infusion
Dacarbazine
protect IV bag and tubing from light
Rituximab
store refrigerated, do not freeze
Bevacizumab
refrigerate; avoid shaking
Capecitabine (oral)
store at room temp, away from moisture and heat
Vesicants (can cause tissue damage)
IV only via central line preferred
Vincristine
Vinblastine
Anthracyclines
PD-1, CTLA-4 inhibitors
Immune checkpoint inhibitors
Cytokines
interleukins, interferons