Chemotherapy uses drugs to kill or stop cancer cells. Traditional cytotoxic classes target rapidly dividing cells, while newer targeted therapies and immunotherapies act on specific molecular pathways or the immune system. Oncologists balance dose and schedule to maximize effect and limit toxicity. Supportive care - antiemetics, growth factors, hydration, and fertility preservation - has improved tolerability and outcomes.
What chemotherapy is and where it began
Chemotherapy uses chemical drugs that kill or stop the growth of cancer cells. The first systemic chemotherapies - nitrogen mustards and folate antagonists - appeared in the 1940s. Since then, cancer drug development has grown into a large global industry and expanded beyond classic cytotoxic agents to include targeted and immune-based therapies.How traditional chemotherapy works
Most traditional chemotherapy drugs interfere with cell division or DNA synthesis, so they preferentially affect rapidly dividing cancer cells. Because these drugs damage cells, they are described as cytotoxic. Some agents also trigger apoptosis (programmed cell death).Common classes of conventional chemotherapy include:
- Alkylating agents
- Antimetabolites
- Anthracyclines
- Plant-derived agents (vinca alkaloids, taxanes)
- Topoisomerase inhibitors
- Antitumor antibiotics
Targeted drugs and immunotherapies
Since the early 2000s, treatments have expanded to include targeted therapies (for example, tyrosine kinase inhibitors such as imatinib for chronic myeloid leukemia and gastrointestinal stromal tumors) and immune-based therapies (immune checkpoint inhibitors and CAR-T cell therapies). These approaches act on specific molecular pathways or the immune system rather than broadly on cell division.
Dosing and administration
Oncologists calculate doses to balance effectiveness and toxicity. Historically clinicians use body-surface-area (BSA) calculations and nomograms, but modern dosing also considers organ function, drug interactions, pharmacogenomics, and sometimes fixed dosing. Most chemotherapy is given intravenously, but many newer agents are oral and administered at home.Combination regimens remain common because using drugs with different mechanisms reduces the chance of resistance and can be more effective than single agents.
Side effects and supportive care
Chemotherapy affects healthy rapidly dividing tissues too. Common acute and subacute effects include nausea and vomiting, hair loss, mouth sores (mucositis), diarrhea or constipation, and myelosuppression (low blood counts) that raises infection risk. Some drugs cause long-term or organ-specific toxicities - cardiotoxicity (anthracyclines), neuropathy (platinum drugs, taxanes), hepatotoxicity, nephrotoxicity, and ototoxicity.Supportive care has improved outcomes: modern antiemetics, growth factors (G-CSF) to reduce neutropenia, hydration protocols, and fertility preservation options are standard parts of treatment planning.
Conclusion
Chemotherapy remains a core tool in cancer care. Over the past decades, it has evolved from broadly cytotoxic drugs to a landscape that also includes targeted agents and immunotherapies. Treatment plans now personalize drug choice, dose, and supportive measures to maximize benefit and limit harm.FAQs about Cancer Chemotherapy
How is chemotherapy different from targeted therapy or immunotherapy?
How do doctors determine the chemotherapy dose?
Are there oral chemotherapy options?
What are the most common side effects, and can they be managed?
Does chemotherapy always aim to cure cancer?
News about Cancer Chemotherapy
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