List of chemotherapeutic agents

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(Redirected from List of antineoplastic agents)

Chemotherapeutic agents are a class of drugs used primarily for treating cancer by killing or inhibiting the growth of cancer cells. These agents encompass a broad range of medications with diverse mechanisms of action and specificity towards cancerous cells. This article provides an overview of chemotherapeutic agents, their classification, mechanisms, applications in cancer treatment, and associated side effects.

Patient receives chemotherapy

Introduction[edit | edit source]

Chemotherapy involves the use of chemical substances, known as chemotherapeutic agents, to treat disease. In the context of cancer, chemotherapy represents a cornerstone of treatment, either as a standalone therapy or in combination with surgery, radiation therapy, and other forms of cancer treatment. The goal of chemotherapy can vary from curative intent to palliation, depending on the cancer type, stage, and overall health of the patient.

Classification of Chemotherapeutic Agents[edit | edit source]

Chemotherapeutic agents are classified based on their chemical structure, mechanism of action, and origin. Major classes include:

Alkylating Agents[edit | edit source]

These compounds work by adding alkyl groups to DNA, leading to DNA damage and preventing cancer cells from dividing. Examples include cyclophosphamide and ifosfamide.

Antimetabolites[edit | edit source]

Mimicking the substrates of metabolic pathways, antimetabolites interfere with DNA and RNA synthesis. Methotrexate and 5-fluorouracil are common examples.

Natural Products[edit | edit source]

Derived from plants, microorganisms, and marine species, these agents include vinca alkaloids (e.g., vincristine), taxanes (e.g., paclitaxel), and anthracyclines (e.g., doxorubicin).

Topoisomerase Inhibitors[edit | edit source]

These agents interfere with the topoisomerases, enzymes that help unwind DNA during replication, leading to DNA damage. Examples are etoposide and irinotecan.

Antitumor Antibiotics[edit | edit source]

Despite the name, these agents are not used for treating infections but for their ability to bind to DNA and inhibit RNA synthesis. Dactinomycin and bleomycin fall into this category.

Targeted Therapies[edit | edit source]

A newer class of drugs that specifically target molecular differences between cancer and normal cells. Examples include imatinib (a tyrosine kinase inhibitor) and trastuzumab (a monoclonal antibody).

Mechanisms of Action[edit | edit source]

The mechanisms of action of chemotherapeutic agents vary widely but generally involve the disruption of cellular processes critical for cancer cell growth and division. These mechanisms include DNA damage, inhibition of DNA or RNA synthesis, disruption of mitotic spindles, and inhibition of specific enzymes or growth factors.

Uses in Cancer Treatment[edit | edit source]

Chemotherapeutic agents are used in various settings across the cancer treatment continuum, including:

Curative Therapy[edit | edit source]

Aimed at curing the cancer, often used in early-stage cancers or specific types of cancer that are highly responsive to chemotherapy.

Adjuvant Therapy[edit | edit source]

Administered after primary treatment (such as surgery) to eliminate any remaining cancer cells and reduce the risk of cancer recurrence.

Neoadjuvant Therapy[edit | edit source]

Given before primary treatment to shrink tumors, making them easier to remove surgically.

Palliative Care[edit | edit source]

Used to relieve symptoms and improve the quality of life in patients with advanced cancer.

Side Effects[edit | edit source]

The side effects of chemotherapy are a consequence of the damage to rapidly dividing cells, including healthy cells. Common side effects include nausea and vomiting, hair loss, fatigue, increased risk of infections, and myelosuppression. The severity and type of side effects vary depending on the specific agents used, the dosage, and the individual patient's response.

Comprehensive list of chemotherapeutic agents[edit | edit source]

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Contributors: Prab R. Tumpati, MD