What is the difference between chemotherapy and immunotherapy?

Chemotherapy and immunotherapy are two distinct approaches to treating cancer, each with its own method of attacking the disease and different effects on the body. Chemotherapy works by directly killing fast-growing cells, including cancer cells, but also affects other rapidly dividing healthy cells. Immunotherapy, on the other hand, boosts or trains the body’s immune system to recognize and attack cancer cells more precisely.

Chemotherapy uses drugs that target all rapidly dividing cells indiscriminately. This means while it effectively kills many cancer cells that grow quickly, it also harms normal healthy cells such as those in hair follicles, digestive tract lining, and bone marrow. This broad action leads to common side effects like hair loss, nausea, fatigue, and increased risk of infection because normal cell populations are damaged alongside cancerous ones. Chemotherapy drugs typically act quickly during treatment sessions to shrink tumors by killing these fast-growing cells directly.

Immunotherapy takes a different approach by enhancing or modifying the immune system’s natural ability to fight disease. Cancer can evade immune detection by disguising itself or suppressing immune responses; immunotherapy removes these “cloaks” or stimulates immune components so they can better identify and destroy tumor cells. Instead of attacking all fast-dividing cells broadly like chemotherapy does, immunotherapies focus on activating specific parts of immunity such as T-cells (a type of white blood cell) or blocking proteins that prevent immune attacks on tumors.

There are several types of immunotherapies used in cancer treatment:

– **Checkpoint inhibitors**: These block proteins used by cancers to turn off immune responses.
– **Adoptive cell therapy**: Immune cells from a patient are modified outside the body then reinfused to better target tumors.
– **Monoclonal antibodies**: Lab-made molecules designed to bind specific targets on cancer cells.
– **Cancer vaccines**: Designed to train the immune system against tumor-specific markers.
– **Immune modulators**: Substances that boost overall immune activity.

Because immunotherapies rely on stimulating an individual’s own defenses rather than directly killing tumor tissue with chemicals or radiation damage, their effects often take longer to appear but may last longer after treatment ends. Some patients experience durable remissions where their cancers remain controlled for extended periods even without ongoing therapy.

The side effect profiles differ significantly between these treatments due primarily to their mechanisms:

– Chemotherapy’s side effects stem from collateral damage done when non-cancerous rapidly dividing tissues are harmed—leading commonly to hair loss (because hair follicle growth is rapid), mouth sores due to mucosal lining damage, gastrointestinal upset causing nausea/vomiting/diarrhea/constipation; bone marrow suppression causing anemia and infections; fatigue; among others.

– Immunotherapies tend not cause those typical chemotherapy toxicities since they do not kill normal dividing tissues directly but instead may provoke autoimmune-like reactions where activated immunity mistakenly attacks healthy organs such as skin rashes or inflammation in lungs (pneumonitis), liver (hepatitis), intestines (colitis), endocrine glands leading hormone imbalances etc., reflecting overactive immunity rather than direct toxicity.

Another important difference lies in how broadly effective each is across various cancers:

Chemotherapy remains a mainstay for many types because most cancers have some degree of rapid growth susceptible at least temporarily—making chemo useful across a wide range including breast cancer, lung cancer generally etc., though resistance often develops over time.

Immunotherapies currently show best results mainly in certain cancers known for being more “immunogenic” — meaning they naturally provoke an immune response — such as melanoma (skin cancer), lung cancers with high mutation rates especially non-small-cell lung carcinoma subtypes kidney/bladder cancers among others where biomarkers predict likely benefit from this approach.

Sometimes doctors combine both therapies along with surgery or radiation depending upon individual patient factors like tumor type/stage/genetic markers/patient health status aiming for synergy — chemo shrinking tumors quickly while immuno ramps up long-term control through immunit