Gene therapy is a promising new method for treating non-small cell lung cancer (NSCLC). It allows doctors to target specific genes to prevent cancerous cells from growing and spreading.
NSCLC is a common form of cancer that causes cancerous cells to form within lung tissues. NSCLC is a serious condition, though many people receive treatment and survive for years.
Generally, treating NSCLC involves interacting with multiple healthcare specialists and receiving a combination of therapies. Specific treatment plans depend on factors that include the tumor size, type of NSCLC, and the extent of its spread to other organs.
Surgery, radiation or chemotherapy, and immunotherapy are examples of key techniques that doctors use to treat NSCLC.
Gene therapy is another promising treatment for NSCLC, which targets genes that contribute to the tumor.
There are two main approaches to using gene therapy to treat cancer:
- targeted medications to stop or interfere with the genetic processes that cause tumors to form and continue growing
- replacing the atypical gene with a healthy and fully functional copy
This article focuses on the second approach to NSCLC gene therapy. Read on to learn more.
Getting genes into cells requires making
Scientists can deactivate parts of the virus that cause infectious diseases. They can then modify the virus to carry genetic material into cancerous cells.
One type of gene therapy for NSCLC targets
Other possible applications include inserting genes that:
- cause cancer cells to die
- keep blood vessels from forming in tumors, slowing their growth
- prevent the growth and spread of cancerous cells
NSCLC gene therapy is a new form of treatment. However, early results are promising.
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According to the
NSCLC gene therapy is a new technique. However, it still has to meet rigorous
Gene therapies that the FDA approves are generally safe. However, they can have side effects, such as:
- fever
- chills
- headache
- nausea
- vomiting
- low blood pressure
According to the
Some limitations to gene therapy include:
- genetic mutations that cause cancer involve
multiple genes - safe and reliable methods of delivering gene therapy are challenging to engineer
- there is a need for caution and extensive testing before these treatments reach FDA approval, which will delay their availability to people who might need them
- the treatments are still new and lack data on how effective these treatments are over time
Doctors will typically develop a treatment plan with people who have NSCLC, depending on their health, age, and other relevant factors. Some common forms of NSCLC treatment
- surgery
- chemotherapy
- radiation therapy
- targeted therapy
- immunotherapy
Doctors may combine these treatments to maximize their effectiveness. This will involve undergoing multiple treatments at once, back-to-back treatments, or both.
For example, doctors may use a therapy to treat cancer in one part of the body and another therapy to treat where it is spreading.
Doctors typically describe the outlook for people with cancer using the percentage of people alive at least 5 years after their diagnosis compared to those without that type of cancer. This is the relative 5-year survival rate. They may further break down 5-year survival rates according to specific NSCLC diagnoses.
According to the
- 65% for localized NSCLC, which means that the tumor has not spread
- 37% for regional NSCLC, which means that the tumor has spread to nearby organs
- 9% for distant NSCLC, which means that cancerous cells are present far from the original tumor
- 28% for all NSCLC diagnoses together
Non-small cell lung cancer (NSCLC) is a common form of lung cancer in the United States. Gene therapy for people with NSCLC is a promising new treatment that targets specific genes that contribute to disease progression. There is evidence that gene therapy can slow the growth of tumors in people with NSCLC.
Gene therapy is new but has the potential to change the way doctors treat cancer. Scientists and doctors must first overcome limitations, including finding reliable methods to deliver gene therapy.