Cells take their instructions from proteins regarding cellular growth, division, and apoptosis (programmed cell death). Often in targeted therapy, specific proteins are targeted with a goal of interfering with or preventing instructions from reaching their recipients. Targeted therapy is designed to alter or inhibit the typical function of a specific protein.
According to a 2022 journal article by Shuel, S., most targeted therapies fall into one of two categories:
However, targeted therapies can also be classified as:
Side Effects:
The side effects that accompany targeted therapies are based on the mechanism of action of the therapy.
Cutaneous toxicities (skin toxicities: rash and paronychia, inflammation of skin around nails) are common with EGFR inhibitors (epidermal growth factor receptor). This is because these receptors, EGFRs, are also on the surface of cells that make up the epidermis, or skin. Reducing and limiting sun exposure, prophylactic antibiotics, and topical treatments have all been recommended for the prevention and/or reduction of these skin toxicities.
Some additional targeted therapy side effects include high blood pressure (hypertension), congestive heart failure, impaired wound healing, deep vein thrombosis or pulmonary embolism, and increased risk of bleeding.
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Shuel, Sian L. “Targeted cancer therapies: Clinical pearls for primary care.” Canadian family physician Medecin de famille canadien vol. 68,7 (2022): 515-518. doi:10.46747/cfp.6807515
Current & Recent Research Involving Prochlorperazine & Targeted Therapies in Cancer Care:
A February 2024 publication in the journal of Nanomedicine: Nanotechnology, Biology and Medicine describes research that's being conducted on the use of prochlorperazine (PCZ), a common anti-emetic/anti-nausea medication, in combination with monoclonal antibodies (moAb) like EGFR inhibitors to enhance efficacy. The response rates for moAb treatments are quite low, hovering around 15% and increasing up to 40% when used with other antineoplastic drugs. If this PCZ-moAb combination proves successful it could open the door for a larger population of patients to experience a clinically significant response from monoclonal antibody therapy.
Prochlorperazine (PCZ) has been studied for reducing resistance to radiation therapy in NSCLC (non-small cell lung cancer) populations with KRAS mutations. You can read the 2021 study from the journal of Free Radical Biology and Medicine here.
Prochlorperazine has been studied for its potential to reduce migration and invasion (metastasis) of multiforme glioblastoma cancer cells. You can read the 2022 study in Oncology Letters here.
There's much more in store for this page. I have piles of notes and studies to compile and share. In the meantime, please check out the resources below.
If you haven't yet, please visit our Newly Diagnosed page for a thorough overview of the early cancer experience.
We regularly review these resources to make sure that all links work correctly and are of value to our visitors. If you find a link that isn't working, please email coral@oncologyoffense.com. If you would like us to consider adding a resource to our list, please email us with details.
List of Targeted Therapy Drugs Approved for Specific Types of Cancer (National Cancer Institute, updated December 2023)
https://www.cancer.gov/about-cancer/treatment/types/targeted-therapies/approved-drug-list
Targeted Therapy for Cancer (NCI)
https://www.cancer.gov/about-cancer/treatment/types/targeted-therapies
Targeted Therapy: Monoclonal Antibodies, Anti-angiogenesis, and Other Cancer Therapies (ChemoCare)
https://chemocare.com/what-is-chemotherapy/targeted-therapy
Targeted Therapy (ACS)
https://www.cancer.org/cancer/managing-cancer/treatment-types/targeted-therapy.html
PARP Inhibitors (Komen)
PARP Inhibitors - Susan G. Komen®
PARP Inhibitors as targeted therapy for people with inherited mutations (FORCE)
PARP inhibitors as targeted therapy for people with inherited mutations (facingourrisk.org)
PARP Inhibitors: Clinical Relevance, Mechanisms of Action and Tumor Resistance (Frontiers, Cell Dev. Biol. 2020)
Angiogenesis Inhibitors (NCI)
https://www.cancer.gov/about-cancer/treatment/types/immunotherapy/angiogenesis-inhibitors-fact-sheet
Monoclonal Antibodies (NCI)
https://www.cancer.gov/about-cancer/treatment/types/immunotherapy/monoclonal-antibodies
Tyrosine Kinase Inhibitors (Cleveland Clinic)
https://my.clevelandclinic.org/health/treatments/24984-tyrosine-kinase-inhibitors
Cancer Drugs Database (Anticancer Fund) CancerDrugs_DB is a curated listing of licensed cancer drugs produced by the Anticancer Fund. Source data comes from the NCI, FDA, EMA and other data sources. The intention is to provide researchers, clinicians and regulators with an easily filtered database of licensed drugs used in the treatment of cancer. Drugs which are used in cancer treatments to alleviate symptoms or other supportive care uses or which are used for diagnostic purposes are not included. Investigational agents and experimental treatments being used in clinical trials are also not included. (This list includes whether or not there is a generic equivalent on the market for each drug.)
https://www.anticancerfund.org/en/cancerdrugs-db
Editorial: Novel small molecules in targeted cancer therapy (Li, R. et al., Front. Pharmacol., 14 August 2023 Sec. Pharmacology of Anti-Cancer Drugs Volume 14 - 2023)
https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2023.1272523/full
Shuel, Sian L. “Targeted cancer therapies: Clinical pearls for primary care.” Canadian family physician Medecin de famille canadien vol. 68,7 (2022): 515-518. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9842142/
Zahavi D, Weiner L. Monoclonal Antibodies in Cancer Therapy. Antibodies. 2020; 9(3):34. https://doi.org/10.3390/antib9030034
Bhullar, K.S., Lagarón, N.O., McGowan, E.M. et al. Kinase-targeted cancer therapies: progress, challenges and future directions. Mol Cancer 17, 48 (2018). https://doi.org/10.1186/s12943-018-0804-2
Zhong, L., Li, Y., Xiong, L. et al. Small molecules in targeted cancer therapy: advances, challenges, and future perspectives. Sig Transduct Target Ther 6, 201 (2021).
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