Targeted Cancer Therapies: Questions and Answers. Key Points

Similar documents
Introduction to Targeted Therapy

Drug-targeted therapies and Predictive Prognosis: Changing Role for the Pathologist

Biological Therapies for Cancer: Questions and Answers

Cancer: Questions and Answers

Backgrounder. 1. What are targeted therapies? 2. How do targeted therapies work?

BLOOD AND LYMPH CANCERS

TARGETED THERAPY FOR CHILDHOOD CANCERS

Targeted Therapy Vijay Narang

Chemoprevention. Chemoprevention is the use of natural or synthetic substances to reduce the risk of

Clinical Trials: Questions and Answers

What is DNA? DNA is a double helix formed by base pairs attached to a sugar-phosphate backbone.

Review Journal of The Korean Ger iatr ics Soci 2004:8(3):

Personalized Therapy for Acute Myeloid Leukemia. Patrick Stiff MD Loyola University Medical Center

Care for Children and Adolescents With Cancer: Questions and Answers. Key Points

Introduction to Basic Oncology

Where do these cells come from?

Cancer Cells. It would take another 20 years and a revolution in the techniques of biological research to answer these questions.

CELL BIOLOGY - CLUTCH CH CANCER.

Questions and Answers About the Prostate-Specific Antigen (PSA) Test

Question #1 Controls on cell growth and division turned on and off

Targeted Medicine and Molecular Therapeutics. Angus McIntyre, M.D. Medical Oncologist, Addison Gilbert Hospital and Beverly Hospital October 6, 2009

CANCER 1.7 M 609,000 26% 15.5 M 73% JUST THE FACTS. More Than 1,100 Cancer Treatments in Clinical Testing Offer Hope to Patients

Acute: Symptoms that start and worsen quickly but do not last over a long period of time.

IMMUNOTHERAPY FOR LUNG CANCER

Bihong Zhao, M.D, Ph.D Department of Pathology

Cancer Facts. Complementary and Alternative Medicine. Complementary and Alternative Medicine in Cancer Treatment: Questions and Answers.

Cancer and Gene Regulation

Cancer. October is National Breast Cancer Awareness Month

Improving Methods for Breast Cancer Detection and Diagnosis. The National Cancer Institute (NCI) is funding numerous research projects to improve

Soft Tissue Sarcomas: Questions and Answers

National Cancer Institute Studies of Hydrazine Sulfate. In the 1980s and early 1990s, the National Cancer Institute (NCI) sponsored studies of

Cancer Studies at the National Institutes of Health Clinical Center: Questions and Answers. Key Points

REGULATING the CELL CYCLE.

Breast Cancer Prevention Studies. Key Points. Breast cancer prevention studies are clinical trials (research studies conducted with

Cell, Volume 141. Supplemental Information Cell Signaling by Receptor Tyrosine Kinases Mark A. Lemmon and Joseph Schlessinger

Human Papillomaviruses and Cancer: Questions and Answers. Key Points. 1. What are human papillomaviruses, and how are they transmitted?

Regulating the Cell Cycle. Lesson Overview THINK ABOUT IT. How do cells know when to divide? Review: Why do cells divide?

Introduction to Cancer

1.5. Research Areas Treatment Selection

Screening Mammograms: Questions and Answers

Cancer Facts. Complementary And Alternative Medicine. Cancell/Entelev: Questions and Answers

New Developments in Cancer Treatment. Dulcinea Quintana, MD

Chapter 18- Oncogenes, tumor suppressors & Cancer

2013 Holiday Lectures on Science Medicine in the Genomic Era

oncogenes-and- tumour-suppressor-genes)

Active Cancer Studies by Approval Date For additional information on any one of these studies contact the Lancaster General Cancer Center

Chronic Myelogenous Leukemia (Hematology) By DEISSEROTH READ ONLINE

Cancer and Tyrosine Kinase Inhibition

H&HD ANTINEOPLASTIC DRUG CARD ASSEMBLY INSTRUCTIONS

Testicular Cancer: Questions and Answers. Testicular cancer is a disease in which cells become malignant (cancerous) in one or both testicles.

Bortezomib (Velcade)

Information for Patients. Guidance on the use of trastuzumab for the treatment of advanced breast cancer

CoQ10 and Cancer Treatment

Lecture 1: Carcinogenesis

Peking University People's Hospital, Peking University Institute of Hematology

Claudia Adams Barr Program in Innovative Cancer Research Dana-Farber Cancer Institute BARR PROGRAM IMPACT STATEMENTS

Breast Cancer: Who Gets It? Who Survives? The Latest Information

2015 AP Biology Unit #4 Test Cell Communication, Cancer, Heredity and The Cell Cycle Week of 30 November

THE CANCER/MITOSIS CONNECTION

IMATINIB MESYLATE (Gleevec or Glivec, Novartis,

Cryosurgery in Cancer Treatment: Questions and Answers

Children s Hospital of Philadelphia Annual Progress Report: 2011 Formula Grant

In this program you will learn

Media Release. Basel, 12 December 2017

number Done by Corrected by Doctor Maha Shomaf

Almost every cell in the human body has an identical set of 46 chromosomes, produced through the process of mitosis.

Gleevec. Gleevec (imatinib) Description

SPECIAL AUTHORIZATION REQUEST FOR COVERAGE OF HIGH COST CANCER DRUGS

Formaldehyde and Cancer: Questions and Answers. Key Points

2015 AP Biology Unit #4 Quiz 1 Cell Communication, Cancer and The Cell Cycle Week of November

Engineering Nanomedical Systems

INTERIM MANAGEMENT STATEMENT Q3 2017

The Study of Tamoxifen and Raloxifene (STAR): Questions and Answers. Key Points

Pharmacyclics Reports Updated Clinical Results from its Phase IA Trial of its First in Human BTK- Inhibitor PCI-32765

Revlimid. Revlimid (lenalidomide) Description. Section: Prescription Drugs Effective Date: July 1, 2015

Metastatic Colorectal Cancer

Deregulation of signal transduction and cell cycle in Cancer

Dr. C. Tom Kouroukis. New and upcoming treatments for Lymphoma

THE EUKARYOTIC CELL CYCLE AND CANCER

BL-8040: BEST-IN-CLASS CXCR4 ANTAGONIST FOR TREATMENT OF ONCOLOGICAL MALIGNANCIES. Overview and Mechanism of Action Dr.

ACTR (Antibody Coupled T-cell Receptor): A universal approach to T-cell therapy

National Horizon Scanning Centre. Imatinib (Glivec) for adjuvant therapy in gastrointestinal stromal tumours. August 2008

What is a hematological malignancy? Hematology and Hematologic Malignancies. Etiology of hematological malignancies. Leukemias

Cancer arises from the mutation of a normal gene. A factor which brings about a mutation is called a mutagen.

BIT 120. Copy of Cancer/HIV Lecture

UnitedHealthcare Pharmacy Clinical Pharmacy Programs

Molecular Oncology, oncology parameters see each test

MITOCW S05-L30

Current management of multiple myeloma. Jorge J. Castillo, MD Assistant Professor of Medicine Harvard Medical School

HSCT - Minimum Essential Data - A FOLLOW UP REPORT - ANNUAL

Functional Limitations

Stratified medicine in practice: Review of predictive biomarkers in European Medicines Agency (EMA) indications

GLEEVEC (imatinib mesylate) Capsules FACT SHEET

Curable cancers: Progress in Oncology. Prof.Dilip Kumar Dhar Princicipal & Professor of Medicine MH Samorita Hospital & Medical College, Dhaka.

BR for previously untreated or relapsed CLL

Radiation Therapy for Cancer: Questions and Answers

The Future of Cancer. Lawrence Tsui Global Risk Products Actuary Swiss Reinsurance Company Hong Kong. Session Number: WBR8

OMONDI OGUDE MEDICAL ONCOLOGY

New Developments in Cancer Treatment. Ian Rabinowitz MD

Specialist Referral Service Willows Information Sheets. Cancer in cats and dogs: Assessment of the patient

Transcription:

CANCER FACTS N a t i o n a l C a n c e r I n s t i t u t e N a t i o n a l I n s t i t u t e s o f H e a l t h D e p a r t m e n t o f H e a l t h a n d H u m a n S e r v i c e s Targeted Cancer Therapies: Questions and Answers Key Points Targeted cancer therapies use drugs that block the growth and spread of cancer by interfering with specific molecules involved in carcinogenesis (the process by which normal cells become cancer cells) and tumor growth (see Questions 1, 2, and 3). Because scientists call these molecules molecular targets, therapies that interfere with them are sometimes called molecular-targeted drugs, molecularly targeted therapies, or other similar names (see Question 1). The National Cancer Institute s Molecular Targets Development Program is working to identify and evaluate molecular targets (see Question 6). 1. What are targeted cancer therapies? Targeted cancer therapies use drugs that block the growth and spread of cancer. They interfere with specific molecules involved in carcinogenesis (the process by which normal cells become cancer cells) and tumor growth. Because scientists call these molecules molecular targets, these therapies are sometimes called molecular-targeted drugs, molecularly targeted therapies, or other similar names. By focusing on molecular and cellular changes that are specific to cancer, targeted cancer therapies may be more effective than current treatments and less harmful to normal cells. Most targeted cancer therapies are in preclinical testing (research with animals), but some are in clinical trials (research studies with people), or have been approved by the U.S. Food and Drug Administration (FDA). Targeted cancer therapies are being studied for use alone, in combination with each other, and in combination with other cancer treatments, such as chemotherapy. C a n c e r R e s e a r c h B e c a u s e L i v e s D e p e n d O n I t Page 1

2. What are some of the cellular changes that lead to cancer? Normally, cells grow and divide to form new cells as the body needs them. When cells grow old, they die, and new cells take their place. Sometimes this orderly process goes wrong. New cells form when the body does not need them, and old cells do not die when they should. These extra cells can form a mass of tissue called a growth or tumor. The cells in malignant (cancerous) tumors are abnormal and divide without control or order. They can invade and damage nearby tissues and organs. Also, cancer cells can break away from a malignant tumor and spread to other parts of the body. Normal cell growth and division are largely under the control of a network of chemical and molecular signals that give instructions to cells. Genetic alterations (changes) can disrupt the signaling process so that cells no longer grow and divide normally, or no longer die when they should. Alterations in two types of genes can contribute to the cancer process. Proto-oncogenes are normal genes that are involved in cell growth and division. Changes in these genes lead to the development of oncogenes, which can promote or allow excessive and continuous cell growth and division. Tumor suppressor genes are normal genes that slow down cell growth and division. When a tumor suppressor gene does not work properly, cells may be unable to stop growing and dividing, which leads to tumor growth. To use the metaphor of a car, the presence of an oncogene is like having a gas pedal that is stuck to the floorboard, causing cells to continually grow and divide. Tumor suppressor genes act like a brake pedal. The loss of a functioning tumor suppressor gene is like having a brake pedal that does not work properly, allowing cells to continually grow and divide. Genetic changes that are not corrected by the cell can lead to the production of abnormal proteins. Normally, proteins interact with each other as a kind of relay team to carry out the work of the cell. For example, when molecules called growth factors (GFs) attach to their corresponding growth factor receptors (GFRs) on the surface of the cell, a process carried out by proteins signals the cell to divide. Damaged proteins may not respond to normal signals, may over-respond to normal signals, or otherwise fail to carry out their normal functions. Cancer develops when abnormal proteins inside a cell cause it to reproduce excessively and allow that cell to live longer than normal cells. 3. How do targeted cancer therapies work? Targeted cancer therapies interfere with cancer cell growth and division in different ways and at various points during the development, growth, and spread of cancer. Many of these therapies focus on proteins that are involved in the signaling process. By blocking the signals that tell cancer cells to grow and divide uncontrollably, targeted cancer therapies can help to stop the growth and division of cancer cells. Page 2

4. What are some types of targeted cancer therapies? Targeted cancer therapies include several types of drugs. Some examples are listed below: Small-molecule drugs block specific enzymes and GFRs involved in cancer cell growth. These drugs are also called signal-transduction inhibitors. Gleevec (STI 571 or imatinib mesylate) is a small-molecule drug approved by the FDA to treat gastrointestinal stromal tumor (a rare cancer of the gastrointestinal tract) and certain kinds of chronic myeloid leukemia (1, 2). Gleevec targets abnormal proteins, or enzymes, that form inside cancer cells and stimulate uncontrolled growth. Iressa (ZD1839 or gefitinib) is approved by the FDA to treat advanced non-small cell lung cancer. This drug targets the epidermal growth factor receptor (EGFR), which is overproduced by many types of cancer cells. Other small-molecule drugs are being studied in clinical trials in the United States. Apoptosis-inducing drugs cause cancer cells to undergo apoptosis (cell death) by interfering with proteins involved in the process. Velcade (bortezomib) is approved by the FDA to treat multiple myeloma that has not responded to other treatments (3). Velcade causes cancer cells to die by blocking enzymes called proteasomes, which help to regulate cell function and growth. Another apoptosis-inducing drug called Genasense (oblimersen), which is only available in clinical trials, is being studied to treat leukemia, non-hodgkin s lymphoma, and solid tumors. Genasense blocks the production of a protein known as BCL 2, which promotes the survival of tumor cells. By blocking BCL 2, Genasense leaves the cancer cells more vulnerable to anticancer drugs. Monoclonal antibodies, cancer vaccines, angiogenesis inhibitors, and gene therapy are considered by some to be targeted therapies because they interfere with the growth of cancer cells. Information about these treatments can be found in the following NCI fact sheets, which are available on the Internet or by calling the Cancer Information Service (CIS) (see below): Biological Therapies: Using the Immune System To Treat Cancer includes information about monoclonal antibodies and cancer vaccines. This fact sheet is available at http://cis.nci.nih.gov/fact/7_2.htm on the Internet. Herceptin (Trastuzumab): Questions and Answers contains information about Herceptin, which is a monoclonal antibody. This fact sheet can be found at http://cis.nci.nih.gov/fact/7_45.htm on the Internet. Angiogenesis Inhibitors in the Treatment of Cancer is available at http://cis.nci.nih.gov/fact/7_42.htm on the Internet. Gene Therapy for Cancer: Questions and Answers can be found at http://cis.nci.nih.gov/fact/7_18.htm on the Internet. Page 3

5. What impact will targeted therapies have on cancer treatment? Targeted cancer therapies will give doctors a better way to tailor cancer treatment. Eventually, treatments may be individualized based on the unique set of molecular targets produced by the patient s tumor. Targeted cancer therapies also hold the promise of being more selective, thus harming fewer normal cells, reducing side effects, and improving the quality of life. 6. What are some resources for more information? The NCI s Molecular Targets Development Program (MTDP) is working to identify and evaluate molecular targets that may be candidates for drug development. As part of the NCI s Center for Cancer Research, the MTDP provides research support for NCI-designated, high-priority drug discovery, development, and research focused on specific molecular targets, pathways, or processes. The MTDP s Web site is http://home.ncifcrf.gov/mtdp/ on the Internet. Information about clinical trials is available from the CIS (see below). Information specialists at the CIS use PDQ, the NCI s cancer information database, to identify and provide detailed information about specific ongoing clinical trials. PDQ includes all NCI-funded clinical trials and some studies conducted by independent investigators at hospitals and medical centers in the United States and other countries around the world. People also have the option of searching for clinical trials on their own. The clinical trials page of the NCI s Web site, located at http://www.cancer.gov/clinicaltrials/ on the Internet, provides information about clinical trials and links to PDQ. Selected References 1. Demetri GD, von Mehren M, Blanke CD, et al. Efficacy and safety of imatinib mesylate in advanced gastrointestinal stromal tumors. New England Journal of Medicine 2002; 347(7):472 480. 2. Kantarjian H, Sawyers C, Hochhaus A, et al. Hematologic and cytogenetic responses to imatinib mesylate in chronic myelogenous leukemia. New England Journal of Medicine 2002; 346(9):645 652. 3. Richardson PG, Barlogie B, Berenson J, et al. A phase 2 study of bortezomib in relapsed, refractory myeloma. New England Journal of Medicine 2003; 348(26):2609 2617. # # # Page 4

Related Resources Publications (available at http://www.cancer.gov/publications) Cancer Facts 2.11, Clinical Trials: Questions and Answers Cancer Facts 7.2, Biological Therapies: Using the Immune System To Treat Cancer Cancer Facts 7.18, Gene Therapy for Cancer: Questions and Answers Cancer Facts 7.42, Angiogenesis Inhibitors in the Treatment of Cancer Cancer Facts 7.45, Herceptin (Trastuzumab): Questions and Answers What You Need To Know About Cancer National Cancer Institute (NCI) Resources Cancer Information Service (toll-free) Telephone: 1 800 4 CANCER (1 800 422 6237) TTY: 1 800 332 8615 Online NCI s Web site: http://www.cancer.gov LiveHelp, NCI s live online assistance: https://cissecure.nci.nih.gov/livehelp/welcome.asp This fact sheet was reviewed on Page 5