Abstract
The Cancer Bundle includes the following reports:
- Biomarker Technology Platforms for Cancer Diagnoses and Therapies.
- Cancer Cell Therapy Markets.
- Cancer Diagnostic Testing World Markets.
- Cancer Therapeutics Markets.
- Companion Diagnostics in Personalized Medicine and Cancer Therapy.
- Cytology and HPV Testing World Markets.
Biomarker Technology Platforms for Cancer Diagnoses and Therapies
Until superior therapeutic treatments are developed to prevent, treat and cure
cancer, the best means of reducing mortality and morbidity in a disease this
complex is early detection and diagnosis. In the major solid cancer types such
as lung, breast, colon and prostate, long-term survival rates drop
precipitously once metastatis has occurred. The case is clear for development
of biomarkers for early detection and screening tests for diseases such as
breast, colon, ovarian and lung cancer. In addition, diagnostic measurement of
cancer disease progression is essential to successful disease management. For
these reasons, development of new and effective biomarkers for cancer
detection and diagnosis is central to the cancer problem. The use of nucleic
acid biomarker diagnostics have begun to answer these questions. Protein
biomarkers are also useful. The purpose of this TriMark Publications report is
to describe the specific segment of the cancer diagnostics market which
develops new biomarker technology platforms for diagnosing and treating
cancer. Biomarkers are useful in following the course of cancer and evaluating
which therapeutic regimes are most effective for a particular type of cancer,
as well as determining long-term susceptibility to cancer or recurrence. This
study particularly examines those clinical measurement devices, and their
reagents and supplies, which are meant to be used in hospitals, clinics,
commercial laboratories and doctor' s offices to diagnose and monitor cancer.
The examination also provides an in-depth discussion of the application of
biomarkers in developing novel targeted cancer therapeutics, their predication
response and efficacy, as well as their use in diagnosis of cancer.
This report answers the questions:
- Which companies are utilizing cutting-edge technologies to develop,
validate, and implement cancer biomarkers for clinical use?
- What impediments still exist to incorporating promising research into
clinical practice?
- Which cancer biomarkers show the most promise for approval?
- What are the economic challenges to approval?
- How can regulatory oversight drive approval and adoption of new
technologies?
- Which alliances show the greatest synergy in bringing valid biomarkers to
market?
- Which shared technologies are driving the most encouraging development?
Cancer Cell Therapy Markets
Traditionally, treatment of disease is carried out by small molecules that
target specific cell types. In diseases such as cancer, the treatment is meant
to kill cancer cells, leading to the removal or at least the inhibition of
cancer cell proliferation. In other circumstances, a variety of therapeutic
molecules have been utilized lead the disease cells to perform a specific
function that they normally do not. These include small molecules, peptides,
proteins, antibodies, anti-sense RNAs and ribozymes. In the case of cell
therapy, as the name indicates, treatment is carried out with cells instead of
small molecules. In cell therapy, cells are given to the patient as the
therapeutic delivery system for a specific disease to achieve therapeutic
benefit. The purpose of this TriMark Publications report is to describe the
market segment of the cell therapy market aimed specifically at cancer
therapy. Moreover, a review of cellular agents that are related to the
chemical and cellular constituents of blood or other tissues for cancer care
of the patient is addressed in this study. The two most important areas where
such agents are used are in the hospital and the clinic. Emphasis is on those
companies and products that are actively developing and marketing cell
therapeutic agents and supplies for treating cancer patients.
Cancer Diagnostic Testing World Markets
Cancer testing is one of the most important growth opportunities for the next
three to five years in the diagnostics segment. The National Cancer Institute
estimates that about ten million Americans have or have had some form of
cancer. Overall costs of the disease are $126 billion annually. Pharmaceutical
companies are developing more than 300 new medicines for cancer, some of which
are in development for more than one type of the disease, for a total of more
than 500 ongoing R&D projects. The goal of this TriMark Publications report is
to review the market for tumor marker testing equipment and supplies using
screening reagents and instruments for analysis of individual components in
blood, serum or plasma. It defines the dollar volume of sales, both worldwide
and in the U.S., and analyzes the factors that influence the size and the
growth of the market segments. Also examined are the subsections of each
market segment, including: the physician office labs, hospital labs and
commercial laboratories. Additionally, the numbers of institutions using this
type of testing and the factors that influence purchases are discussed. The
report surveys almost all of the companies known to be marketing,
manufacturing or developing instruments and reagents for the clinical
point-of-care market in the U.S. Each company is discussed in depth with a
section on its history, product line, business and marketing analysis, and a
subjective commentary of the company' s market position.
This report answers the following questions in this report:
- What are the near-term business opportunities in the cancer diagnostics
market?
- What are the current and forecasted sizes of the cancer diagnostics market?
- What are the business models currently used by companies in cancer
diagnostics?
- How will manufacturers, researchers, physicians, patients and payers
influence the cancer diagnostics market?
- What are the drivers and bottlenecks influencing the cancer diagnostics
market?
- What are the technologies used in the cancer diagnostics sector?
- Who holds the proprietary rights to cancer diagnostics market technology?
- What are current applications of this technology?
- What regulatory processes must cancer diagnostics undergo in the United
States, Japan and Europe?
- How will new cancer diagnostics change treatment and payment paradigms?
- How will cancer diagnostic testing reduce healthcare expenditures?
Cancer Therapeutics Markets
Cancer is the second leading cause of death by disease in the United States,
exceeded only by heart disease. Traditionally cancer has been treated with
surgery, chemotherapy, hormones and radiation therapy, alone or in
combination. Emerging technologies include photodynamic therapy, gene therapy,
biological therapy (immunotherapy) and angiogenesis inhibitors. Pharmaceutical
and biotechnology companies are investing billions of dollars to search out
and develop weapons for the arsenal in the war against cancer. This TriMark
Publications report provides an overview of the global market for cancer
therapeutics. The examination focuses on the efforts of biotechnology
companies and pharmaceutical firms to incorporate new technologies for
developing anti-cancer drugs into their corporate strategies. This study
examines cancer therapeutic products now on the market, as well as those
currently under development that might be commercialized in the near future.
Additionally, the report profiles a number of firms that are actively involved
in marketing and developing of products to be used in the treatment of
cancer-both large multinational corporations. The analysis also provides an
overview of the disease and data on cancers by site or type. It provides
incidence and mortality data for different types of the disease. In addition,
the report provides a summary of each of the therapies that are being used to
treat cancer.
Companion Diagnostics in Personalized Medicine and Cancer Therapy
A near-term market opportunity for cancer companion diagnostic tests exists in
drug selection for cancer therapy. Co-development of molecular diagnostics and
targeted therapeutics has already been proven to be a successful strategy in
the development of novel anti-cancer drugs. Adoption of biomarker development
in clinical research provides great opportunities to identify patient
subpopulations with differential drug responses and to uncover the underlying
mechanisms. These data could help to explain if clinical trials of new drugs
are adequate, and offer the possibility of creating a clear prescription path
based on predictive biomarkers. The purpose of this TriMark Publications
report is to describe the specific segment of the diagnostics market that
develops new technology platforms for evaluating the metabolism of therapeutic
agents, or for evaluating which therapeutic regimes are most effective for a
particular type of disease. The term companion diagnostic means that the
particular diagnostic test under evaluation is specifically linked to a known
therapeutic drug. This linkage could be important in the therapeutic
application and clinical outcome of a drug (personalized medicine), or an
important component of the drug development process. This report focuses on
the former linkage, i.e., the use of companion diagnostic tests in
personalized medicine.
Cytology and HPV Testing World Markets
Cancer is a group of diseases characterized by uncontrolled growth and spread
of abnormal cells. If the spread is not controlled, it can result in death.
Cancer is caused by both external (chemicals, radiation and viruses) and
internal (hormones, immune conditions and inherited mutations) factors. Causal
factors may act together or in sequence to initiate or promote carcinogenesis.
Ten or more years often pass between exposures or mutations and detectable
cancer. Cancer is treated by surgery, radiation, chemotherapy, hormones and
immunotherapy. The purpose of this TriMark Publications report is to describe
the specific segment of the diagnostic market aimed at analysis cytology (the
examination of cells using optical microscopy methods) specimens derived from
the human female reproductive tract. It examines the measurement devices and
their reagents and supplies used in hospitals, clinics, commercial
laboratories and research institutions to detect cells and proteins for the
diagnosis and monitoring of disease. The study describes the analytical
methods used to separate, isolate, characterize and quantitate cells, DNA and
proteins complex in biological systems related to the diagnosis and treatment
of disease of the female reproductive tract, such as the cervix and vagina.
The emphasis is on those companies and products that are actively developing
and marketing laboratory instrumentation, reagents and supplies for performing
cytology and related molecular diagnostic tests, such as human papillomavirus
(HPV) and other inflammatory and sexually-transmitted diseases.
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