北米の卵巣がん診断市場 – 業界動向と2030年までの予測

北米の卵巣がん診断市場の分析と洞察

卵巣がんは、卵巣（卵子が形成される一対の女性生殖腺の 1 つ）の組織に発生するがんの一種です。卵巣がんのほとんどは、卵巣上皮がん（卵巣の表面の細胞から発生するがん）または悪性胚細胞腫瘍（卵細胞から発生するがん）のいずれかです。卵巣がんの診断に使用される検査と手順には、骨盤検査、画像検査、血液検査、手術などがあります。骨盤検査では、医師が手袋をはめた指を膣に挿入し、同時に腹部に手を押して骨盤内臓器を触診します。

北米の卵巣がん診断市場は、2023年から2030年の予測期間に成長すると予想されています。データブリッジマーケットリサーチは、市場は2023年から2030年の予測期間に7.8%のCAGRで成長し、2022年の31億2,406万米ドルから2030年には56億7,536万米ドルに達すると分析しています。

北米卵巣がん診断市場の市場定義

Ovarian cancer is most common in women between the ages of 50 and 79. It is becoming more prevalent as the world's geriatric population grows and there is a greater emphasis on early detection and treatment, which is expected to accelerate ovarian cancer diagnostic market development. Increasing government investment in raising awareness about early cancer detection as well as increasing health-care spending would also propel business growth. Obesity appears to play a significant role in the development of ovarian cancer. Other lifestyle choices that can raise the risk include smoking, drinking, and not having children. Since ovarian cancer is not easily detectable, women who are at risk of developing the disease must undergo routine testing to identify the disease early, allowing the market to expand.

The North America ovarian cancer diagnostic market is growing in the forecast year due to the rise in market players and the availability of advanced services. Along with this, manufacturers are engaged in R&D activity for launching novel services in the market. The increasing research in ovarian cancer diagnostics and development is further boosting the market growth. However, difficulties in ovarian cancer screening techniques might hamper the growth of the North America ovarian cancer diagnostic market in the forecast period.

North America Ovarian Cancer Diagnostics Market Dynamics

Drivers

• Growing Ovarian Cancer Awareness

Growing ovarian cancer awareness has led to an increased demand for timely cancer detection, leading to market growth.

Ovarian cancer is one of the major causes of rising mortality rates among female populations worldwide, which is fuelling market growth over the next five years. Cancer in the ovaries and cysts is becoming more common due to various factors such as environmental factors and genetic mutations.

Ovarian cancer is a type of cancer that affects women’s egg-producing organs, the ovaries. Ovarian cancer is difficult to diagnose because the symptoms are vague and are often detected only after cancer has spread through the stomach and pelvis, making it difficult to cure.

As a result, improved diagnostic processes and techniques are required to determine the cancer stage to treat. Furthermore, the rising mortality rate from ovarian cancer is concerning, emphasizing the importance of early detection so that treatment can be provided.

Due to an increase in awareness about ovarian cancer, it is expected to act as a driving factor for market growth.

• Improved Diagnostic Processes and Techniques

Screening tests and exams are used to detect a disease, such as cancer, in people who do not have any symptoms. There has been a lot of research to develop a screening test for ovarian cancer, but there has not been much success so far. The two tests used most often (in addition to a complete pelvic exam) to screen for ovarian cancer are Transvaginal Ultrasound (TVUS) and the CA-125 blood test.

TVUS is a test that uses sound waves to look at the uterus, fallopian tubes, and ovaries by putting an ultrasound wand into the vagina. It can help find a mass (tumor) in the ovary, but it cannot actually tell if a mass is cancer or benign. When it is used for screening, most of the masses found are not cancer.

The CA-125 blood test measures the amount of a protein called CA-125 in the blood. Many women with ovarian cancer have high levels of CA-125. This test can be useful as a tumor marker to help guide treatment in women known to have ovarian cancer because a high level often goes down if treatment is working. But checking CA-125 levels is not as useful as a screening test for ovarian cancer.

Thus, due to the increase in improved diagnostic processes and techniques, it is expected to act as a driving factor for market growth.

RESTRAINTS

High Cost of Diagnosis

Worldwide, the costs of cancer treatment have increased. Health industries are facing several challenges like medical costs for cancer care. The cost of cancer care in 2010 was USD 124.60 billion which was projected to increase to USD 173.00 billion by 2020 with cancer drug prices and acute hospital care as the main drivers. Hence, the increased cost of diagnostic agents production is hampering the market growth.

Lack of Skilled Professionals

Healthcare professionals involved in the diagnostic process have an obligation and ethical responsibility to employ clinical reasoning skills, evaluate, and manage a patient's medical problems. When a diagnosis is accurate and made in a timely manner, a patient has the best opportunity for a positive health outcome because clinical decision-making will be tailored to a correct understanding of the patient's health problem. The lack of skilled professionals may hinder the recovery process of the patient and thus, may hamper the market growth.

OPPORTUNITIES

Increasing Healthcare Expenditure for Cancer Diagnosis and Treatment

Across the globe, R&D activities are escalating owing to public health expenditure with economic performances whereas, the healthcare industry ranks second among all industries when it comes to the amount spent on healthcare. Rising healthcare expenditure can result in better provision of R&D opportunities. It is anticipated to upsurge the demand for ovarian cancer diagnostics.

Increasing healthcare expenditure for cancer treatment also helps patients to take hassle-free advanced diagnostics and treatment for fast recovery. The spending on healthcare is made up of the combination of out-of-pocket payments (people paying for their own care), government expenditure, and sources including health insurance and activities by Non-Governmental Organizations (NGOs). Due to this increasing healthcare expenditure for cancer treatment, it acts as an opportunity for market growth.

CHALLENGES

Strict Regulations and Standards for the Approval and Commercialization of Cancer Diagnostic Products

The stringent regulations for commercialization of any product in the market are proving to be a big challenge for manufacturers of cancer diagnostic products in the U.S. and European region. Every country has its own regulations and has a different body for regulatory procedures.

In the U.S., manufacturers require marketing authorization approval for IVD products for human use. The product must be labeled in accordance with labeling regulations. Establishments involved in the production and distribution of medical devices intended for commercial distribution in the U.S. are required to register with the FDA. Registration provides the FDA with the location of medical device manufacturing facilities and importers. Registration of an establishment is not an approval of the establishment or its devices by the FDA, that is, it does not provide FDA authorization to market the device. Unless exempted, premarketing authorization is required before a device can be placed into commercial distribution in the U.S.

The regulatory requirement for approvals of marketing as well as the declaration of conformity and the time required for regulatory review may vary for different products. The company which fails to get regulatory approval harms the business because without getting approval on the products, manufacturers are not able to launch their product in the market and for this reason, strict regulations and standards for the approval and commercialization of cancer diagnostic products act as a restraining factor for market growth.

Recent Developments

• In November 2022, Myriad genetics Inc. announced that it has acquired Gateway Genomics, LLC, The acquisition strengthens Myriad Genetics’ portfolio of Women’s Health products, expanding access to personalized genetic tests during the reproductive stage of a women’s life and beyond. With SneakPeek, Myriad now serves women earlier in their pregnancy, providing data-driven genetic insights through their lifetime with the Prequel non-invasive prenatal screen, Foresight carrier screen, and MyRisk Hereditary Cancer Test with Risk Score for all ancestries, this will help the company to increase their revenue.
• In October 2022, Quest Diagnostics announced the new phase of collaboration with Decode health, in the starting phase of collaboration, the two parties developed RNA (transcriptome) sequencing capabilities based on both parties' next-generation sequencing, analytics and clinical expertise. The collaboration is significant as biomarker-based data can help reduce the time and cost of developing novel diagnostic tests and identifying new drug targets for different types of cancers (breast, prostate and ovarian cancer). This collaboration helps the company to find innovative paths in the field of R&D and increases the North America presence of the company.

North America Ovarian Cancer Diagnostics Market Scope

北米の卵巣がん診断市場は、製品タイプ、手順タイプ、がんタイプ、エンドユーザーに分類されています。これらのセグメントの成長は、業界のわずかな成長セグメントの分析に役立ち、ユーザーに貴重な市場概要と市場洞察を提供して、コア市場アプリケーションを特定するための戦略的決定を下すのに役立ちます。

製品タイプ

• 楽器
• キットと試薬

製品タイプに基づいて、北米の卵巣がん診断市場は、機器とキットおよび試薬に分類されます。

手順の種類

• 血液マーカー検査
• 医療画像検査
• 生検検査
• 遺伝子検査

手順の種類に基づいて、北米の卵巣がん診断市場は、血液マーカー検査、医療画像検査、生検検査、遺伝子検査に分類されます。

がんの種類

• 上皮性腫瘍
• 生殖細胞
• 間質細胞腫瘍

がんの種類に基づいて、北米の卵巣がん診断市場は、上皮性腫瘍、生殖細胞および間質細胞腫瘍に分類されます。

エンドユーザー

• がん診断センター
• 病院の検査室
• 研究機関
• その他

エンドユーザーに基づいて、北米の卵巣癌診断市場は、癌診断センター、病院の研究所、研究機関、その他に分類されます。

北米の卵巣がん診断市場の地域分析/洞察        

北米の卵巣がん診断市場が分析され、上記のように国、製品タイプ、手順タイプ、がんタイプ、エンドユーザー別に市場規模の洞察と傾向が提供されます。

この市場レポートでカバーされている国は、米国、カナダ、メキシコです。

米国は、市場シェアと収益の面で北米の卵巣がん診断市場を支配しており、予測期間中もその優位性は高まり続けるでしょう。これは、この地域での神経疾患の有病率と発症率が高いためであり、研究開発投資の増加と新製品の発売が市場を押し上げています。

レポートの国別セクションでは、市場の現在および将来の傾向に影響を与える個別の市場影響要因と市場規制の変更も提供しています。新規および交換販売、国の人口統計、疾病疫学、輸出入関税などのデータ ポイントは、個々の国の市場シナリオを予測するために使用される主要な指標の一部です。さらに、国別データの予測分析を提供する際には、北米ブランドの存在と入手可能性、地元および国内ブランドとの競争により直面する課題、販売チャネルの影響が考慮されています。

競争環境と北米の卵巣がん診断市場シェア分析

卵巣がん診断市場の競争状況は、競合他社ごとに詳細を提供します。詳細には、会社概要、会社の財務状況、収益、市場の可能性、研究開発への投資、新しい市場への取り組み、北米でのプレゼンス、生産拠点と施設、生産能力、会社の強みと弱み、製品の発売、製品の幅と広さ、アプリケーションの優位性が含まれます。提供されている上記のデータ ポイントは、卵巣がん診断市場に関連する会社の焦点にのみ関連しています。

北米の卵巣がん診断市場で活動している主要企業には、F. Hoffmann-la roche ltd、Tosoh india pvt. Ltd.、Luminex corporation、Quest diagnostics corporate、Thermo fisher Scientific Inc.、Ngenebio、Abbott、Siemens healthcare private limited、Myriad genetics Inc.、Bio-rad laboratories, Inc.、R&d systems, Inc.、Foundation medicine, Inc.、Abcam plc.、Monobind Inc.、Mp biomedicals、Biovision Inc.、Boster bionomic technology、Biogenix Inc. Pvt. Ltd.、Genway biotech、Lifespan biosciences, Inc などがあります。

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