IQVIA Institute: Innovative Therapies and Strong Pipeline to Combat Rise in Cancer Diagnoses
The IQVIA Institute has released a report detailing the global rise in cancer diagnoses and the corresponding increase in innovative cancer therapies. Cancer incidence is projected to reach 32 million new cases annually by 2050, especially in lower-income countries.
Global spending on cancer medicines rose to $223 billion in 2023 and is expected to hit $409 billion by 2028. The year 2023 saw the launch of 25 novel active substances (NASs) in oncology, bringing the total to 193 since 2014.
Over 2,000 new oncology clinical trials began in 2023, featuring advanced therapies like cell and gene therapies, antibody-drug conjugates, and radioligand therapies. Despite advancements, geographic disparities in access to these therapies persist.
Oncology trials have become less complex, increasing the success rate to 10% in 2023 from 4% the previous year. However, the pace of bringing new therapies to patients remains uneven due to differences in healthcare infrastructure and adoption rates.
- Global spending on cancer medicine increased by $25 billion in 2023, reaching $223 billion.
- Projected spending on cancer medicines expected to rise to $409 billion by 2028.
- Launch of 25 novel active substances (NASs) in 2023, totaling 193 since 2014.
- Over 2,000 new oncology clinical trials started in 2023.
- Emerging biopharma companies now account for 60% of new trials, up from 33% in 2013.
- Oncology composite success rate increased to 10% in 2023 from 4% the prior year.
- Reduced complexity in oncology trials by 8% since 2019.
- Improvement in productivity in oncology clinical development by 23% in 2023.
- PD-1/PD-L1 inhibitors accounted for $52 billion in spending in 2023.
- Cancer incidence expected to rise to 32 million new cases annually by 2050.
- Large geographic variations exist in the availability of NASs.
- Despite reduced trial durations, overall length of oncology programs only shortened by five months.
- Significant disparities in five-year cancer survival rates across countries with similar GDP levels.
- The pace of novel cancer therapies reaching patients is uneven due to infrastructural and adoption differences.
- European Medicines Agency approved fewer NASs in 2023 compared to 2022, indicating a slowdown in Europe.
- Complexity in other disease areas increased by 2% while oncology trials decreased in complexity.
Insights
The substantial rise in global spending on oncology medicines, from
Key takeaways for investors: The oncology sector's growth presents significant opportunities for companies actively involved in cancer drug development and distribution. However, disparities in global drug availability and the uneven pace of new therapy adoption might affect revenue streams differently based on geographic markets. Investors should monitor companies with a strong pipeline of novel therapies and particularly those investing in next-generation biotherapeutics.
The initiation of over 2,000 new oncology clinical trials in 2023 highlights the intense research activity in the field. Novel modalities, such as cell and gene therapies, antibody-drug conjugates (ADCs) and multispecific antibodies, represent promising advancements in treatment options. The increase in trials involving PD-1/PD-L1 inhibitors and CAR T-cell therapies underscores the emphasis on targeted therapies.
For investors: Companies leading in these innovative treatment modalities may see substantial future returns. The improved success rates and reduced complexity of oncology trials point to enhanced R&D efficiency, potentially accelerating the time to market for new therapies. However, geographical variations in the availability and adoption of these therapies, particularly in regions like Europe compared to the U.S. and China, could influence market accessibility and profitability.
The report's emphasis on the rising incidence of cancer, projected to reach 32 million new cases annually by 2050, particularly in lower-income countries, presents a critical challenge in global healthcare. The ongoing development and rapid introduction of advanced therapies reflect the medical community's response to this growing burden. However, the report also highlights significant disparities in access to treatments, influenced by healthcare infrastructure, biomarker testing rates and the economic capacity of different regions.
Implications for investors: Investing in companies that prioritize expanding access to innovative treatments in underserved markets could not only address a significant healthcare need but also open new revenue streams. Moreover, continued improvements in cancer survival rates through tailored healthcare strategies present compelling opportunities for investment in companies focusing on early detection and personalized medicine approaches.
- Cancer incidence is expected to rise significantly through 2050, particularly in lower-income countries, to 32 million new cases annually – a potential increase of more than 12 million new annual cases
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Global spending on cancer medicine increased to
in 2023,$223 billion more than in 2022, and is projected to reach$25 billion by 2028$409 billion - In 2023, 25 oncology novel active substances (NASs) were launched globally, reaching a total of 193 since 2014 – however, large geographic variations exist in availability of these medicines
- More than 2,000 new oncology clinical trials started in 2023 with novel modalities and significant promise for cancer treatment, including cell and gene therapies, antibody-drug conjugates, multispecific antibodies, and radioligand therapies
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Cancer treatments have increased
9% annually since 2019 but the pace of bringing novel therapies to patients is uneven due to differences in biomarker testing rates, adoption of novel therapies and lack of infrastructure capacity to deliver some of the most advanced therapies
“The global oncology ecosystem is operating near peak levels to address increasing challenges. New therapies for advanced cancers, including some of the most advanced novel science in the industry, are under development or have been recently launched,” said Murray Aitken, Executive Director, the IQVIA Institute for Human Data Science. “These therapies represent the largest area of collective research and drug spending across all of healthcare. Yet despite significant advances in treatment and better access to care, the global oncology community and patients continue to struggle with disparities in access and care.”
A few key highlights in the report include:
- Trends in cancer incidence and mortality: Cancer incidence is expected to rise significantly through 2050, particularly in lower-income countries, to 32 million new cases annually – a potential increase of more than 12 million new annual cases. The growing disease burden underscores the urgent need for new treatments to enhance survival and quality of life. Disparities in five-year cancer survival across countries with similar GDP levels indicate that different healthcare strategies may lead to better outcomes for certain cancers. The variability in cancer severity and progression, along with healthcare system differences, suggests that tailored strategies, such as focusing on early detection or enhancing survivorship and quality of life, could be more effective for certain cancers.
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Oncology research and development activities: In 2023, more than 2,000 oncology trials started, fewer than the past two years of rebounding from the COVID-19 pandemic and
11% higher than in 2019. Emerging biopharma companies accounted for60% of these trials, a significant increase from33% in 2013. Novel modalities, including cell and gene therapies, antibody-drug conjugates (ADCs) and multispecific antibodies, show significant promise for cancer treatment and represent a growing share of clinical research. Trials involving PD-1/PD-L1 inhibitors grew29% over the last five years, investigating across more tumors and in earlier lines of therapy. More than 250 trials testing CAR T-cell therapies in oncology started in 2023 and while the majority investigated for hematological cancers, the therapies were increasingly viewed across a range of solid tumors. Fifteen ADCs have been approved globally and the number of ADC trials grew26% from 2022 to 2023 as more companies invested in these targeted chemotherapeutics. Development of these novel treatments is being accelerated by regulator and industry initiatives, including the use of artificial intelligence to advance new therapies.
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Oncology clinical development productivity: The oncology composite success rate increased to
10% in 2023 from4% the year prior, with improvements across all phases, especially in rare oncology and solid tumor research. While oncology trials remain complex, their level of complexity – a comparison of a number of factors, including the number of countries, sites, patients, eligibility criteria, and clinical endpoints – has decreased by8% since 2019, in contrast to a2% increase in complexity for other disease areas. The number of subjects enrolled in oncology trials is down11% in 2023 from the peak in 2021. Western European countries are included in trials the most often, althoughChina and North American country inclusion has increased significantly in recent years. Despite a reduction in trial durations, the overall length of all oncology programs was only shortened by an average of five months due to an increase in the time between trial completion and starting the next phase. Improved success and declining complexity resulted in a23% improvement in productivity in oncology clinical development in 2023.
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Novel active substances (NASs) in oncology: In 2023, 25 oncology NASs were launched globally, reaching a total of 193 since 2014 – however, large geographic variations exist in the availability of these medicines. The number of NAS launches in
China over the last five years exceeded those in theU.S. While many of these new medicines inChina are driven by domestic innovation, most have previously launched globally. New medicine launches inEurope have slowed, resulting in delays in the availability of innovative medicines compared to theU.S. –38% ofU.S. oncology NASs in the past 10 years are not yet available inEurope . Eighteen new cancer medicines were introduced in theU.S. in 2023 and these new drugs are largely targeting rare cancers, are recombinant and are often approved based on a single clinical trial. The European Medicines Agency approved eight NASs for hematological cancers and five for solid tumors in 2023, fewer than the 14 approved in 2022.
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Cancer patient access and use of scientific advances: The total number of cancer treatment regimens provided globally – defined as the number of patients treated with a regimen in a time period, whether one cycle or multiple – has increased by an average of
9% annually since 2019 due to higher cancer rates and better access to care. Despite this growth, the pace of novel cancer therapies arriving to patients is uneven across countries, with differences in biomarker testing rates, adoption of novel therapies, and the lack of infrastructure capacity to deliver some of the most advanced therapies. Treatment of women’s cancers, prostate cancer and late-stage multiple myeloma has advanced in recent years as novel modalities, including antibody-drug conjugates, radiopharmaceuticals, bispecifc antibodies and CAR T-cell therapies have been introduced – providing better outcomes for patients.
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Spending on oncology medicines: Global spending on cancer medicine increased to
in 2023,$223 billion more than in 2022, and is projected to rise to$25 billion by 2028. This growth is attributed to the volume of protected brands and the introduction of new products in the past five years, despite losses of exclusivity for some treatments. Biosimilars have been widely adopted in major markets, leading to significant cost savings. Notably, six major tumor categories experienced double-digit growth in spending due to breakthrough medicines and improved patient access. PD-1/PD-L1 inhibitors, which are widely used in solid tumor treatments, accounted for$409 billion in spending in 2023, with expectations to increase to more than$52 billion by 2028. The future of next-generation biotherapeutics in oncology is marked by clinical and commercial uncertainties, yet annual spending could still potentially rise from$90 billion to$4 billion by 2028.$23 billion
About the IQVIA Institute for Human Data Science
The IQVIA Institute for Human Data Science contributes to the advancement of human health globally through timely research, insightful analysis and scientific expertise applied to granular non-identified patient-level data.
Fulfilling an essential need within healthcare, the Institute delivers objective, relevant insights and research that accelerate understanding and innovation critical to sound decision making and improved human outcomes. With access to IQVIA’s institutional knowledge, advanced analytics, technology and unparalleled data, the Institute works in tandem with a broad set of healthcare stakeholders to drive a research agenda focused on Human Data Science, including government agencies, academic institutions, the life sciences industry, and payers. More information about the IQVIA Institute can be found at www.IQVIAInstitute.org.
About IQVIA
IQVIA (NYSE:IQV) is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. IQVIA creates intelligent connections across all aspects of healthcare through its analytics, transformative technology, big data resources and extensive domain expertise. IQVIA Connected Intelligence™ delivers powerful insights with speed and agility — enabling customers to accelerate the clinical development and commercialization of innovative medical treatments that improve healthcare outcomes for patients. With approximately 87,000 employees, IQVIA conducts operations in more than 100 countries.
IQVIA is a global leader in protecting individual patient privacy. The company uses a wide variety of privacy-enhancing technologies and safeguards to protect individual privacy while generating and analyzing information on a scale that helps healthcare stakeholders identify disease patterns and correlate with the precise treatment path and therapy needed for better outcomes. IQVIA’s insights and execution capabilities help biotech, medical device and pharmaceutical companies, medical researchers, government agencies, payers and other healthcare stakeholders tap into a deeper understanding of diseases, human behaviors, and scientific advances, in an effort to advance their path toward cures. To learn more, visit www.iqvia.com.
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Kerri Joseph, IQVIA Investor Relations (kerri.joseph@iqvia.com)
+1.973.541.3558
Trent Brown, IQVIA Media Relations (trent.brown@iqvia.com)
+1.919.780.3221
Source: IQVIA
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