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Cell and Gene Therapy for Oncology Market Advanced Gene Therapies Unlocking the Future of Oncology Treatment

Cell and Gene Therapy for Oncology Market (By Therapy Type: Cell Therapy, Gene Therapy, Non-Viral Gene Therapy, Gene Editing Therapy; By Cancer Type: Hematological Malignancies, Solid Tumors; By Therapy Source: Autologous Therapies, Allogeneic Therapies; By Delivery Vector: Viral Vectors; By Application: Therapeutic Application, Research Applications; By End User: Hospitals, Cancer Treatment Centers, academic & Research Institutes, Biotechnology & Pharmaceutical Companies, Specialty Clinics; By Manufacturing Type: In-House Manufacturing, Contract Manufacturing; By Route of Administration: Intravenous, Intratumoral, Intraosseous, Others; By Region: North America, Asia Pacific, Europe, Latin America, Middle East and Africa) Global Analysis, Size, Trends, Leading Companies, Regional Outlook and Forecast 2026 to 2035.

Last Updated : 20 May 2026 Category: Therapeutic Area Insight Code: 6896 Format: PDF / PPT / Excel
Revenue, 2025
USD 14.82 Billion
Forecast, 2035
USD 134.53 Billion
CAGR, 2026-2035
24.68%
Report Coverage
Global

The global cell and gene therapy for oncology market size was estimated at USD 14.82 billion in 2025 and is predicted to increase from USD 18.48 billion in 2026 to approximately USD 134.53 billion by 2035, expanding at a CAGR of 24.68% from 2026 to 2035. The market is expanding rapidly due to increasing cancer cases and rising demand for personalized and targeted cancer treatments. Advancements in CAR-T therapy, gene editing technologies, and growing investments in oncology research are further supporting market growth.

Cell and Gene Therapy for Oncology Market Size is USD 18.48 Billion in 2026.

Key Takeaways

  • The cell and gene therapy for oncology market will likely exceed USD 18.48 billion by 2026.
  • Valuation is projected to hit USD 134.53 billion by 2035.
  • Estimated to grow at a CAGR of 24.68% starting from 2026 to 2035.
  • North America dominated the cell and gene therapy for oncology market with a share of 46% in 2025.
  • Asia Pacific held 21% share in 2025 and is expected to grow at the fastest CAGR in the market during the forecast period.
  • By therapy type, the cell therapy segment held a dominant share of 68% in 2025.
  • By therapy type, the gene therapy segment held the second-largest share of 27% in 2025 and is expected to grow at the fastest CAGR in the market during the forecast period.
  • By cancer type, the hematological malignancies segment led the market with a share of 64% in 2025.
  • By cancer type, the solid tumors segment held the second-largest share of 36% in 2025 and is expected to grow at the fastest CAGR in the market during the forecast period.
  • By end user, the hospitals segment held a dominant share of 38% in 2025.
  • By end user, the biotechnology & pharmaceutical companies segment held 16% share in 2025 and is expected to grow at the fastest CAGR in the market during the forecast period.
  • By manufacturing type, the in-house manufacturing segment dominated the cell and gene therapy for oncology market with a share of 58% in 2025.
  • By manufacturing type, the contract manufacturing segment held the second-largest share of 42% in 2025 and is expected to grow at the fastest CAGR in the market during the forecast period.

Rising Demand for Personalized Cancer Treatments Driving Market Growth

Cell and gene therapy for oncology is an advanced cancer treatment approach that uses modified cells or genetic material to target, destroy, or prevent cancer cells more effectively. The cell and gene therapy for oncology market is growing rapidly due to the increasing prevalence of cancer and the rising demand for personalized and targeted treatment options. Advancements in CAR-T cell therapy, gene editing technologies, and immunotherapy are improving treatment outcomes and expanding clinical applications. In addition, growing investments in oncology research, supportive regulatory initiatives, and increasing clinical trials are further accelerating market expansion globally.

How Can AI Affect the Cell and Gene Therapy for Oncology Market?

Artificial intelligence is transforming the market by accelerating drug discovery, improving patient selection, and enhancing treatment precision. AI-powered data analysis helps identify genetic targets, optimize clinical trials, and predict therapy responses more effectively. This supports faster development of personalized cancer therapies while reducing research costs and improving overall treatment outcomes.

Trend and Future Outlook of the Cell and Gene Therapy for Oncology Market?

Growing Adoption of Personalized Cancer Therapies

Increasing focus on precision medicine is driving demand for personalized cell and gene therapies tailored to individual patient profiles. This trend is improving treatment effectiveness, reducing side effects, and expanding the use of advanced oncology therapies across multiple cancer indications.

Advancements in Gene Editing and CAR-T Technologies

Continuous innovations in CRISPR gene editing, CAR-T cell therapy, and next-generation immunotherapies are enhancing treatment accuracy and clinical outcomes. These advancements are expected to accelerate product development and create new opportunities in the oncology treatment landscape.

Rising Investments and Expanding Clinical Trials

Growing investments from pharmaceutical companies, biotechnology firms, and government organizations are supporting large-scale research and clinical trials. This is expected to strengthen commercialization efforts, improve therapy accessibility, and drive long-term market growth globally.

Executive Summary Table

Table Scope
Market Size in 2026 USD 18.48 Billion
Projected Market Size in 2035 USD 134.53 Billion
CAGR (2026 - 2035) 24.68%
Leading Region North America by 46%
Historical Data 2020 - 2023
Base Year 2025
Forecast Period 2026 - 2035
Measurable Values USD Millions/Units/Volume
Market Segmentation By Therapy Type, By Cancer Type, By Therapy Source, By Delivery Vector, By Application, By End User, By Manufacturing Type, By Route of Administration, By Region
Top Key Players Amgen Inc., Novartis AG, Gilead Sciences, Inc., bluebird bio, Inc., Bristol Myers Squibb Company, Legend Biotech, JW Therapeutics

Segmental Insights

By Therapy Type Insights

Cell and Gene Therapy for Oncology Market By Therapy Type, (Cell Therapy) Segment Dominates by 68% in 2025.

Segment Share 2025 (%)
Cell Therapy 68%
Gene Therapy 32%

The Cell Therapy Segment Dominated the Cell and Gene Therapy for Oncology Market in 2025

The cell therapy segment held a dominant share of 68% in 2025 due to the strong adoption of CAR-T cell therapies and their proven effectiveness in treating various hematologic cancers. Increasing regulatory approvals, expanding clinical applications, and growing investment in personalized cancer treatments further supported segment growth. In addition, advancements in cell engineering technologies and rising demand for targeted immunotherapies strengthened the market position of cell-based oncology therapies.

The gene therapy segment held the second-largest share of 27% in 2025 and is expected to grow at the fastest CAGR in the cell and gene therapy for oncology market during the forecast period due to its strong potential to directly modify or correct cancer-causing genetic mutations. Increasing clinical trials, growing success in treating rare and solid tumors, and rapid advancements in gene-editing technologies are driving adoption. However, higher development costs and regulatory complexities slightly limit faster commercialization compared to established cell therapy approaches.

By Cancer Type Insights

Cell and Gene Therapy for Oncology Market By Cancer Type, (Hematological Malignancies) Segment Dominates by 64% in 2025.

Segment Share 2025 (%)
Hematological Malignancies 64%
Solid Tumors 36%

The Hematological Malignancies Segment Led the Market in 2025 with the Largest Share

The hematological malignancies segment led the cell and gene therapy for oncology market with a share of 64% in 2025 due to the high success rate of CAR-T and other cell-based therapies in blood cancers such as leukemia, lymphoma, and multiple myeloma. These cancers are more accessible for treatment compared to solid tumors, allowing better therapy delivery and outcomes. Strong clinical approvals and expanding use of targeted immunotherapies further reinforced segment dominance.

The solid tumors segment held the second-largest share of 36% in 2025 and is expected to grow at the fastest CAGR in the cell and gene therapy for oncology market during the forecast period due to the high global burden oc cancers such as breast, lung, and colorectal cancer. Increasing research in overcoming tumor microenvironment barriers, along with advancements in gene editing and engineered cell therapies, is improving treatment potential. However, complex tumor structures and delivery challenges have limited faster adoption compared to hematological malignancies.

By End User Insights

Cell and Gene Therapy for Oncology Market By End User, (Hospitals) Segment Dominates by 38% in 2025.

Segment Share 2025 (%)
Hospitals 38%
Cancer Treatment Centers 27%
Academic & Research Institutes 14%
Biotechnology & Pharmaceutical Companies 16%
Specialty Clinics 5%

The Hospitals Segment Led the Market in 2025 with the Largest Share

The hospitals segment held a dominant share of 38% of the cell and gene therapy for oncology market in 2025 due to the availability of advanced infrastructure, specialized oncology departments, and skilled healthcare professionals required for complex therapies like CAR-T and gene therapy. Hospitals also handle a high volume of cancer patients and have better access to clinical trials and regulatory approvals, making them the primary centers for administering and managing advanced cancer treatment.

The cancer treatment centers segment held the second-largest share of 27% in 2025 due to their strong specialization in oncology care and access to advanced therapeutic technologies. These centers offer focused expertise, shorter treatment pathways, and better patient monitoring for complex therapies like CAR-T and gene therapy. However, the limited infrastructure compared to large hospitals slightly restricts their overall patient handling capacity.

The biotechnology & pharmaceutical companies segment held 16% share in 2025 and is expected to grow at the fastest CAGR in the market during the forecast period due to their strong focus on R&D, pipeline expansion, and strategic collaborations for advanced therapies. Increasing investments in gene editing, CAR-T development, and clinical trials for commercial innovations. Additionally, rising demand for commercial-scale manufacturing and faster regulatory approvals is further driving segment growth.

The academic & research Institutes segment held a 14% of cell and gene therapy for oncology market share due to increasing focus on early-stage research, innovation, and discovery of novel cancer treatment approaches. Strong government funding, collaborations with biotech firms, and expanding clinical trial activities are supporting growth. These institutes play a key role in developing advanced gene editing techniques and understanding cancer biology, driving long-term therapies advancements.

By Manufacturing Type Insights

Cell and Gene Therapy for Oncology Market By Manufacturing Type, (In-House Manufacturing) Segment Dominates by 58% in 2025.

Segment Share 2025 (%)
In-House Manufacturing 58%
Contract Manufacturing 42%

The In-House Manufacturing Segment Led the Market in 2025 with the Largest Share

The in-house manufacturing segment dominated the cell and gene therapy for oncology market with a share of 58% in 2025 due to companies' need for strict quality control, process consistency, and protection of sensitive intellectual property. Producing therapies internally helps reduce dependency on third-party CDMOs, ensures faster production timelines, and supports complex personalized treatments like CAR-T. Additionally, high initial investments are justified by better scalability, regulatory compliance, and long-term cost efficiency.

The contract manufacturing segment held the second-largest share of 42% in 2025 and is expected to grow at the fastest CAGR in the cell and gene therapy for oncology market during the forecast period due to increasing outsourcing by biotech and pharmaceutical companies to specialized CDMOs. These providers offer advanced manufacturing capabilities, scalability, and regulatory expertise, reducing time-to-market and capital investments. However, dependence on third parties and concerns over process control and confidentiality slightly limit broader adoption compared to in-house manufacturing.

Regional Insights

Cell and Gene Therapy for Oncology Market Shares for North America, Europe, Asia Pacific, Latin America and Middle East and Africa, 2025 (%).

Strong Innovation Ecosystems Driving North America Market Leadership

Cell and Gene Therapy for Oncology Market Size is USD 8.44 Billion in 2026.

North America dominated the cell and gene therapy for oncology market with a share of 46% in 2025 due to its advanced healthcare infrastructure, strong presence of leading biotech and pharmaceutical companies, and high investment in R&D. Early regulatory approvals, widespread adoption of CAR-T therapies, and robust clinical trials activity further support growth. Additionally, favorable reimbursement policies and increasing cancer prevalence strengthen the region’s leadership in advanced oncology treatments.

U.S. Market Trends

The U.S. leads the cell and gene therapy for oncology market due to strong R&D investments, presence of major biotech and pharmaceutical companies, and rapid adoption of advanced therapies like CAR-T. Supportive FDA approvals, a well-established clinical trials ecosystem, and high cancer prevalence further drive growth. Additionally, strong funding, innovative startups, and advanced healthcare infrastructure reinforced the U.S. dominance in this market.

Rapid Healthcare Expansion Driving Asia Pacific Growth Surge

Asia Pacific captured 21% share in 2025 and is anticipated to grow at the fastest CAGR in the cell and gene therapy for oncology market due to rising cancer prevalence, improving healthcare infrastructure, and increasing adoption of advanced therapies. Growing government support, expanding clinical trials, and rising investments from global biotech firms are further accelerating growth. Additionally, increasing patient awareness and improving access to innovative treatments are boosting regional market expansion.

India Market Trends

India is expected to grow at the fastest CAGR in the cell and gene therapy for oncology market due to its large patient pool, rising cancer burden, and improving healthcare infrastructure. Increasing government support for biotechnology, growing clinical trials activity, and expanding investments from global pharma companies are accelerating adoption. Additionally, the rising affordability of advanced therapies and growing awareness of personalized medicine are further boosting market growth.

Supply Chain Analysis

R&D

  • Research and development in cell and gene therapies for oncology is progressing quickly, with a strong focus on improving CAR-T cell effectiveness, expanding applications to solid tumors, and advancing in vivo gene editing technologies to achieve better patient outcomes.
  • Key Players: Novartis, Gilead Sciences (Kite Pharma), Bristol Myers Squibb, and Fate Therapeutics

Clinical Trials

  • Clinical trials in oncology cell and gene therapies are progressing quickly, targeting hard-to-treat cancers such as lung cancer, prostate cancer, and glioblastoma. They focus on innovative approaches like CAR T-cell therapy, oncolytic viruses, and gene-modified stem cells to enhance immune response against tumors.
  • Key players: Novartis, Gilead Sciences, Bristol Myers Squibb, AstraZeneca, and Merck & Co.

Patient Support and Services

  • Patient support in oncology cell and gene therapies is centered on guiding patients through complex treatment journeys like CAR-T therapy by providing personalized care coordination, financial aid, travel assistance, and end-to-end logistical support. These services are often delivered through specialized patient support programs and treatment hubs to ensure smoother access to advanced therapies.
  • Key Players: Novartis, Gilead Sciences (Kite Pharma), Bristol Myers Squibb, and Johnson & Johnson

Top Vendors in the Cell and Gene Therapy for Oncology Market & Their Offerings

Cell and Gene Therapy for Oncology Market Companies are Amgen Inc., Novartis AG, Gilead Sciences, Inc., bluebird bio, Inc., Bristol Myers Squibb Company, Legend Biotech, JW Therapeutics

Companies Headqaurters Offerings
Amgen Inc. California, U.S. Develops CAR-T and bispecific T-cell engager therapies (e.g., Blincyto) and advanced immuno-oncology and cell therapy pipelines for blood cancers.
Novartis AG Basel, Switzerland Pioneer in CAR-T therapy (Kymriah) for leukemia and lymphoma, focusing on personalized cell-based cancer treatments.
Gilead Sciences, Inc. California, U.S. Through Kite Pharma offers CAR-T therapies (Yescarta, Tecartus) for lymphoma and multiple myeloma.
bluebird bio, Inc. Massachusetts, U.S. Specializes in gene and cell therapies for hematologic cancers and genetic diseases using lentiviral gene modification.
Bristol Myers Squibb Company New York, U.S. Provides CAR-T therapies (Breyanzi, Abecma) and invests heavily in next-generation oncology cell therapies.
Legend Biotech Somerset, New Jersey, U.S. Focuses on CAR-T therapy (Carvykti) for multiple myeloma in collaboration with Johnson & Johnson.
JW Therapeutics Shanghai, China Develops CAR-T cell therapies for hematologic malignancies, including relapsed/refractory lymphomas.

SWOT Analysis

Strengths

  • High therapeutic efficacy in treating complex and refractory cancers, especially hematological malignancies.
  • Rapid advancements in CAR-T, gene editing, and personalized medicine technologies.
  • Strong pipeline of innovative therapies supported by leading biotech and pharmaceutical companies.
  • Increasing regulatory approvals, accelerating market adoption.

Weaknesses

  • Extremely high treatment and manufacturing costs limit patient accessibility.
  • Complex production and supply chain requirements for personalized therapies.
  • Limited effectiveness in solid tumors compared to blood cancers.
  • Risk of severe side effects such as cytokine release syndrome in CAR-T therapy.

Opportunities

  • Expansion into solid tumor indications through next-generation technologies
  • Growth in emerging markets with improving healthcare infrastructure.
  • Rising collaborations between biotech firms and research institutes.
  • Advancements in in vivo gene editing and off-the-shelf cell therapies.

Threats

  • Stringent regulatory pathways and lengthy approval timelines.
  • Ethical and safety concerns related to gene editing technologies.
  • High competition among global biotech and pharmaceutical players.
  • Reimbursement challenges due to extremely high therapy costs.

What are the Recent Developments in the Cell and Gene Therapy for Oncology Market?

  • In March 2026, Merck & Co. signed an MoU with Cyto-Facto to strengthen its cell and gene therapy manufacturing capabilities in the Asia-Pacific region. The collaboration focuses on improving lentiviral vector production and optimizing advanced manufacturing processes to support next-generation oncology therapies.
  • In January 2026, Siren Biotechnology received U.S. FDA clearance for its first Investigational New Drug (IND) application, marking its transition into clinical-stage development. The therapy focuses on AAV-based immuno-gene therapy for treating recurrent high-grade glioma, a highly aggressive brain tumor. This milestone highlights growing innovation in oncology gene therapies along with increasing regulatory support for next-generation cancer treatments.

Segments Covered in the Report

By Therapy Type

  • Cell Therapy
    • CAR-T Cell Therapy
      • Autologous CAR-T
      • Allogeneic CAR-T
    • TCR-T Cell Therapy
    • Tumor-Infiltrating Lymphocyte (TIL) Therapy
    • NK Cell Therapy
    • Dendritic Cell Therapy
    • Stem Cell-Based Oncology Therapy
  • Gene Therapy
    • Viral Vector-Based Gene Therapy
      • Lentiviral Vectors
      • retroviral Vectors
      • Adenoviral Vectors
      • AVV Vectors
  • Non-Viral Gene Therapy
    • Lipid Nanoparticles
    • electroporation
    • Polymeric Nanoparticles
  • Gene Editing Therapy
    • CRISPR-Cas9
    • TALEN
    • Zinc-Finger Nucleases

By Cancer Type

  • Hematological Malignancies
    • Leukemia
    • Lymphoma
    • Multiple Myeloma
  • Solid Tumors
    • Lung Cancer
    • Breast Cancer
    • Prostate Cancer
    • Colorectal Cancer
    • Ovarian Cancer
    • Pancreatic Cancer
    • Melanoma
    • Brain Tumors
    • Others

By Therapy Source

  • Autologous Therapies
  • Allogeneic Therapies

By Delivery Vector

  • Viral Vectors
    • Lentivirus
    • Retrovirus
    • Adenovirus
    • Adeno-Associated Virus (AAV)

By Application

  • Therapeutic Application
    • First-Line Therapy
    • Second-Line Therapy
    • Third-Line & Salvage Therapy
  • Research Applications
    • Clinical Research
    • translational Research
    • preclinical Oncology Research

By End User

  • Hospitals
  • Cancer Treatment Centers
  • academic & Research Institutes
  • Biotechnology & Pharmaceutical Companies
  • Specialty Clinics

By Manufacturing Type

  • In-House Manufacturing
  • Contract Manufacturing
    • CDMOs
    • CMOs

By Route of Administration

  • Intravenous
  • Intratumoral
  • Intraosseous
  • Others

By Region

  • North America
    • U.S.
    • Canada
    • Mexico
    • Rest of North America
  • Latin America
    • Brazil
    • Argentina
    • Rest of Latin America
  • Europe
    • Western Europe
      • Germany
      • Italy
      • France
      • Netherlands
      • Spain
      • Portugal
      • Belgium
      • Ireland
      • UK
      • Iceland
      • Switzerland
      • Poland
      • Rest of Western Europe
    • Eastern Europe
      • Austria
      • Russia & Belarus
      • Türkiye
      • Albania
      • Rest of Eastern Europe
  • Asia Pacific
    • China
    • Taiwan
    • India
    • Japan
    • Australia and New Zealand
    • ASEAN Countries (Singapore, Malaysia)
    • South Korea
    • Rest of APAC
  • MEA
    • GCC Countries
      • Saudi Arabia
      • United Arab Emirates (UAE)
      • Qatar
      • Kuwait
      • Oman
      • Bahrain
    • South Africa
    • Egypt
    • Rest of MEA

FAQ's

Finding : The cell and gene therapy for oncology market currently in 2026 records USD 18.48 billion and is anticipated to grow to USD 134.53 billion by 2035, advancing at a CAGR of 24.68% from 2026 to 2035.

Finding : North America is currently leading the cell and gene therapy for oncology market by 46% due to its advanced healthcare infrastructure, strong presence of leading biotech and pharmaceutical companies, and high investment in R&D.

Finding : Ministry of Health and Family Welfare, Government of India, National Institutes of Health, FDA, WHO, PIB.

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Meet the Team

Rohan Patil

Rohan Patil

Principal Consultant

Rohan Patil is a seasoned market research professional with over 5+ years of focused experience in the healthcare sector, bringing deep domain expertise, strategic foresight, and analytical precision to every project he undertakes.

Learn more about Rohan Patil
Aditi Shivarkar

Aditi Shivarkar

Reviewed By

Aditi Shivarkar is a seasoned professional with over 14 years of experience in healthcare market research. As a content reviewer, Aditi ensures the quality and accuracy of all market insights and data presented by the research team.

Learn more about Aditi Shivarkar
Cell and Gene Therapy for Oncology Market
Updated Date: 20 May 2026   |   Report Code: 6896