
Immuno-Oncology & Targeted Therapy Course
Master the science and clinical application of immuno-oncology and targeted therapy, from tumor microenvironment biology to CAR-T cell engineering. This course equips oncology professionals with the mechanistic depth and translational skills needed to navigate today's most complex cancer treatment decisions. Whether you work in clinical practice, drug development, or translational research, this is the definitive program for advancing your expertise in modern cancer therapeutics.
What you will learn:
Understand the molecular mechanisms of immune evasion and how targeted therapies counteract them.
Interpret biomarkers such as PD-L1, TMB, and MSI-H to guide immunotherapy patient selection.
Evaluate CAR-T, TCR-T, and TIL cellular therapy platforms across hematologic and solid tumors.
Apply resistance mechanism frameworks to anticipate treatment failure and select next-line strategies.
Design and critically assess immuno-oncology clinical trials using IO-specific endpoints and response criteria.
Manage immune-related adverse events and combination regimen toxicities using evidence-based algorithms.
How you study in practice Immuno-Oncology & Targeted Therapy Course
How you practice Immuno-Oncology & Targeted Therapy Course
For companies looking to train their teams
With Dedika for businesses, the course includes exercises and examples tailored to your own business and the way your company needs.
Course Content
8 Chapters • 40 LessonsDuration between 4 and 360 hours (you decide)
Chapter 1HideHide detailsSee detailsFoundations of Cancer Biology
Foundations of Cancer Biology
Lesson 1 • Innate Immune Surveillance of Tumors
Describes how NK cells, macrophages, and dendritic cells detect and eliminate nascent tumor cells. Provides the immunological groundwork for understanding checkpoint and innate immune therapies.
Lesson 2 • Immune Evasion Mechanisms
Analyzes how tumors escape immune destruction through checkpoint upregulation, antigen loss, and immunosuppressive cell recruitment. Directly motivates the therapeutic strategies covered in later chapters.
Lesson 3 • Hallmarks of Cancer and Oncogenesis
Covers the molecular events driving malignant transformation, including oncogene activation and tumor suppressor loss. Establishes the biological basis for all targeted and immune therapies.
Lesson 4 • Adaptive Immunity and Tumor Antigens
Explains T and B cell responses to tumor-associated and tumor-specific antigens. Connects antigen presentation to the rationale for checkpoint blockade and cancer vaccines.
Lesson 5 • Tumor Microenvironment Architecture
Examines cellular and molecular components of the tumor microenvironment (TME). Understanding TME composition is essential for interpreting therapy resistance and response.
Chapter 2HideHide detailsSee detailsPrinciples of Targeted Therapy
Principles of Targeted Therapy
Lesson 1 • Resistance Mechanisms to Targeted Therapy
Classifies primary, acquired, and adaptive resistance mechanisms at the molecular level. Prepares students to anticipate resistance and evaluate next-generation inhibitor strategies.
Lesson 2 • Oncogenic Driver Mutations and Biomarkers
Identifies actionable mutations across major cancer types and explains how biomarker testing guides therapy selection. Grounds subsequent drug-class discussions in clinical relevance.
Lesson 3 • Kinase Inhibitor Classes and Mechanisms
Covers ATP-competitive, allosteric, and covalent kinase inhibitors and their selectivity profiles. Provides mechanistic vocabulary needed to evaluate resistance and next-generation agents.
Lesson 4 • Pharmacokinetics of Targeted Agents
Examines absorption, distribution, metabolism, and excretion properties specific to small-molecule inhibitors. Connects PK parameters to dosing schedules and drug interaction risks.
Lesson 5 • Key Signaling Pathways as Drug Targets
Maps RAS/MAPK, PI3K/AKT/mTOR, and RTK pathways to approved inhibitors. Enables students to reason about combination strategies and pathway crosstalk.
Chapter 3HideHide detailsSee detailsImmune Checkpoint Inhibitors
Immune Checkpoint Inhibitors
Lesson 1 • CTLA-4 Pathway Biology and Blockade
Details CTLA-4 co-inhibitory signaling in T cell priming and the mechanism of anti-CTLA-4 antibodies. Sets the stage for comparing CTLA-4 and PD-1 axis blockade.
Lesson 2 • Immune-Related Adverse Event Management
Classifies irAEs by organ system, severity grade, and management algorithm. Equips students to recognize, grade, and treat toxicities while preserving therapeutic benefit.
Lesson 3 • Biomarkers of Checkpoint Response
Evaluates PD-L1 expression, TMB, MSI-H, and gene expression profiles as predictive biomarkers. Connects biomarker interpretation to patient selection and clinical trial design.
Lesson 4 • Emerging Checkpoint Targets
Surveys LAG-3, TIM-3, TIGIT, and other next-generation checkpoint targets under clinical investigation. Positions students to evaluate emerging combination regimens.
Lesson 5 • PD-1/PD-L1 Pathway and Inhibitors
Explains PD-1/PD-L1 co-inhibitory signaling in the TME and the pharmacology of approved anti-PD-1 and anti-PD-L1 antibodies. Directly informs biomarker-driven patient selection.
Chapter 4HideHide detailsSee detailsAntibody-Based Therapeutics in Oncology
Antibody-Based Therapeutics in Oncology
Lesson 1 • Monoclonal Antibody Engineering Principles
Covers antibody structure, isotype selection, and humanization strategies that determine efficacy and immunogenicity. Provides the structural foundation for all antibody-based drug classes.
Lesson 2 • Clinical Development of Antibody Therapeutics
Reviews dose-finding, PK/PD modeling, and regulatory considerations specific to antibody-based drugs. Prepares students to interpret clinical trial data for antibody therapeutics.
Lesson 3 • Bispecific Antibodies and T Cell Engagers
Describes bispecific antibody formats that redirect T cells or NK cells to tumor targets. Connects molecular design to clinical activity and cytokine release syndrome risk.
Lesson 4 • Antibody-Drug Conjugate Design
Examines linker chemistry, payload selection, and drug-to-antibody ratio in ADC design. Explains how ADC architecture determines therapeutic index and resistance mechanisms.
Lesson 5 • Mechanisms of Antitumor Antibody Action
Explains ADCC, CDC, ADCP, and direct signaling blockade as mechanisms of therapeutic antibodies. Connects mechanism to clinical activity and combination rationale.
Chapter 5HideHide detailsSee detailsCellular Immunotherapy Approaches
Cellular Immunotherapy Approaches
Lesson 1 • CAR-T Cell Design and Engineering
Details CAR construct architecture across generations and the impact of costimulatory domains on T cell function. Connects design choices to clinical efficacy and exhaustion risk.
Lesson 2 • TCR-Engineered T Cell Therapy
Explains how TCR-T cells recognize intracellular antigens via MHC and differ from CAR-T cells. Covers HLA restriction as a key design and patient selection constraint.
Lesson 3 • Toxicity and Safety of Cellular Therapies
Classifies CRS, ICANS, and on-target off-tumor toxicities with grading and management algorithms. Prepares students to anticipate and manage life-threatening cellular therapy toxicities.
Lesson 4 • Adoptive Cell Therapy Fundamentals
Introduces the concept of ex vivo cell expansion and reinfusion for antitumor immunity. Establishes the biological rationale distinguishing autologous from allogeneic approaches.
Lesson 5 • Tumor-Infiltrating Lymphocyte Therapy
Covers TIL isolation, expansion protocols, and clinical evidence in solid tumors. Positions TIL therapy relative to CAR-T and TCR-T in the cellular therapy landscape.
Chapter 6HideHide detailsSee detailsCancer Vaccines and Innate Immune Activation
Cancer Vaccines and Innate Immune Activation
Lesson 1 • Principles of Cancer Vaccine Design
Covers antigen selection, adjuvant pairing, and delivery route as determinants of vaccine immunogenicity. Establishes the design framework applied across all vaccine platform sections.
Lesson 2 • Innate Immune Agonists as Cancer Therapeutics
Covers STING, TLR, and RIG-I agonists that activate innate immunity to enhance antitumor responses. Connects innate activation to adaptive immune priming and combination therapy rationale.
Lesson 3 • Peptide and Protein Vaccine Platforms
Examines synthetic long peptide and recombinant protein vaccines, including formulation and MHC presentation requirements. Connects platform limitations to the rationale for nucleic acid approaches.
Lesson 4 • Neoantigen-Based Personalized Vaccines
Explains the pipeline from tumor sequencing to neoantigen prediction and vaccine manufacturing. Positions personalized vaccines as a precision oncology strategy complementing checkpoint blockade.
Lesson 5 • mRNA and Viral Vector Vaccine Platforms
Details mRNA lipid nanoparticle and viral vector delivery systems for cancer antigen expression. Evaluates immunogenicity advantages and manufacturing scalability of each platform.
Chapter 7HideHide detailsSee detailsCombination Strategies and Resistance
Combination Strategies and Resistance
Lesson 1 • Rationale for Combination Immunotherapy
Establishes mechanistic frameworks for combining checkpoint inhibitors, targeted agents, and cellular therapies. Distinguishes synergistic from additive combinations using preclinical and clinical evidence.
Lesson 2 • Chemotherapy and Radiation Immunomodulation
Explains immunogenic cell death, abscopal effects, and how cytotoxic agents sensitize tumors to immunotherapy. Connects these mechanisms to chemo-immunotherapy and radio-immunotherapy combinations.
Lesson 3 • Overcoming Immunotherapy Resistance
Classifies primary and acquired resistance to checkpoint blockade and cellular therapies at the molecular level. Evaluates strategies including alternative checkpoints, TME reprogramming, and combination rescue.
Lesson 4 • Toxicity Management in Combination Regimens
Addresses overlapping and additive toxicity profiles when combining immunotherapy with targeted or cytotoxic agents. Equips students with dose modification and supportive care decision frameworks.
Lesson 5 • Targeted Therapy Plus Immunotherapy
Examines how BRAF/MEK inhibitors, CDK4/6 inhibitors, and VEGF inhibitors modulate immune responses. Provides evidence-based rationale for approved and investigational combinations.
Chapter 8HideHide detailsSee detailsClinical Trial Design and Translational Application
Clinical Trial Design and Translational Application
Lesson 1 • Response Assessment Criteria in IO
Compares RECIST, iRECIST, and irRC criteria for assessing immunotherapy responses. Equips students to select and apply appropriate criteria in trial and clinical practice settings.
Lesson 2 • Biomarker Integration in Clinical Trials
Covers prospective biomarker strategies, co-development of companion diagnostics, and exploratory biomarker analysis. Connects biomarker planning to regulatory approval and precision medicine goals.
Lesson 3 • Endpoint Selection for IO Trials
Evaluates OS, PFS, ORR, DOR, and novel endpoints such as milestone survival for IO trials. Connects endpoint choice to regulatory requirements and clinical meaningfulness.
Lesson 4 • Unique Challenges in IO Trial Design
Identifies how delayed responses, pseudoprogression, and hyperprogression complicate standard oncology trial design. Motivates the use of IO-specific endpoints and response criteria.
Lesson 5 • Translating Preclinical Data to Clinical Practice
Examines how preclinical models, translational biomarkers, and early-phase signals inform go/no-go decisions. Prepares students to critically evaluate the translational validity of IO research.
Your valid completion certificate
This course is for you:
Medical oncologists seeking deeper fluency in immunotherapy mechanisms and resistance.
Pharmaceutical scientists working on early-stage immuno-oncology drug development programs.
Clinical research associates managing IO trials who need stronger scientific grounding.
Pathologists expanding their role in biomarker testing and companion diagnostic interpretation.
Translational researchers bridging laboratory discoveries and patient-facing oncology applications.
Oncology nurses advancing into specialized roles involving cellular therapy patient management.
What our students say
Your classes are perfect. I purchased the one-year package and finally have the opportunity to follow various topics of interest without needing to switch platforms... I thank you for everything you do, I've already recommended you to other people...

I like how the lessons are straight to the point and how I can switch chapters and skip content I don't need.

I like the content and the presentation style and video transcription, which speeds up the process!

The platform is fast, simple to use. The diversity of content and complementary videos really help with learning.

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