Pediatric cancer therapeutics development / Jorge DiMartino, Gregory H. Reaman, Franklin O. Smith, editors.

Format:

Book

Contributor:

DiMartino, Jorge, editor.

Reaman, Gregory H., editor.

Smith, Franklin O., editor.

Series:

Pediatric oncology (Series)

Pediatric Oncology

Language:

English

Subjects (All):

Cancer in children--Treatment.

Cancer in children.

Cancer--Chemotherapy.

Cancer.

Drug development.

Genre:

Electronic books.

Physical Description:

1 online resource.

Place of Publication:

Cham, Switzerland : Springer, 2022.

Summary:

This book provides a comprehensive overview of the scientific, medical, regulatory, and economic considerations associated with the discovery, development, and delivery of novel therapeutics for children with cancer. Co-authored by a diverse team from academic, government, and industry backgrounds, the book describes the steps in the process from the identification of a promising therapeutic target to the evaluation of drug candidates in the various phases of clinical testing and regulatory review. Throughout, special emphasis is placed on the unique biology of pediatric malignancies and the medical and social needs of children and their families. In providing a firm grounding in the drug development process, the book will be of value to all with an interest in how medicines currently used to treat pediatric cancer were made available. This includes trainees as well as established practitioners and others participating in translational and clinical research in the academic setting.

Contents:

Intro

Contents

1: History of Drug Development for Children with Cancer

1.1 Introduction

1.2 Initial Progress

1.3 Rise of the Cancer Cooperative Groups

1.4 Impact of Regulation to Improve Safety and Efficacy Federal Laws Providing a Regulatory Framework for Drug Development in Children

1.5 Indications

1.6 Summary

References

2: Targeted Small Molecule Drug Discovery

2.1 Introduction

2.2 Stage Gating

2.3 Phenotypic Drug Discovery

2.4 Target-Based Drug Discovery: Considerations for Target Selection/Identification

2.5 Target-Based Drug Discovery: Identifying Chemical Starting Points

2.6 Hit-to-Lead

2.7 Lead Optimization

2.8 Candidate Nomination

3: An FDA Oncology Perspective of Juvenile Toxicity Studies to Support Pediatric Drug Development

3.1 Introduction

3.2 Should a JAS Be Considered?

3.2.1 ICH S11: Nonclinical Safety Testing in Support of Development of Pediatric Medicines

3.2.2 ICH S9: Nonclinical Evaluation for Anticancer Pharmaceuticals Questions and Answers

3.3 Dinutuximab and Naxitamab

3.4 TRK Inhibitors

3.5 Conclusion

References

4: Design and Statistical Considerations for Early Phase Clinical Trials in Pediatric Oncology

4.1 Introduction

4.2 Rule-Based Designs

4.2.1 Traditional 3 + 3 Design

4.2.2 Accelerated Titration Design

4.2.3 Rolling Six Design

4.3 Model-Based Designs

4.3.1 Continual Reassessment Method (CRM)

4.3.2 EWOC and BLRM

4.3.3 TITE-CRM and TITE-EWOC

4.4 Model-Assisted Designs

4.4.1 Modified Toxicity Probability Interval (mTPI) Design

4.4.2 Keyboard Design

4.4.3 Bayesian Optimal Interval (BOIN) Design

4.5 New Designs

4.5.1 Modified 4 + 4 Design

4.6 Conclusions

5: Exploratory Clinical Development: From First in Humans to Phase 3 Ready

5.1 Introduction

5.2 The Therapeutic Hypothesis

5.3 Dose and Schedule Determination

5.4 Clinical Proof of Concept (PoC)

5.5 Putting It All Together: Combined Phase 1-2 Studies

5.6 A Role for Pediatric Cancer in Exploratory Drug Development

6: Gene and Cell Therapy: How to Build a BioDrug

6.1 Introduction

6.2 BioDrug ToolKit: Cells

6.2.1 Hematopoietic Stem Cells (HSCs)

6.2.2 T Lymphocytes

6.2.3 Natural Killer (NK) Cells

Notes:

Online resource; title from PDF title page (SpringerLink, viewed December 2, 2022).

ISBN:

9783031063572

3031063570

OCLC:

1351448104

Access Restriction:

Restricted for use by site license.