Resistance to Targeted Therapies in Multiple Myeloma - Clinical
Resistance to Targeted Therapies in Multiple Myeloma - Clinical
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In this review of Resistance to Targeted Therapies in Multiple Myeloma, the authors present a focused look at why targeted treatments fail as disease progresses and how newer agents attempt to overcome that resistance. The book is most useful for clinicians, oncology fellows, and researchers who need a concise, clinically oriented summary of current and emerging targeted approaches in multiple myeloma. The single biggest reason to read it is its practical synthesis of approved classes and investigational options, helping readers connect mechanisms of resistance with therapeutic strategies.
Key Features
- Clear overview of approved classes: Describes Proteasome Inhibitors, Immunomodulatory Drugs and Monoclonal Antibodies and their roles in current treatment algorithms.
- Mechanisms of resistance explained: Links how disease progression and molecular changes lead to refractory disease, aiding clinical decision making.
- Discussion of later-generation agents: Summarizes second and third generation drugs developed to overcome resistance and their distinct mechanisms of action.
- Coverage of emerging therapies: Reviews CAR-T cells, bi-specific antibodies, vaccines, ubiquitin ligase inhibitors and BCL-2 inhibitors that are in clinical trials.
- Clinically focused synthesis: Emphasizes practical implications for sequencing targeted therapies across disease stages rather than exhaustive preclinical detail.
Who It's For
This book is aimed at oncologists, hematologists, oncology fellows and clinical researchers who need a compact reference on targeted therapy resistance in multiple myeloma. The emphasis on approved drug classes and trial-stage approaches makes it a useful bridge between bench science and bedside decisions.
Non-specialist readers seeking a patient-oriented guide or deeply technical molecular biology may want a different text; this volume assumes familiarity with standard multiple myeloma therapies and clinical terminology.
Pros & Cons
Pros
- Concise synthesis of proteasome inhibitors, immunomodulators and monoclonal antibodies and how they are used clinically.
- Helpful explanation of why patients develop refractory disease, linking mechanisms to practice.
- Useful summary of promising investigational options such as CAR-T and bi-specific antibodies for readers tracking trials.
Cons
- Not a deep molecular textbook, so researchers seeking exhaustive bench-level detail may find the coverage high level.
Specifications
| Title | Resistance to Targeted Therapies in Multiple Myeloma |
| Series | Resistance to Targeted Anti-Cancer Therapeutics |
| Authors | Silvia CW Ling, Steven Trieu |
| Primary topics | Proteasome Inhibitors; Immunomodulatory Drugs; Monoclonal Antibodies |
| Investigational therapies covered | CAR-T cells; bi-specific antibodies; vaccines; ubiquitin ligase inhibitors; BCL-2 inhibitors |
| Clinical focus | Mechanisms of resistance and therapeutic sequencing |
Our Verdict
Resistance to Targeted Therapies in Multiple Myeloma is a compact, clinically minded review that helps practitioners connect mechanisms of resistance with real-world treatment choices. It is good value for oncologists and researchers who want a practical update on approved classes and emerging targeted options without wading through exhaustive bench science.
Frequently Asked Questions
Does this book cover CAR-T therapies?
Yes. It reviews CAR-T cells alongside other investigational approaches such as bi-specific antibodies and vaccines.
Is the focus clinical or basic science?
The emphasis is clinical, explaining resistance mechanisms in the context of therapeutic sequencing and approved drug classes.
Who are the intended readers?
The intended audience is clinicians, oncology fellows and clinical researchers interested in targeted therapies for multiple myeloma.
Editor's Take
A compact, clinically focused review that links mechanisms of resistance in multiple myeloma to practical treatment strategies, useful for oncologists and researchers tracking approved and emerging targeted therapies.

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