Handbook of Statistics in Clinical Oncology
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Beszerezhetőség
Becsült beszerzési idő: A Prosperónál jelenleg nincsen raktáron, de a kiadónál igen. Beszerzés kb. 3-5 hét..
A Prosperónál jelenleg nincsen raktáron.
Why don't you give exact delivery time?
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A termék adatai:
- Kiadás sorszáma 4
- Kiadó Chapman and Hall
- Megjelenés dátuma 2025. december 31.
- ISBN 9781032596952
- Kötéstípus Keménykötés
- Terjedelem540 oldal
- Méret 254x178 mm
- Súly 1160 g
- Nyelv angol
- Illusztrációk 94 Illustrations, black & white; 14 Halftones, black & white; 80 Line drawings, black & white 700
Kategóriák
Rövid leírás:
This revised edition features contributions from leading cancer trial statisticians, providing expert insights into modern oncology trial design and methodology and provides a comprehensive resource for researchers, clinicians, and statisticians involved in the evolving landscape of oncology clinical trials.
TöbbHosszú leírás:
Since the third edition of this handbook, significant advances have transformed the field of oncology. Most cancer types now offer multiple treatment options, with immunotherapies and targeted therapies becoming the standard of care. Master protocols, which allow the addition of new treatment arms without requiring new protocols, have gained popularity—not only to expedite the approval process for new therapies but also to ensure that patients receive the most beneficial treatments tailored to their individual needs. This revised edition features contributions from leading cancer trial statisticians, providing expert insights into modern oncology trial design and methodology. The handbook is structured into five key parts:
- Part 1: Cancer prevention and screening trial designs, including risk prediction models and prevention trials
- Part 2: Early-phase trial designs, covering dose-finding studies, selection designs, and multi-strata trials
- Part 3: Late-stage trial designs, including approaches for IO therapies, cure-rate models, targeted agents, and considerations for pediatric oncology trials
- Part 4: Trial conduct and operations, addressing best practices for Data Monitoring Committees (DMCs), SWOG/CRAB calculators, pragmatic trials, and clinical trial innovation
- Part 5: Beyond primary endpoints, exploring surrogate endpoints, microbiome research, patient-reported outcomes (PROs), and tree-based partitioning methods
This updated edition provides a comprehensive resource for researchers, clinicians, and statisticians involved in the evolving landscape of oncology clinical trials.
TöbbTartalomjegyzék:
SECTION 1 Cancer Prevention & Screening
Chapter 1 Cancer Screening Trials
Chapter 2 Cancer Risk Prediction Models
Chapter 3 Incorporating External Registry Data Into Cohort-based Cancer Risk Prediction Tools
SECTION 2 Trial Design | Early-Phase Trials
Chapter 4 Phase I – Overview and Recent Trial Designs
Chapter 5 Statistical and Machine Learning Methods for Phase I Dose-Finding
Chapter 6 Seamless Phase I/II Trial Design for Assessing Toxicity and Efficacy for Targeted Agents
Chapter 7 Designs Using Time to Event Endpoints / Single Arm versus Randomized Phase II Designs
Chapter 8 Phase II Selection Designs
Chapter 9 Phase II Trials with Multiple Strata
SECTION 3 Trial Design | Late-Phase Trials
Chapter 10 Cure Rate Survival Models
Chapter 11 Phase III Trials for Targeted Agents
Chapter 12 Phase II and III Clinical Trial Designs for Precision Medicine
Chapter 13 SMARTs in Oncology
Chapter 14 Statistical Considerations in the Design and Analysis of Cancer Trials with Immune-Oncology Therapies
Chapter 15 Alpha Splitting
Chapter 16 Early Stopping of Clinical Trials Evaluating Targeted Therapies
Chapter 17 Noninferiority Trials
Chapter 18 Considerations for Pediatric Oncology Trials
SECTION 4 Trial Conduct
Chapter 19 An Overview of Master Protocols
Chapter 20 On Use of Covariates in Randomization and Analysis of Clinical Trials
Chapter 21 Pragmatic Clinical Trials in Clinical Oncology: A Statistical Perspective
Chapter 22 Dynamic Treatment Regimens and Sequential Multiple Assignment Randomized Trial in Cancer Research
Chapter 23 Outcome-Adaptive Randomization
Chapter 24 Current Suggested Practices and Issues for Data and Safety Monitoring Committees in Cancer Clinical Trials
Chapter 25 Improving Data Collection: EHR-to-EDC Assisted Data Transfer
Chapter 26 Barriers and Disparities in Access to Cancer Clinical Trials – Causes and Implications
Chapter 27 SWOG Statistical Calculators for Design and Analysis of Clinical Trials
Chapter 28 Streamlining Data Collection and Trial Conduct
SECTION 5 Beyond the Primary Endpoint
Chapter 29 Use of Circulating Tumor DNA in Oncology – ctMoniTR
Chapter 30 Statistical Analysis of -Omics Data
Chapter 31 Principles of Design and Analysis for Patient-Reported Outcomes
Chapter 32 X Intermediate and Surrogate Endpoints in Phase III Randomized
Chapter 33 Prognostic Groups via Interpretable Function Approximation: Tree-based and Extreme Regression Models
Több
