{"product_id":"handbook-of-statistics-in-clinical-oncology","title":"Handbook of Statistics in Clinical Oncology","description":"\u003cp\u003eMany new challenges have arisen in the area of oncology clinical trials. New cancer therapies are often based on cytostatic or targeted agents, which pose new challenges in the design and analysis of all phases of trials. The literature on adaptive trial designs and early stopping has been exploding. Inclusion of high-dimensional data and imaging techniques have become common practice, and statistical methods on how to analyse such data have been refined in this area. A compilation of statistical topics relevant to these new advances in cancer research, this third edition of \u003cstrong\u003eHandbook of Statistics in Clinical Oncology\u003c\/strong\u003e focuses on the design and analysis of oncology clinical trials and translational research. \u003c\/p\u003e\u003cp\u003eAddressing the many challenges that have arisen since the publication of its predecessor, this third edition covers the newest developments involved in the design and analysis of cancer clinical trials, incorporating updates to all four parts:\u003c\/p\u003e\u003cul\u003e \u003cp\u003e \u003c\/p\u003e \u003cli\u003e \u003cem\u003ePhase I trials:\u003c\/em\u003e Updated recommendations regarding the standard 3 + 3 and continual reassessment approaches, along with new chapters on phase 0 trials and phase I trial design for targeted agents.\u003c\/li\u003e \u003cli\u003e \u003cem\u003ePhase II trials\u003c\/em\u003e: Updates to current experience in single-arm and randomized phase II trial designs. New chapters include phase II designs with multiple strata and phase II\/III designs.\u003c\/li\u003e \u003cli\u003e \u003cem\u003ePhase III trials\u003c\/em\u003e: Many new chapters include interim analyses and early stopping considerations, phase III trial designs for targeted agents and for testing the ability of markers, adaptive trial designs, cure rate survival models, statistical methods of imaging, as well as a thorough review of software for the design and analysis of clinical trials.\u003c\/li\u003e \u003cli\u003e \u003cem\u003eExploratory and high-dimensional data analyses\u003c\/em\u003e: All chapters in this part have been thoroughly updated since the last edition. New chapters address methods for analyzing SNP data and for developing a score based on gene expression data. In addition, chapters on risk calculators and forensic bioinformatics have been added.\u003c\/li\u003e \u003c\/ul\u003e\u003cp\u003eAccessible to statisticians and oncologists interested in clinical trial methodology, the book is a single-source collection of up-to-date statistical approaches to research in clinical oncology. \u003c\/p\u003e","brand":"Taylor \u0026 Francis","offers":[{"title":"Default Title","offer_id":45542203752686,"sku":"9781138199491","price":92.8,"currency_code":"AUD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0630\/9612\/7726\/files\/9781138199491.jpg?v=1720121837","url":"https:\/\/bookland.com.au\/products\/handbook-of-statistics-in-clinical-oncology","provider":"Book Land AU","version":"1.0","type":"link"}