Mitigating long-term and delayed adverse events associated with cancer treatment: implications for survivorship.

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2023-08

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Abstract

Despite the importance of chemotherapy-associated adverse events in oncology practice and the broad range of interventions available to mitigate them, limited systematic efforts have been made to identify, critically appraise and summarize the totality of evidence on the effectiveness of these interventions. Herein, we review the most common long-term (continued beyond treatment) and late or delayed (following treatment) adverse events associated with chemotherapy and other anticancer treatments that pose major threats in terms of survival, quality of life and continuation of optimal therapy. These adverse effects often emerge during and continue beyond the course of therapy or arise among survivors in the months and years following treatment. For each of these adverse effects, we discuss and critically evaluate their underlying biological mechanisms, the most commonly used pharmacological and non-pharmacological treatment strategies, and evidence-based clinical practice guidelines for their appropriate management. Furthermore, we discuss risk factors and validated risk-assessment tools for identifying patients most likely to be harmed by chemotherapy and potentially benefit from effective interventions. Finally, we highlight promising emerging supportive-care opportunities for the ever-increasing number of cancer survivors at continuing risk of adverse treatment effects.

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Humans, Neoplasms, Quality of Life, Survivorship

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Published Version (Please cite this version)

10.1038/s41571-023-00776-9

Publication Info

Lustberg, Maryam B, Nicole M Kuderer, Aakash Desai, Cristiane Bergerot and Gary H Lyman (2023). Mitigating long-term and delayed adverse events associated with cancer treatment: implications for survivorship. Nature reviews. Clinical oncology, 20(8). pp. 527–542. 10.1038/s41571-023-00776-9 Retrieved from https://hdl.handle.net/10161/31556.

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Scholars@Duke

Lyman

Gary Herbert Lyman

Adjunct Professor in the Department of Medicine

Dr. Gary Lyman is Adjunct Professor of Medicine in the Division of Medical Oncology, Department of Internal Medicine at Duke University School of Medicine . He is a nationally and internationally recognized authority on comparative effectiveness and health services and outcomes research. Lyman research has been funded by the National Cancer Institute, the National Heart Lung and Blood Institute, the American Society of Clinical Oncology along with industry grants related to supportive cancer care. Dr Lyman has published some 700 research articles in in the professional medical literature. 

Personal Statement
I have been extremely privileged to work with some of the worlds best biostatisticians and clinical trialists over the years including a postdoctoral fellowship with Professor Marvin Zelen, chair of Biostatistics at the Harvard School of Public Health and as a Visiting Professor with Professor Stuart Pocock at the the London School of Hygiene and Tropical Medicine and Professor Doug Altman at the Oxford Centre for Health Statistics as well as many others now in the Division of Public Health Sciences at the Fred Hutchinson Cancer Research Center. It has been very humbling and a true honor to work with and learn from such professionals. These wonderful colleagues have made it possible for me to be listed among the top 1% of most highly cited investigators by Web of Science for the past 8 years with well over 100,000 professional citations.  Thank you all. https://en.wikipedia.org/wiki/Gary_Herbert_Lyman

Dr Lyman’s research interests include:
Personalized Medicine and Cancer Supportive Care: In addition to the conduct of randomized controlled trials of new cancer diagnostic, prognostic, treatment and supportive care approaches, Dr Lyman’s research interests include the personalized management of early-stage breast cancer and supportive care of patients receiving cancer chemotherapy, most notably those at risk for febrile neutropenia and venous thromboembolism. Based on clinical trial results, Dr Lyman is actively involved in the development and validation of clinical risk models for patient selection and targeted intervention and preventive strategies. Dr Lyman is co-PI on an NCI on comparative effectiveness of cancer pharmacogenomics grant to discover and validate new genomic tools for guiding more personalized cancer treatments and on an NHLBI trial of thromboprophylaxis in high risk ambulatory patients receiving cancer chemotherapy.

Evidence synthesis, clinical practice guidelines and health policy: Dr Lyman conducts systematic reviews and meta-analyses of major clinical issues in support of clinical practice guidelines. Dr Lyman chairs several guidelines for the American Society of Clinical Oncology including those on antiemetics, venous thromboembolism, sentinel node biopsy in patients with breast cancer and cutaneous melanoma and on weight based dosing of chemotherapy. Dr Lyman also conducts analyses of large population studies of clinical outcomes associated with of current cancer patient management in a real world setting with a particular focus on cancer management in the elderly patient with cancer. Dr Lyman leads several decision simulation studies for improved clinical decision making and cost-effectiveness analysis of new and novel therapies based on results of clinical trials, systematic reviews and population studies. He serves as an advisor on new oncologic agents to the US FDA. Dr Lyman also serves as Editor-in-Chief of Cancer Investigation and on the editorial boards of several prestigious research journals.


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