Blood and Marrow Transplantation Long Term Management

Blood and Marrow Transplantation Long Term Management
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Hematopoietic cell transplantation (HCT) provides curative therapy for a variety of diseases. Over the past several decades, significant advances have been made in the field of HCT, to the point where HCT has become an integral part of treatment modality for a variety of hematologic malignancies and some nonmalignant diseases. HCT remains an important treatment option for a wide variety of hematologic and nonhematologic disorders, despite recent advances in the field of immunologic therapies. Factors driving this growth include expanded disease indications, greater donor options (expanding unrelated donor registries and haploidentical HCT), and accommodation of older and less fit recipients.  The development of less toxic pretransplant conditioning regimens, more effective prophylaxis of graft-versus-host disease (GVHD), improved infection control, and other advances in transplant technology have resulted in a rapidly growing number of transplant recipients surviving long-term free of the disease for which they were transplanted. The changes over decades in the transplant recipient population and in the practice of HCT will have almost inevitably altered the composition of the long-term survivor population over time. Apart from an increasingly older transplant recipient cohort, the pattern of transplant indications has shifted from the 1990s when chronic myeloid leukemia made up a significant proportion of allo-HCT indications. Changes in cell source, donor types, conditioning regimens, GVHD prophylaxis, and supportive care have all occurred, with ongoing reductions in both relapse and non-relapse mortality (NRM) have been demonstrated.  These patients have increased risks for a variety of late complications, which can cause morbidity and mortality. Most long-term survivors return to the care of their local hematologists/oncologists or primary care physicians, who may not be familiar with specialized monitoring and management of long complications after HCT for this patient population. As HCT survivorship increases, the focus of care has shifted to the identification and treatment of long-term complications that may affect quality of life and long-term morbidity and mortality.  Preventive care as well as early detection and treatments are important aspects to reducing morbidity and mortality in long-term survivors after allo-HCT. This second edition,  Blood and Marrow Transplantation Long-Term Management: Survivorship after Transplant , provides up-to-date information about diagnosis, screening, treatment, and long-term surveillance of long-term survivors after HCT.

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Группа авторов. Blood and Marrow Transplantation Long Term Management

Table of Contents

List of Tables

List of Illustrations

Guide

Pages

Blood and Marrow Transplantation Long Term Management. Survivorship after Transplant

Foreword to the Second Edition

Foreword (from first edition)

List of Contributors

CHAPTER 1 Introduction to long‐term survivorship after hematopoietic cell transplantation

Background

Rapidly rising numbers of long‐term transplant survivors

Long‐term issues in long‐term survivors

Developing resources and a guide for long‐term survivors

Declaration of commercial interest

References

CHAPTER 2 International Blood and Marrow Registries: trends on long‐term data collection

Overview of the Role of Registries in HCT

Overview of Late Effects Data Collection through Registries. Registry Strengths

Registry Challenges

Future of Data Collection in Survivorship

Center for International Blood and Marrow Transplant Research (CIBMTR)

Introduction to the registry

Data collection

Late effects specific data collection

Future plans

The Registry of the European Society for Blood and Marrow Transplantation (EBMT)

Introduction to the registry

Data collection

Late effects specific data collection

Future plans

Asia‐Pacific Blood and Marrow Transplant Group (APBMT)

Introduction of the registry

Data collection

Late effects specific data collection

Future plans

The Registry of the Eastern Mediterranean Blood and Marrow Transplantation Group (EMBMT)

Introduction to the registry

Data collection

Late Effects Specific Data Collection

Future plans

References

CHAPTER 3 Long‐term follow‐up program and transplant clinic setup

Introduction

Concept of long‐term survivorship

Late effects after HSCT

Timing and transition to long‐term survivorship care

The transition from pediatric to adult long‐term care

Long‐term follow‐up program

Long‐term follow‐up Clinic

Long‐term transplant team and the annual LTFU visit

Preparation of the visit

The LTFU visit

Post‐visit follow‐up

Recommendation for screening and preventive practices

Organizing a long‐term follow‐up clinic in resource‐limited countries

Essential need for a LTFU clinic in resource limited countries

Unique challenges for survivorship in the resource limited countries

References

CHAPTER 4 Telemedicine in patient care of long‐term transplant survivors

Introduction

Principles of telehealth. Components of Telehealth

Practical applications for Telehealth

Legal, ethical and regulatory considerations for Telehealth

Reimbursement and financial considerations for Telehealth

Challenges to Telehealth adoption

What we know about current models for hct survivorship

Example of a LTFU telemedicine model

Future directions

References

CHAPTER 5 Long‐term follow‐up calendar

Introduction

Survivorship care plan

Schedule of the long‐term follow‐up visit

Screening and preventive recommendations

References

CHAPTER 6 Late effects post‐allogeneic hematopoietic stem cell transplantation

Introduction

Identification of late effects

Late effects. Acute and chronic infections

Cutaneous complications

Oral/dental complications

Hepatic complications

Gastrointestinal complications

Genital complications

Renal complications

Ocular complications

Endocrine complications

Hypogonadism, fertility loss, pregnancy, and lactation issues

Musculoskeletal and bone complications

Pulmonary complications

Neurologic complications

Psychological and social complications

Sexual dysfunction

Subsequent hematologic malignancies

Very late effects. Cardiovascular complications

Subsequent neoplasms

Future directions

Summary

References

CHAPTER 7 Late effects post‐autologous hematopoietic stem cell transplantation

Introduction

Pulmonary Complications

Cardiovascular Complications

Secondary Malignancies

Endocrine and Metabolic Complications. Thyroid Dysfunction

Bone Complications

Gonadal Dysfunction

Kidney Complications

Infectious Complications

Quality of Life and Psychosocial Effects

Cognitive Dysfunction

Special Considerations in Lymphoma and Myeloma

Conclusion

References

CHAPTER 8 Long‐term follow‐up of children

Introduction

Common posttransplant screening and prevention guidelines

Engraftment

Iron overload

Chronic GVHD

Infection and immunity

Ocular

Oral/dental

Pulmonary

Cardiovascular or metabolic

Gastrointestinal or hepatic

Renal or genitourinary

Muscle or connective tissue

Bone

Skin

Endocrinopathies

Growth Hormone deficiency

Hypogonadism, pubertal delay and infertility

Thyroid dysfunction

Iatrogenic Cushing’s Syndrome and Adrenal insufficiency

Insulin Resistance and Diabetes Mellitus

Neurocognitive

Psychological and quality of life

Subsequent neoplasms (SMN)

Survivorship care plans

References

CHAPTER 9 Graft‐versus‐host disease and late effects after hematopoietic stem cell transplantation

Introduction

cGVHD and nonmalignant late effects. Ocular effects [18]

Pulmonary effects [29,30]

Restrictive lung disease

Chronic obstructive lung disease

Complications of bones and joints [36] Avascular necrosis of bone (AVN)

Osteoporosis

Late cardiovascular complications [48]

Secondary Malignancies

Secondary leukemia after allogeneic HSCT

Lymphomas

Solid Tumors[53]

Pathogenesis

Skin and mucosal carcinoma and cGVHD

Thyroid carcinoma and cGVHD

References

CHAPTER 10 Screening and prevention guidelines for hematopoietic cell transplant survivors

Introduction

Published guidelines for screening and prevention of late complications in hsct survivors

Non‐infectious late effects. Neurocognitive

Eye

Oral and dental

Respiratory

Cardiovascular and metabolic

Gastrointestinal and liver

Renal and genitourinary

Musculoskeletal and connective tissue

Bone

Gonadotoxicity and fertility

Endocrine

Skin

Psychological complications and quality of life

Infectious and immunologic

Subsequent neoplasms

Treatment summary and survivorship care plans

Areas for future research

References

CHAPTER 11 Biology of survivorship after blood or marrow transplantation

Introduction

Anthracycline‐related heart failure

Genetics of heart failure

Therapy‐related myeloid neoplasia

Pathogenesis of t‐MDS/AML

Germline Polymorphisms

Candidate genes

Gene‐gene interactions

Genome‐wide association studies (GWAS)

Differential Gene Expression Profiles

Clonal Hematopoiesis with Somatic Mutations detected by DNA Sequencing

Cognitive outcomes

Genetic susceptibility to cognitive impairment

Conclusions

References

CHAPTER 12 Second malignancies

Introduction

Estimating the risk of second cancers

Pathophysiology

Risk factors for secondary malignancies. MDS & AML

Lymphoma

Solid tumors. Single center studies

Collaborative studies

Analysis on specific tumor types. Skin cancers

Liver cancers

Thyroid cancers

Breast cancers

Diagnosis, screening and prevention

Management; Treatment and Recommendations

References

CHAPTER 13 Anti‐infective prophylaxis, immunization and prevention of late infectious complications

Introduction

Vaccination

Antimicrobial prophylaxis

Immunoglobulin

Prevention of bacterial infections. Pneumococci

Haemophilus influenzae type B (HIB)

Meningococci

Other bacterial infections

Prevention of viral infections. Varicella‐zoster virus

CMV

Influenza

Papilloma virus

Hepatitis B virus

Hepatitis C virus

Hepatitis E virus

Prevention of fungal infections

Travel medicine

References

CHAPTER 14 Seasonal respiratory viral infections

Introduction

Community Respiratory Virus Infections in HCT Recipients. Influenza

2009 H1N1

Respiratory Syncytial Virus infections

Human Parainfluenza Virus

Human Metapneumovirus

Human Coronavirus

Human Rhinovirus

Other CRVs

Respiratory viruses and alloimmune lung syndrome

Diagnostic Evaluation

Treatment Options

Influenza

RSV

HPIV

Other CRVs

Preventing exposure

Infection Control Practices in the hospital, clinic and at home

Preventing Disease and Progression to LRTI

Influenza Vaccination

Chemoprophylaxis and Pre‐emptive Therapy

Future Considerations

References

CHAPTER 15 Monitoring and management of hepatitis B, C, and HIV infection before and after transplantation

Hepatitis B Virus (HBV) HBV screening

Patient and donor HBV status at HCT and risk of complications

Antiviral therapy/prophylaxis

Monitoring HBV after HCT [22]

Vaccination

Summary of HBV and HCT

Hepatitis C Virus (HCV)

HCV screening

Patients with HCV infection and risk of complications after HCT

Donor with HCV infection and risk of complications

Antiviral treatment (ASBMT Taskforce recommendations) [27]

Monitoring after HCT

Summary of HCV and HCT

Human Immunodeficiency Virus (HIV)

HIV Screening

Patients with HIV at HCT and risk of complications

Monitoring HIV patients during HCT

Acknowledgment

References

CHAPTER 16 Skin chronic GVHD

Introduction

cGVHD pathophyisiology

Animal models

Generation of specific T‐cell clones

T regs impairment and aberrant B‐cells activity

Fibrotic damage and tissue remodeling

Biomarkers

Pathological findings in cutaneous cGVHD

Clinical manifestations

Clinical management. Diagnosis

Scoring

Imaging and instrumental tools in skin cGVHD

Systemic treatment

Ancillary and topical treatment

Topical steroids

Topical calcineurin inhibitors

Phototherapy. PUVA

Other treatments

References

CHAPTER 17 Ocular complications

Introduction

Ocular graft‐versus‐host disease

Pathophysiology

Diagnosis

Incidence

Risk factors

Screening and prevention

Treatment

Cataract formation

Pathophysiology

Frequency and risk factors

Screening, prevention and management

Other non‐GVHD ocular complications. Ocular infections. Incidence and risk factors

Screening, prevention, and treatment

Ischemic microvascular retinopathy (IMR) Incidence and risk factors

Screening, prevention and treatment

Recommendations for the survivors / general practitioner

References

CHAPTER 18 Management of oral and dental complications

Introduction

Xerostomia and salivary gland hypofunction

Management of xerostomia

Oral graft‐versus‐host disease

Management of oral cGVHD

Jaw/bisphosphonate osteonecrosis

Secondary malignancies

Management

Conclusions

References

CHAPTER 19 Thyroid disease: monitoring and management guidelines

Introduction

Hypothyroidism. Pathophysiology

Frequency/ Cumulative Incidence

Risk Factors

Surveillance/ Screening

Treatment

Recommendation for Survivors

Hyperthyroidism. Pathophysiology

Frequency/ Cumulative Incidence

Risk Factors

Surveillance/ Screening

Treatment

Recommendation for Survivors

Thyroid nodules. Pathophysiology

Frequency/ Cumulative Incidence

Risk Factors

Surveillance/ Screening

Treatment

Recommendation for Survivors

Thyroid disorders and pregnancy post‐HSCT

References

CHAPTER 20 Pretransplant considerations in gender, reproductive, and sexual health

Introduction

General principles

Females: Ovarian physiology and potential for primary ovarian insufficiency and failure

Ovarian protection during HSCT

Fertility preservation

Contraception in men

Menstrual suppression and contraception for women

Pre‐HSCT cervical cytology and HPV disease

Pre‐HSCT STI screening and prevention

Sexuality

Summary

References

CHAPTER 21 Posttransplant Considerations in Gender, Reproductive, and Sexual Health

Introduction

Genital chronic graft‐versus‐host disease

Sex‐specific Signs and Symptoms of Genital GVHD. Females

Girls and young female adolescents

Males

Diagnosis and Staging

Management

Females

Males

Chronic GVHD and Sexual Dysfunction

Hypogonadism. General Considerations for females

Non‐gynecologic consequences of POI

Hormonal treatment of POI: general considerations

Hormonal therapy versus hormonal contraception

Contraceptive alternatives other than oral hormones post‐HSCT

Hypogonadism in Males

Special considerations for children and adolescents. POI for prepubertal girls and puberty induction

Pediatric and Adolescent Gynecologic Examination

Reproductive Health Visit, Consent, Confidentiality for female adolescents

Post‐HSCT HPV, cervical cancer and breast cancer prevention

Sexuality and fertility post‐HSCT

Summary

References

CHAPTER 22 Fertility issues, fertility preservation, and pregnancy outcome in long‐term survivors

Female fertility after HSCT

Fertility preservation options

Male fertility after HSCT

Fertility preservation options

Pregnancy after HSCT. Prevalence of conception and pregnancy

Outcome of pregnancy

Frequency of pregnancy after assisted conception in HSCT

Pregnancy outcome after assisted conception in HSCT

Maternal health during pregnancy following HSCT

Fertility Prevention Counseling

References

CHAPTER 23 Sexual Dysfunction in Long‐Term Survivors

Introduction

Sexual Well‐Being and Sexual Distress

Sexual Dysfunction

Sexual Arousal Disorder

Orgasmic Dysfunction

Dyspareunia

Risk Factors. Treatment‐Related Effects

Conditioning regimens

Chronic genital GVHD

Cardiovascular disease

Hormonal disorders

Medications

Psychosocial Distress

Body image distress

Screening and Prevention

Treatment

Addressing Psychosocial Factors. Cognitive Behavioral Therapy

Integrative sex therapy approaches

Couples therapy

Pharmacologic Interventions

Topical therapy

Systemic therapy

Other Methods

Considerations for Sexual Minority Populations

Recommendations for Practitioners Regarding SM Patients

Recommendations for Practitioners. Managing Polypharmacy

Routine Assessment of Sexual Functioning

Recommendations for Survivors

References

CHAPTER 24 Late non‐infectious pulmonary complications

Introduction

Early Non‐infectious Pulmonary Complications

Bronchiolitis Obliterans Syndrome

Cryptogenic Organizing Pneumonia

Interstitial Lung Disease:

Thoracic Air Leak Syndrome

Pulmonary Drug Toxicity

Pleural effusions

Venous Thromboembolic Disease (VTE)

Pulmonary Hypertension

Posttransplant Lymphoproliferative Disorder (PTLD)

Diagnostic considerations of non‐infectious pulmonary complications following HSCT

Conclusion

References

CHAPTER 25 Cardiac and arterial complications

Late cardiac dysfunction

Cardiotoxicity in cancer survivors

Congestive heart failure and cardiomyopathy. Incidence

Risk factors for congestive heart failure

Other cardiac complications

Screening, monitoring and management of cardiac dysfunction

Arterial disease

Arterial disease after HSCT

Risk factors for arterial disease

Pathogenesis of arterial disease after HSCT

Endocrine dysfunction

Endothelial injury and other factors

Screening and preventive recommendations for survivors at risk for arterial disease

Patients at risk for arterial disease

Type and timing of screening

Prevention and treatment of cardiovascular risks

Disclosures

References

CHAPTER 26 Cardiovascular risk factors

Introduction

Dyslipidemia

Pathophysiology

Estimated incidence

Screening, Prevention and Treatment

Hypertension

Pathophysiology

Estimated incidence

Screening, Prevention and Treatment

Diabetes

Pathophysiology

Estimated incidence

Screening, Prevention and Treatment

Other Endocrinopathies

Hypothyroidism

Growth hormone deficiency

Gonadal failure

Metabolic syndrome

Pathophysiology

Estimated incidence

Sarcopenic obesity

Screening, Prevention and Treatment

Summary

References

CHAPTER 27 Gastrointestinal complications

Introduction

Pre‐existing gastrointestinal conditions

Preconditioning‐related GI complications

Acute and subacute complications. Oral pain. Conditioning‐induced mucositis

Oral infections

Dysphagia and odynophagia

Nausea, vomiting, and diarrhea. Chemotherapy effects

aGVHD. Background

Symptoms

Biomarkers

Endoscopy

Histology

Radiology

Infection

Management

Abdominal pain. Neutropenic enterocolitis

Posttransplant lymphoproliferative disease

GI bleeding

Chronic complications. Introduction

Oral complications

Esophageal complications

Nausea, vomiting, abdominal pain, diarrhea

Late acute GI GVHD

Overlap cGVHD

Chronic GI GVHD

Infections

Medication adverse events

Pancreaticobiliary disease

Future directions

Financial support

Disclosures

References

CHAPTER 28 Hepatic Complications

Introduction

Initial evaluation

Iron overload. Background

Diagnosis

Management

Chronic hepatic graft‐versus‐host disease (GVHD) Background

Diagnosis

Management

Chronic hepatitis B (HBV) Background

Diagnosis

Management

Chronic hepatitis C (HCV) Background

Diagnosis

Management

Chronic hepatitis E (HEV) Background

Diagnosis

Management

Non‐alcoholic fatty liver disease (NAFLD) Background

Diagnosis

Management

Focal nodular hyperplasia (FNH) Background

Diagnosis

Management

Nodular regenerative hyperplasia (NRH) Background

Diagnosis

Management

Cirrhosis. Background

Diagnosis

Management

Hepatocellular carcinoma (HCC) Background

Diagnosis

Management

References

CHAPTER 29 Renal complications

Introduction

Acute kidney injury

Chronic kidney disease

Pathophysiology

Thrombotic microangiopathy

Proteinuria

Podocytopathy

Bk nephropathy

End stage renal disease

Strategies to prevent and mitigate kidney injury post HSCT

References

CHAPTER 30 Posttransplantation bone disease: prevalence, surveillance, prevention, and management

Introduction

Low Bone Mineral Density, Osteopenia and Osteoporosis. Pathophysiology

Radiation Therapy

Chemotherapy

Glucocorticoids

Calcineurin Inhibitors

Frequency/Cumulative Incidence

Risk Factors

Surveillance/Screening

Prevention

Treatment

Treatment Considerations in Children and Adolescents

Other Agents

Parathyroid hormone‐derived peptides

Selective Estrogen Receptor Modulators

RANK Ligand (RANKL) Inhibitors

Recommendation for the Survivor/General Practitioner

Avascular Necrosis. Pathophysiology

Frequency/Incidence

Risk Factors

Screening/Surveillance

Prevention

Treatment

Vascularized fibular graft (VFG)

Osteotomy

Recommendations for the Survivor and General Practitioner

References

CHAPTER 31 Late neurologic complications

Introduction

Pathophysiology

Frequency/cumulative incidence

Risk Factors

Clinical Entities. Infections

Cerebrovascular disease

Immune‐mediated disorders

Neurocognitive dysfunctions

Secondary CNS tumors

CNS disease relapse

Surveillance/ screening

Prevention

Recommendation for the survivors / general practitioner

References

CHAPTER 32 Neurocognitive dysfunction

Introduction

Definition and critical domains of neurocognitive dysfunction

Risk factors and correlates

Primary Disease

Conditioning Regimen

GVHD Prophylaxis and Immunosuppressive Therapies

Infections

Other Risk Factors and Correlates

Biomarkers as potential mechanisms

Biomarkers of CNS injury and neuroinflammation

Neuroimaging biomarkers

Neurocognitive dysfunction in adult patients with HCT

Presentation prior to HCT

Presentation throughout the course of HCT

Relevance of Neurocognitive Dysfunction

Neurocognitive dysfunction in special populations

Children

Youngest and Adolescent Young Adult (AYA) HCT Survivors

Older Adults

Assessment. General Recommendations

Test Measures

Self‐Report Measures and Clinical Interview

Recommendations regarding adult HCT survivors

Recommendations regarding pediatric HCT survivors

Interventions

Interventions to minimize therapy‐related neurocognitive toxicity

Management of acute CNS toxicities

Non‐pharmacologic interventions

Pharmacologic Interventions

Concluding remarks

References

CHAPTER 33 Psychological Distress

Introduction

Late survivorship

Screening for distress

Treatment

Pharmacological interventions

Non pharmacological interventions

Recommendations for the survivors/general practitioner

References

CHAPTER 34 Evaluation and management of fatigue in survivors of allogeneic hematopoietic stem cell transplantation

Introduction

Pathophysiology of Fatigue in HSCT Survivors

Frequency and Cumulative Incidence

Risk Factors

Screening and Evaluation

Pharmacologic and Non‐Pharmacologic Treatments for Fatigue

Pharmacologic interventions

Non‐pharmacologic interventions. Exercise, Physical Activity, and Structured Rehabilitation

Management of Concurrent Symptoms

Psychoeducational Interventions

Interventions to Improve Sleep Quality and Circadian Rhythmicity

Complementary and integrative therapies

Survivor Self‐Management Recommendations

Recommendations for Primary Care

Summary

References

CHAPTER 35 Social Issues

Introduction

Social Factors Associated with HCT Access and Outcomes. Socioeconomic and Sociodemographic Factors

Educational Status and Health Literacy

Geographical Factors

Caregiver Availability

Insurance Status

Influence of HCT on Social Well‐being. Financial Burden

Return to Previous Social Roles

Family Relationships

Relationship Between Social and Psychological Factors

Instruments to Assess Social Risks

Conclusion

References

CHAPTER 36 Health‐related quality of life in adult and pediatric survivors

Introduction

Quality of life

Clinical Features of Treatment with Allogeneic HSCT

Health‐related Quality of Life. Adults

Pediatrics

Physical Function. Adults

Pediatrics

Psychological function. Adult

Pediatric

Parental psychological function

Social and role functioning. Adults

Pediatrics

Benefit‐finding and post‐traumatic growth

Healthy lifestyle and health‐promoting behaviors

Application to practice. Adults

Pediatrics

Interventions. Adults

Pediatrics

Summary

References

CHAPTER 37 Immunosuppressive agents and monitoring in long‐term survivors

GVHD Prophylaxis Agents:

Calcineurin Inhibitors

Mycophenolate Mofetil

Sirolimus

Cyclophosphamide

Antithymocyte globulin

GVHD Treatment Agents

Corticosteroids

Ruxolitinib

Ibrutinib

Imatinib

Monoclonal Antibodies. Alemtuzumab

Tumor necrosis factor (TNF)‐α blockade

Rituximab

Basiliximab

References

CHAPTER 38 Nutritional support and nutritional supplementation

Introduction (Definition; subgroups)

Pathophysiology

Frequency/cumulative incidence

Risk factors

Surveillance/ screening

Prevention

Treatment

Recommendation for the survivors / general practitioner

References

CHAPTER 39 Daily routines and healthy lifestyle guidelines

Background

Education

Exercise

Diet

Physical safety and substances

Infection Prevention

Compliance with Scheduled Follow Up

Health Maintenance Screenings

Community/Home Support

Summary

References

CHAPTER 40 Prevalent psychosocial adjustment issues and solutions: lifestyle and social challenges

Introduction

The patient and their support system: coping with stress in the long‐term care setting

The patient and caregiver: facing intimacy issues

Other quality of life issues for the stem‐cell transplant patient

Conclusion

References

CHAPTER 41 Complementary and alternative medicine in HSCT

Introduction

Natural products in HCT recipients

Mind and body practices in HCT recipients

Mindfulness meditation, psychoeducation, and relaxation

Acupunctures and massage therapy

Music therapy and Art interventions

Other complementary and alternative medicine

Safety of complementary and alternative medicine

Approach to CAM discussions

Future directions

References

CHAPTER 42 Impact of adherence in outcome of long‐term survivors

Introduction. Case of unintentional non‐adherence

Case of intentional non‐adherence

Adherence

Non‐Adherence

Non‐intentional and intentional non‐adherence

HSCT a risk factor for non‐adherence

Recommendation for healthcare providers

How to assess and monitor adherence/incorporate adherence in daily care?

How to support survivors?

Future research

Conclusion

References

CHAPTER 43 Prominent role of allied health professionals

Introduction

Immunizations

First visit

Subsequent first‐year visits

Annual visits

References

CHAPTER 44 Patient reported outcomes

Introduction

Basic concepts about PROs

Perceived health status

Physical function and symptom burden post‐HCT

Psychological aspects post‐HCT

Social aspects post‐HCT

Behavioral aspects post‐HCT

PROs and GVHD

PROs as predictors of HCT survival

Conclusion

References

CHAPTER 45 Caregivers of long‐term survivors

Introduction

Frequency/cumulative incidence

Risk factors

Surveillance/ screening

Recommendation for the survivors/caregivers/general practitioner

References

CHAPTER 46 Patient’s perspective: memoir of a recovered lymphomaniac

Lilian

Living a normal Life

Hello Cancer

So, here we go!

Staging the Cancer

Staging and Sarah Cannon

Clinical Trials

Lymphomaniac

Remission

PET Scan and What's Next?

Vanderbilt Hematology and Stem Cell Clinic

Transplant Day

Now for the Fun Part: Four Months of Treatment

Going Home

Returning to Everyday Life

Twenty‐Three and Me / Ancestory.Com

Medical Surprises and Life for the past 10 Years

Blood Clots

More Post‐Transplant Medical Surprises

Colonoscopy

Colon Cancer Surgery

Tumor Board

Wake Up Call

Radiation Treatments

The Puppy from Hell

The Move to Florida

The last of the Cancer‐Related Episodes

The Continuation of the Story but not the End

So Much to be Thankful For

APPENDIX 1 Commonly used transplant‐related medications in long‐term survivors

References

APPENDIX 2 The eGVHD App

References

Index. A

B

C

D

E

F

G

H

I

J

K

L

M

N

O

P

Q

R

S

T

U

V

W

X

Y

Z

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Second Edition

.....

Christopher Koh MD, MHS Liver Disease Branch National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) National Institutes of Health Bethesda, MD, USA

Minako Iida MD Department of Promotion for Blood and Marrow Transplantation Aichi Medical University School of Medicine Nagakute, Japan

.....

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