Table 1

Summary of SIGN recommendations on long-term follow-up of survivors of childhood cancer

Late effectHigh-risk factorsSpecific late effectsScreening methods/ managementEvidence level/grade
Subsequent primary cancers (SPCs)Genetic predisposition, eg, NF-1Dependent on syndromeAs per guidance for specific syndromes
RadiotherapyDelayed presentation >5 years from treatment, at edge of radiation field (eg, mediastinal radiotherapy and breast SPCs)No consensus
Promote healthy lifestyle behaviours
3/C
Chemotherapy* (alkylating agents, epipodophyllotoxins)Increased risk of all SPCsNo consensus
Promote healthy lifestyle behaviours
3/C
Sub-/infertilityBoth sexes
 Cranial radiotherapyHypogonadotropic hypogonadism (pubertal arrest/ delay)See individual sections for assessment depending on sex3
 Pelvic radiotherapySexual dysfunctionConsider psychological referral3–4/D
Boys
 Chemotherapy* (alkylating agents)AzoospermiaSemen analysis±cryopreservation, FSH, inhibin B3/D
 Gonadal radiotherapy/ total body irradiation (TBI)Azoospermia
Hypergonadotropic hypogonadism (less likely—pubertal arrest/ delay, sexual dysfunction)
Semen analysis±cryopreservation, FSH, inhibin B
Regular pubertal assessment, LH, testosterone
±pubertal induction/ testosterone supplementation
2±3/D
Girls
 Chemotherapy* (alkylating agents)Hypergonadotropic hypogonadism (pubertal arrest/ delay/ oligoamenorrhoea)Regular pubertal assessment, FSH, AMH
±pubertal induction/ female hormone replacement therapy
±oocyte cryopreservation if postpubertal
3/D
 Abdominopelvic radiotherapyHypergonadotropic hypogonadism
Uterine dysfunction (premature delivery, low birth weight)
Cardiac effectsChemotherapy (anthracyclines)Congestive heart failureEchocardiography: Fractional shortening (FS) and ejection fraction (EF) measurements
2–3 yearly if anthracycline dose >250 mg/m2
5 yearly if anthracycline dose <250 mg/m2
Treat as per regular heart failure/cardiovascular disease guidelines
Promote healthy lifestyle behaviours
3–4/D
3/D
Cardiac/mediastinal radiotherapy Cardiovascular (especially coronary artery) disease
Bone healthChemotherapy (glucocorticoids, high dose methotrexate, 6-mercaptopurine)
Cranial radiotherapy
Bone marrow transplantation
Endocrine dysfunction (GH deficiency, hypogonadism, hypothyroidism)
Osteoporosis (osteonecrosis with glucocorticoids)Dual energy X-ray absorptiometry (DXA)/ peripheral quantitative CT/ quantitative ultrasound: BMD or bone mineral content (BMC) Z-scores adjusted for age, sex and height 2 years post-end of treatment
Serial measurements not required unless abnormal or clinical change
Sex steroid replacement
Promote healthy lifestyle behaviours
3/D
Metabolic syndromeALL (especially after bone marrow transplantation)
Brain tumours (especially after cranial radiotherapy and growth hormone deficiency)
Obesity
Dyslipidaemia
Insulin resistance
Cardiovascular disease
BP and BMI: Annually in all survivors
Fasting glucose, insulin, lipid profile:
2-yearly if obese/ overweight
5-yearly if normal weight
Treat as per regular obesity guidelines
3–4/D
Cognitive outcomesCranial radiotherapyCognitive decline
Psychosocial dysfunction
Neuropsychological assessment: Pretreatment and then annually3/D
GrowthCraniopharyngiomas (and other hypothalamopituitary tumours)Growth hormone deficiency
Pubertal delay/ arrest
Regular height monitoring
Pituitary function testing at diagnosis and regularly thereafter
2+/B-C
Cranial radiotherapyGrowth hormone deficiency
Precocious puberty
Pubertal delay/ arrest
Other pituitary hormone deficiencies
Regular height monitoring and pubertal assessment
Paediatric endocrinology referral if reduced height velocity
2+-2++/B-C
(Cranio) spinal radiotherapySpinal growth retardationRegular height monitoring+sitting height2+/B
Thyroid dysfunctionNeck, (cranio) spinal and total body irradiation
MIBG therapy
Primary hypothyroidism
Thyroid nodules
Thyroid cancer
Thyroid function tests: At end of treatment and then annually
Thyroid hormone replacement
No consensus about thyroid nodules/ cancer—patient education
2±2++/D
Cranial radiotherapySecondary/tertiary hypothyroidism
Chemotherapy?Unclear mechanism
  • *Clinicans should note that all chemotherapy may be associated with an increased risk of SPCs and sub-/infertility. ALL, acute lymphoblastic leukaemia; AMH, anti-Mullerian hormone; BMD, bone mineral density; BMI, body mass index; FSH, follicle-stimulating hormone; LH, luteinising hormone; MIBG, metaiodobenzylguanidine; NF-1, neurofibromatosis type 1; SIGN, Scottish Intercollegiate Guidelines Network.