Paeds · haematology-oncology-and-transfusion
Cancer therapy complications and supportive care
Also known as Chemotherapy-induced nausea and vomiting · Oral mucositis · Anthracycline cardiotoxicity · Chemotherapy supportive care · Tumour lysis syndrome · Febrile neutropenia
Fellowship guide to the complications of anticancer therapy and the supportive care that surrounds it in children. Covers chemotherapy-induced nausea and vomiting risk-stratified and treated with a 5-HT3 antagonist plus dexamethasone plus aprepitant, oral mucositis graded on the WHO scale and prevented with cryotherapy, photobiomodulation, and palifermin, anthracycline cardiotoxicity prevented and surveilled with dexrazoxane and echocardiography, febrile neutropenia defined by a temperature at or above 38.3 degrees with an absolute neutrophil count under 500 treated with empiric antibiotics within one hour, and tumour lysis syndrome classified by the Cairo-Bishop criteria and prevented with hydration, allopurinol, and rasburicase.
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- A child on chemotherapy with a single oral temperature at or above 38.3 degrees, or at or above 38.0 degrees sustained for an hour, has febrile neutropenia when the absolute neutrophil count is under 500, and needs cultures and an empiric broad-spectrum antipseudomonal beta-lactam within one hour
- A child receiving an anthracycline who develops a gallop, a rising heart rate, breathlessness, or a falling ejection fraction has anthracycline cardiotoxicity and needs urgent echocardiography and cardiology review
- A child with high tumour burden starting therapy who develops a rising potassium, phosphate, or uric acid with a falling urine output has tumour lysis syndrome and needs aggressive hydration and rasburicase
- Severe oral mucositis of WHO grade 3 or 4 that stops a child eating or drinking risks dehydration, secondary sepsis, and opioid need, and warrants analgesia, nutritional support, and infection surveillance
- A chemotherapy drug that extravasates outside the vein causes local tissue necrosis, and anthracycline extravasation needs prompt dexrazoxane treatment within six hours rather than waiting for the lesion to declare itself
- Uncontrolled acute chemotherapy-induced nausea and vomiting on day one predicts refractory nausea through the whole cycle, so prophylaxis is matched to the emetogenic risk of the regimen before the first dose
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- Risk-stratifies chemotherapy regimens by emetogenic potential and matches the antiemetic combination to the risk
- Grades oral mucositis on the WHO scale and gives cryotherapy, oral care, and analgesia for prevention and treatment
- Recognises that a febrile child on chemotherapy needs cultures and an empiric antipseudomonal beta-lactam within one hour
- Explains how anticancer agents injure tissue through free-radical and cytokine pathways, producing nausea, mucosal breakdown, cardiomyocyte death, and tumour lysis
- Coordinates dexrazoxane cardioprotection and echocardiographic surveillance across the anthracycline exposure and into survivorship
- Appraises the Dupuis pediatric antiemetic guideline, the MASCC and ISOO mucositis guideline, the dexrazoxane harmonisation and Chow studies, and the Cairo-Bishop tumour lysis classification
- High emetogenic regimens such as cisplatin and high-dose cyclophosphamide receive a 5-HT3 antagonist plus dexamethasone plus aprepitant
- Febrile neutropenia is a single temperature at or above 38.3 degrees with an absolute neutrophil count under 500, treated with empiric antibiotics within one hour
- Anthracycline cardiotoxicity risk is dose-dependent and reduced by dexrazoxane at a ten-to-one ratio with the doxorubicin dose
- Leads the supportive-care bundle for a child receiving high-dose conditioning for transplant, linking mucositis, neutropenia, and nutrition
- Builds the tumour lysis prevention plan for a child with high tumour burden, choosing rasburicase over allopurinol after excluding G6PD deficiency
- Counsels a family on the long-term cardiac surveillance that follows anthracycline exposure through childhood into survivorship
- Level 1: Recognition of the unwell child on chemotherapy and the need to escalate for fever, dehydration, or cardiac signs
- Level 2: Applies the febrile neutropenia pathway, the antiemetic risk stratification, and the mucositis grading at the bedside
- Level 3: Coordinates the multidisciplinary supportive-care and survivorship plan across anthracycline cardioprotection and tumour lysis prevention
- The emetogenic risk categories and the matching antiemetic combinations for each
- The WHO mucositis grading scale and the evidence-based preventive interventions of cryotherapy, photobiomodulation, and palifermin
- The Cairo-Bishop classification of tumour lysis syndrome and the role of rasburicase for high-risk patients
- Structured assessment of the child on chemotherapy presenting with fever, oral pain, vomiting, breathlessness, or reduced urine output
- Communication with the family about the predictable side effects of a regimen and the supportive plan that manages each one
- Recognition of the red flags of febrile neutropenia, anthracycline cardiotoxicity, and tumour lysis syndrome at the bedside
- Chemotherapy-induced nausea and vomiting risk stratification and the three-drug prophylaxis for high emetogenic regimens
- Dexrazoxane for anthracycline cardioprotection and echocardiographic surveillance in survivors
- Empiric antipseudomonal beta-lactam for febrile neutropenia and the definition of the low-risk child eligible for oral therapy
- Recognition of the major toxicity classes of anticancer therapy and the supportive intervention for each
- Application of the Dupuis and MASCC antiemetic, MASCC and ISOO mucositis, dexrazoxane, and fever-and-neutropenia guidelines
- Avoidance of harm from delayed antibiotics in febrile neutropenia, from urinary alkalinisation in tumour lysis, and from unrecognised extravasation
- Canadian approach to febrile neutropenia with the IPSG criteria for low-risk oral management
- Dexrazoxane cardioprotection and the long-term cardiac follow-up of the childhood cancer survivor
- The supportive-care bundle that keeps the child on chemotherapy safe from nausea, mucositis, cardiotoxicity, and tumour lysis
Overview & Definition
A child who begins treatment for cancer steps into a landscape of predictable toxicity, and the team that knows the terrain can keep the child safe while the antineoplastic drugs do their work. The cure of childhood cancer now exceeds 80 percent across the high-income world, and a large share of that survival rests not on the chemotherapy alone but on the supportive care that surrounds it. Anticancer agents are blunt by design, because they target the rapidly dividing cell, and the same property that kills the leukaemic blast or the lymphoma cell also strips the gastrointestinal mucosa, suppresses the marrow, irritates the vomiting centre, and scars the heart. The fellow who masters the supportive care of childhood cancer masters the difference between a child who completes treatment and one who is broken by it. [3][9]
Three toxicities carry the highest yield for the exam and the highest stakes at the bedside, and they form the spine of this topic. The first is chemotherapy-induced nausea and vomiting, complication child fears most before treatment begins, which is prevented by matching the antiemetic combination to the emetogenic risk of the regimen. The second is oral mucositis, the painful ulceration of the mucosal barrier that opens the door to dehydration, opioid need, and bloodstream infection, graded on the World Health Organization scale and prevented with cryotherapy, photobiomodulation, and palifermin. The third is anthracycline cardiotoxicity, the cumulative injury to the cardiomyocyte that threatens the survivor long after the cancer is cured, reduced by dexrazoxane and watched with echocardiography. [1][4][6]
Three further supportive-care domains sit alongside these three and complete the picture. Febrile neutropenia is the emergency that arises when the marrow is suppressed and a single fever signals a possible bloodstream infection, and it is treated with an empiric antibiotic within the hour. Tumour lysis syndrome is the metabolic storm that follows the rapid destruction of a sensitive tumour, classified by the Cairo-Bishop criteria and prevented with hydration and uric-acid control. Extravasation is the local catastrophe of a vesicant drug that leaks outside the vein, and the anthracycline spill needs dexrazoxane within hours rather than watchful waiting. The fellow who holds these six domains holds the supportive care of childhood cancer. [9][10][7]
References12ShowHide
- [1]Dupuis LL, Boodhan S, Holdsworth M Guideline for the prevention of acute nausea and vomiting due to antineoplastic medication in pediatric cancer patients. Pediatr Blood Cancer, 2013.PMID 23512831
- [2]Molassiotis A, Aapro M, Herrstedt J MASCC/ESMO Antiemetic Guidelines: Introduction to the 2016 guideline update. Support Care Cancer, 2017.PMID 27501964
- [3]Navari RM Management of Chemotherapy-Induced Nausea and Vomiting in Pediatric Patients. Paediatr Drugs, 2017.PMID 28447301
- [4]Elad S, Cheng KKF, Lalla RV MASCC/ISOO clinical practice guidelines for the management of mucositis secondary to cancer therapy. Cancer, 2020.PMID 32786044
- [5]Robijns J, Nair RG, Lodewijckx J Photobiomodulation therapy in management of cancer therapy-induced side effects: WALT position paper 2022. Front Oncol, 2022.PMID 36110957
- [6]de Baat EC, van Dalen EC, Mulder RL Primary cardioprotection with dexrazoxane in patients with childhood cancer who are expected to receive anthracyclines: recommendations from the International Late Effects of Childhood Cancer Guideline Harmonization Group. Lancet Child Adolesc Health, 2022.PMID 36174614
- [7]Chow EJ, Aggarwal S, Doody DR Dexrazoxane and Long-Term Heart Function in Survivors of Childhood Cancer. J Clin Oncol, 2023.PMID 36669148
- [8]Mavinkurve-Groothuis AMC, de Baat EC, Feijen EAM Comment on: Cardiotoxicity in children with cancer treated with anthracyclines: A position statement on dexrazoxane. Pediatr Blood Cancer, 2023.PMID 37505793
- [9]Lehrnbecher T, Robinson PD, Ammann RA Guideline for the Management of Fever and Neutropenia in Pediatric Patients With Cancer and Hematopoietic Cell Transplantation Recipients: 2023 Update. J Clin Oncol, 2023.PMID 36689694
- [10]Cairo MS, Bishop M Tumour lysis syndrome: new therapeutic strategies and classification. Br J Haematol, 2004.PMID 15384972
- [11]Bansal N, Joshi C, Adams MJ Cardiotoxicity in pediatric lymphoma survivors. Expert Rev Cardiovasc Ther, 2021.PMID 34958622
- [12]Freifeld AG, Pizzo PA The outpatient management of febrile neutropenia in cancer patients. Oncology (Williston Park), 1996.PMID 8723296