Clinical Tools and Resources for Self-Study and Patient Education

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Clinical Tools and Resources for Self-Study and Patient Education CHEMOTHERAPY-INDUCED NAUSEA AND VOMITING CLINICIAN'S RESOURCE GUIDE The clinical tools and resources contained herein are provided as

1 Clinical Tools and Resources for Self-Study and Patient Education CHEMOTHERAPY-INDUCED NAUSEA AND VOMITING CLINICIAN'S RESOURCE GUIDE The clinical tools and resources contained herein are provided as educational adjuncts to the CE-certified online activity, Preventing and Mitigating Chemotherapy-Induced Nausea and Vomiting in High-Risk Patients. To access the activity and earn CE credit visit: CONTENTS I: MASCC Antiemesis Tool (MAT)... 2 II: NCI-CTCAE Version 4.03: Chemotherapy-Induced Nausea and Vomiting... 3 III: Functional Living Index-Emesis (FLIE)... 4 IV: Rhodes Index of Nausea, Vomiting, and Retching (INVR)... 5 V: Emetic Risk of Intravenous Antineoplastic Agents: High and Moderate... 6 VI: Emetic Risk of Oral Antineoplastic Agents... 7 VII: Online Nausea and Vomiting Risk Assessment Tool: 8 VIII: Types of Chemotherapy-Induced Nausea and Vomiting... 9

2 071CINV Reference Guide Page 2 of 9 I: MASCC ANTIEMESIS TOOL (MAT) Multinational Association of Supportive Care in Cancer.

3 071CINV Reference Guide Page 3 of 9 II: NCI-CTCAE VERSION 4.03: CHEMOTHERAPY-INDUCED NAUSEA AND VOMITING Adverse Event Grade 1 Grade 2 Grade 3 Grade 4 Grade 5 Nausea Loss of appetite without alteration in eating habits Oral intake decreased without significant weight loss, dehydration, or malnutrition Inadequate oral caloric or fluid intake; tube feeding, TPN, or hospitalization indicated - - Vomiting 1 2 episodes (separated by 5 min) in 24 hr 3 5 episodes (separated by 5 min) in 24 hr 6 episodes (separated by 5 min) in 24 hr; tube feeding, TPN, or hospitalization indicated Lifethreatening consequences; urgent intervention indicated Death National Cancer Institute (2010). National Cancer Institute Common Terminology Criteria for Adverse Events. V4.03. Available at: NCI-CTCAE = National Cancer Institute Common Terminology Criteria for Adverse Events. TPN = Total parenteral nutrition.

4 071CINV Reference Guide Page 4 of 9 III: FUNCTIONAL LIVING INDEX-EMESIS (FLIE) Item How much nausea (vomiting) have you had in the past 3 days? a Has nausea (vomiting) affected your ability to maintain usual recreation or leisure activities in the past 3 days? Has nausea (vomiting) affected your ability to complete your usual household tasks during the past 3 days? How much has nausea (vomiting) affected your ability to enjoy a meal in the past 3 days? How much has nausea (vomiting) affected your ability to enjoy liquid refreshment in the past 3 days? How much has nausea (vomiting) affected your willingness to see and spend time with family and friends in the past 3 days? Rating 1 = None/Not at all; 7 = A great deal Has nausea (vomiting) affected your daily functioning in the past 3 days? Rate the degree to which nausea (vomiting) has imposed a hardship on you (personally) in the past 3 days. Rate the degree to which nausea (vomiting) has imposed a hardship on those closest to you in the past 3 days. a The phrase "in the past 3 days" can be adjusted. Adapted from O Brien BJ, Rusthoven J, Rocchi A, et al (1993). Impact of chemotherapy-associated nausea and vomiting on patients functional status and on costs: survey of five Canadian centres. CMAJ, 149(3):

5 071CINV Reference Guide Page 5 of 9 IV: RHODES INDEX OF NAUSEA, VOMITING, AND RETCHING (INVR) Molassiotis A, Russell W, Hughes J, et al (2013). The effectiveness and cost-effectiveness of acupressure for the control and management of chemotherapy-related acute and delayed nausea: assessment of nausea in chemotherapy research (ANCHoR), a randomised controlled trial. Health Technol Assess, 17(26): DOI:10.331/hta17260

6 071CINV Reference Guide Page 6 of 9 V: EMETIC RISK OF INTRAVENOUS ANTINEOPLASTIC AGENTS: HIGH AND MODERATE Emetic Risk Agents High Emesis has been documented to occur in more than 90% of patients AC combination defined as any chemotherapy regimen that contains an anthracycline and cyclophosphamide Carboplatin AUC 4 Carmustine >250 mg/m 2 Cisplatin Cyclophosphamide 1,500 mg/m 2 Dacarbazine Doxorubicin 60 mg/m 2 Epirubicin >90 mg/m 2 Ifosfamide 2 g/m 2 per dose Mechlorethamine Streptozotocin Moderate Emesis has been documented to occur in 30% to 90% of patients Aldesleukin >12-15 million IU/m 2 Amifostine >300 mg/m 2 Arsenic trioxide Azacitidine Bendamustine Busulfan Carboplatin AUC <4 Carmustine 250 mg/m 2 Clofarabine Cyclophosphamide (<1,500 mg/m 2 ) Cytarabine >200 mg/m 2 Dactinomycin Daunorubicin Dinotuximab Doxorubicin <60 mg/m 2 Epirubicin 90 mg/m 2 Idarubicin Ifosfamide <2 g/m 2 per dose Interferon alfa 10 million IU/m 2 Irinotecan Melphalan Methotrexate 250 mg/m 2 Oxaliplatin Temozolomide Trabectedin Adapted from National Comprehensive Cancer Network (2017). NCCN Clinical Practice Guidelines in Oncology: antiemesis. Version Available at: AC = doxorubicin hydrochloride/cyclophosphamide; AUC = area under the concentration-time curve; IU = international unit.

7 071CINV Reference Guide Page 7 of 9 VI: EMETIC RISK OF ORAL ANTINEOPLASTIC AGENTS Emetic Risk Agents Moderate to High 30% frequency of emesis Altretamine Busulfan 4 mg/d Ceritinib Crizotinib Cyclophosphamide 100 mg/m 2 /d Estramustine Etoposide Lenvatinib Lomustine (single day) Mitotane Olaparib Panobinostat Procarbazine Rucaparib Temzolomide >75 mg/m 2 /d Trifluridine/tipiracil Adapted from National Comprehensive Cancer Network (2017). NCCN Clinical Practice Guidelines in Oncology: antiemesis. Version Available at:

8 071CINV Reference Guide Page 8 of 9 VII: ONLINE NAUSEA AND VOMITING RISK ASSESSMENT TOOL:

9 071CINV Reference Guide Page 9 of 9 VIII: TYPES OF CHEMOTHERAPY-INDUCED NAUSEA AND VOMITING Acute Delayed Anticipatory Breakthrough Refractory Occurs and resolves within 24 hours of chemotherapy Typically peaks within 5-6 hours Occurs 1-5 days after chemotherapy Common with administration of cisplatin, carboplatin, cyclophosphamide, and doxorubicin Feeling of nausea or vomiting prior to chemotherapy Conditioned response Occurs in 25-50% of patients Occurs despite prophylactic treatment Requires rescue therapy Can be acute or delayed Occurs during chemotherapy cycle after prophylaxis and/or rescue therapy has failed in earlier cycles Adapted from National Comprehensive Cancer Network (2017). NCCN Clinical Practice Guidelines in Oncology: antiemesis. Version Available at:

Corporate Medical Policy

Antiemetic Injection Therapy Corporate Medical Policy File Name: Origination: Last CAP Review: Next CAP Review: Last Review: antiemetic_injection_therapy 5/2015 3/2017 3/2018 3/2017 Description of Procedure