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EMETOGENIC POTENTIAL OF ANTINEOPLASTIC AGENTS INTRAVENOUS/INJECTABLE AGENTS HIGH RISK (>90% frequency)† AC combination: any regimen containing anthracycline + Dacarbazine cyclophosphamide Doxorubicin ≥60mg/m² Carboplatin AUC ≥4 Epirubicin (Ellence) >90mg/m² Carmustine (BiCNU) >250mg/m² Ifosfamide (Ifex) ≥2g/m² per dose Cisplatin Mechlorethamine (Mustargen) Cyclophosphamide >1,500mg/m² Streptozocin (Zanosar) MODERATE RISK (>30–90% frequency)† Aldesleukin (Proleukin) >12−15 million IU/m² Dual-drug liposomal cytarabine + daunorubicin (Vyxeos) Amifostine (Ethyol) >300mg/m² (Unituxin) Arsenic trioxide (Trisenox) Doxorubicin <60mg/m²* Azacitidine (Vidaza) Epirubicin (Ellence) ≤90mg/m²* Bendamustine (Treanda) Idarubicin (Idamycin PFS) Busulfan (Busulfex) Ifosfamide (Ifex) <2g/m² per dose* Carboplatin AUC <4* Interferon alfa (Intron A) ≥10 million IU/m² Carmustine (BiCNU) ≤250mg/m²* (Camptosar)* Clofarabine (Clolar) Melphalan (Alkeran, Evomela) Cyclophosphamide ≤1,500mg/m² ≥250 mg/m²* Cytarabine >200mg/m² (Eloxatin)* Dactinomycin (Cosmegen)* Temozolomide (Temodar) Daunorubicin (Cerubidine)* Trabectedin (Yondelis)* LOW RISK (10–30% frequency)† Ado- emtansine (Kadcyla) Irinotecan liposomal (Onivyde) Aldesleukin (Proleukin) ≤12 million IU/m² Ixabepilone (Ixempra) Amifostine (Ethyol) ≤300mg/m² Methotrexate >50mg/m²−<250mg/m² Atezolizumab (Tecentriq) Mitomycin Belinostat (Beleodaq) Mitoxantrone (Blincyto) (Portrazza) (Adcetris) (Lartruvo) Cabazitaxel (Jevtana) Omacetaxine (Synribo) Carfilzomib (Kyprolis) Paclitaxel (Taxol) Cytarabine (low dose) 100−200mg/m² Paclitaxel-albumin (Abraxane) Docetaxel (Taxotere) Pemetrexed (Alimta) Doxorubicin liposomal (Doxil) Pentostatin Eribulin (Halaven) Pralatrexate (Folotyn) Etoposide (Etopophos) Romidepsin (Istodax) Floxuridine Talimogene laherparepvec (Imlygic) (5-FU) Thiotepa (Tepadina) Gemcitabine (Gemzar) Topotecan (Hycamtin) alfa (Intron A) >5−<10 million IU/m² Ziv-aflibercept (Zaltrap) MINIMAL RISK (<10% frequency)† Alemtuzumab (Campath) Nivolumab (Opdivo) (Bavencio) (Gazyva) Asparaginase (Erwinaze) (Arzerra) (Avastin) (Vectibix) Bleomycin Pegasparagase (Oncaspar) Bortezomib (Velcade) Peginterferon (Sylatron) (Erbitux) (Keytruda) (Perjeta) Cytarabine <100mg/m² Ramucirumab (Cyramza) Daratumumab (Darzalex) (Rituxan) Decitabine (Dacogen) Rituximab + hyaluronidase (Rituxan Hycela) (Ontak) (Sylvant) Dexrazoxane (Totect, Zinecard) (Torisel) (Imfinzi) Trastuzumab (Herceptin) (Empliciti) Valrubicin (Valstar) Fludarabine Vinblastine (Intron A) ≤5 million IU/m² Vincristine (Yervoy) Vincristine liposomal (Marqibo) Methotrexate ≤50mg/m² Vinorelbine (Navelbine) Nelarabine (Arranon) (continued) EMETOGENIC POTENTIAL OF ANTINEOPLASTIC AGENTS ORAL AGENTS MODERATE TO HIGH RISK (≥30% frequency)† Altretamine (Hexalen) (Rydapt) Busulfan (Myleran) ≥4mg/day Mitotane (Lysodren) (Zykadia) Niraparib (Zejula) (Xalkori) Olaparib (Lynparza) Cyclophosphamide ≥100mg/m²/day Panobinostat (Farydak) (Idhifa) Procarbazine (Matulane) Estramustine (Emcyt) Rucaparib (Rubraca) Etoposide Temozolomide (Temodar) >75mg/m²/day (Lenvima) Trifluridine/tipiracil (Lonsurf) Lomustine single day (Gleostine) MINIMAL TO LOW RISK (<30% frequency)† Abemaciclib (Verzenio) Mercaptopurine (Purinethol) (Gilotrif) Methotrexate (Alecensa) (Nerlynx) (Inlyta) (Tasigna) Bexarotene (Targretin) (Tagrisso) (Alunbrig) (Ibrance) (Bosulif) (Votrient) Busulfan (Myleran) <4mg/day Pomalidomide (Pomalyst) Cabozantinib (Cabometyx, Cometriq) (Iclusig) Capecitabine (Xeloda) (Stivarga) Chlorambucil (Leukeran) (Kisqali) (Cotellic) (Jakafi) Cyclophosphamide <100mg/m²/day Sonidegib (Odomzo) Dasatinib (Sprycel) (Nexavar) (Tafinlar) (Sutent) (Tarceva) Temozolomide (Temodar) ≤75mg/m²/day (Afinitor) (Thalomid) (Iressa) Thioguanine Hydroxyurea (Hydrea) Topotecan (Hycamtin) (Imbruvica) (Mekinist) Idelalisib (Zydelig) Tretinoin (Gleevec) (Caprelsa) Ixazomib (Ninlaro) (Zelboraf) (Tykerb) (Venclexta) (Revlimid) (Erivedge) Melphalan (Alkeran) Vorinostat (Zolinza) NOTES † Frequency of emesis in the absence of effective antiemetic prophylaxis. * May be highly emetogenic in certain patients. REFERENCES National Comprehensive Cancer Network. NCCN Clinical Practice Guidelines in Oncology: Antiemesis. Version 1.2018 – March 14, 2018. https://www.nccn.org/professionals/physician_gls/pdf/antiemesis.pdf. Accessed March 27, 2018. (Rev. 4/2018)