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Emetogenic Potential of Antineoplastic Agents

Emetogenic Potential of Antineoplastic Agents

EMETOGENIC POTENTIAL OF ANTINEOPLASTIC AGENTS High Risk (>90% frequency without ) AC combination: or (Ellence) + Doxorubicin IV: >60mg/m2 (Cytoxan) IV Epirubicin (Ellence) IV: >90mg/m2 (HMM, Hexalen) oral (Ifex) IV: ≥2g/m2 per dose (BCNU, BiCNU) IV: >250mg/m2 Mechlorethamine (Mustargen) IV (CDDP) IV (Matulane) oral Cyclophosphamide (CTX, Cytoxan) IV: >1,500mg/m2 Streptozocin (Zanosar) IV (DTIC, DTIC-Dome) IV Moderate Risk (30–90% frequency without antiemetics) Aldesleukin (IL-2, Proleukin) IV: >12–15 million IU/m2 Doxorubicin IV: ≤60mg/m2 Amifostine (Ethyol) IV: >300mg/m2 Epirubicin (Ellence) IV: ≤90mg/m2 trioxide (As2O3, Trisenox) IV Estramustine (Emcyt) oral (Vidaza) IV (VP-16) oral (Treanda) IV (Idamycin) IV (Busulfex) IV; oral: >4mg/day Ifosfamide (Ifex) IV: <2g/m2 Carboplatin IV Interferon alpha (IFN-alfa, Intron A) IV: ≥10 million IU/m2 Carmustine (BCNU, BiCNU) IV: ≤250mg/m2 (CPT-11, Camptosar) IV (Clolar) IV (CCNU, CeeNU) oral Cyclophosphamide (CTX, Cytoxan) IV: ≤1,500mg/m2 (L-PAM, Alkeran) IV Cyclophosphamide (CTX) oral ≥100mg/m2/day (MTX) IV: ≥250mg/m2 (ARA-C) IV: >200mg/m2 (Eloxatin) IV (Cosmegen) IV (Temodar) IV; oral >75mg/m2/day (Cerubidine) IV Low Risk (10–30% frequency without antiemetics) Aldesleukin (IL-2, Proleukin) IV: ≤12 million IU/m2 (Gemzar) IV Amifostine (Ethyol) IV: ≤300mg alpha (IFN-alfa, Intron A) IV: >5–<10 million IU/m2 Bexarotene (Targretin) oral (Ixempra) IV (Jevtana) IV Methotrexate (MTX) IV: >50mg/m2 to <250mg/m2 Capecitabine (Xeloda) oral Mitomycin (MTC) IV Cyclophosphamide (CTX) oral <100mg/m2/day Mitoxantrone (DHAD) IV Cytarabine (ARA-C) IV: 100–200mg/m2 (Taxol) IV (Taxotere) IV Paclitaxel albumin (Abraxane) IV Doxorubicin liposomal (Doxil) IV (Alimta) IV (Halaven) IV IV Etoposide (VP-16, Etopophos) IV (Folotyn) IV IV (Istodax) IV (Fludara) oral IV (5-FU) IV (Hycamtin) IV, oral Minimal Risk (<10% frequency without antiemetics) Alemtuzumab (Campath) IV Methotrexate (MTX) IV: ≤50mg/m2; oral (Avastin) IV (Arranon) IV IV Niltoinib (Tasigna) oral (Velcade) IV (Arzerra) IV Busulfan (Busulfex) oral: <4mg/day Panitumumab (Vectibix) IV Cetuximab (Erbitux) IV Pazopanib (Votrient) oral (Leukeran) oral Pegasparagase (Oncaspar) IV (2-CdA) IV Peginterferon IV Cytarabine (ARA-C) IV: <100mg/m2 Rituximab (Rituxan) IV Dasatinib (Sprycel) oral Sorafenib (Nexavar) oral (Dacogen) IV Sunitinib (Sutent) oral Denileukin diftitox (Ontak) IV (Torisel) IV (Totect, Zinecard) IV Temozolamide (Temodar) oral: ≤75mg/m2/day (Tarceva) oral (Thalomid) oral (Afinitor, Zortress) oral Thioguanine (6-TG, Tabloid) oral Fludarabine (Fludara) IV Trastuzumab (Herceptin) IV Hydroxyurea (Hydrea) oral (Vesanoid) oral (Gleevec) oral (Valstar) IV Interferon alpha (IFN-alfa, Intron A) IV: ≤5 million IU/m2 Vandetanib (Caprelsa) oral (Yervoy) IV (VLB) IV (Tykerb) oral (VCR) IV (Revlimid) oral (Navelbine) IV Melphalan (L-PAM, Alkeran) oral (Zolinza) oral (Purinethol) oral Daily use of antiemetics is not recommended based on clinical experience. REFERENCES Adapted from: 1. Kris MG, Hesketh PJ, Somerfield MR, et al. American Society of Clinical Guideline for Antiemetics in Oncology: Update 2006. J Clin Oncol 2006;24:2932–2947. 2. National Comprehensive Network. NCCN Clinical Practice Guidelines in Oncology; v.1.2012: Antiemesis. Available at: http://www.nccn.org/professionals/physician_gls/PDF/antiemesis.pdf. Accessed August 8, 2012. (Rev. 6/2014)