01Covered for commercial medical plans when each cancer's initial approval criteria are met: Kaposi sarcoma; breast cancer that is recurrent or metastatic, has no response to preoperative systemic therapy, or where albumin-bound paclitaxel substitutes for paclitaxel or docetaxel because of hypersensitivity or contraindication to standard hypersensitivity premedications; subsequent treatment of metastatic or unresectable cutaneous melanoma, alone or with carboplatin; subsequent single-agent treatment of endometrial carcinoma; epithelial ovarian, fallopian tube or primary peritoneal cancer that is persistent or recurrent, or where it substitutes for paclitaxel due to hypersensitivity; biliary tract cancer with gemcitabine when unresectable, R2 or metastatic, or as neoadjuvant therapy for resectable locoregionally advanced gallbladder cancer that does not present as jaundice; non-small cell lung cancer that is recurrent, advanced or metastatic, or where it substitutes for paclitaxel or docetaxel due to hypersensitivity; pancreatic adenocarcinoma with gemcitabine with or without cisplatin; advanced or metastatic small bowel adenocarcinoma; uveal melanoma that is metastatic or unresectable; ampullary adenocarcinoma with gemcitabine; subsequent single-agent treatment of persistent, recurrent or metastatic cervical cancer; subsequent treatment of platinum-resistant locally advanced or metastatic bladder cancer; and subsequent single-agent treatment of recurrent or metastatic vaginal cancer.
02Claims for these need documentation that the criteria for the specific cancer are met.
03HCPCS J9264 (injection, paclitaxel protein-bound particles, 1 mg) is covered when those selection criteria are met.
04Dosing: 260 mg/m2 intravenously over 30 minutes every 3 weeks for metastatic breast cancer; 100 mg/m2 intravenously over 30 minutes on days 1, 8 and 15 of each 21-day cycle, with carboplatin given on day 1 immediately after, for non-small cell lung cancer; and 125 mg/m2 intravenously over 30 to 40 minutes on days 1, 8 and 15 of each 28-day cycle, with gemcitabine given immediately after, for pancreatic adenocarcinoma.
05Dose adjustments vary by indication and are described in the full prescribing information.
06ICD-10 codes C33 through C34.92 are covered for non-small cell lung cancer but not for small cell lung cancer.
07ICD-10 codes C43.0 through C43.9 and D03.0 through D03.9 for melanoma are not covered for hepatic arterial infusion of albumin-bound paclitaxel for metastatic melanoma to the liver.
08Hepatic arterial infusion for metastatic melanoma to the liver is experimental, investigational, or unproven.
09The combination of albumin-bound paclitaxel and sintilimab is experimental, investigational, or unproven for gastric cancer and soft tissue sarcoma.
10Medicare criteria are not in this policy and are found in the separate Medicare Part B criteria.