Information requested to support prior authorization review; not explicit coverage rules but used for medical necessity evaluation.
Patient identifying information: patient name, Cigna ID, date of birth, address, phone
Physician information: physician name, specialty, DEA, NPI or TIN, office contact, phone, fax, address
Urgency selection: Standard or Urgent (if Urgent attest that standard review may seriously jeopardize life/health/ability to regain function)
Medication requested: Erbitux (cetuximab); indicate new start Yes/No, start date, dose, frequency, length of therapy
Treatment logistics: where medication will be obtained (Accredo Specialty Pharmacy, prescriber's office stock, retail pharmacy, home health/home infusion vendor, other)
Facility/dispensing info: facility name, state, tax ID, address
Home infusion candidate and availability of in-office infusion site
Indication selection: colorectal cancer (CRC), head/neck cancer, non-small cell lung cancer (NSCLC), penile cancer, skin cancer, other (specify)
Biomarker and disease-specific questions (KRAS/NRAS wild-type; if CRC advanced/metastatic; EGFR expression; BRAF V600E presence and metastatic disease; combination with encorafenib (Braftovi) if V600E)
Head/neck specific: whether given with radiation as primary treatment; new start vs continuation; if continuation, weeks already received; whether squamous cell carcinoma (head/neck or skin); for skin whether regional recurrence, distant metastases or inoperable positive regional lymph nodes
Penile specific: will be used as single agent therapy; metastatic disease if NSCLC or penile; NSCLC: second-line chemotherapy; NSCLC: combination with afatinib (Gilotrif); NSCLC EGFR-positive disease and prior progression on Gilotrif, Iressa, Tarceva
Additional clinical information: disease stage, prior therapy, performance status, names/doses/admin schedule of concurrent agents
Prescriber attestation and signature with date