How to Get Somatuline Depot (lanreotide) Covered by Blue Cross Blue Shield in Ohio: Prior Authorization Forms, Appeals, and Timeline Guide

Answer Box: Getting Somatuline Depot Covered in Ohio

Blue Cross Blue Shield (BCBS) plans in Ohio typically require prior authorization for Somatuline Depot (lanreotide) with specific criteria for acromegaly, GEP-NETs, and carcinoid syndrome. Most plans limit coverage to one syringe per 28 days (maximum 120 mg every 4 weeks) and may require step therapy with octreotide first.

Fastest path to approval:

  1. Verify your exact BCBS Ohio plan type (Anthem is the primary licensee)
  2. Download the lanreotide prior authorization form from your plan's provider portal
  3. Submit complete documentation including diagnosis, prior treatments, and specialist consultation

Start today: Call the member services number on your ID card to confirm formulary status and obtain the current PA form.

Table of Contents

  1. What This Guide Covers
  2. Before You Start: Plan Verification
  3. Gather Required Documentation
  4. Submit the Prior Authorization Request
  5. Follow-Up and Tracking
  6. Typical Approval Timelines
  7. Handling Requests for Additional Information
  8. If Your Request is Denied
  9. Renewal and Reauthorization
  10. Quick Reference Checklist
  11. FAQ

What This Guide Covers

This comprehensive guide helps patients, caregivers, and healthcare providers navigate the prior authorization process for Somatuline Depot (lanreotide) with Blue Cross Blue Shield plans in Ohio. We'll walk through each step from initial verification to appeals, including specific forms, timelines, and contact information for Ohio BCBS plans.

Who this helps:

  • Patients with acromegaly, gastroenteropancreatic neuroendocrine tumors (GEP-NETs), or carcinoid syndrome
  • Healthcare providers submitting PA requests
  • Caregivers advocating for family members

Expected outcomes: With proper documentation and adherence to plan criteria, most medically appropriate requests for FDA-approved indications are approved within 72 hours to 15 business days.

Before You Start: Plan Verification

Identify Your Exact BCBS Ohio Plan

Ohio's primary Blue Cross Blue Shield licensee is Anthem Blue Cross and Blue Shield. However, plan requirements vary by product type:

  • Commercial/Employer plans (individual, small group, large group)
  • ACA Marketplace plans
  • Medicare Advantage (MAPD)
  • Medicaid managed care

Action step: Look at your ID card for the specific product name (e.g., "Anthem Blue Access PPO," "Medicare Preferred PPO") and note any pharmacy benefit manager (PBM) listed.

Check Formulary Status

Before submitting a PA request, verify that Somatuline Depot is on your plan's formulary:

  1. Visit Anthem Ohio's drug list search (verify with the source linked)
  2. Search for "Somatuline Depot" or "lanreotide"
  3. Note the tier placement (typically Specialty/Tier 4) and any restrictions (PA, ST, QL)

Coverage at a Glance:

Requirement What It Means Typical Status
Prior Authorization (PA) Clinical review required before coverage Required for most BCBS plans
Formulary Tier Cost-sharing level Specialty Tier 4 (highest copay)
Step Therapy (ST) Must try preferred alternative first Often required - octreotide trial
Quantity Limits (QL) Maximum amount per fill period 1 syringe per 28 days
Site of Care Where drug can be administered Office, outpatient hospital, or home

Gather Required Documentation

Essential Clinical Information

Based on BCBS/FEP Blue's 2024 lanreotide policy, prepare the following:

For all indications:

  • Patient age ≥18 years
  • Specific ICD-10 diagnosis code
  • Prescriber specialty (endocrinology, oncology, or gastroenterology preferred)
  • Planned dose and frequency (60-120 mg every 4 weeks)

For Acromegaly:

  • Inadequate response or contraindication to surgery and/or radiotherapy
  • Elevated GH and/or IGF-1 levels (with reference ranges)
  • Endocrinology consultation notes

For GEP-NETs:

  • Confirmed neuroendocrine tumor of GI tract, pancreas, lung, thymus, or adrenal gland
  • Metastatic or unresectable disease status
  • Positive somatostatin scintigraphy or hormone-related symptoms
  • Oncology or gastroenterology consultation

For Carcinoid Syndrome:

  • Clinical symptoms (flushing, diarrhea)
  • Elevated 24-hour urinary 5-HIAA or chromogranin A
  • Documentation of NET with hormone-related symptoms

Prior Therapy Documentation

Many BCBS plans require step therapy with octreotide. Document:

  • Previous octreotide (short-acting or LAR) use and response
  • Reasons for inadequate response, intolerance, or contraindication
  • Other prior treatments attempted (surgery, radiation, dopamine agonists)

Submit the Prior Authorization Request

Step-by-Step Submission Process

Step 1: Obtain the PA Form

  • Access your plan's provider portal or call the provider services number
  • Request the "lanreotide (Somatuline Depot)" or "somatostatin analogs" PA form
  • Anthem providers can access forms here (verify current link)

Step 2: Complete Documentation

  • Fill out all required fields completely
  • Attach supporting clinical notes, lab results, and imaging reports
  • Include prescriber attestation and signature

Step 3: Submit via Preferred Channel

  • Provider portal: Most efficient method with real-time tracking
  • Fax: Use the fax number specified on the PA form
  • Phone: For urgent cases, call the number on the provider portal

Step 4: Request Expedited Review if Appropriate

Tip: Submit requests early in the week and before 2 PM to avoid weekend delays in processing.

Follow-Up and Tracking

When to Follow Up

  • Initial follow-up: 48-72 hours after submission for urgent cases
  • Standard follow-up: 5-7 business days for routine requests
  • If no response: Contact member services using the number on your ID card

What to Track

  • PA reference number
  • Date of submission
  • Reviewer contact information
  • Any additional information requests
  • Decision date and authorization number (if approved)

Sample Follow-Up Script: "I'm calling to check on a prior authorization request for lanreotide (Somatuline Depot) submitted on [date]. The reference number is [number]. Can you provide a status update and expected decision date?"

Typical Approval Timelines

Ohio-Specific Requirements

For BCBS plans regulated by Ohio:

Commercial Plans:

  • Standard PA: Up to 15 business days
  • Expedited PA: 72 hours with medical urgency certification

Medicare Advantage:

Factors That Speed Approval

  • Complete documentation on first submission
  • FDA-approved indication with clear medical necessity
  • Specialist (endocrinologist/oncologist) involvement
  • Prior therapy documentation that meets step therapy requirements

Factors That Slow Approval

  • Missing clinical information
  • Off-label use without compendial support
  • Incomplete prior therapy documentation
  • Non-specialist prescriber for complex cases

Handling Requests for Additional Information

Common Information Requests

Medical Necessity Questions:

  • Specific lab values (GH, IGF-1, 5-HIAA)
  • Imaging results showing tumor burden or progression
  • Detailed prior therapy history with dates and outcomes

Dosing Clarifications:

  • Justification for doses >120 mg every 4 weeks
  • Explanation of dosing frequency (every 4 vs. 6-8 weeks)
  • Site of care requirements for administration

Response Strategy

  1. Respond quickly - usually within 5-10 business days
  2. Address each question specifically with clinical rationale
  3. Include relevant guidelines (FDA label, NCCN, endocrine society recommendations)
  4. Provide additional specialist consultation if requested
Note: Counterforce Health helps patients and providers turn insurance denials into targeted, evidence-backed appeals by analyzing denial letters and plan policies to draft point-by-point rebuttals with the right clinical evidence and procedural requirements.

If Your Request is Denied

Common Denial Reasons and Solutions

Denial Reason How to Address
"Criteria not met" Review plan policy point-by-point; provide missing documentation
"Step therapy required" Document octreotide trial/failure or contraindication
"Off-label use" Provide compendial references (NCCN) or peer-reviewed literature
"Quantity limit exceeded" Justify dosing with FDA label and clinical necessity

Appeals Process in Ohio

Level 1: Internal Appeal

  • File within plan's specified timeframe (usually 180 days)
  • Include additional clinical evidence and specialist letters
  • Request expedited review for urgent cases

Level 2: External Review

Ohio Department of Insurance Resources:

Peer-to-Peer Review

Many BCBS plans offer peer-to-peer review before formal appeals:

How to request:

  • Call the medical director or utilization management department
  • Request a clinical discussion between prescriber and plan medical director
  • Prepare clinical rationale and be ready to discuss alternatives

Renewal and Reauthorization

When to Reauthorize

Most BCBS plans approve Somatuline Depot for:

  • Initial approval: 3 months
  • Renewal approval: 12 months

Calendar reminder: Submit renewal requests 30-45 days before expiration to avoid gaps in coverage.

Renewal Documentation

For continued approval, provide:

  • Clinical benefit documentation (lab improvements, symptom control)
  • No disease progression or unacceptable toxicity
  • Continued specialist management
  • Updated dosing if changed from initial approval

Quick Reference Checklist

Before Submitting PA:

  • Verify exact BCBS Ohio plan type
  • Confirm Somatuline Depot is on formulary
  • Check for step therapy requirements
  • Gather all clinical documentation

PA Submission Packet:

  • Completed PA form
  • Diagnosis with ICD-10 code
  • Prior therapy documentation
  • Specialist consultation notes
  • Recent lab results
  • Prescriber attestation

After Submission:

  • Record PA reference number
  • Set follow-up reminder (5-7 days)
  • Prepare for potential information requests
  • Know your appeal rights and deadlines

FAQ

How long does BCBS prior authorization take in Ohio? Standard requests: up to 15 business days for commercial plans, 72 hours for Medicare Advantage. Expedited requests: 24-72 hours depending on plan type.

What if Somatuline Depot is non-formulary on my plan? You can request a formulary exception with clinical justification. Provide documentation that preferred alternatives are inappropriate or have failed.

Can I request an expedited appeal in Ohio? Yes, if delay would seriously jeopardize your health. Your prescriber must certify medical urgency, and Ohio law provides for expedited external review within 72 hours.

Does step therapy apply if I failed octreotide outside Ohio? Yes, most BCBS plans recognize prior therapy failures from other states if properly documented with dates, doses, and clinical outcomes.

What manufacturer support is available for Somatuline Depot? Ipsen offers patient assistance programs and copay cards for eligible patients. Visit the Somatuline Depot patient resources page for current programs.

Can specialty pharmacies help with prior authorization? Yes, many specialty pharmacies have dedicated PA departments that work with prescribers to submit and track requests. Coordinate with your prescriber to designate the specialty pharmacy as an authorized representative.


Counterforce Health specializes in helping patients, clinicians, and specialty pharmacies navigate complex prior authorization and appeals processes. Our platform analyzes denial letters and plan policies to create targeted, evidence-backed appeals that align with payer requirements and clinical guidelines. Learn more about our services.


Sources & Further Reading


Disclaimer: This guide is for informational purposes only and does not constitute medical or legal advice. Coverage policies vary by plan and change over time. Always verify current requirements with your specific BCBS plan and consult with your healthcare provider regarding appropriate treatment options. For assistance with appeals and coverage issues in Ohio, contact the Ohio Department of Insurance at 1-800-686-1526.

Powered by Counterforce Health—AI that turns drug denials into evidence-based appeals patients and clinicians can submit today.