Glioblastoma denials in California external review

In the California DMHC record, independent physician reviewers decided 44 published external-review cases involving glioblastomaand overturned the plan’s denial in 47.7%. That is a historical result among cases that reached this program, not a forecast for an individual appeal.

California DMHC decisions
44
2005–2025
Overturned
47.7%
21 denials reversed

Most-fought treatments for glioblastoma

What insurers denied — and how those fights ended.
CategoryDecisionsOverturned
Optune8
87.5%
Avastin5
20%

What the insurer actually argued

Denials fall into different categories, and they don’t succeed equally — so the reason on your letter changes how you should answer it.
Reason givenDecisionsOverturned
Experimental/Investigational
The plan called the treatment unproven. These turn on published evidence, so the appeal is a literature argument.
27
51.9%
Medical Necessity
The plan said the care wasn’t medically necessary. The most common fight, and the most winnable.
16
37.5%
Typical time to a decision
7 days
Most land between 5 and 14 days
Handled as urgent
70.5%
Expedited when a delay would cause harm

What the reviewers wrote

Excerpts from the independent reviewers’ published findings — the actual reasoning, quoted, not summarised.

Where the denial was overturned

Physician 1: The patient is an 18-year-old young man first noted to have some numbness in his right arm in November 2005. It progressively worsened over the next few months, and by April 2006 he had right arm numbness and weakness along with neck pain. An MRI of the spine revealed a 3.9 x 1.2 x 1.4 cm enhancing lesion at C2 to C4. The lesion was partially excised in early May 2006. The final histopathologic diagnosis is glioblastoma (GBM). The June 2006 spine MRI shows no change in the size of the enhancing lesion (suggesting that less was removed than thought or that the tumor has grown back to its original size). The patient improved after the operation, but according to his mother, his neurologic symptoms (tingling and weakness) are returning. The patient’s providers have recommended Avastin and CPT-11 as initial therapy.
Experimental/Investigational · 2006 · IMR EI06-5628
Findings: The physician reviewer found that Nature of Statutory Criteria/Case Summary: The patient requested authorization and coverage for Intensity-modulated radiation therapy (IMRT) (30 units/visits).IMRT offers several significant advantages over standard 3-dimensional conformal radiation therapy (3D-CRT) for the treatment of glioblastoma. One of the primary benefits is improved target coverage. Studies have consistently shown that IMRT provides better coverage of the planning target volume (PTV) compared to 3D-CRT. This enhanced coverage allows for more precise delivery of the prescribed radiation dose to the tumor while minimizing exposure to surrounding healthy tissues.
Experimental/Investigational · 2024 · IMR EI24-42679

Where the denial was upheld

Worth reading too — these show what an appeal has to overcome.
Physician 1: The patient is a 51-year-old man diagnosed with glioblastoma in July 2004. He was treated with surgery, radiation therapy, and chemotherapy. The patient underwent further surgery in January 2005 followed by treatment with interleukin-13 pseudomonas exotoxin. An MRI performed in September 2005 demonstrated progressive disease and it has been recommended that the patient be treated with CPT-11 and Avastin. The Health Plan has denied authorization for Avastin on the basis the therapy is considered investigational in this clinical setting.The included evidence includes two abstracts/papers that have been submitted for publication. One of these papers noted that in 21 patients treated with CPT-11 and Avastin, 9 had some sort of response. This was suggestive of an improved response to the combination when compared to CPT-11 alone.
Experimental/Investigational · 2005 · IMR EI05-5005
Nature of Statutory Criteria/Case Summary: An enrollee has requested authorization and coverage for Tibsovo. The use of next-generation sequencing (NGS) panel testing as a means of selecting anti-cancer therapy in advanced cancer has been progressing over the past few years and is an area of active research with ongoing studies. The concept of this approach is that all cancers are unique and that each cancer has a specific individual molecular driver which can be identified using this testing. Once identified, specific therapy can be given to the patient that directly treats their tumor. In this case, the patient was originally diagnosed with anaplastic astrocytoma. Notes dated 6/28/22 reported that the patient had a recurrence that was categorized as glioblastoma, World Health Organization (WHO) grade IV.
Experimental/Investigational · 2022 · IMR EI22-37758

Figures and quotations on this page come from 42,749 published decisions in the California DMHC Independent Medical Review dataset. These are California external-review outcomes. Other state and federal programs have different eligibility rules, processes, and current availability; the rates here do not transfer to those programs or predict an individual result. Excerpts are quoted verbatim from the public record and describe this condition generally, not any individual case.

How to use this in your appeal

These outcomes describe eligible cases completed through California DMHC’s Independent Medical Review program. They do not estimate the chance that an internal appeal, an external review in another jurisdiction, or your individual case will succeed. Use the record to identify evidence patterns involving glioblastoma, then check the rights and deadlines that apply to your plan.

SOURCE: CALIFORNIA DMHC INDEPENDENT MEDICAL REVIEW OUTCOMES (CHHS OPEN DATA) · AGGREGATES + DEIDENTIFIED DECISION EXCERPTS/REFERENCE IDS · METHODOLOGY

Not legal or medical advice. Coverage Rights is a self-help tool that helps you prepare your own appeal. For advice about your specific situation, talk to a licensed attorney or your doctor.

Fighting a denial for glioblastoma? Use the California record to prepare.

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