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Gaps in Access to Patient Care for Patients with Rare Hematological Disorders

2011· article· en· W2585495775 on OpenAlexaffabout
Renee Lachance, Douglas A. Stewart, Katie Worthington, Beena Mistry, S. Yunger, Jose M Garnica, Shelagh Knight, D. Milliken

Bibliographic record

VenueBlood · 2011
Typearticle
Languageen
FieldImmunology and Microbiology
TopicImmunodeficiency and Autoimmune Disorders
Canadian institutionsUniversity of CalgaryRoche (Canada)
Fundersnot available
KeywordsMedicineRituximabReimbursementThrombocytopenic purpuraMedicaidPediatricsFamily medicineIntensive care medicineHealth careInternal medicine

Abstract

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Abstract Abstract 4752 Background In Canada, gaps exist in access to therapy for patients with rare hematological disorders. Although a growing body of evidence exists for these rare disorders, they remain off-label as they are not Health Canada approved and as a result, limited drug funding options are available through Canadian funding bodies. For patients suffering with Warm Autoimmune Hemolytic Anemia (AIHA), Cold Agglutinin Disease (CAD), Cryoglobulinemia, Graft versus Host Disease (GvHD), Idiopathic Thrombocytopenic Purpura (ITP), Thrombotic Thrombocytopenic Purpura (TTP) and Waldenstrom's, challenges exist for physicians to access appropriate treatment for these patients. With no formalized public or private reimbursement available for these off-label indications, patients must pay for costly treatments out-of-pocket, or be left untreated. In response to this unmet medical need, Roche Canada initiated a patient assistance program to ease the burden for physicians and their patients seeking limited treatment options for these rare disorders. Roche Canada's Patient Assistance Program (RPAP), managed by a 3rd party, assists patients with timely access to treatment through reimbursement navigation, financial assistance and private infusion clinics. To address the gap in patient care, Roche Canada piloted a non-promoted Compassionate Use (CU) program to provide access to therapy for patients with rare hematological disorders enrolled in RPAP after all public and private funding options have been exhausted. At the discretion of a 3rd party adjudication panel, the CU program provides rituximab on a case-by-case basis to patients with the above stated rare hematological disorders, where substantial evidence exists to suggest its safety and efficacy (Garvey B, BJH, 2008). All participating physicians enter a contractual agreement acknowledging the off-label use of rituximab. Response outcome data was not collected or required for the program. Objective This observational study compares, across two consecutive years, physician enrollment of patients in RPAP and patients' subsequent access to therapy in an environment with and without a compassionate use program. Methods An analysis of anonymized data from RPAP and the CU program was conducted, comparing 1 year of RPAP without the CU program, May 2009-April 2010(Y1), to 1 year of RPAP with the CU program, May 2010-April 2011(Y2). Patients were assessed by enrollment, indication, reimbursement coverage type, reimbursement approval, and access to rituximab. Results Total enrollment into RPAP over the 2 year period was 218 patients. 65 (30%) patients were enrolled in Y1, while 153 (70%) patients were enrolled in Y2, indicating a 153% (88 patient) increase in enrollment. Of the 218 patients enrolled, 154 (71%) subsequently received rituximab therapy. In Y1, 36 of 65 enrolled patients received rituximab therapy (55%), while 118 of the 153 patients enrolled in Y2 received rituximab therapy (77%). This indicates a 228% (82 patient) increase in access to therapy. Table 1 illustrates the number of patients who received access to therapy after enrollment in RPAP, and the type of reimbursement they received. Table 2 illustrates the enrollment and access to therapy by year and disease area. Conclusion The pilot compassionate program has highlighted that an unmet medical need exists for patients with rare hematological disorders. There remains a need for additional regulatory and provincial programs to help address the gaps in care for these patients. Disclosures: Lachance: Hoffman-La Roche Limited: Employment. Off Label Use: Rituximab is a chimeric mouse/human monoclonal antibody that binds specifically to the transmembrane antigen CD20. Rituxan is indicated in Canada for Non-Hodgkin's Lymphoma (NHL), Chronic Lymphocytic Leukemia (CLL) and Rheumatoid Arthritis (RA). This abstract describes the use of rituximab in the following rare hematological disorders: Warm Autoimmune Hemolytic Anemia (AIHA), Cold Agglutinin Disease (CAD), Cryoglobulinemia, Graft versus Host Disease (GvHD), Idiopathic Thrombocytopenic Purpura (ITP), Thrombotic Thrombocytopenic Purpura (TTP) and Waldenstrom's. Stewart:Hoffmann-La Roche Limited: Honoraria. Worthington:Hoffmann-La Roche Limited: Employment. Mistry:Hoffmann-La Roche Limited: Employment. Yunger:Hoffmann-La Roche Limited: Employment. Garnica:Hoffmann-La Roche Limited: Employment. Knight:Hoffmann-La Roche Limited: Employment. Milliken:Hoffmann-La Roche Limited: Employment.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.004
metaresearch head score (Gemma)0.026
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: none
GenreCandidate signal: Empirical · Consensus signal: none
Teacher disagreement score0.825
Threshold uncertainty score0.353

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0040.026
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.001
Bibliometrics0.0010.002
Science and technology studies0.0040.002
Scholarly communication0.0040.002
Open science0.0020.005
Research integrity0.0020.003
Insufficient payload (model declined to judge)0.0330.002

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.009
GPT teacher head0.214
Teacher spread0.205 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Citations1
Published2011
Admission routes2
Has abstractyes

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