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In France, French citizens with an annual income less than 10339 euros are considered living with low-income and are eligible to benefit from a public universal healthcare insurance coverage called C2S (complémentaire santé solidaire). C2S covers primary care and hospital care. Non-citizens with low income, like some migrants, can also benefit from a public healthcare insurance coverage called AME ("Aide Medicale d'Etat" for State Medical Aid). These criteria are used as a marker of precarity settings (i.e., socio-economic vulnerability) in France. In France, HIV-related care and treatments are reimbursed at 100% (ALD30), whatever the level of precariousness. ART adherence has been shown significantly lower in PLWH with C2S health insurance coverage. Although BIC/FTC/TAF is a recommended preferred option in naive PLWH and in switch or maintenance therapy in most settings, due to the forgiveness profile and the high genetic barrier to resistance, boosted darunavir (DRV/r) remains even more widely used than 2nd generation InSTIs in populations in precarity settings, and Real World Effectiveness (RWE) with BIC/FTC/TAF is missing to better support its use in these settings.
Paris Bichat Hospital (located in one of the poorest districts in the Ile-de-France region) and Nantes university hospital (West France region) follow a cohort of PLWH with a high proportion of populations in precarity settings (i.e with C2S and AME health insurance coverage): Paris Bichat hospital: N=5143 PLWH (December 2021), sex ratio F/M 37/56%, Transgender Women 7%, and born in sub-Saharan African countries 49%. Nantes university hospital: N=2227 PLWH (December 2021), sex ratio F/M 35/65% and born in sub-Saharan African countries 33%. In this cohort of 7370 PLWH in both sites 50% are receiving an InSTI-based ART regimen, regardless of prior treatment history, and at least 40% are receiving care through the C2S or AME, respectively.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Treatment naive,virologically suppressed and unsuppressed treatment experienced in 2nd line |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Biktarvy | Drug | this study applies secondary use of data collected from medical health records |
|
| Measure | Description | Time Frame |
|---|---|---|
| i. HIV RNA ≥50 copies/mL at week 48 within the time window OR One HIV RNA ≥50 copies/mL followed by treatment discontinuation before week 48 after reaching HIV RNA < 50 copies/mL | Week 48 | |
| ii. Discontinuation due to treatment related adverse event | week 48 | |
| iii. Discontinuation due to non-treatment related adverse event, death or other reasons | week 48 | |
| iv. On study but missing data in window | Week 48+/- 8 weeks | |
| i. Two consecutive HIV RNA VL ≥200 copies/mL after reaching a HIV RNA < 50 copies/mL | week 48 | |
| ii. One HIV RNA VL ≥200 copies/mL followed by baseline treatment discontinuation after reaching HIV RNA < 50 copies/mL | week 48 | |
| iii. HIV RNA VL ≥200 copies/mL at week 48 and no other value for confirmation | week 48 |
| Measure | Description | Time Frame |
|---|---|---|
| • Evaluate the time to treatment discontinuation and reason for discontinuation with BIC/FTC/TAF among TN, VS TE and VU TE PLWH. | week 48 | |
| • Describe subsequent regimens among individuals discontinued BIC/FTC/TAF among TN, VS TE and VU TE. | week 48 |
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Inclusion Criteria:
Exclusion Criteria:
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Treatment naïve (TN) and Virologically Suppressed Treatment Experienced (VS TE) in 2d line treatment, or Virologically Unsuppressed Treatment Experienced (VU TE) in 2d line treatment patients within Paris Bichat and CHU Nantes hospitals who were covered by C2S/AME heath insurance during study period.
- Those using BIC/FTC/TAF We will conduct descriptive analyses only. Analyses will be disaggregated by TN, VS TE, and VU TE groups.
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Roland LANDMAN | Contact | 40 25 63 54 | +33 1 | landman.roland@gmail.com |
| Aïda BENALYCHERIF | Contact | aida.benalycherif@fondation-imea.org |
| Name | Affiliation | Role |
|---|---|---|
| Roland LANDMAN | Institut de Médecine et d'Epidémiologie Appliquée - Fondation Internationale Léon M'Ba | Principal Investigator |
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| • Describe the number of hospital medical HIV appointments, and participants baseline characteristics with BIC/FTC/TAF among TN, VS TE and VU TE PLWH | week 48 |
| • Describe treatment emergent resistance profile among participants with confirmed virologic failure with BIC/FTC/TAF among TN, VS TE and VU TE PLWH. | week 48 |
| • Describe the change of CD4 | CD4 description | week 48 |
| • Factors associated with virologic suppression (HIV RNA<50 copies/mL, FDA Snapshot), confirmed virologic failure (HIV RNA ≥200 copies/mL), discontinuation, and emergence of resistance-associated mutations at failure among TN, VS TE and VU TE. | week 48 |
| • Describe the change of CD8 cell counts | CD8 description | Week 48 |
| • Describe the change CD4/CD8 ratio | description CD4/CD8 ratio | Week 48 |
| • Describe the change of BMI | BMI description | Week 48 |
| • Describe the change of body weight | Body weight description | Week 48 |
| ID | Term |
|---|---|
| C000654125 | bictegravir, emtricitabine, tenofovir alafenamide, drug combination |
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