Cerebrospinal Fluid Early Fungicidal Activity as a Surrogate Endpoint for Cryptococcal Meningitis Survival in Clinical Trials. (8th January 2020)
- Record Type:
- Journal Article
- Title:
- Cerebrospinal Fluid Early Fungicidal Activity as a Surrogate Endpoint for Cryptococcal Meningitis Survival in Clinical Trials. (8th January 2020)
- Main Title:
- Cerebrospinal Fluid Early Fungicidal Activity as a Surrogate Endpoint for Cryptococcal Meningitis Survival in Clinical Trials
- Authors:
- Pullen, Matthew F
Hullsiek, Katherine Huppler
Rhein, Joshua
Musubire, Abdu K
Tugume, Lillian
Nuwagira, Edwin
Abassi, Mahsa
Ssebambulidde, Kenneth
Mpoza, Edward
Kiggundu, Ruben
Akampurira, Andrew
Nabeta, Henry W
Schutz, Charlotte
Evans, Emily E
Rajasingham, Radha
Skipper, Caleb P
Pastick, Katelyn A
Williams, Darlisha A
Morawski, Bozena M
Bangdiwala, Ananta S
Meintjes, Graeme
Muzoora, Conrad
Meya, David B
Boulware, David R - Abstract:
- Abstract: Background: In cryptococcal meningitis phase 2 clinical trials, early fungicidal activity (EFA) of Cryptococcus clearance from cerebrospinal fluid (CSF) is used as a surrogate endpoint for all-cause mortality. The Food and Drug Administration allows for using surrogate endpoints for accelerated regulatory approval, but EFA as a surrogate endpoint requires further validation. We examined the relationship between rate of CSF Cryptococcus clearance (EFA) and mortality through 18 weeks. Methods: We pooled individual-level CSF data from 3 sequential cryptococcal meningitis clinical trials conducted during 2010–2017. All 738 subjects received amphotericin + fluconazole induction therapy and had serial quantitative CSF cultures. The log10 -transformed colony-forming units (CFUs) per mL CSF were analyzed by general linear regression versus day of culture over the first 10 days. Results: Mortality through 18 weeks was 37% for EFA > = 0.60 (n = 170), 36% for 0.40–0.59 (n = 182), 39% for 0.30–0.39 (n = 112), 35% for 0.20–0.29 (n = 87), and 50% for those with EFA < 0.20 CFU/mL/day (n = 187). The hazard ratio for 18-week mortality, comparing those with EFA < 0.20 to those with EFA > = 0.20, was 1.60 (95% confidence interval, 1.25, 2.04; P = .002). The lowest EFA group had lower median CD4 T-cell counts ( P < .01) and lower proportion of patients with CSF pleocytosis ( P < .001). Conclusions: EFA is associated with all-cause mortality in cryptococcal meningitis. An EFAAbstract: Background: In cryptococcal meningitis phase 2 clinical trials, early fungicidal activity (EFA) of Cryptococcus clearance from cerebrospinal fluid (CSF) is used as a surrogate endpoint for all-cause mortality. The Food and Drug Administration allows for using surrogate endpoints for accelerated regulatory approval, but EFA as a surrogate endpoint requires further validation. We examined the relationship between rate of CSF Cryptococcus clearance (EFA) and mortality through 18 weeks. Methods: We pooled individual-level CSF data from 3 sequential cryptococcal meningitis clinical trials conducted during 2010–2017. All 738 subjects received amphotericin + fluconazole induction therapy and had serial quantitative CSF cultures. The log10 -transformed colony-forming units (CFUs) per mL CSF were analyzed by general linear regression versus day of culture over the first 10 days. Results: Mortality through 18 weeks was 37% for EFA > = 0.60 (n = 170), 36% for 0.40–0.59 (n = 182), 39% for 0.30–0.39 (n = 112), 35% for 0.20–0.29 (n = 87), and 50% for those with EFA < 0.20 CFU/mL/day (n = 187). The hazard ratio for 18-week mortality, comparing those with EFA < 0.20 to those with EFA > = 0.20, was 1.60 (95% confidence interval, 1.25, 2.04; P = .002). The lowest EFA group had lower median CD4 T-cell counts ( P < .01) and lower proportion of patients with CSF pleocytosis ( P < .001). Conclusions: EFA is associated with all-cause mortality in cryptococcal meningitis. An EFA threshold of > = 0.20 log10 CFU/mL/day was associated with similar 18-week mortality (37%) compared to 50% mortality with EFA < 0.20. This EFA threshold may be considered a target for a surrogate endpoint. This builds upon existing studies to validate EFA as a surrogate endpoint. Abstract : In cryptococcal meningitis trials, early fungicidal activity (EFA) reflecting Cryptococcus cerebrospinal fluid (CSF) clearance is used as a surrogate endpoint. We examined the relationship between EFA and survival in 738 Africans receiving amphotericin-based therapy: EFA < 0.20 log10 CFU/mL/day has decreased 18-week survival. … (more)
- Is Part Of:
- Clinical infectious diseases. Volume 71:Number 7(2020)
- Journal:
- Clinical infectious diseases
- Issue:
- Volume 71:Number 7(2020)
- Issue Display:
- Volume 71, Issue 7 (2020)
- Year:
- 2020
- Volume:
- 71
- Issue:
- 7
- Issue Sort Value:
- 2020-0071-0007-0000
- Page Start:
- e45
- Page End:
- e49
- Publication Date:
- 2020-01-08
- Subjects:
- cryptococcus -- meningitis -- cryptococcal meningitis -- early fungicidal activity -- surrogate endpoint
Communicable diseases -- Periodicals
616.905 - Journal URLs:
- http://cid.oxfordjournals.org ↗
http://ukcatalogue.oup.com/ ↗
http://www.journals.uchicago.edu/CID/journal ↗
http://www.jstor.org/journals/10584838.html ↗ - DOI:
- 10.1093/cid/ciaa016 ↗
- Languages:
- English
- ISSNs:
- 1058-4838
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3286.293860
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- 21400.xml