Cargando…
Utility of colposcopy in a phase 2 portion of a microbicide clinical trial of BufferGel and 0.5% PRO 2000 Gel
BACKGROUND: The majority of new HIV infections are acquired through heterosexual transmission. There is urgent need for prevention methods to compliment behavior change and condom use. Topical microbicide represent a potential strategy for reduction of HIV transmission in women. METHODS: Monthly Col...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International AIDS Society
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3494172/ https://www.ncbi.nlm.nih.gov/pubmed/22944480 http://dx.doi.org/10.7448/IAS.15.2.17376 |
_version_ | 1782249372266790912 |
---|---|
author | Chirenje, Zvavahera M Mâsse, Benoît R Maslankowski, Lisa A Ramjee, Gita Coletti, Anne S Tembo, Tchangani N Magure, Tsitsi M Soto-Torres, Lydia Kelly, Cliff Hillier, Sharon Karim, Abdool |
author_facet | Chirenje, Zvavahera M Mâsse, Benoît R Maslankowski, Lisa A Ramjee, Gita Coletti, Anne S Tembo, Tchangani N Magure, Tsitsi M Soto-Torres, Lydia Kelly, Cliff Hillier, Sharon Karim, Abdool |
author_sort | Chirenje, Zvavahera M |
collection | PubMed |
description | BACKGROUND: The majority of new HIV infections are acquired through heterosexual transmission. There is urgent need for prevention methods to compliment behavior change and condom use. Topical microbicide represent a potential strategy for reduction of HIV transmission in women. METHODS: Monthly Colposcopy evaluations were performed during pelvic examinations among 299 women enrolled in the Phase 2 portion of HPTN 035 study at four sites (1 in USA, 3 in Southern Africa). This was a phase 2/2b, multisite, randomized, and controlled clinical trial with four arms: BufferGel, 0.5% PRO2000 Gel, placebo gel and no gel. At two of the sites, pelvic examinations were conducted by the use of naked eye without colposcopy. RESULTS: A colposcopy finding of any kind was detected in 48% of participants at baseline compared to 40% at 3 months (p =0.04). The lower rates were also observed in vaginal discharge (22% at baseline, 16% at 3 months, p=0.06), erythema (15% at baseline, 8% at 3 months, p=0.004). The trend towards significance at p=0.05 disappear when utilizing stringent statistical significance levels. A pelvic finding of any kind was detected in 71% of colposcopy participants compared to 41% of participants who had naked eye examination only conducted at two sites that performed both colposcopy and naked eye without colposcopy. Use of colposcopy yielded significantly higher rates of participants with deep epithelial disruption, erythema and ecchymosis. We observed no cases of incident Chlamydia, Gonorrhea, or Syphilis during the three month follow up. There were 2 cases of incident HIV during 3-month study period neither of which was associated with any abnormal colposcopy evaluation findings. CONCLUSION: No safety signals were observed in the 4 study arms, allowing seamless transition from phase 2 to 2b. Colposcopy utility in microbicide clinical trials has minimal value given high rates of background noise findings of no relevant clinical significance. |
format | Online Article Text |
id | pubmed-3494172 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International AIDS Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-34941722012-11-26 Utility of colposcopy in a phase 2 portion of a microbicide clinical trial of BufferGel and 0.5% PRO 2000 Gel Chirenje, Zvavahera M Mâsse, Benoît R Maslankowski, Lisa A Ramjee, Gita Coletti, Anne S Tembo, Tchangani N Magure, Tsitsi M Soto-Torres, Lydia Kelly, Cliff Hillier, Sharon Karim, Abdool J Int AIDS Soc Research Article BACKGROUND: The majority of new HIV infections are acquired through heterosexual transmission. There is urgent need for prevention methods to compliment behavior change and condom use. Topical microbicide represent a potential strategy for reduction of HIV transmission in women. METHODS: Monthly Colposcopy evaluations were performed during pelvic examinations among 299 women enrolled in the Phase 2 portion of HPTN 035 study at four sites (1 in USA, 3 in Southern Africa). This was a phase 2/2b, multisite, randomized, and controlled clinical trial with four arms: BufferGel, 0.5% PRO2000 Gel, placebo gel and no gel. At two of the sites, pelvic examinations were conducted by the use of naked eye without colposcopy. RESULTS: A colposcopy finding of any kind was detected in 48% of participants at baseline compared to 40% at 3 months (p =0.04). The lower rates were also observed in vaginal discharge (22% at baseline, 16% at 3 months, p=0.06), erythema (15% at baseline, 8% at 3 months, p=0.004). The trend towards significance at p=0.05 disappear when utilizing stringent statistical significance levels. A pelvic finding of any kind was detected in 71% of colposcopy participants compared to 41% of participants who had naked eye examination only conducted at two sites that performed both colposcopy and naked eye without colposcopy. Use of colposcopy yielded significantly higher rates of participants with deep epithelial disruption, erythema and ecchymosis. We observed no cases of incident Chlamydia, Gonorrhea, or Syphilis during the three month follow up. There were 2 cases of incident HIV during 3-month study period neither of which was associated with any abnormal colposcopy evaluation findings. CONCLUSION: No safety signals were observed in the 4 study arms, allowing seamless transition from phase 2 to 2b. Colposcopy utility in microbicide clinical trials has minimal value given high rates of background noise findings of no relevant clinical significance. International AIDS Society 2012-08-27 /pmc/articles/PMC3494172/ /pubmed/22944480 http://dx.doi.org/10.7448/IAS.15.2.17376 Text en © 2012 Zvavahera M Chirenje et al; licensee International AIDS Society http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 3.0 Unported License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Chirenje, Zvavahera M Mâsse, Benoît R Maslankowski, Lisa A Ramjee, Gita Coletti, Anne S Tembo, Tchangani N Magure, Tsitsi M Soto-Torres, Lydia Kelly, Cliff Hillier, Sharon Karim, Abdool Utility of colposcopy in a phase 2 portion of a microbicide clinical trial of BufferGel and 0.5% PRO 2000 Gel |
title | Utility of colposcopy in a phase 2 portion of a microbicide clinical trial of BufferGel and 0.5% PRO 2000 Gel |
title_full | Utility of colposcopy in a phase 2 portion of a microbicide clinical trial of BufferGel and 0.5% PRO 2000 Gel |
title_fullStr | Utility of colposcopy in a phase 2 portion of a microbicide clinical trial of BufferGel and 0.5% PRO 2000 Gel |
title_full_unstemmed | Utility of colposcopy in a phase 2 portion of a microbicide clinical trial of BufferGel and 0.5% PRO 2000 Gel |
title_short | Utility of colposcopy in a phase 2 portion of a microbicide clinical trial of BufferGel and 0.5% PRO 2000 Gel |
title_sort | utility of colposcopy in a phase 2 portion of a microbicide clinical trial of buffergel and 0.5% pro 2000 gel |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3494172/ https://www.ncbi.nlm.nih.gov/pubmed/22944480 http://dx.doi.org/10.7448/IAS.15.2.17376 |
work_keys_str_mv | AT chirenjezvavaheram utilityofcolposcopyinaphase2portionofamicrobicideclinicaltrialofbuffergeland05pro2000gel AT massebenoitr utilityofcolposcopyinaphase2portionofamicrobicideclinicaltrialofbuffergeland05pro2000gel AT maslankowskilisaa utilityofcolposcopyinaphase2portionofamicrobicideclinicaltrialofbuffergeland05pro2000gel AT ramjeegita utilityofcolposcopyinaphase2portionofamicrobicideclinicaltrialofbuffergeland05pro2000gel AT colettiannes utilityofcolposcopyinaphase2portionofamicrobicideclinicaltrialofbuffergeland05pro2000gel AT tembotchanganin utilityofcolposcopyinaphase2portionofamicrobicideclinicaltrialofbuffergeland05pro2000gel AT maguretsitsim utilityofcolposcopyinaphase2portionofamicrobicideclinicaltrialofbuffergeland05pro2000gel AT sototorreslydia utilityofcolposcopyinaphase2portionofamicrobicideclinicaltrialofbuffergeland05pro2000gel AT kellycliff utilityofcolposcopyinaphase2portionofamicrobicideclinicaltrialofbuffergeland05pro2000gel AT hilliersharon utilityofcolposcopyinaphase2portionofamicrobicideclinicaltrialofbuffergeland05pro2000gel AT karimabdool utilityofcolposcopyinaphase2portionofamicrobicideclinicaltrialofbuffergeland05pro2000gel |