Oops, you're using an old version of your browser so some of the features on this page may not be displaying properly.

MINIMAL Requirements: Google Chrome 24+Mozilla Firefox 20+Internet Explorer 11Opera 15–18Apple Safari 7SeaMonkey 2.15-2.23

Poster session 13

511P - HIV impact in localized anal carcinoma: A matched cohort study

Date

10 Sep 2022

Session

Poster session 13

Topics

AIDS-Associated Malignancies

Tumour Site

Anal Cancer

Presenters

Amanda Acioli de Almeida

Citation

Annals of Oncology (2022) 33 (suppl_7): S227-S232. 10.1016/annonc/annonc1052

Authors

A. Acioli de Almeida1, E. Rocha1, R. Colombo Bonadio2, D. Galhera2, M.I. Braghiroli2, L.B. ALBAN2, C.R. Victor2, A.F.L. Dornellas3, M. Polo Mingueti e Silva2, C.S. Araujo de Carvalho4, A. Bueno4, C. Nahas4, K. Ibrahim2, A. Chen4, P.M. Hoff3, C. Motta Venchiarutti Moniz3

Author affiliations

  • 1 Oncologia, ICESP - Instituto do Cancer do Estado de Sao Paulo, 01246-000 - Sao Paulo/BR
  • 2 Medical Oncology, ICESP - Instituto do Cancer do Estado de Sao Paulo, 01246-000 - Sao Paulo/BR
  • 3 Oncology Department, University of Sao Paulo - Faculty of Medicine, 01246-903 - Sao Paulo/BR
  • 4 Oncology Department, ICESP - Instituto do Cancer do Estado de Sao Paulo, 01246-000 - Sao Paulo/BR

Resources

Login to get immediate access to this content.

If you do not have an ESMO account, please create one for free.

Abstract 511P

Background

Despite a higher incidence of HPV-related cancer in HIV-positive (HIV+) patients (pts), pivotal studies with curative chemoradiation (CRT) in anal cancer do not include this population. The impact of HIV infection remains unknown in this scenario. This study aimed to compare overall survival (OS) according to HIV status.

Methods

In this retrospective matched cohort study, we reviewed electronic medical records in Sao Paulo State Cancer Institute between 2010 and 2021 and selected available patients (pts) with anal cancer T1-4 N0-1 M0 by AJCCVIII. For each HIV+ pts, we selected one or two HIV- cases matched by age, stage (T, N), and ECOG. The primary endpoint was OS; estimated using Kaplan-Meir and compared with the log-rank test.

Results

Our final sample was 122 patients, 45 being HIV+. We included 2 HIV-:1 HIV+ (n=96) plus 1 HIV-:1 HIV+ (n=26) match. The median follow-up was 37 months (m). The majority of patients n=119, 98%, received concomitant CRT with curative intent and had ECOG 0/1, n=116, 95%. Stage III was seen in n=85 pts, 69% with T4 (n=41, 33%) or T3 tumors (n=36, 29%). Positive nodes were detected in 76 pts, 62%. No difference was observed in complete response (CR) at 6 months post QT/RDT, which was 68% in HIV+ vs. 63% in HIV- (p=0.6). Median RFS was not reached; 3yRFS rates was 60.7% in HIV+ vs. HIV- (HR 1.20, 95% CI 0.66 - 2.17, p=0.538). Median OS was not reached; 3yOS was 66.4% HIV+ vs. 72.2% in HIV- (HR 1.23, 95% CI 0.61 - 2.47, p=0.546). HIV+ pts presented significantly more hospital admission due to toxicity 29% (n=12/41) than HIV- 13% (n=10/74) (p=0.04).

Conclusions

HIV+ pts with anal carcinoma treated with CRT presented similar CR, RFS, and OS outcomes compared with HIV- pts. Optimal therapy should be attempted in the HIV+ population. More hospital admission due to toxicity occurs in the HIV+ group.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

C. Motta Venchiarutti Moniz.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

This site uses cookies. Some of these cookies are essential, while others help us improve your experience by providing insights into how the site is being used.

For more detailed information on the cookies we use, please check our Privacy Policy.

Customise settings
  • Necessary cookies enable core functionality. The website cannot function properly without these cookies, and you can only disable them by changing your browser preferences.