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E-Poster Display

518P - Treatment outcome and prognostic factors after chemoradiotherapy for anal cancer

Date

17 Sep 2020

Session

E-Poster Display

Topics

Cytotoxic Therapy

Tumour Site

Colon and Rectal Cancer

Presenters

Kathinka Slørdahl

Citation

Annals of Oncology (2020) 31 (suppl_4): S409-S461. 10.1016/annonc/annonc270

Authors

K.S. Slørdahl1, J. Olsen1, D. Klotz2, E. Skovlund3, C. Undseth1, H.L. Abildgaard1, M. Brændengen1, A. Nesbakken4, S.G. Larsen4, B. Hanekamp5, L. Holmboe5, R. Tvedt1, E. Malinen6, S. Kaasa1, M.G. Guren1

Author affiliations

  • 1 Department Of Oncology, Oslo University Hospital, 0424 - Oslo/NO
  • 2 Department Of Pathology, Oslo University Hospital, 0424 - Oslo/NO
  • 3 Department Of Public Health And Nursing, Norwegian University of Science and Technology, 7491 - Trondheim/NO
  • 4 Department Of Gastrointestinal Surgery, Oslo University Hospital, 0424 - Oslo/NO
  • 5 Department Of Radiology And Nuclear Medicine, Oslo University Hospital, 0424 - Oslo/NO
  • 6 Department Of Physics, University of Oslo, 0316 - Oslo/NO

Resources

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Abstract 518P

Background

Squamous cell carcinoma of the anus (SCCA) is a rare cancer. Chemoradiotherapy (CRT) is the recommended curative treatment for SCCA stage I-III. The aim of the study was to investigate the 3- and 5-year disease-free survival (DFS) and overall survival (OS), locoregional treatment failure rate, and determine prognostic factors for DFS.

Methods

141 patients were entered in a prospective observational study (ANCARAD; NCT 01937780) at Oslo University Hospital from Oct 2013 to Sept 2017. Main inclusion criteria were histologically proven SCCA, planned radiotherapy, and performance status (ECOG) ≤ 2. CRT was delivered to doses of 54–58 Gy with concomitant mitomycin and 5-fluorouracil or capecitabine, with 5-year follow-up. Disease stage, patient characteristics, treatment, response and survival were prospectively registered. Human papilloma virus (HPV) status was assessed. Disease-free and overall survival were analyzed by the Kaplan-Meier method and Cox’ proportional hazard model.

Results

Of the 141 patients included, 132 were eligible for final analyses. Median age was 63 years (range 39-90), 73% were women, 42% had T3-T4 tumors and 44% had N1-3 disease. Median follow up time was 49.3 months (range 3-71). Eighteen patients (14%) had treatment failure, 9 locoregional, 4 distant and 5 both locoregional and distant failure. Of these, 15 patients underwent surgery, 12 had salvage abdomino-perineal resection and 3 resection of metastases. Eleven of the 18 patients were alive with no evidence of disease at last follow-up. DFS at 3 and 5 years was 85% and 77%, respectively. OS was 93% at 3 years and 85% at 5 years. HPV negative tumors (Hazard Ratio (HR) = 2.9, p <0.01), N3 disease (HR = 2.5, p <0.05), tumor size >4cm (HR = 2.2, p <0.05) and male gender (HR = 2.2, p <0.05) were statistically significant negative prognostic factors in univariate analyses for DFS. HPV negativity, N3 disease, and tumor size >4cm remained significant after adjusting for age and gender in multivariate analyses for DFS.

Conclusions

Chemoradiotherapy for SCCA resulted in excellent clinical outcomes in this prospective study, with less than 15% observed treatment failures and an estimated 3-years DFS of over 80%. Known prognostic factors were confirmed.

Clinical trial identification

NCT 01937780.

Editorial acknowledgement

Legal entity responsible for the study

Oslo University Hospital.

Funding

Oslo University Hospital.

Disclosure

All authors have declared no conflicts of interest.

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