Definitive local therapy in solitary liver metastatic anal squamous cell carcinoma.

T Teerada Siripoon (Ramathibodi Hospital, Mahidol University, Ratchathewi, Thailand) C Conor O'Donnell (School of Physics, University College Dublin 1 , Dublin 4, Dublin D04 P7W1,) M Michael H. Storandt (Mayo Clinic Rochester, Rochester, MN) P Patrick Starlinger (Mayo Clinic Rochester, Rochester, MN) N Nguyen H. Tran (Mayo Clinic Florida, Jacksonville, FL) T Thomas D. Atwell (Mayo Clinic Rochester, Rochester, MN) K Krishan Jethwa (Mayo Clinic, Rochester, MN) Z Zhaohui Jin

Abstract

5 Background: Metastatic anal squamous cell carcinoma is rare and associated with a poor prognosis. There is limited evidence on the impact of local interventions on survival outcomes in patients with metastatic disease. We aimed to evaluate the survival of patients with liver-only metastatic anal cancer following definitive local management of liver lesions. Methods: This is a single-institution retrospective cohort study of patients with liver-limited metastatic anal cancer who underwent curative-intent local therapy. Clinical characteristics were collected and analyzed. The Kaplan-Meier method was used to calculate disease-free survival (DFS) and overall survival (OS). Prognostic factors associated with DFS and OS were assessed using Cox-proportional hazards models. Results: Twenty-five patients were included, median age was 59 years, and 92% were female. None of the patients had known HIV infection, 92% had HPV-positive disease and 76% had metachronous liver metastases following locoregional disease. All patients received chemoradiation for the primary lesion Unilobar hepatic involvement was present in 76% of the patients, with 56% having a single metastatic lesion. Pre-intervention systemic therapy was provided to 52% of the patients, including 8 who received carboplatin and paclitaxel, with a median duration of 3 months and ORR of 69%. Definitive treatment of metastatic disease included surgical resection (60%), non-surgical interventions (20%), and multimodal therapy (20%). All patients had viable tumor in the pathological specimen. With a median follow-up of 22 months, median DFS was 7.3 months, and median OS was 51.3 months. An ECOG performance status of 2, poorly differentiated histology, and extrahepatic recurrence were identified as significant prognostic factors in the univariate analysis, but not in the multivariate analysis. Conclusions: Our results demonstrate potential for long-term survival in liver-limited metastatic anal squamous cell carcinoma amenable to local therapeutic intervention combined with systemic therapy. These findings warrant further prospective study of local therapy in oligometastatic anal cancer. Characteristics N=25 (%) Median number of liver metastases (range), lesions- 1- 2-3- >3 1 (1-20)14 (56)8 (32)3 (12) Median maximal diameter of liver metastases (range), cm 3 (0.9-11.9) Best response of liver metastases to chemotherapy (N=13)- Complete response- Partial response- Stable disease- Progressive disease 2 (15)7 (54)3 (23)1 (8) Surgical procedure (N=20)- Right/left hemi-hepatectomy- Segmentectomy- Wedge resection 4 (20)14 (70)2 (10) Non-surgical procedure (N=10)- Local ablation- Radiotherapy- Other 5 (50)3 (30)2 (20) Hepatic surgical margins (N=20)- Positive margins- Close margins (<1mm)- Negative margins 02 (10)18 (90) Recurrent disease- Yeso Intrahepatico Extrahepatic- No 20 (80)14 (70)6 (30)5 (20)

Article Details

Volume / Issue Vol. 43, Issue 4_suppl
Published February 01, 2025
Pages 5-5
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (8)

T

Teerada Siripoon

Ramathibodi Hospital, Mahidol University, Ratchathewi, Thailand

C

Conor O'Donnell

School of Physics, University College Dublin 1 , Dublin 4, Dublin D04 P7W1,

M

Michael H. Storandt

Mayo Clinic Rochester, Rochester, MN

P

Patrick Starlinger

Mayo Clinic Rochester, Rochester, MN

N

Nguyen H. Tran

Mayo Clinic Florida, Jacksonville, FL

T

Thomas D. Atwell

Mayo Clinic Rochester, Rochester, MN

K

Krishan Jethwa

Mayo Clinic, Rochester, MN

Z

Zhaohui Jin