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Inicio Annals of Hepatology P-32 ACCESSIBILITY TO SEQUENTIAL SYSTEMIC TREATMENT AFTER TACE: IMPACT ON SURVIV...
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Vol. 29. Issue S3.
Abstracts of the 2023 Annual Meeting of the ALEH
(December 2024)
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Vol. 29. Issue S3.
Abstracts of the 2023 Annual Meeting of the ALEH
(December 2024)
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P-32 ACCESSIBILITY TO SEQUENTIAL SYSTEMIC TREATMENT AFTER TACE: IMPACT ON SURVIVAL IN A LATIN AMERICAN PROSPECTIVE COHORT
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FEDERICO PIÑERO1Margarita Anders2Carla Bermúdez3Diego Arufe4Adriana Varón5Ana Palazzo6Jorge Rodríguez7Oscar Beltrán5Patricio Palavecino Rubilar8Leonardo Gomes da Fonseca9Ezequiel Ridruejo10Norberto Tamagnone11Hugo Cheinquer12Nicolás Cortés Medina13Juan Ignacio Marín14Estela Manero15Federico Orozco Ganem2Jaime Poniachik8Sebastián Marciano3Virginia Reggiardo11Manuel Mendizabal1
1 HOSPITAL UNIVERSITARIO AUSTRAL, Pilar, Argentina
2 Hospital Alemán, Buenos Aires, Argentina
3 Hospital Italiano de Buenos Aires, Buenos Aires, Argentina
4 Sanatorio Sagrado Corazón, Buenos Aires, Argentina
5 Fundación Cardioinfantil, Bogotá, Colombia
6 Hospital Padilla, Tucumán, Argentina
7 Hospital Central, Mendoza, Argentina
8 Hospital Clínico de la Universidad Chile, Santiago, Chile
9 Instituto do Cancer do Estado de São Paulo, Hospital das Clínicas, Universidade São Paulo, Sao Paulo, Brasil
10 Centro de Educación Médica e Investigaciones Clínicas (CEMIC), Buenos Aires, Argentina
11 Hospital Centenario, Rosario, Argentina
12 Hospital das Clínicas de Porto Alegre, Universidade Federal do Rio Grande do Sul., Porto Alegre, Brasil
13 Hospital Universitario Fundación Santa Fe de Bogotá, Bogotá, Colombia
14 Hospital Pablo Tobón Uribe, Medellín, Colombia
15 Hospital Pablo Soria, San Salvador de Jujuy, Argentina
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Vol. 29. Issue S3

Abstracts of the 2023 Annual Meeting of the ALEH

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Introduction and Objectives

Stopping rules following transarterial chemoembolization (TACE), either tumor progression or “unTACEable” progression are needed. Avoiding liver decompensation after TACE may lead better access to systemic treatment and survival. These scenarios are unknown in our region. We aimed to evaluate accessibility to systemic therapy following TACE and its impact on survival.

Patients / Materials and Methods

A multicenter prospective cohort study conducted in Latin America, included HCC patients receiving TACE from May 15, 2018 to March 15, 2024. We excluded patients on the liver transplant waiting list, or Child Pugh C. Survival since first TACE was compared between groups accessing (A) and not accessing (no-A) to systemic therapy after TACE through Cox proportional hazard survival analysis, and adjusted treatment effect was further evaluated using a propensity score (PS) and inverse probability treatment weighting (IPTW).

Results and Discussion

rom 258 receiving TACE, 188 were included after excluding 33 patients on the waiting list and 37 Child C (Table). Access to any systemic therapy was 46.8% (95% CI 39.5-54.2%), within a median time from TACE to first line of 9 months (range 3.7-17.0). In group A (n=88) systemic treatments following TACE were sorafenib 62.5%, atezolizumab + bevacizumab 31.8%, and lenvatinib 4.5%. Paradoxically, while presenting better liver function reserve, liver decompensation after TACE was more frequent in group A (7% vs 0%; P=0.004), without significant differences regarding median number of TACEs, modality, or tumor burden. Median survival since first TACE between groups was A 37.4 months vs no-A 29.8 months [HR 0.69 (95% CI 0.44-1.10), adjusted for the HAP score (Figure), which was unchanged after PS and IPTW.

Conclusions

In our region, less than half of HCC systemic treatment candidates acceded to sequential TACE-systemic therapy. Although not statistically significant, due to underpowered estimations, numerically higher survival was achieved with TACE-systemic therapies.

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Comparison between patients acceding and not acceding to systemic therapies

Survival comparison between patients acceding and not acceding to systemic

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