The impact of previous local therapy (LT) on overall survival (OS) in patients with advanced hepatocellular carcinoma (aHCC) treated with atezolizumab/bevacizumab (A+B) as first line systemic therapy.

Authors

null

Maria Elena Fierro

University of Texas Health Science Center at San Antonio, San Antonio, TX

Maria Elena Fierro , Munaf Alkadimi , Lauren Diaz Boyle , Kana Lucero , Michael Mader , Kathleen Franklin , Zohra Nooruddin

Organizations

University of Texas Health Science Center at San Antonio, San Antonio, TX, University of Texas Health Science Center at San Antonio, San Anonio, TX, The University of Texas Health Science Center-San Antonio, San Antonio, TX, Audie L Murphy VA Medical Center, San Antonio, TX, South Texas Veterans Health Care System, San Antonio, TX, University of Texas Health San Antonio, San Antonio, TX

Research Funding

No funding received
None.

Background: Treatment options for aHCC have drastically improved over the past few years with immunotherapy at the forefront. Ongoing studies aim to identify the benefit of immunotherapy in combination with local therapies, but there are no studies that analyze the impact of previous local therapy on OS in patients who later receive A+B for treatment of aHCC. This study aims to analyze the impact of previous local therapy on OS in patients with aHCC treated with first line A+B within the Veterans Health Administration (VHA). Methods: Patients with aHCC receiving first line systemic therapy with A+B at VHA between Dec 1, 2019 through Mar 1, 2022 were identified from the electronic medical record (EMR) using ICD-9 and ICD-10 codes. Abstractors reviewed the EMR and followed the patients from the date of diagnosis, date of local treatment and date of A+ B initiation until death or their last VHA visit with the study period ending on Jan 31, 2023. The Chi-Squared test was used to compare rates and the Mann-Whitney test was used to compare medians. Results: 332 patients with aHCC received A+B. 67% of patients received prior LT. Patients who received LT had better ECOG status, Child-Pugh classification, and BCLC staging at time of diagnosis. There was no difference in age at diagnosis, race/ethnicity, ALBI score at time of diagnosis or at time of starting A+B, or presence of extrahepatic spread at time of starting A+B. There was a statistically significant difference in time from HCC diagnosis to start of A+B, with patients who received LT having a longer interval time. There was a small but not statistically significant difference in median OS from the start of A+B, favoring people who received LT. Conclusions: Our unique retrospective study confirms that patients receiving LT have better OS from the time of diagnosis. Disease biology and LT response may be contributing to this survival benefit. However, the OS was similar from the time of initiation of A+B in patients receiving LT versus patients who did not receive any LT.

Comparison of aHCC Patients Who Received Local Therapy Vs. No Local Therapy.

Characteristic No Local TherapyLocal Therapy P-value
N110222NA
ECOG at diagnosis (%)
0
1
2 or 3

27 (25%)
60 (55%)
23 (21%)

85 (38%)
119 (54%)
18 ( 8%)

0.001
Barcelona Clinic Liver Cancer stage (%)
at diagnosis
A
B
C

13 (12%)
28 (26%)
67 (62%)

100 (50%)
61 (30%)
41 (20%)

<0.0001
Barcelona Clinic Liver Cancer stage (%)
prior to starting A+B
A
B
C

3 ( 3%)
29 (26%)
78 (71%)

8 ( 4%)
67 (30%)
146 (66%)

0.66
OS from HCC Diagnosis, months13.3 (7.3 – 22.4)38.2 (25.2 – 57.6)<0.0001
Time from HCC Diagnosis to start of A+B, months1.5 (0.8 – 4.3)22.9 (10.8 – 45.6)<0.0001
OS from start of A+B, months9.8 (4.2 – 18.6)11.5 (6.2 – 19.1)0.18

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Abstract Details

Meeting

2023 ASCO Annual Meeting

Session Type

Publication Only

Session Title

Publication Only: Gastrointestinal Cancer—Gastroesophageal, Pancreatic, and Hepatobiliary

Track

Gastrointestinal Cancer—Gastroesophageal, Pancreatic, and Hepatobiliary

Sub Track

Hepatobiliary Cancer - Advanced/Metastatic Disease

Citation

J Clin Oncol 41, 2023 (suppl 16; abstr e16129)

DOI

10.1200/JCO.2023.41.16_suppl.e16129

Abstract #

e16129

Abstract Disclosures

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