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Multicenter Study
. 2022 Nov:8:e2200205.
doi: 10.1200/GO.22.00205.

Efficacy, Safety, and Patient-Reported Outcomes of Atezolizumab Plus Bevacizumab for Unresectable Hepatocellular Carcinoma in Thailand: A Multicenter Prospective Study

Affiliations
Multicenter Study

Efficacy, Safety, and Patient-Reported Outcomes of Atezolizumab Plus Bevacizumab for Unresectable Hepatocellular Carcinoma in Thailand: A Multicenter Prospective Study

Chanchai Charonpongsuntorn et al. JCO Glob Oncol. 2022 Nov.

Abstract

Purpose: Atezolizumab plus bevacizumab treatment is a first-line therapy for unresectable hepatocellular carcinoma (HCC) worldwide. The efficacy, safety, and patient-reported outcomes (PROs) of HCC in Thailand have not yet been reported. This study aimed to evaluate the efficacy, safety, and PROs of atezolizumab plus bevacizumab.

Materials and methods: From September 2020 to August 2021, 30 patients with unresectable HCC who met the inclusion criteria of atezolizumab plus bevacizumab as first-line treatment were enrolled. Analysis was assessed for progression-free survival, overall survival, adverse events (AEs), and quality of life (QoL).

Results: The median progression-free survival and overall survival periods were 6.7 and 10.2 months, respectively. The disease control rate was 63.3%. The frequent AEs were proteinuria, hypertension, and hepatitis. Serious AEs included gastrointestinal bleeding, but none of the patients died from serious AEs. The discontinuation rate was 23.3%, and the median number of treatment cycles was 10.5 cycles. In total, 23.3% of the patients continued treatment after 1 year of therapy. The global health status/QoL and physical function scores showed less deterioration at baseline than at 3 and 6 months (median scores = 76.7, 71.6, and 64.1 in QoL and 84.7, 79.6, and 79.0 in physical function, respectively). The HCC18 symptom score index data showed a slow progression of symptom scores from baseline to 3 and 6 months (12.7, 19.6, and 22.3, respectively).

Conclusion: This study demonstrates that atezolizumab plus bevacizumab is effective and has a safety profile comparable with that of previous studies as first-line therapy for unresectable HCC in a real-world setting and in Thai populations. Data on PROs also demonstrate benefits in terms of patients' QoL and symptoms.

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Conflict of interest statement

The following represents disclosure information provided by authors of this manuscript. All relationships are considered compensated unless otherwise noted. Relationships are self-held unless noted. I = Immediate Family Member, Inst = My Institution. Relationships may not relate to the subject matter of this manuscript. For more information about ASCO's conflict of interest policy, please refer to www.asco.org/rwc or ascopubs.org/go/authors/author-center.

Open Payments is a public database containing information reported by companies about payments made to US-licensed physicians (Open Payments).

Chanchai Charonpongsuntorn

Research Funding: AstraZeneca

Suebpong Tanasanvimon

Honoraria: Eisai, MSD, Roche Canada, Bristol Myers Squibb/Celgene, Amgen, Lilly, Merck, Novartis, Ipsen, AstraZeneca

Consulting or Advisory Role: Eisai, MSD, Bristol Myers Squibb/Celgene, Merck, Amgen

Travel, Accommodations, Expenses: Fresinius Krabi

Ekkamol Phaibulvatanapong

Honoraria: Roche

Consulting or Advisory Role: Roche

Naiyarat Prasongsook

Consulting or Advisory Role: AstraZeneca, Boehringer Ingelheim, Roche, Novartis, Bristol Myers Squibb/Celgene

Travel, Accommodations, Expenses: AstraZeneca, Roche

Nuttapong Ngamphaiboon

Consulting or Advisory Role: MSD, Novartis, Amgen, Eisai, Merck

Speakers' Bureau: Roche, Eisai, MSD, Novartis

Research Funding: MSD (Inst), Pfizer (Inst), Roche (Inst), Exelixis (Inst), RAPT Therapeutics (Inst), BeiGene (Inst)

Travel, Accommodations, Expenses: Roche

Ekaphop Sirachainan

Honoraria: MSD, Sanofi/Aventis, Merck, Amgen, Roche, Mundipharma, AstraZeneca, LF Asia, Diethelm Keller Group, Bristol Myers Squibb, Boehringer Ingelheim, Taiho Pharmaceutical, Dr Reddy's Laboratories, Zuellig Pharma, Meda Pharmaceuticals, Pfizer, Novo Nordisk, Novartis

Consulting or Advisory Role: Roche, Taiho Oncology, MSD Oncology, Novartis, Bristol Myers Squibb/Celgene

Travel, Accommodations, Expenses: MSD, AstraZeneca, Pfizer, Amgen, American Taiwan Biopharm, Taiho Pharmaceutical, Eisai

No other potential conflicts of interest were reported.

Figures

FIG 1
FIG 1
(A) OS and (B) PFS curves of the patients treated with atezolizumab plus bevacizumab. OS, overall survival; PFS, progression-free survival.
FIG 2
FIG 2
Assessment of the overall response rate using the Response Evaluation Criteria in Solid Tumors. PD, progressive disease; PR, partial response; SD, stable disease.
FIG 3
FIG 3
(A) The global health status/QoL and (B) physical function score based on the EORTC-QLC C30 and (C) HCC symptoms score index using the EORTC-QLQ-HCC18 at baseline, 3, 6, 9, and 12 months of atezolizumab and bevacizumab treatment. EORTC-QLC C30, European Organization for the Research and Treatment of Cancer Quality of Life Questionnaire; HCC, hepatocellular carcinoma; QoL, quality of life.

References

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