Evidence map›Paper›PMID 42052149›Full record

ArticleSurgical case reports2026

Conversion Liver Resection for Hepatocellular Carcinoma with Portal Vein Tumor Thrombus after Single Tremelimumab Regular Interval Durvalumab Regimen as a Second-Line Therapy: A Case Report.

Diyar Akhmet, Akihiko Soyama, Ayaka Kinoshita, Hajime Matsushima, Hajime Imamura, Takashi Hamada, Ayaka Satoh, Kazushige Migita, Shun Nakamura, Baglan Askeyev and 5 more

Abstract readCase Reports
In one paragraph

Article in Surgical case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Diyar AkhmetDepartment of Surgery, Division of Digestive Surgery and Transplantology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Nagasaki, Japan.
Akihiko SoyamaDepartment of Surgery, Division of Digestive Surgery and Transplantology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Nagasaki, Japan.
Ayaka KinoshitaDepartment of Surgery, Division of Digestive Surgery and Transplantology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Nagasaki, Japan.
Hajime MatsushimaDepartment of Surgery, Division of Digestive Surgery and Transplantology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Nagasaki, Japan.
Hajime ImamuraDepartment of Surgery, Division of Digestive Surgery and Transplantology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Nagasaki, Japan.
Takashi HamadaDepartment of Surgery, Division of Digestive Surgery and Transplantology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Nagasaki, Japan.
Ayaka SatohDepartment of Surgery, Division of Digestive Surgery and Transplantology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Nagasaki, Japan.
Kazushige MigitaDepartment of Surgery, Division of Digestive Surgery and Transplantology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Nagasaki, Japan.
Shun NakamuraDepartment of Surgery, Division of Digestive Surgery and Transplantology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Nagasaki, Japan.
Baglan AskeyevDepartment of Surgery, Division of Digestive Surgery and Transplantology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Nagasaki, Japan.
Masanori FukushimaDepartment of Gastroenterology and Hepatology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Nagasaki, Japan.
Tomohiko AdachiDepartment of Surgery, Division of Digestive Surgery and Transplantology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Nagasaki, Japan.
Shinji OkanoDepartment of Pathology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Nagasaki, Japan.
Hisamitsu MiyaakiDepartment of Gastroenterology and Hepatology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Nagasaki, Japan.
Susumu EguchiDepartment of Surgery, Division of Digestive Surgery and Transplantology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Nagasaki, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionHepatocellular carcinoma (HCC) is a leading cause of cancer-related mortality, with limited treatment options for advanced, unresectable cases. Although immune checkpoint inhibitors (ICI), particularly the combination of atezolizumab plus bevacizumab (Atezo+Bev), have improved outcomes, many patients ultimately experience disease progression. The single tremelimumab regular interval durvalumab (STRIDE) regimen has emerged as a promising alternative, yet evidence of its efficacy as a second-line therapy remains limited. CASE PRESENTATION: A 74-year-old man presented with recurrent HCC and liver cirrhosis complicated by portal vein tumor thrombosis (PVTT). Following 2 cycles of Atezo+Bev and 1 additional cycle of atezolizumab monotherapy, the tumor progressed rapidly. The patient was subsequently treated with dual ICIs (durvalumab and tremelimumab) under the STRIDE regimen, resulting in significant tumor shrinkage and normalization of serum tumor markers. After 4 cycles of STRIDE, conversion surgery was performed, including segment VI resection and portal vein branch thrombectomy. Histopathological analysis revealed >95% tumor necrosis and confirmed R0 resection.

conclusionsThis case illustrates the importance of a multidisciplinary approach in the treatment of advanced HCC and shows that a successful response to the STRIDE regimen, even as a second-line therapy can enable curative conversion surgery while maintaining safety and tolerability in patients with limited hepatic reserve.

Indexed as

hepatocellular carcinomaportal vein tumor thrombosissequential immunotherapysingle tremelimumab regular interval durvalumab regimen

Identifiers

PMID42052149
PMCPMC13112089

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.