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논문 기본 정보

자료유형
학술저널
저자정보
Anand V. Kulkarni (Department of Hepatology, AIG Hospitals, Hyderabad) Parthasarathy Kumaraswamy (Department of Liver Transplant Surgery, AIG Hospitals, Hyderabad) Balachandran Menon (Department of Liver Transplant Surgery, AIG Hospitals, Hyderabad) Anuradha Sekaran (Department of Pathology, AIG Hospitals, Hyderabad) Anuhya Rambhatla (Department of Liver Transplant Anaesthesia, AIG Hospitals, Hyderabad, India) Sowmya Iyengar (Department of Hepatology, AIG Hospitals, Hyderabad) Manasa Alla (Department of Hepatology, AIG Hospitals, Hyderabad) Shantan Venishetty (Department of Hepatology, AIG Hospitals, Hyderabad) Sumana Kolar Ramachandra (Department of Liver Transplant Surgery, AIG Hospitals, Hyderabad) Giri V. Premkumar (Department of Liver Transplant Anaesthesia, AIG Hospitals, Hyderabad, India) Mithun Sharma (Department of Hepatology, AIG Hospitals, Hyderabad) P. Nagaraja Rao (Department of Hepatology, AIG Hospitals, Hyderabad) Duvvur Nageshwar Reddy (Department of Hepatology, AIG Hospitals, Hyderabad) Amit G. Singal (Department of Internal Medicine, UT Southwestern Medical Center, Dallas, TX, USA)
저널정보
대한간암학회 Journal of Liver Cancer Journal of Liver Cancer 제24권 제2호
발행연도
2024.9
수록면
224 - 233 (10page)
DOI
10.17998/jlc.2024.05.12

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Backgrounds/Aims: Hepatocellular carcinoma (HCC) is generally diagnosed at an advanced stage, which limits curative treatment options for these patients. Locoregional therapy (LRT) is the standard approach to bridge and downstage unresectable HCC for liver transplantation (LT). Atezolizumab-bevacizumab (atezo-bev) can induce objective responses in nearly one-third of patients; however, the role and outcomes of downstaging using atezo-bev remains unknown. Methods: In this retrospective single-center study, we included consecutive patients between November 2020 and August 2023, who received atezo-bev with or without LRT and were subsequently considered for resection/LT after downstaging. Results: Of the 115 patients who received atezo-bev, 12 patients (10.4%) achieved complete or partial response and were willing to undergo LT; they (age, 58.5 years; women, 17%; Barcelona Clinic Liver Cancer stage system B/C, 5/7) had received 3-12 cycles of atezo-bev, and four of them had received prior LRT. Three patients died before LT, while three were awaiting LT. Six patients underwent curative therapies: four underwent living donor LT after a median of 79.5 days (range, 54-114) following the last atezo-bev dose, one underwent deceased donor LT 38 days after the last dose, and one underwent resection. All but one patient had complete pathologic response with no viable HCC. Three patients experienced wound healing complications, and one required re-exploration and succumbed to sepsis. After a median follow-up of 10 months (range, 4-30), none of the alive patients developed HCC recurrence or graft rejection. Conclusions: Surgical therapy, including LT, is possible after atezo-bev therapy in well-selected patients after downstaging.

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