Ablative radiation therapy for hepatocellular carcinoma is associated with reduced treatment- and tumor-related liver failure and improved survival.

Hepatocellular carcinoma (HCC) ablative radiation therapy liver failure stereotactic radiation therapy

Journal

Journal of gastrointestinal oncology
ISSN: 2078-6891
Titre abrégé: J Gastrointest Oncol
Pays: China
ID NLM: 101557751

Informations de publication

Date de publication:
Aug 2021
Historique:
received: 03 03 2021
accepted: 08 06 2021
entrez: 17 9 2021
pubmed: 18 9 2021
medline: 18 9 2021
Statut: ppublish

Résumé

More than 70% of patients with hepatocellular carcinoma (HCC) are not candidates for curative therapy or recur after curative-intent therapy. There is growing evidence on the use of ablative radiation therapy (RT) for liver tumors. We aimed to analyze outcomes of HCC patients treated with conventional versus ablative RT. We retrospectively analyzed medical records of HCC patients treated with liver RT from 2001 to 2019. We defined ablative RT as biologically effective dose (BED) ≥80 Gy. RECIST 1.1 was used to define early responses at 3-6 months after RT, and local control (LC) at last follow-up (FU). Data was analyzed using Fisher exact test, Kaplan-Meier, cumulative incidence rates, Cox proportional hazards model and Fine-Gray competing risks. Forty-five patients were identified, of whom 14 (31.1%) received ablative RT using a stereotactic technique. With median FU of survivors of 10.1 months, 1-year cumulative incidence of LC was 91.7% for ablative and 75.2% for BED <80 Gy. At early FU, patients treated with ablative RT had better responses compared to BED <80 Gy, with 7% progressing versus 19%, and 21.4% with complete response versus none (P=0.038). On univariate analysis (UVA), Child-Pugh (CP) score [hazard ratio (HR): 3 for CP-B, HR: 16 for CP-C] and BED (HR: 7.69 for BED <80 Gy) correlated with deterioration of liver function, leading to liver failure. Most liver failure cases were due to disease progression. No RT-related liver failure occurred in the ablative RT group. On UVA, only BED ≥80 Gy was associated with improved overall survival (OS) (HR: 0.4; P=0.044). Median OS (mOS) and 1-year OS were 7 months and 35% respectively for BED <80 Gy compared to 28 months and 66% for BED ≥80 Gy. No grade 3+ bowel toxicity was reported in either group. Greater than 90% LC was achieved after stereotactic ablative RT, which was associated with minimized tumor- and treatment-related liver failure and improved survival for highly selected inoperable HCC patients.

Sections du résumé

BACKGROUND BACKGROUND
More than 70% of patients with hepatocellular carcinoma (HCC) are not candidates for curative therapy or recur after curative-intent therapy. There is growing evidence on the use of ablative radiation therapy (RT) for liver tumors. We aimed to analyze outcomes of HCC patients treated with conventional versus ablative RT.
METHODS METHODS
We retrospectively analyzed medical records of HCC patients treated with liver RT from 2001 to 2019. We defined ablative RT as biologically effective dose (BED) ≥80 Gy. RECIST 1.1 was used to define early responses at 3-6 months after RT, and local control (LC) at last follow-up (FU). Data was analyzed using Fisher exact test, Kaplan-Meier, cumulative incidence rates, Cox proportional hazards model and Fine-Gray competing risks.
RESULTS RESULTS
Forty-five patients were identified, of whom 14 (31.1%) received ablative RT using a stereotactic technique. With median FU of survivors of 10.1 months, 1-year cumulative incidence of LC was 91.7% for ablative and 75.2% for BED <80 Gy. At early FU, patients treated with ablative RT had better responses compared to BED <80 Gy, with 7% progressing versus 19%, and 21.4% with complete response versus none (P=0.038). On univariate analysis (UVA), Child-Pugh (CP) score [hazard ratio (HR): 3 for CP-B, HR: 16 for CP-C] and BED (HR: 7.69 for BED <80 Gy) correlated with deterioration of liver function, leading to liver failure. Most liver failure cases were due to disease progression. No RT-related liver failure occurred in the ablative RT group. On UVA, only BED ≥80 Gy was associated with improved overall survival (OS) (HR: 0.4; P=0.044). Median OS (mOS) and 1-year OS were 7 months and 35% respectively for BED <80 Gy compared to 28 months and 66% for BED ≥80 Gy. No grade 3+ bowel toxicity was reported in either group.
CONCLUSIONS CONCLUSIONS
Greater than 90% LC was achieved after stereotactic ablative RT, which was associated with minimized tumor- and treatment-related liver failure and improved survival for highly selected inoperable HCC patients.

Identifiants

pubmed: 34532124
doi: 10.21037/jgo-21-116
pii: jgo-12-04-1743
pmc: PMC8421883
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1743-1752

Subventions

Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : AHRQ HHS
ID : T32 HS000063
Pays : United States

Informations de copyright

2021 Journal of Gastrointestinal Oncology. All rights reserved.

Déclaration de conflit d'intérêts

Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at https://dx.doi.org/10.21037/jgo-21-116). The authors have no conflicts of interest to declare

Références

Ann Surg. 2015 May;261(5):947-55
pubmed: 25010665
Cancers (Basel). 2019 Jun 22;11(6):
pubmed: 31234476
Radiat Oncol. 2019 Oct 22;14(1):180
pubmed: 31640728
Int J Radiat Oncol Biol Phys. 2011 Nov 15;81(4):1039-45
pubmed: 20888707
J Clin Oncol. 2016 Feb 10;34(5):460-8
pubmed: 26668346
BMJ. 2018 Jul 18;362:k2817
pubmed: 30021785
Radiat Oncol. 2018 Nov 26;13(1):234
pubmed: 30477560
World J Gastrointest Oncol. 2019 May 15;11(5):367-376
pubmed: 31139307
Br J Surg. 1973 Aug;60(8):646-9
pubmed: 4541913
J Clin Oncol. 2013 May 1;31(13):1631-9
pubmed: 23547075
Eur J Cancer. 2009 Jan;45(2):228-47
pubmed: 19097774
J Clin Oncol. 2016 Jan 20;34(3):219-26
pubmed: 26503201
J Clin Oncol. 2005 Mar 20;23(9):1839-46
pubmed: 15774777
Cancer. 2011 Jul 1;117(13):3053-9
pubmed: 21264826

Auteurs

Lara Hilal (L)

Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Marsha Reyngold (M)

Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Abraham J Wu (AJ)

Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Abdallah Araji (A)

Department of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Ghassan K Abou-Alfa (GK)

Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Department of Medicine, Weill Cornell Medical College, New York, NY, USA.

William Jarnagin (W)

Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

James J Harding (JJ)

Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Department of Medicine, Weill Cornell Medical College, New York, NY, USA.

Maya Gambarin (M)

Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Department of Medicine, Weill Cornell Medical College, New York, NY, USA.

Imane El Dika (I)

Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Department of Medicine, Weill Cornell Medical College, New York, NY, USA.

Paul Brady (P)

Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

John Navilio (J)

Department of Medical Physics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Sean L Berry (SL)

Department of Medical Physics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Jessica Flynn (J)

Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Zhigang Zhang (Z)

Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Richard Tuli (R)

Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Melissa Zinovoy (M)

Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Paul B Romesser (PB)

Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

John J Cuaron (JJ)

Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Christopher H Crane (CH)

Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Carla Hajj (C)

Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Classifications MeSH