Ablative liver radiotherapy for unresected intrahepatic cholangiocarcinoma: Patterns of care and survival in the United States.

liver failure local therapy locally advanced metastatic primary liver cancer stereotactic body radiotherapy

Journal

Cancer
ISSN: 1097-0142
Titre abrégé: Cancer
Pays: United States
ID NLM: 0374236

Informations de publication

Date de publication:
01 07 2022
Historique:
revised: 01 03 2022
received: 19 01 2022
accepted: 22 03 2022
pubmed: 14 4 2022
medline: 11 6 2022
entrez: 13 4 2022
Statut: ppublish

Résumé

Single-institution studies have shown the oncologic benefit of ablative liver radiotherapy (A-RT) for patients with unresectable intrahepatic cholangiocarcinoma (ICC). However, adoption of A-RT across the United States and its associated outcomes are unknown. We queried the National Cancer Data Base for nonsurgically managed patients with ICC diagnosed between 2004 and 2018. Patients were labeled A-RT for receipt of biologically effective doses (BED Of 27,571 patients, the most common treatments were chemotherapy without liver RT (45%), no chemotherapy or liver RT (42%), and liver RT ± chemotherapy (13%). Use of liver RT remained constant over time. Of 1112 patients receiving liver RT with known doses, RT was 73% Conv-RT (median BED Although A-RT has been increasingly used, use of liver RT as a whole in the United States remained constant despite growing evidence supporting its use, suggesting continued unmet need. A-RT is associated with longer survival versus Conv-RT. Bile duct cancer is a rare, deadly disease that often presents at advanced stages. Single-institution retrospective studies have demonstrated that use of high-dose radiotherapy may be associated with longer survival, but larger studies have not been conducted. We used a large, national cancer registry of patients diagnosed between 2004 and 2018 to show that liver radiotherapy use remains low in the United States, despite growing evidence that patients who receive it live longer. Furthermore, we showed that patients who received high-dose radiotherapy lived longer than those who received lower doses. Greater awareness of the benefits of liver radiotherapy is needed to improve patient outcomes.

Sections du résumé

BACKGROUND
Single-institution studies have shown the oncologic benefit of ablative liver radiotherapy (A-RT) for patients with unresectable intrahepatic cholangiocarcinoma (ICC). However, adoption of A-RT across the United States and its associated outcomes are unknown.
METHODS
We queried the National Cancer Data Base for nonsurgically managed patients with ICC diagnosed between 2004 and 2018. Patients were labeled A-RT for receipt of biologically effective doses (BED
RESULTS
Of 27,571 patients, the most common treatments were chemotherapy without liver RT (45%), no chemotherapy or liver RT (42%), and liver RT ± chemotherapy (13%). Use of liver RT remained constant over time. Of 1112 patients receiving liver RT with known doses, RT was 73% Conv-RT (median BED
CONCLUSIONS
Although A-RT has been increasingly used, use of liver RT as a whole in the United States remained constant despite growing evidence supporting its use, suggesting continued unmet need. A-RT is associated with longer survival versus Conv-RT.
LAY SUMMARY
Bile duct cancer is a rare, deadly disease that often presents at advanced stages. Single-institution retrospective studies have demonstrated that use of high-dose radiotherapy may be associated with longer survival, but larger studies have not been conducted. We used a large, national cancer registry of patients diagnosed between 2004 and 2018 to show that liver radiotherapy use remains low in the United States, despite growing evidence that patients who receive it live longer. Furthermore, we showed that patients who received high-dose radiotherapy lived longer than those who received lower doses. Greater awareness of the benefits of liver radiotherapy is needed to improve patient outcomes.

Identifiants

pubmed: 35417569
doi: 10.1002/cncr.34223
pmc: PMC9177808
mid: NIHMS1793169
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

2529-2539

Subventions

Organisme : NCI NIH HHS
ID : U01 CA200468
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA016672
Pays : United States
Organisme : NCI NIH HHS
ID : U54 CA210181
Pays : United States
Organisme : NCI NIH HHS
ID : U01 CA252965
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA218004
Pays : United States
Organisme : NCI NIH HHS
ID : U54 CA143837
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA248917
Pays : United States
Organisme : NCI NIH HHS
ID : U01 CA196403
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA221971
Pays : United States
Organisme : NCI NIH HHS
ID : P50 CA221707
Pays : United States
Organisme : NCI NIH HHS
ID : P50 CA217674
Pays : United States
Organisme : NCI NIH HHS
ID : U01 CA214263
Pays : United States

Informations de copyright

© 2022 American Cancer Society.

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Auteurs

Brian De (B)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Hop S Tran Cao (HS)

Department of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Jean-Nicolas Vauthey (JN)

Department of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Gohar S Manzar (GS)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Kelsey L Corrigan (KL)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Kanwal P S Raghav (KPS)

Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Sunyoung S Lee (SS)

Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Ching-Wei D Tzeng (CD)

Department of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Bruce D Minsky (BD)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Grace L Smith (GL)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Department of Health Services Research, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Emma B Holliday (EB)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Cullen M Taniguchi (CM)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Albert C Koong (AC)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Prajnan Das (P)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Milind Javle (M)

Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Ethan B Ludmir (EB)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Eugene J Koay (EJ)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

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