Phase I Trial of SPECT-Guided Liver-Directed Radiotherapy for Patients with Low Functional Liver Volume.


Journal

JNCI cancer spectrum
ISSN: 2515-5091
Titre abrégé: JNCI Cancer Spectr
Pays: England
ID NLM: 101721827

Informations de publication

Date de publication:
10 May 2024
Historique:
received: 29 12 2023
revised: 28 03 2024
accepted: 03 05 2024
medline: 11 5 2024
pubmed: 11 5 2024
entrez: 11 5 2024
Statut: aheadofprint

Résumé

Traditional constraints specify that 700 cc of liver should be spared a hepatotoxic dose when delivering liver-directed radiotherapy to reduce the risk of inducing liver failure. We investigated the role of single photon emission computed tomography (SPECT) to identify and preferentially avoid functional liver during liver-directed radiation treatment planning in patients with preserved liver function but limited functional liver volume after receiving prior hepatotoxic chemotherapy or surgical resection. This phase I trial with a 3 + 3 design evaluated the safety of liver-directed radiotherapy using escalating functional liver radiation dose constraints in patients with liver metastases. Dose limiting toxicities (DLTs) were assessed 6-8 weeks and 6 months after completing radiotherapy. All twelve patients had colorectal liver metastases and received prior hepatotoxic chemotherapy. Eight patients underwent prior liver resection. Median computed tomography (CT) anatomical non-tumor liver volume was 1,584 cc (range 764-2,699 cc). Median SPECT functional liver volume was 1,117 cc (range 570-1,928cc). Median non-target CT and SPECT liver volumes below the volumetric dose constraint were 997 cc (range 544-1,576 cc) and 684 cc (range 429-1,244 cc), respectively. The prescription dose was 67.5-75 Gy in 15 fractions or 75-100 Gy in 25 fractions. No DLTs were observed during follow-up. One-year in-field control was 57%. One-year overall survival was 73%. Liver-directed radiotherapy can be safely delivered to high doses when incorporating functional SPECT into the radiation treatment planning process which may enable sparing of lower volumes of liver than traditionally accepted in patients with preserved liver function. NCT02626312.

Sections du résumé

BACKGROUND BACKGROUND
Traditional constraints specify that 700 cc of liver should be spared a hepatotoxic dose when delivering liver-directed radiotherapy to reduce the risk of inducing liver failure. We investigated the role of single photon emission computed tomography (SPECT) to identify and preferentially avoid functional liver during liver-directed radiation treatment planning in patients with preserved liver function but limited functional liver volume after receiving prior hepatotoxic chemotherapy or surgical resection.
METHODS METHODS
This phase I trial with a 3 + 3 design evaluated the safety of liver-directed radiotherapy using escalating functional liver radiation dose constraints in patients with liver metastases. Dose limiting toxicities (DLTs) were assessed 6-8 weeks and 6 months after completing radiotherapy.
RESULTS RESULTS
All twelve patients had colorectal liver metastases and received prior hepatotoxic chemotherapy. Eight patients underwent prior liver resection. Median computed tomography (CT) anatomical non-tumor liver volume was 1,584 cc (range 764-2,699 cc). Median SPECT functional liver volume was 1,117 cc (range 570-1,928cc). Median non-target CT and SPECT liver volumes below the volumetric dose constraint were 997 cc (range 544-1,576 cc) and 684 cc (range 429-1,244 cc), respectively. The prescription dose was 67.5-75 Gy in 15 fractions or 75-100 Gy in 25 fractions. No DLTs were observed during follow-up. One-year in-field control was 57%. One-year overall survival was 73%.
CONCLUSION CONCLUSIONS
Liver-directed radiotherapy can be safely delivered to high doses when incorporating functional SPECT into the radiation treatment planning process which may enable sparing of lower volumes of liver than traditionally accepted in patients with preserved liver function.
TRIAL REGISTRATION BACKGROUND
NCT02626312.

Identifiants

pubmed: 38730548
pii: 7668446
doi: 10.1093/jncics/pkae037
pii:
doi:

Banques de données

ClinicalTrials.gov
['NCT02626312']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press.

Auteurs

Enoch Chang (E)

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

Franklin C L Wong (FCL)

Nuclear Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Beth A Chasen (BA)

Nuclear Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

William D Erwin (WD)

Imaging Physics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Prajnan Das (P)

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

Emma B Holliday (EB)

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

Albert C Koong (AC)

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

Ethan B Ludmir (EB)

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

Bruce D Minsky (BD)

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

Sonal S Noticewala (SS)

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

Grace L Smith (GL)

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

Cullen M Taniguchi (CM)

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

Maria J Rodriguez (MJ)

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

Sam Beddar (S)

Radiation Physics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Rachael M Martin-Paulpeter (RM)

Radiation Physics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Joshua S Niedzielski (JS)

Radiation Physics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Gabriel O Sawakuchi (GO)

Radiation Physics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Emil Schueler (E)

Radiation Physics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Luis A Perles (LA)

Radiation Physics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Lianchun Xiao (L)

Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Janio Szklaruk (J)

Diagnostic Imaging, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Peter C Park (PC)

Radiology Physics, University of California, Davis, Davis, CA, USA.

Arvind N Dasari (AN)

Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Ahmed O Kaseb (AO)

Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Bryan K Kee (BK)

Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Sunyoung S Lee (SS)

Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Michael J Overman (MJ)

Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Jason A Willis (JA)

Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Robert A Wolff (RA)

Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Ching-Wei D Tzeng (CD)

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

Jean-Nicolas Vauthey (JN)

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

Eugene J Koay (EJ)

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

Classifications MeSH