The normal tissue complication probability model-based approach considering uncertainties for the selective use of radiation modality in primary liver cancer patients. (June 2019)
- Record Type:
- Journal Article
- Title:
- The normal tissue complication probability model-based approach considering uncertainties for the selective use of radiation modality in primary liver cancer patients. (June 2019)
- Main Title:
- The normal tissue complication probability model-based approach considering uncertainties for the selective use of radiation modality in primary liver cancer patients
- Authors:
- Prayongrat, Anussara
Kobashi, Keiji
Ito, Yoichi M.
Katoh, Norio
Tamura, Masaya
Dekura, Yasuhiro
Toramatsu, Chie
Khorprasert, Chonlakiet
Amornwichet, Napapat
Alisanant, Petch
Shirato, Hiroki
Shimizu, Shinichi - Abstract:
- Highlights: Normal tissue complication probability (NTCP) model can guide treatment selection. NTCP for radiation-induced liver toxicity (RILT) has been developed. RILT risk varied among different Child–Pugh and viral hepatitis infection status. Estimated NTCP model and ΔNTCP for RILT are specific to the patient subgroups. ΔNTCP with uncertainty in individualized subgroups is helpful to select treatment. Abstract: Purpose: To predict the probability of radiation-induced liver toxicity (RILT) and implement the normal tissue complication probability (NTCP) model-based approach considering confidence intervals (CIs) to select patients for new treatment techniques, such as proton beam therapy, based on a certain NTCP reduction (ΔNTCP) threshold for primary liver cancer patients. Methods and materials: Common Toxicity Criteria for Adverse Events (CTCAE) grade ≥2 RILT was scored. The Lyman NTCP models predicting the probability of CTCAE grade ≥2 RILT as a function of the fraction-size adjusted mean liver dose (MLD), using reference fraction size = 2 Gy/fraction and α / β ratio = 2 Gy, were fitted using the maximum likelihood method. At certain combinations of MLDs, ΔNTCP with a CI was evaluated by the delta method. Results: Of the 239 patients, the incidence of CTCAE grade ≥2 RILT was 55% (46% in the Child–Pugh (CP)-A vs. 81% in the CP-B/C, p < 0.001). Among 180 CP-A patients, 40% who had viral hepatitis infections experienced toxicity vs. 32% in the nonhepatitis subgroup. TheHighlights: Normal tissue complication probability (NTCP) model can guide treatment selection. NTCP for radiation-induced liver toxicity (RILT) has been developed. RILT risk varied among different Child–Pugh and viral hepatitis infection status. Estimated NTCP model and ΔNTCP for RILT are specific to the patient subgroups. ΔNTCP with uncertainty in individualized subgroups is helpful to select treatment. Abstract: Purpose: To predict the probability of radiation-induced liver toxicity (RILT) and implement the normal tissue complication probability (NTCP) model-based approach considering confidence intervals (CIs) to select patients for new treatment techniques, such as proton beam therapy, based on a certain NTCP reduction (ΔNTCP) threshold for primary liver cancer patients. Methods and materials: Common Toxicity Criteria for Adverse Events (CTCAE) grade ≥2 RILT was scored. The Lyman NTCP models predicting the probability of CTCAE grade ≥2 RILT as a function of the fraction-size adjusted mean liver dose (MLD), using reference fraction size = 2 Gy/fraction and α / β ratio = 2 Gy, were fitted using the maximum likelihood method. At certain combinations of MLDs, ΔNTCP with a CI was evaluated by the delta method. Results: Of the 239 patients, the incidence of CTCAE grade ≥2 RILT was 55% (46% in the Child–Pugh (CP)-A vs. 81% in the CP-B/C, p < 0.001). Among 180 CP-A patients, 40% who had viral hepatitis infections experienced toxicity vs. 32% in the nonhepatitis subgroup. The MLD was 18 Gy in the toxicity group vs. 16.1 Gy in the nontoxicity group ( p = 0.002). The estimated NTCP model parameters specific to the patient subgroups and the ΔNTCP with CI assuming a particular CP classification and viral hepatitis infection status were considerably different which possible changed treatment decision. Conclusions: Patients with CP-A and viral hepatitis infection or CP-B/C cirrhosis had greater susceptibility to CTCAE grade ≥2 RILT. The estimated NTCP and ΔNTCP for individual patients along with a consideration of uncertainties improve the reliability of the NTCP model-based approach. … (more)
- Is Part Of:
- Radiotherapy and oncology. Volume 135(2019)
- Journal:
- Radiotherapy and oncology
- Issue:
- Volume 135(2019)
- Issue Display:
- Volume 135, Issue 2019 (2019)
- Year:
- 2019
- Volume:
- 135
- Issue:
- 2019
- Issue Sort Value:
- 2019-0135-2019-0000
- Page Start:
- 100
- Page End:
- 106
- Publication Date:
- 2019-06
- Subjects:
- CPT charged particle therapy -- PBT proton beam therapy -- RT radiotherapy -- XRT X-ray treatment -- MBA model-based approach -- NTCP normal tissue complication probability -- ΔNTCP NTCP reduction -- RILT radiation-induced liver toxicity -- HCC hepatocellular carcinoma -- CCA cholangiocarcinoma -- 3D three-dimensional -- CP Child–Pugh -- HBV hepatitis B virus -- HCV hepatitis C virus -- 3D-CRT 3D-conformal radiotherapy -- IMRT intensity-modulated radiotherapy -- CT computed tomography -- ITV internal target volume -- DEBH deep expiratory breath hold -- IRB institutional review board -- AST aspartate aminotransferase -- ALT alanine aminotransferase -- ALP alkaline phosphatase -- UNL upper normal limit -- CTCAE Common Toxicity Criteria for Adverse Events -- RILD radiation-induced liver disease -- DVHs Dose–volume histograms -- FED fraction-size equivalent dose -- MLD mean liver dose -- Vx volume receiving x Gy -- OS Overall survival -- HL Hosmer–Lemeshow -- CI confidence interval -- ΔNTCP68%CI LB 68%CI lower boundary of the ΔNTCP
Normal tissue complication probability (NTCP) -- Radiation-induced liver disease (RILD) -- Treatment selection -- Model
Oncology -- Periodicals
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Tumors -- Periodicals
Medical Oncology -- Periodicals
Neoplasms -- radiotherapy -- Periodicals
Radiotherapy -- Periodicals
Radiothérapie -- Périodiques
Cancérologie -- Périodiques
Tumeurs -- Périodiques
Electronic journals
616.9940642 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01678140 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/01678140 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/01678140 ↗
http://www.estro.org/ ↗
http://www.elsevier.com/journals ↗
http://www.journals.elsevier.com/radiotherapy-and-oncology/ ↗ - DOI:
- 10.1016/j.radonc.2019.03.003 ↗
- Languages:
- English
- ISSNs:
- 0167-8140
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- Legaldeposit
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