Photons, protons or carbon ions for stage I non-small cell lung cancer – Results of the multicentric ROCOCO in silico study
To compare dose to organs at risk (OARs) and dose-escalation possibility for 24 stage I non-small cell lung cancer (NSCLC) patients in a ROCOCO (Radiation Oncology Collaborative Comparison) trial. For each patient, 3 photon plans [Intensity-modulated radiotherapy (IMRT), volumetric modulated arc the...
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Published in: | Radiotherapy and oncology Vol. 128; no. 1; pp. 139 - 146 |
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Abstract | To compare dose to organs at risk (OARs) and dose-escalation possibility for 24 stage I non-small cell lung cancer (NSCLC) patients in a ROCOCO (Radiation Oncology Collaborative Comparison) trial.
For each patient, 3 photon plans [Intensity-modulated radiotherapy (IMRT), volumetric modulated arc therapy (VMAT) and CyberKnife], a double scattered proton (DSP) and an intensity-modulated carbon-ion (IMIT) therapy plan were created. Dose prescription was 60 Gy (equivalent) in 8 fractions.
The mean dose and dose to 2% of the clinical target volume (CTV) were lower for protons and ions compared with IMRT (p < 0.01). Doses to the lungs, heart, and mediastinal structures were lowest with IMIT (p < 0.01), doses to the spinal cord were lowest with DSP (p < 0.01). VMAT and CyberKnife allowed for reduced doses to most OARs compared with IMRT. Dose escalation was possible for 8 patients. Generally, the mediastinum was the primary dose-limiting organ.
On average, the doses to the OARs were lowest using particles, with more homogenous CTV doses. Given the ability of VMAT and CyberKnife to limit doses to OARs compared with IMRT, the additional benefit of particles may only be clinically relevant in selected patients and thus should be carefully weighed for every individual patient. |
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AbstractList | To compare dose to organs at risk (OARs) and dose-escalation possibility for 24 stage I non-small cell lung cancer (NSCLC) patients in a ROCOCO (Radiation Oncology Collaborative Comparison) trial.
For each patient, 3 photon plans [Intensity-modulated radiotherapy (IMRT), volumetric modulated arc therapy (VMAT) and CyberKnife], a double scattered proton (DSP) and an intensity-modulated carbon-ion (IMIT) therapy plan were created. Dose prescription was 60 Gy (equivalent) in 8 fractions.
The mean dose and dose to 2% of the clinical target volume (CTV) were lower for protons and ions compared with IMRT (p < 0.01). Doses to the lungs, heart, and mediastinal structures were lowest with IMIT (p < 0.01), doses to the spinal cord were lowest with DSP (p < 0.01). VMAT and CyberKnife allowed for reduced doses to most OARs compared with IMRT. Dose escalation was possible for 8 patients. Generally, the mediastinum was the primary dose-limiting organ.
On average, the doses to the OARs were lowest using particles, with more homogenous CTV doses. Given the ability of VMAT and CyberKnife to limit doses to OARs compared with IMRT, the additional benefit of particles may only be clinically relevant in selected patients and thus should be carefully weighed for every individual patient. To compare dose to organs at risk (OARs) and dose-escalation possibility for 24 stage I nonsmall cell lung cancer (NSCLC) patients in a ROCOCO (Radiation Oncology Collaborative Comparison) trial. Methods: For each patient, 3 photon plans [Intensity-modulated radiotherapy (IMRT), volumetric modulated arc therapy (VMAT) and CyberKnife], a double scattered proton (DSP) and an intensity-modulated carbon-ion (IMIT) therapy plan were created. Dose prescription was 60 Gy (equivalent) in 8 fractions. Results: The mean dose and dose to 2% of the clinical target volume (CTV) were lower for protons and ions compared with IMRT (p < 0.01). Doses to the lungs, heart, and mediastinal structures were lowest with IMIT (p < 0.01), doses to the spinal cord were lowest with DSP (p < 0.01). VMAT and CyberKnife allowed for reduced doses to most OARs compared with IMRT. Dose escalation was possible for 8 patients. Generally, the mediastinum was the primary dose-limiting organ. Conclusion: On average, the doses to the OARs were lowest using particles, with more homogenous CTV doses. Given the ability of VMAT and CyberKnife to limit doses to OARs compared with IMRT, the additional benefit of particles may only be clinically relevant in selected patients and thus should be carefully weighed for every individual patient. PURPOSETo compare dose to organs at risk (OARs) and dose-escalation possibility for 24 stage I non-small cell lung cancer (NSCLC) patients in a ROCOCO (Radiation Oncology Collaborative Comparison) trial.METHODSFor each patient, 3 photon plans [Intensity-modulated radiotherapy (IMRT), volumetric modulated arc therapy (VMAT) and CyberKnife], a double scattered proton (DSP) and an intensity-modulated carbon-ion (IMIT) therapy plan were created. Dose prescription was 60 Gy (equivalent) in 8 fractions.RESULTSThe mean dose and dose to 2% of the clinical target volume (CTV) were lower for protons and ions compared with IMRT (p < 0.01). Doses to the lungs, heart, and mediastinal structures were lowest with IMIT (p < 0.01), doses to the spinal cord were lowest with DSP (p < 0.01). VMAT and CyberKnife allowed for reduced doses to most OARs compared with IMRT. Dose escalation was possible for 8 patients. Generally, the mediastinum was the primary dose-limiting organ.CONCLUSIONOn average, the doses to the OARs were lowest using particles, with more homogenous CTV doses. Given the ability of VMAT and CyberKnife to limit doses to OARs compared with IMRT, the additional benefit of particles may only be clinically relevant in selected patients and thus should be carefully weighed for every individual patient. |
Author | Jelen, Urszula Jansen, Nicolas Wink, Krista C.J. Roelofs, Erik Solberg, Timothy Avery, Stephen Simone, Charles B. van der Stoep, Judith Smits, Julia Santiago, Alina Ammazzalorso, Filippo de Ruysscher, Dirk Dechambre, David Dries, Wim Troost, Esther G.C. |
Author_xml | – sequence: 1 givenname: Krista C.J. surname: Wink fullname: Wink, Krista C.J. email: krista.wink@maastro.nl organization: Department of Radiation Oncology (MAASTRO), GROW – School for Oncology and Developmental Biology, Maastricht University Medical Centre, The Netherlands – sequence: 2 givenname: Erik surname: Roelofs fullname: Roelofs, Erik organization: Department of Radiation Oncology (MAASTRO), GROW – School for Oncology and Developmental Biology, Maastricht University Medical Centre, The Netherlands – sequence: 3 givenname: Charles B. surname: Simone fullname: Simone, Charles B. organization: Hospital of the University of Pennsylvania, Department of Radiation Oncology, Philadelphia, USA – sequence: 4 givenname: David surname: Dechambre fullname: Dechambre, David organization: University Hospital of Liege (CHU), Department of Radiation Oncology, Belgium – sequence: 5 givenname: Alina surname: Santiago fullname: Santiago, Alina organization: Department of Radiotherapy and Radiation Oncology, University of Marburg, Germany – sequence: 6 givenname: Judith surname: van der Stoep fullname: van der Stoep, Judith organization: Department of Radiation Oncology (MAASTRO), GROW – School for Oncology and Developmental Biology, Maastricht University Medical Centre, The Netherlands – sequence: 7 givenname: Wim surname: Dries fullname: Dries, Wim organization: Catharina Hospital, Department of Radiation Oncology, Eindhoven, The Netherlands – sequence: 8 givenname: Julia surname: Smits fullname: Smits, Julia organization: Catharina Hospital, Department of Radiation Oncology, Eindhoven, The Netherlands – sequence: 9 givenname: Stephen surname: Avery fullname: Avery, Stephen organization: Hospital of the University of Pennsylvania, Department of Radiation Oncology, Philadelphia, USA – sequence: 10 givenname: Filippo surname: Ammazzalorso fullname: Ammazzalorso, Filippo organization: Department of Radiotherapy and Radiation Oncology, University of Marburg, Germany – sequence: 11 givenname: Nicolas surname: Jansen fullname: Jansen, Nicolas organization: University Hospital of Liege (CHU), Department of Radiation Oncology, Belgium – sequence: 12 givenname: Urszula surname: Jelen fullname: Jelen, Urszula organization: Department of Radiotherapy and Radiation Oncology, University of Marburg, Germany – sequence: 13 givenname: Timothy surname: Solberg fullname: Solberg, Timothy organization: Hospital of the University of Pennsylvania, Department of Radiation Oncology, Philadelphia, USA – sequence: 14 givenname: Dirk surname: de Ruysscher fullname: de Ruysscher, Dirk organization: Department of Radiation Oncology (MAASTRO), GROW – School for Oncology and Developmental Biology, Maastricht University Medical Centre, The Netherlands – sequence: 15 givenname: Esther G.C. surname: Troost fullname: Troost, Esther G.C. organization: Department of Radiation Oncology (MAASTRO), GROW – School for Oncology and Developmental Biology, Maastricht University Medical Centre, The Netherlands |
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Keywords | Stage I NSCLC Radiotherapy In silico planning study Particle therapy Multicentric trial |
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Snippet | To compare dose to organs at risk (OARs) and dose-escalation possibility for 24 stage I non-small cell lung cancer (NSCLC) patients in a ROCOCO (Radiation... PURPOSETo compare dose to organs at risk (OARs) and dose-escalation possibility for 24 stage I non-small cell lung cancer (NSCLC) patients in a ROCOCO... To compare dose to organs at risk (OARs) and dose-escalation possibility for 24 stage I nonsmall cell lung cancer (NSCLC) patients in a ROCOCO (Radiation... |
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SubjectTerms | carbo-ions compararive dosimetry Hematology Human health sciences IMRT In silico planning study lung cancer Multicentric trial NSCLC Oncologie Oncology Particle therapy protons Radiology, Nuclear Medicine and imaging Radiotherapy Sciences de la santé humaine Stage I NSCLC Stage I NSCLC Radiotherapy Particle therapy In silico planning study Multicentric trial VMAT |
Title | Photons, protons or carbon ions for stage I non-small cell lung cancer – Results of the multicentric ROCOCO in silico study |
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