Single institution experience of MRI-guided radiotherapy for thoracic tumors and clinical characteristics impacting treatment duty cycle

MRI-guided radiotherapy (MRgRT) allows for direct motion management and real-time radiation treatment plan adaptation. We report our institutional experience using low strength 0.35T MRgRT for thoracic malignancies, and evaluate changes in treatment duty cycle between first and final MRgRT fractions...

Full description

Saved in:
Bibliographic Details
Published in:Frontiers in oncology Vol. 14; p. 1401703
Main Authors: Miccio, Joseph A, Potter, Nicholas J, Showkat, Anaum, Yao, Min, Mahase, Sean, Ferenci, Michele, Sisley, Kaitlin, Dailey, Amy, Knipple, Jamie, Blakely, Amy, Tuanquin, Leonard, Machtay, Mitchell
Format: Journal Article
Language:English
Published: Switzerland Frontiers Media S.A 2024
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Abstract MRI-guided radiotherapy (MRgRT) allows for direct motion management and real-time radiation treatment plan adaptation. We report our institutional experience using low strength 0.35T MRgRT for thoracic malignancies, and evaluate changes in treatment duty cycle between first and final MRgRT fractions. All patients with intrathoracic tumors treated with MRgRT were included. The primary reason for MRgRT (adjacent organ at risk [OAR] vs. motion management [MM] vs. other) was recorded. Tumor location was classified as central (within 2cm of tracheobronchial tree) vs. non-central, and further classified by the Expanded HILUS grouping. Gross tumor volume (GTV) motion, planning target volume expansions, dose/fractionation, treatment plan time, and total delivery time were extracted from the treatment planning system. Treatment plan time was defined as the time for beam delivery, including multileaf collimator (MLC) motion, and gantry rotation. Treatment delivery time was defined as the time from beam on to completion of treatment, including treatment plan time and patient respiratory breath holds. Duty cycle was calculated as treatment plan time/treatment delivery time. Duty cycles were compared between first and final fraction using a two-sample t-test. Twenty-seven patients with thoracic tumors (16 non-small cell lung cancer and 11 thoracic metastases) were treated with MRgRT between 12/2021 and 06/2023. Fifteen patients received MRgRT due to OAR and 11 patients received MRgRT for motion management. 11 patients had central tumors and all were treated with MRgRT due to OAR risk. The median dose/fractionation was 50 Gy/5 fractions. For patients treated due to OAR (n=15), 80% had at least 1 adapted fraction during their course of radiotherapy. There was no plan adaptation for patients treated due to motion management (n=11). Mean GTV motion was significantly higher for patients treated due to motion management compared to OAR (16.1mm vs. 6.5mm, =0.011). Mean duty cycle for fraction 1 was 54.2% compared to 62.1% with final fraction ( =0.004). Mean fraction 1 duty cycle was higher for patients treated due to OAR compared to patients treated for MM (61% vs. 45.0%, =0.012). Duty cycle improved from first fraction to final fraction possibly due to patient familiarity with treatment. Duty cycle was improved for patients treated due to OAR risk, likely due to more central location and thus decreased target motion.
AbstractList MRI-guided radiotherapy (MRgRT) allows for direct motion management and real-time radiation treatment plan adaptation. We report our institutional experience using low strength 0.35T MRgRT for thoracic malignancies, and evaluate changes in treatment duty cycle between first and final MRgRT fractions. All patients with intrathoracic tumors treated with MRgRT were included. The primary reason for MRgRT (adjacent organ at risk [OAR] vs. motion management [MM] vs. other) was recorded. Tumor location was classified as central (within 2cm of tracheobronchial tree) vs. non-central, and further classified by the Expanded HILUS grouping. Gross tumor volume (GTV) motion, planning target volume expansions, dose/fractionation, treatment plan time, and total delivery time were extracted from the treatment planning system. Treatment plan time was defined as the time for beam delivery, including multileaf collimator (MLC) motion, and gantry rotation. Treatment delivery time was defined as the time from beam on to completion of treatment, including treatment plan time and patient respiratory breath holds. Duty cycle was calculated as treatment plan time/treatment delivery time. Duty cycles were compared between first and final fraction using a two-sample t-test. Twenty-seven patients with thoracic tumors (16 non-small cell lung cancer and 11 thoracic metastases) were treated with MRgRT between 12/2021 and 06/2023. Fifteen patients received MRgRT due to OAR and 11 patients received MRgRT for motion management. 11 patients had central tumors and all were treated with MRgRT due to OAR risk. The median dose/fractionation was 50 Gy/5 fractions. For patients treated due to OAR (n=15), 80% had at least 1 adapted fraction during their course of radiotherapy. There was no plan adaptation for patients treated due to motion management (n=11). Mean GTV motion was significantly higher for patients treated due to motion management compared to OAR (16.1mm vs. 6.5mm, =0.011). Mean duty cycle for fraction 1 was 54.2% compared to 62.1% with final fraction ( =0.004). Mean fraction 1 duty cycle was higher for patients treated due to OAR compared to patients treated for MM (61% vs. 45.0%, =0.012). Duty cycle improved from first fraction to final fraction possibly due to patient familiarity with treatment. Duty cycle was improved for patients treated due to OAR risk, likely due to more central location and thus decreased target motion.
MRI-guided radiotherapy (MRgRT) allows for direct motion management and real-time radiation treatment plan adaptation. We report our institutional experience using low strength 0.35T MRgRT for thoracic malignancies, and evaluate changes in treatment duty cycle between first and final MRgRT fractions.IntroductionMRI-guided radiotherapy (MRgRT) allows for direct motion management and real-time radiation treatment plan adaptation. We report our institutional experience using low strength 0.35T MRgRT for thoracic malignancies, and evaluate changes in treatment duty cycle between first and final MRgRT fractions.All patients with intrathoracic tumors treated with MRgRT were included. The primary reason for MRgRT (adjacent organ at risk [OAR] vs. motion management [MM] vs. other) was recorded. Tumor location was classified as central (within 2cm of tracheobronchial tree) vs. non-central, and further classified by the Expanded HILUS grouping. Gross tumor volume (GTV) motion, planning target volume expansions, dose/fractionation, treatment plan time, and total delivery time were extracted from the treatment planning system. Treatment plan time was defined as the time for beam delivery, including multileaf collimator (MLC) motion, and gantry rotation. Treatment delivery time was defined as the time from beam on to completion of treatment, including treatment plan time and patient respiratory breath holds. Duty cycle was calculated as treatment plan time/treatment delivery time. Duty cycles were compared between first and final fraction using a two-sample t-test.MethodsAll patients with intrathoracic tumors treated with MRgRT were included. The primary reason for MRgRT (adjacent organ at risk [OAR] vs. motion management [MM] vs. other) was recorded. Tumor location was classified as central (within 2cm of tracheobronchial tree) vs. non-central, and further classified by the Expanded HILUS grouping. Gross tumor volume (GTV) motion, planning target volume expansions, dose/fractionation, treatment plan time, and total delivery time were extracted from the treatment planning system. Treatment plan time was defined as the time for beam delivery, including multileaf collimator (MLC) motion, and gantry rotation. Treatment delivery time was defined as the time from beam on to completion of treatment, including treatment plan time and patient respiratory breath holds. Duty cycle was calculated as treatment plan time/treatment delivery time. Duty cycles were compared between first and final fraction using a two-sample t-test.Twenty-seven patients with thoracic tumors (16 non-small cell lung cancer and 11 thoracic metastases) were treated with MRgRT between 12/2021 and 06/2023. Fifteen patients received MRgRT due to OAR and 11 patients received MRgRT for motion management. 11 patients had central tumors and all were treated with MRgRT due to OAR risk. The median dose/fractionation was 50 Gy/5 fractions. For patients treated due to OAR (n=15), 80% had at least 1 adapted fraction during their course of radiotherapy. There was no plan adaptation for patients treated due to motion management (n=11). Mean GTV motion was significantly higher for patients treated due to motion management compared to OAR (16.1mm vs. 6.5mm, p=0.011). Mean duty cycle for fraction 1 was 54.2% compared to 62.1% with final fraction (p=0.004). Mean fraction 1 duty cycle was higher for patients treated due to OAR compared to patients treated for MM (61% vs. 45.0%, p=0.012).ResultsTwenty-seven patients with thoracic tumors (16 non-small cell lung cancer and 11 thoracic metastases) were treated with MRgRT between 12/2021 and 06/2023. Fifteen patients received MRgRT due to OAR and 11 patients received MRgRT for motion management. 11 patients had central tumors and all were treated with MRgRT due to OAR risk. The median dose/fractionation was 50 Gy/5 fractions. For patients treated due to OAR (n=15), 80% had at least 1 adapted fraction during their course of radiotherapy. There was no plan adaptation for patients treated due to motion management (n=11). Mean GTV motion was significantly higher for patients treated due to motion management compared to OAR (16.1mm vs. 6.5mm, p=0.011). Mean duty cycle for fraction 1 was 54.2% compared to 62.1% with final fraction (p=0.004). Mean fraction 1 duty cycle was higher for patients treated due to OAR compared to patients treated for MM (61% vs. 45.0%, p=0.012).Duty cycle improved from first fraction to final fraction possibly due to patient familiarity with treatment. Duty cycle was improved for patients treated due to OAR risk, likely due to more central location and thus decreased target motion.DiscussionDuty cycle improved from first fraction to final fraction possibly due to patient familiarity with treatment. Duty cycle was improved for patients treated due to OAR risk, likely due to more central location and thus decreased target motion.
IntroductionMRI-guided radiotherapy (MRgRT) allows for direct motion management and real-time radiation treatment plan adaptation. We report our institutional experience using low strength 0.35T MRgRT for thoracic malignancies, and evaluate changes in treatment duty cycle between first and final MRgRT fractions.MethodsAll patients with intrathoracic tumors treated with MRgRT were included. The primary reason for MRgRT (adjacent organ at risk [OAR] vs. motion management [MM] vs. other) was recorded. Tumor location was classified as central (within 2cm of tracheobronchial tree) vs. non-central, and further classified by the Expanded HILUS grouping. Gross tumor volume (GTV) motion, planning target volume expansions, dose/fractionation, treatment plan time, and total delivery time were extracted from the treatment planning system. Treatment plan time was defined as the time for beam delivery, including multileaf collimator (MLC) motion, and gantry rotation. Treatment delivery time was defined as the time from beam on to completion of treatment, including treatment plan time and patient respiratory breath holds. Duty cycle was calculated as treatment plan time/treatment delivery time. Duty cycles were compared between first and final fraction using a two-sample t-test.ResultsTwenty-seven patients with thoracic tumors (16 non-small cell lung cancer and 11 thoracic metastases) were treated with MRgRT between 12/2021 and 06/2023. Fifteen patients received MRgRT due to OAR and 11 patients received MRgRT for motion management. 11 patients had central tumors and all were treated with MRgRT due to OAR risk. The median dose/fractionation was 50 Gy/5 fractions. For patients treated due to OAR (n=15), 80% had at least 1 adapted fraction during their course of radiotherapy. There was no plan adaptation for patients treated due to motion management (n=11). Mean GTV motion was significantly higher for patients treated due to motion management compared to OAR (16.1mm vs. 6.5mm, p=0.011). Mean duty cycle for fraction 1 was 54.2% compared to 62.1% with final fraction (p=0.004). Mean fraction 1 duty cycle was higher for patients treated due to OAR compared to patients treated for MM (61% vs. 45.0%, p=0.012).DiscussionDuty cycle improved from first fraction to final fraction possibly due to patient familiarity with treatment. Duty cycle was improved for patients treated due to OAR risk, likely due to more central location and thus decreased target motion.
Author Ferenci, Michele
Sisley, Kaitlin
Showkat, Anaum
Mahase, Sean
Tuanquin, Leonard
Miccio, Joseph A
Blakely, Amy
Knipple, Jamie
Dailey, Amy
Potter, Nicholas J
Machtay, Mitchell
Yao, Min
Author_xml – sequence: 1
  givenname: Joseph A
  surname: Miccio
  fullname: Miccio, Joseph A
  organization: Department of Radiation Oncology, Penn State Cancer Institute, Hershey, PA, United States
– sequence: 2
  givenname: Nicholas J
  surname: Potter
  fullname: Potter, Nicholas J
  organization: Department of Radiation Oncology, Penn State Cancer Institute, Hershey, PA, United States
– sequence: 3
  givenname: Anaum
  surname: Showkat
  fullname: Showkat, Anaum
  organization: Department of Arts and Letters, University of Notre Dame, South Bend, IN, United States
– sequence: 4
  givenname: Min
  surname: Yao
  fullname: Yao, Min
  organization: Department of Radiation Oncology, Penn State Cancer Institute, Hershey, PA, United States
– sequence: 5
  givenname: Sean
  surname: Mahase
  fullname: Mahase, Sean
  organization: Department of Radiation Oncology, Penn State Cancer Institute, Hershey, PA, United States
– sequence: 6
  givenname: Michele
  surname: Ferenci
  fullname: Ferenci, Michele
  organization: Department of Radiation Oncology, Penn State Cancer Institute, Hershey, PA, United States
– sequence: 7
  givenname: Kaitlin
  surname: Sisley
  fullname: Sisley, Kaitlin
  organization: Department of Radiation Oncology, Penn State Cancer Institute, Hershey, PA, United States
– sequence: 8
  givenname: Amy
  surname: Dailey
  fullname: Dailey, Amy
  organization: Department of Radiation Oncology, Penn State Cancer Institute, Hershey, PA, United States
– sequence: 9
  givenname: Jamie
  surname: Knipple
  fullname: Knipple, Jamie
  organization: Department of Radiation Oncology, Penn State Cancer Institute, Hershey, PA, United States
– sequence: 10
  givenname: Amy
  surname: Blakely
  fullname: Blakely, Amy
  organization: Department of Radiation Oncology, Penn State Cancer Institute, Hershey, PA, United States
– sequence: 11
  givenname: Leonard
  surname: Tuanquin
  fullname: Tuanquin, Leonard
  organization: Department of Radiation Oncology, Penn State Cancer Institute, Hershey, PA, United States
– sequence: 12
  givenname: Mitchell
  surname: Machtay
  fullname: Machtay, Mitchell
  organization: Department of Radiation Oncology, Penn State Cancer Institute, Hershey, PA, United States
BackLink https://www.ncbi.nlm.nih.gov/pubmed/38919525$$D View this record in MEDLINE/PubMed
BookMark eNpNkctu1TAQhi1URC_0AdggL9nk4PgSx0tUUThSERIXiV00scfnuErs4DgS5w14bCzaImYz9-8faS7JWUwRCXnVsp0QvXnrU7Q7zrjctZK1moln5IJzIRsjxY-z_-Jzcr2u96xap1jLxAtyXvdbo7i6IL-_hniYkIa4llC2ElKk-GvBHDBapMnTT1_2zWELDh3N4EIqR8ywnKhPmZZjymCDpWWbU14pREftFGKwMFF7hNosFVXRdqVhXmpa5WjJCGXGWKjbyonak53wJXnuYVrx-tFfke-377_dfGzuPn_Y37y7axxXrDTGKi6BK2_RKjeqTo8wWq6kk1IbrbyzjouuFSMH0MJjZ1B6QC-tReM7cUX2D1yX4H5Ycpghn4YEYfhbSPkwQK73TjiAcpp7A4J1nUToe2w7hdqj5Kbvel5Zbx5YS04_N1zLMIfV4jRBxLStg2Cac8O1UXX09ePoNs7o_gk_fUL8Ad2Mkjc
ContentType Journal Article
Copyright Copyright © 2024 Miccio, Potter, Showkat, Yao, Mahase, Ferenci, Sisley, Dailey, Knipple, Blakely, Tuanquin and Machtay.
Copyright_xml – notice: Copyright © 2024 Miccio, Potter, Showkat, Yao, Mahase, Ferenci, Sisley, Dailey, Knipple, Blakely, Tuanquin and Machtay.
DBID NPM
7X8
DOA
DOI 10.3389/fonc.2024.1401703
DatabaseName PubMed
MEDLINE - Academic
Directory of Open Access Journals
DatabaseTitle PubMed
MEDLINE - Academic
DatabaseTitleList PubMed
MEDLINE - Academic

Database_xml – sequence: 1
  dbid: DOA
  name: Directory of Open Access Journals
  url: http://www.doaj.org/
  sourceTypes: Open Website
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 2234-943X
ExternalDocumentID oai_doaj_org_article_a5d72f9a30664ea88e165e7fe4298682
38919525
Genre Journal Article
GroupedDBID 53G
5VS
9T4
AAFWJ
AAKDD
ACGFO
ACGFS
ACXDI
ADBBV
ADRAZ
AFPKN
ALMA_UNASSIGNED_HOLDINGS
AOIJS
BAWUL
BCNDV
DIK
EBS
EJD
EMOBN
GROUPED_DOAJ
GX1
HYE
IAO
IEA
IHR
IHW
IPNFZ
KQ8
M48
M~E
NPM
OK1
PGMZT
RIG
RNS
RPM
7X8
ID FETCH-LOGICAL-d250t-9c524a25fcec5db567babc254d447975fdcd23613b2aa73fe69e4faef4cce9f63
IEDL.DBID DOA
ISSN 2234-943X
IngestDate Tue Oct 22 14:56:26 EDT 2024
Sat Oct 26 04:53:15 EDT 2024
Sat Nov 02 12:24:45 EDT 2024
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Keywords radiotherapy
MRI guidance
duty cycle
thoracic
SBRT
Language English
License Copyright © 2024 Miccio, Potter, Showkat, Yao, Mahase, Ferenci, Sisley, Dailey, Knipple, Blakely, Tuanquin and Machtay.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-d250t-9c524a25fcec5db567babc254d447975fdcd23613b2aa73fe69e4faef4cce9f63
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
OpenAccessLink https://doaj.org/article/a5d72f9a30664ea88e165e7fe4298682
PMID 38919525
PQID 3072292795
PQPubID 23479
ParticipantIDs doaj_primary_oai_doaj_org_article_a5d72f9a30664ea88e165e7fe4298682
proquest_miscellaneous_3072292795
pubmed_primary_38919525
PublicationCentury 2000
PublicationDate 2024-00-00
PublicationDateYYYYMMDD 2024-01-01
PublicationDate_xml – year: 2024
  text: 2024-00-00
PublicationDecade 2020
PublicationPlace Switzerland
PublicationPlace_xml – name: Switzerland
PublicationTitle Frontiers in oncology
PublicationTitleAlternate Front Oncol
PublicationYear 2024
Publisher Frontiers Media S.A
Publisher_xml – name: Frontiers Media S.A
SSID ssj0000650103
Score 2.381531
Snippet MRI-guided radiotherapy (MRgRT) allows for direct motion management and real-time radiation treatment plan adaptation. We report our institutional experience...
IntroductionMRI-guided radiotherapy (MRgRT) allows for direct motion management and real-time radiation treatment plan adaptation. We report our institutional...
SourceID doaj
proquest
pubmed
SourceType Open Website
Aggregation Database
Index Database
StartPage 1401703
SubjectTerms duty cycle
MRI guidance
radiotherapy
SBRT
thoracic
Title Single institution experience of MRI-guided radiotherapy for thoracic tumors and clinical characteristics impacting treatment duty cycle
URI https://www.ncbi.nlm.nih.gov/pubmed/38919525
https://www.proquest.com/docview/3072292795
https://doaj.org/article/a5d72f9a30664ea88e165e7fe4298682
Volume 14
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV05T-wwELZ4FIjmifstlwaJNrB4fcQlp6CAgkOiixx7DCs9ErSbFPsP-NmM12EFBaKhSREp9mg-Zw6P_Q1j-2h5KYI5ymw_8ExYwqJ0ln48U6q8RN1XPm4NXN7pm8f87DzS5MxafcUzYYkeOCnu0EqveTCWQlslkMbCIyVRByRDmqs8Wd9-_imZSjZYxgYGqYxJWZg5DHUVGQu5OIgphY5NsqYk_d9HllMPc7HE_nahIRwnkZbZHFYrbOG6K36vsrc7cjP_EYZdfZ80CjhjKoY6wPXtVfbUDj16GFk_7C5XTYACU2ieCWw3dNC0L_VoDLby8HEtEtxX2mZIdydpOpgdRAffNhNwExJtjT1cnN-fXmZdI4XMU4TTZMZJLiyXwaGTvpRKl7Z0lBp6IbTRMnjnIwnLoOTW6kFAZVAEi0E4hyaowTqbr-oK_zGgT_I80MPQkCr6e4UC0fEgc4oVVY-dRK0Wr4kro4js1dMXhGnRYVr8hGmP7X1gUtBqjyUMW2HdjguySJwbro3ssY0E1myqWHElqeTmb4iwxRbjYkmbLdtsvhm1uMP-jH27O11p72wq210
link.rule.ids 315,782,786,866,2108,4030,27934,27935,27936
linkProvider Directory of Open Access Journals
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Single+institution+experience+of+MRI-guided+radiotherapy+for+thoracic+tumors+and+clinical+characteristics+impacting+treatment+duty+cycle&rft.jtitle=Frontiers+in+oncology&rft.au=Miccio%2C+Joseph+A&rft.au=Potter%2C+Nicholas+J&rft.au=Showkat%2C+Anaum&rft.au=Yao%2C+Min&rft.date=2024&rft.issn=2234-943X&rft.eissn=2234-943X&rft.volume=14&rft.spage=1401703&rft_id=info:doi/10.3389%2Ffonc.2024.1401703&rft.externalDBID=NO_FULL_TEXT
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2234-943X&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2234-943X&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2234-943X&client=summon