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...
Saved in:
Published in: | Frontiers in oncology Vol. 14; p. 1401703 |
---|---|
Main Authors: | , , , , , , , , , , , |
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 |