Christos Moustakis, Oliver Blanck, Maximilian Grohmann, Dirk Albers, Dennis Bartels, Bastian Bathen, Giuseppina Rita Borzì, Sara Broggi, Andrea Bruschi, Michelina Casale, Anna Delana, Paul Doolan, Fatemeh Ebrahimi Tazehmahalleh, Stefania Fabiani, Maria Daniela Falco, Roman Fehr, Melissa Friedlein, Susanne Gutser, Abdul Malek Hamada, Timothy Hancock, Janett Köhn, Christine Kornhuber, Thomas Krieger, Ulrike Lambrecht, Sara Lappi, Eugenia Moretti, Annalena Mirus, Thomas Muedder, Sandija Plaude, Bernd Polvika, Valentina Ravaglia, Roberto Righetto, Giuseppe Rinaldin, Henrik Schachner, Alessandro Scaggion, Philipp Schilling, Philipp Szeverinski, Elena Villaggi, Mathias Walke, Lotte Wilke, Peter Winkler, Nils H Nicolay, Hans Theodor Eich, Eleni Gkika, Thomas B Brunner, Daniela Schmitt
{"title":"Planning Benchmark Study for Stereotactic Body Radiation Therapy of Pancreas Carcinomas With Simultaneously Integrated Boost and Protection: Results of the DEGRO/DGMP Working Group on Stereotactic Radiation Therapy and Radiosurgery.","authors":"Christos Moustakis, Oliver Blanck, Maximilian Grohmann, Dirk Albers, Dennis Bartels, Bastian Bathen, Giuseppina Rita Borzì, Sara Broggi, Andrea Bruschi, Michelina Casale, Anna Delana, Paul Doolan, Fatemeh Ebrahimi Tazehmahalleh, Stefania Fabiani, Maria Daniela Falco, Roman Fehr, Melissa Friedlein, Susanne Gutser, Abdul Malek Hamada, Timothy Hancock, Janett Köhn, Christine Kornhuber, Thomas Krieger, Ulrike Lambrecht, Sara Lappi, Eugenia Moretti, Annalena Mirus, Thomas Muedder, Sandija Plaude, Bernd Polvika, Valentina Ravaglia, Roberto Righetto, Giuseppe Rinaldin, Henrik Schachner, Alessandro Scaggion, Philipp Schilling, Philipp Szeverinski, Elena Villaggi, Mathias Walke, Lotte Wilke, Peter Winkler, Nils H Nicolay, Hans Theodor Eich, Eleni Gkika, Thomas B Brunner, Daniela Schmitt","doi":"10.1016/j.ijrobp.2024.08.038","DOIUrl":"10.1016/j.ijrobp.2024.08.038","url":null,"abstract":"<p><strong>Purpose: </strong>The proximity or overlap of planning target volume (PTV) and organs-at-risk (OARs) poses a major challenge in stereotactic body radiation therapy (SBRT) of pancreatic cancer (PACA). This international treatment planning benchmark study investigates whether simultaneous integrated boost (SIB) and simultaneous integrated protection (SIP) concepts in PACA SBRT can lead to improved and harmonized plan quality.</p><p><strong>Methods and materials: </strong>A multiparametric specification of desired target doses (gross target volume [GTV]<sub>D50%</sub>, GTV<sub>D99%</sub>, PTV<sub>D95%</sub>, and PTV<sub>0.5cc</sub>) with 2 prescription doses of GTV<sub>D50%</sub> = 5 × 9.2Gy (46 Gy) and GTV<sub>D50%</sub> = 8 × 8.25 Gy (66 Gy) and OAR limits were distributed with planning computed tomography and contours from 3 PACA patients. In phase 1, plans were ranked using a scoring system for comparison of trade-offs between GTV/PTV and OAR. In phase 2, replanning was performed for the most challenging case and prescription with dedicated SIB and SIP contours provided for optimization after group discussion.</p><p><strong>Results: </strong>For all 3 cases and both phases combined, 292 plans were generated from 42 institutions in 5 countries using commonly available treatment planning systems. The GTV<sub>D50%</sub> prescription was performed by only 76% and 74% of planners within 2% for 5 and 8 fractions, respectively. The GTV<sub>D99%</sub> goal was mostly reached, while the balance between OAR and target dose showed initial SIB/SIP-like optimization strategies in about 50% of plans. For plan ranking, 149 and 217 score penalties were given for 5 and 8 fractions, pointing to improvement possibilities. For phase 2, the GTV<sub>D50%</sub> prescription was performed by 95% of planners within 2%, and GTV<sub>D99%</sub> as well as OAR doses were better harmonized with notable less score penalties. Fourteen of 19 planners improved their plan rank, 9 of them by at least 2 ranks.</p><p><strong>Conclusions: </strong>Dedicated SIB/SIP concepts in combination with multiparametric prescriptions and constraints can lead to overall harmonized and high treatment plan quality for PACA SBRT. Standardized SIB/SIP treatment planning in multicenter clinical trials appears feasible after group consensus and training.</p>","PeriodicalId":14215,"journal":{"name":"International Journal of Radiation Oncology Biology Physics","volume":" ","pages":"547-557"},"PeriodicalIF":6.4,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142119781","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Robert W Mutter, Michael A Golafshar, Matthew R Buras, Bryce P Comstock, Maddi Jacobson, Todd DeWees, Nicholas B Remmes, Leah N Francis, Judy C Boughey, Kathryn J Ruddy, Lisa A McGee, Arslan Afzal, Laura A Vallow, Keith M Furutani, Christopher L Deufel, Dean A Shumway, Haeyoung Kim, Minetta C Liu, Amy C Degnim, James W Jakub, Tamara Z Vern-Gross, William W Wong, Samir H Patel, Carlos E Vargas, Bradley J Stish, Mark R Waddle, Deanna H Pafundi, Michele Y Halyard, Kimberly S Corbin, Tina J Hieken, Sean S Park
{"title":"Dose Deintensified 3-Day Photon, Proton, or Brachytherapy: A Nonrandomized Controlled Partial Breast Irradiation Trial.","authors":"Robert W Mutter, Michael A Golafshar, Matthew R Buras, Bryce P Comstock, Maddi Jacobson, Todd DeWees, Nicholas B Remmes, Leah N Francis, Judy C Boughey, Kathryn J Ruddy, Lisa A McGee, Arslan Afzal, Laura A Vallow, Keith M Furutani, Christopher L Deufel, Dean A Shumway, Haeyoung Kim, Minetta C Liu, Amy C Degnim, James W Jakub, Tamara Z Vern-Gross, William W Wong, Samir H Patel, Carlos E Vargas, Bradley J Stish, Mark R Waddle, Deanna H Pafundi, Michele Y Halyard, Kimberly S Corbin, Tina J Hieken, Sean S Park","doi":"10.1016/j.ijrobp.2024.09.019","DOIUrl":"10.1016/j.ijrobp.2024.09.019","url":null,"abstract":"<p><strong>Purpose: </strong>The optimal approach for partial breast irradiation (PBI) is unknown. We investigated a novel de-intensified 3-fraction PBI regimen for photons, protons, and brachytherapy.</p><p><strong>Methods and materials: </strong>A multicenter nonrandomized controlled trial with the primary outcome of adverse cosmesis at 3 years versus before PBI. Eligibility criteria were age ≥50 years treated with breast-conserving surgery for node-negative estrogen receptor-positive (ER+) invasive breast cancer or any ductal carcinoma in situ (DCIS) measuring ≤2.5 cm. Photon and proton PBI were prescribed 21.9 Gy (relative biological effectiveness) and brachytherapy 21 Gy in 3 fractions. Radiation therapy technique and adjuvant endocrine therapy were selected at physician and patient discretion.</p><p><strong>Results: </strong>Between June 17, 2015, and July 13, 2017, 161 eligible patients were treated with photons (56), protons (49), or brachytherapy (56). Median patient age was 66.8 years. One hundred twenty-six (78.3%) had invasive breast cancer (all ER+) and 35 (21.7%) had DCIS (88.6% ER+). Fifty-four percent of patients with invasive breast cancer and 25.8% of patients with ER+ DCIS initiated and adhered to the prescribed endocrine therapy. The proportion of patients with adverse cosmesis (by trained nurse assessment) was 14.5% at baseline and 2.3% at 3 years (difference, -12.2%; 95% CI, -100% to -6.4%). Adverse cosmesis at the last follow-up, with a median follow-up of 5 years, was 5.7% by nurse assessment, 5.6% by panel assessment of digital photographs, and 5.2% by patient self-report. There were no observed clinically meaningful changes in other patient-reported outcomes, and just 2 grade 2 or higher adverse events, both grade 2, in the brachytherapy cohort. Five-year local recurrence-free survival and progression-free survival were 98.0% and 95.5%, respectively. There were no local recurrences among 60 patients with invasive breast cancer and Ki67 ≤13.25%.</p><p><strong>Conclusions: </strong>Deintensified 3-day PBI provided favorable disease control, tolerability, and cosmetic outcomes, meeting the prespecified criteria for acceptability. This approach is an attractive option for patients with small node-negative ER+ breast cancer and DCIS.</p>","PeriodicalId":14215,"journal":{"name":"International Journal of Radiation Oncology Biology Physics","volume":" ","pages":"352-364"},"PeriodicalIF":6.4,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142287107","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Sarah Braga-Cohen, Jérémy Lavigne, Morgane Dos Santos, Georges Tarlet, Valérie Buard, Jan Baijer, Olivier Guipaud, Vincent Paget, Eric Deutsch, Mohamed Amine Benadjaoud, Michele Mondini, Fabien Milliat, Agnès François
{"title":"Evidence of Alveolar Macrophage Metabolic Shift Following Stereotactic Body Radiation Therapy -Induced Lung Fibrosis in Mice.","authors":"Sarah Braga-Cohen, Jérémy Lavigne, Morgane Dos Santos, Georges Tarlet, Valérie Buard, Jan Baijer, Olivier Guipaud, Vincent Paget, Eric Deutsch, Mohamed Amine Benadjaoud, Michele Mondini, Fabien Milliat, Agnès François","doi":"10.1016/j.ijrobp.2024.09.018","DOIUrl":"10.1016/j.ijrobp.2024.09.018","url":null,"abstract":"<p><strong>Purpose: </strong>Radiation-induced pneumopathy is the main dose-limiting factor in cases of chest radiation therapy. Macrophage infiltration is frequently observed in irradiated lung tissues and may participate in lung damage development. Radiation-induced lung fibrosis can be reproduced in rodent models using whole thorax irradiation but suffers from limits concerning the role played by unexposed lung volumes in damage development.</p><p><strong>Methods and materials: </strong>Here, we used an accurate stereotactic body radiation therapy preclinical model irradiating 4% of the mouse lung. Tissue damage development and macrophage populations were followed by histology, flow cytometry, and single-cell RNA sequencing. Wild-type and CCR2 KO mice, in which monocyte recruitment is abrogated, were exposed to single doses of radiation, inducing progressive (60 Gy) or rapid (80 Gy) lung fibrosis.</p><p><strong>Results: </strong>Numerous clusters of macrophages were observed around the injured area, during progressive as well as rapid fibrosis. The results indicate that probably CCR2-independent recruitment and/or in situ proliferation may be responsible for macrophage invasion. Alveolar macrophages experience a metabolic shift from fatty acid metabolism to cholesterol biosynthesis, directing them through a possible profibrotic phenotype. Depicted data revealed that the origin and phenotype of macrophages present in the injured area may differ from what has been previously described in preclinical models exposing large lung volumes, representing a potentially interesting trail in the deciphering of radiation-induced lung damage processes.</p><p><strong>Conclusions: </strong>Our study brings new possible clues to the understanding of macrophage implications in radiation-induced lung damage, representing an interesting area for exploration in future studies.</p>","PeriodicalId":14215,"journal":{"name":"International Journal of Radiation Oncology Biology Physics","volume":" ","pages":"506-519"},"PeriodicalIF":6.4,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142287109","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Kathrin Kirchheiner, Alexandru Zaharie, Stéphanie Smet, Sofia Spampinato, Cyrus Chargari, Christine Haie-Meder, Umesh Mahantshetty, Barbara Šegedin, Kjersti Bruheim, Bhavana Rai, Rachel Cooper, Elzbieta Van der Steen-Banasik, Ericka Wiebe, Richard Pötter, Alina Sturdza, Maximilian P Schmid, Kari Tanderup, Astrid De Leeuw, Ina M Jürgenliemk-Schulz, Remi A Nout
{"title":"Association Between the Regular Use of Vaginal Dilators and/or Sexual Activity and Vaginal Morbidity in Locally Advanced Cervical Cancer Survivors: An EMBRACE-I Study Report.","authors":"Kathrin Kirchheiner, Alexandru Zaharie, Stéphanie Smet, Sofia Spampinato, Cyrus Chargari, Christine Haie-Meder, Umesh Mahantshetty, Barbara Šegedin, Kjersti Bruheim, Bhavana Rai, Rachel Cooper, Elzbieta Van der Steen-Banasik, Ericka Wiebe, Richard Pötter, Alina Sturdza, Maximilian P Schmid, Kari Tanderup, Astrid De Leeuw, Ina M Jürgenliemk-Schulz, Remi A Nout","doi":"10.1016/j.ijrobp.2024.09.011","DOIUrl":"10.1016/j.ijrobp.2024.09.011","url":null,"abstract":"<p><strong>Purpose: </strong>The purpose of this study was to provide risk estimations for vaginal morbidity with regard to vaginal dilation (summarizing the use of dilators and/or sexual activity) in patients with locally advanced cervical cancer treated with definitive radiochemotherapy and image guided adaptive brachytherapy within the prospective, multi-institutional EMBRACE-I study.</p><p><strong>Methods and materials: </strong>Physician-assessed vaginal morbidity (National Cancer Institute Common Terminology Criteria for Adverse Events version 3.0), use of vaginal dilators, and patient-reported sexual activity (EORTC-CX24) were prospectively assessed at baseline and during regular follow-ups. Frequency analysis for vaginal dilation was performed in a subcohort of patients with ≥3 follow-ups. Regular dilation was defined if reported in ≥50% of follow-ups, and no/infrequent dilation if reported in <50%. Actuarial estimates were calculated with Kaplan-Meier method; comparisons were evaluated with the log-rank test. Univariate and multivariable Cox proportional hazard regressions were used to evaluate risk factors for vaginal stenosis G≥2.</p><p><strong>Results: </strong>The EMBRACE-I study included a total of 1416 patients (2008-2015); 882 were evaluated in the present report with a median follow-up of 60 months. Of those, 565 (64%) reported regular dilation. This was associated with a significantly lower 5-year risk of vaginal stenosis G≥2 compared with no/infrequent dilation (23% vs 37%, P ≤ .001). This univariate finding was confirmed by multivariable analysis, after adjusting for other risk factors (hazard ratio, 0.630; P = .001). Regular vaginal dilation was also associated with a significantly higher risk for vaginal dryness G≥1 (72% vs 67%, P = .028) and bleeding G≥1 (61% vs 34%, P ≤ .001).</p><p><strong>Conclusions: </strong>Vaginal stenosis represents irreversible fibrotic changes that can cause pain during gynecologic examination and dyspareunia in locally advanced cervical cancer patients survivors. Regular vaginal dilation (defined as the use of dilators and/or sexual activity) is associated with a significantly lower risk for G≥2 vaginal stenosis, suggesting a potential improvement of vaginal patency. It is also associated with a significantly higher risk for mild G≥1 dryness and bleeding (no higher risk for G≥2), which can be clinically managed.</p>","PeriodicalId":14215,"journal":{"name":"International Journal of Radiation Oncology Biology Physics","volume":" ","pages":"452-464"},"PeriodicalIF":6.4,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142287190","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pier Paolo Avolio, Ronald Kool, Bobby Shayegan, Gautier Marcq, Peter C Black, Rodney H Breau, Michael Kim, Ionut Busca, Hamidreza Abdi, Mark Dawidek, Michael Uy, Gagan Fervaha, Fabio L Cury, Rafael Sanchez-Salas, Nimira Alimohamed, Jonathan Izawa, Claudio Jeldres, Ricardo Rendon, Robert Siemens, Girish S Kulkarni, Wassim Kassouf
{"title":"Effect of Complete Transurethral Resection on Oncologic Outcomes After Radiation Therapy for Muscle-Invasive Bladder Cancer.","authors":"Pier Paolo Avolio, Ronald Kool, Bobby Shayegan, Gautier Marcq, Peter C Black, Rodney H Breau, Michael Kim, Ionut Busca, Hamidreza Abdi, Mark Dawidek, Michael Uy, Gagan Fervaha, Fabio L Cury, Rafael Sanchez-Salas, Nimira Alimohamed, Jonathan Izawa, Claudio Jeldres, Ricardo Rendon, Robert Siemens, Girish S Kulkarni, Wassim Kassouf","doi":"10.1016/j.ijrobp.2024.08.036","DOIUrl":"10.1016/j.ijrobp.2024.08.036","url":null,"abstract":"<p><strong>Purpose: </strong>To compare the oncologic outcomes of patients with nonmetastatic muscle-invasive bladder cancer (MIBC) undergoing complete versus incomplete transurethral tumor resection (TURBT) before radiation therapy.</p><p><strong>Methods and materials: </strong>Patients with nonmetastatic MIBC who underwent curative-intent radiation therapy between 2002 and 2018 at 10 Canadian institutions were retrospectively evaluated. Inverse probability of treatment weighting was performed using baseline characteristics. Differences in survival outcomes by complete and incomplete TURBT were analyzed.</p><p><strong>Results: </strong>Of the 757 patients included, 66% (498) had documentation of a complete and 34% (259) an incomplete TURBT. Before adjustment, 121 (47%) and 45 (9%) patients who underwent incomplete and complete TURBT, respectively, were diagnosed with cT3-4 tumor (P <.001). After weight-adjustment, all baseline cohort characteristics were balanced (absolute standardized differences < 0.1). The adjusted median follow-up was 27 months. Adjusted survival analyses showed no significant difference in 5-year overall survival (48% vs 52%, 1.03 [0.82-1.29]; P = .8), cancer-specific survival (64% vs 61%, 0.93 [0.70-1.25]; P = .7), metastasis-free survival (43% vs 46%, 0.97 [0.79-1.19]; P = .8), and disease-free survival (32% vs 35%, 0.95 [0.79-1.15]; P = .7) between the 2 groups.</p><p><strong>Conclusions: </strong>Complete TURBT may be associated with clinical organ-confined disease. Extent of TURBT was not independently associated with oncologic outcomes in patients with MIBC treated with radiation therapy.</p>","PeriodicalId":14215,"journal":{"name":"International Journal of Radiation Oncology Biology Physics","volume":" ","pages":"317-324"},"PeriodicalIF":6.4,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142072752","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Zeinab Abou Yehia, Zohaib Sherwani, Molly Chakraborty, Nisha Ohri, Alison Grann, Firas Eladoumikdachi, Maria Kowzun, Shicha Kumar, Lindsay Potdevin, Michele Blackwood, Deborah Toppmeyer, Bruce G Haffty
{"title":"First Results of the Primary Outcome of a Phase 2 Prospective Clinical Trial to Assess the Feasibility of Preoperative Radiation Boost in Patients With Breast Cancer.","authors":"Zeinab Abou Yehia, Zohaib Sherwani, Molly Chakraborty, Nisha Ohri, Alison Grann, Firas Eladoumikdachi, Maria Kowzun, Shicha Kumar, Lindsay Potdevin, Michele Blackwood, Deborah Toppmeyer, Bruce G Haffty","doi":"10.1016/j.ijrobp.2024.08.043","DOIUrl":"10.1016/j.ijrobp.2024.08.043","url":null,"abstract":"<p><strong>Purpose: </strong>A radiation therapy (RT) boost to the tumor bed is an important component of breast-conserving therapy in early breast cancer. This prospective phase 2 study assessed the feasibility of delivering the RT boost before surgery. We hypothesize wound complication rates to be comparable with postoperative RT and the target boost volume to be smaller than standard postoperative RT.</p><p><strong>Methods and materials: </strong>This prospective phase 2 trial accrued 55 patients with clinically node-negative breast cancer eligible for breast-conserving therapy. Patients were treated with preoperative RT boost of 1332 cGy in 4 fractions, followed by lumpectomy and postoperative adjuvant whole breast RT to 3663 cGy in 11 fractions. The primary outcome was to demonstrate the incidence of grade 3 or more wound complications was not inferior to lumpectomy with standard postoperative whole breast RT and boost (6%-20%). We also compared the preop boost volume with a mock boost volume that would have been done after surgery.</p><p><strong>Results: </strong>Fifty-five women were enrolled between June 2021 and October 2022. Median age was 64 years old (range, 40-77 years). Forty-three patients had invasive cancers, and 5 had ductal carcinoma in situ. Median clinical tumor size was 13 mm (range, 5-26 mm). Grade 3 wound dehiscence requiring surgical revision occurred in 1 patient (2%). There were no other grade 3 adverse events. Three patients (6%) had grade 2 infections requiring antibiotics. The target boost volume was significantly lower than mock postoperative volume (11 cc vs 56 cc; P < .001) Cosmetic outcome at the first follow-up was very good or excellent in 87% of patients, and none had poor cosmetic outcomes.</p><p><strong>Conclusion: </strong>The use of a preoperative RT boost followed by whole breast RT as administered here resulted in an acceptable primary outcome with a similar rate of postoperative wound complications and smaller boost volume compared with standard postoperative RT. This approach is currently under consideration for cooperative group phase 3 trial.</p>","PeriodicalId":14215,"journal":{"name":"International Journal of Radiation Oncology Biology Physics","volume":" ","pages":"333-340"},"PeriodicalIF":6.4,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142145631","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
YiXing Chen, Yong Hu, Jie Shen, ShiSuo Du, Jing Yan, LeYuan Zhou, Zhe Wang, HaiJie Lu, Lei Xiao, Ping Yang, WenChao Zhu, Jun Wang, GuoWei Yang, JianFeng Luo, Rong Liu, ZhaoChong Zeng
{"title":"External Beam Radiation therapy After Transarterial Chemoembolization Versus Transarterial Chemoembolization Alone for Treatment of Inoperable Hepatocellular Carcinoma: A Randomized Phase 3 Trial.","authors":"YiXing Chen, Yong Hu, Jie Shen, ShiSuo Du, Jing Yan, LeYuan Zhou, Zhe Wang, HaiJie Lu, Lei Xiao, Ping Yang, WenChao Zhu, Jun Wang, GuoWei Yang, JianFeng Luo, Rong Liu, ZhaoChong Zeng","doi":"10.1016/j.ijrobp.2024.09.021","DOIUrl":"10.1016/j.ijrobp.2024.09.021","url":null,"abstract":"<p><strong>Purpose: </strong>To compare the outcomes of transarterial chemoembolization (TACE) alone with those of TACE combined with external beam radiation therapy (EBRT) in patients with hepatocellular carcinoma (HCC) in a multicenter randomized study.</p><p><strong>Methods and materials: </strong>From 2017 to 2022, 74 HCC patients with tumors confined to the liver without vascular invasion were treated with either TACE only (TACE group, 39 patients) or TACE combined with EBRT (TACE + EBRT group, 35 patients). The primary outcome measured was overall survival (OS). Secondary outcomes included progression-free survival (PFS), local tumor control, and the assessment of treatment-related toxicity.</p><p><strong>Results: </strong>Due to slow accrual, the trial was closed prematurely after enrolling 74 patients. All patients received 2 cycles of TACE before randomization. The TACE and TACE + EBRT groups showed comparable patient and tumor characteristics. The TACE group underwent a median of 3 TACE cycles, and the TACE + EBRT group received 2 cycles of TACE, and a median of 5500 cGy in 15 fractions. For the TACE group, the median local control (LC) duration was 13.1 months, whereas for the TACE + EBRT group, the median LC was not achieved (P < .001). The PFS was recorded at 11.6 months in the TACE group compared with 15.4 months in the TACE + EBRT group (P = .072). The median OS reached 36.8 months for the TACE group and extended to 47.1 months for the TACE + EBRT group (P = .654). The incidence of toxicity was comparable between both groups.</p><p><strong>Conclusions: </strong>Although the number of patients enrolled in this clinical trial did not meet expectations. TACE combined with EBRT was shown to be more effective than TACE alone in improving LC without increasing toxicity, whereas PFS and OS were slightly improved. TACE + EBRT can be used as a standard treatment option for patients with inoperable but confined intrahepatic HCC.</p>","PeriodicalId":14215,"journal":{"name":"International Journal of Radiation Oncology Biology Physics","volume":" ","pages":"414-422"},"PeriodicalIF":6.4,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142287111","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Antiangiogenic Treatment Facilitates the Abscopal Effect of Radiation Therapy Combined With Anti-PD-1 in Hepatocellular Carcinoma.","authors":"Hailong Sheng, Yongyi Luo, Liting Zhong, Zhiyi Wang, Zhichao Sun, Xinna Gao, Xinrong He, Zhenru Zhu, Dehua Wu, Jingyuan Sun, Chuanhui Cao","doi":"10.1016/j.ijrobp.2024.09.024","DOIUrl":"10.1016/j.ijrobp.2024.09.024","url":null,"abstract":"<p><strong>Purpose: </strong>Metastasis is one of the most important factors contributing to poor prognosis in hepatocellular carcinoma. Radiation therapy (RT), along with its induced abscopal effect, is a promising treatment for metastatic patients. However, the incidence of abscopal effect in clinical practice is rare, even when RT is combined with immune checkpoint inhibitors (ICIs). In this study, we aim to investigate the role of antiangiogenic treatment on the abscopal effect induced by RT + ICIs.</p><p><strong>Methods and materials: </strong>Bilateral subcutaneous and orthotopic Hepa1-6 and Hep53.4 models were established and treated with different combination treatments. We evaluated changes in the immune microenvironment and vascular normalization by flow cytometry, T cell receptor sequencing, chemotactic gene array, enzyme linked immunosorbent assays, and immunofluorescence.</p><p><strong>Results: </strong>Our studies showed that antiangiogenic treatment with RT + ICIs increased the antitumor response of the unirradiated lesions. Mechanistically, the blockade of vascular endothelial receptor 2 (anti-VEGFR2) increased the activation and maturation of dendritic cells and promoted the production of CD8<sup>+</sup> T cells in irradiated tumors. These CD8<sup>+</sup> T cells were attracted by anti-VEGFR2-induced CCL5 secretion from M1 macrophages in unirradiated tumors. Besides that, anti-VEGFR2 enhanced the function of CD8<sup>+</sup> T cells by reducing myeloid-derived suppressor cells and regulatory T cells.</p><p><strong>Conclusions: </strong>This study demonstrated that the combination of antiangiogenic treatment with RT and ICIs enhanced the abscopal effects. The application of triple therapy and its induced abscopal effect may offer a novel therapeutic approach for hepatocellular carcinoma, particularly for cases with multiple metastatic lesions.</p>","PeriodicalId":14215,"journal":{"name":"International Journal of Radiation Oncology Biology Physics","volume":" ","pages":"534-546"},"PeriodicalIF":6.4,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142287189","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
William C Y Lo, Cristian W Villas Boas, Truc T Huynh, Amanda Klaas, Felicia Grogan, Lori Strong, Pamela Samson, Clifford G Robinson, Buck E Rogers, Carmen Bergom
{"title":"Using Integrin α<sub>v</sub>β<sub>6</sub>-Targeted Positron Emission Tomography Imaging to Longitudinally Monitor Radiation-Induced Pulmonary Fibrosis In Vivo.","authors":"William C Y Lo, Cristian W Villas Boas, Truc T Huynh, Amanda Klaas, Felicia Grogan, Lori Strong, Pamela Samson, Clifford G Robinson, Buck E Rogers, Carmen Bergom","doi":"10.1016/j.ijrobp.2024.08.034","DOIUrl":"10.1016/j.ijrobp.2024.08.034","url":null,"abstract":"<p><strong>Purpose: </strong>Radiation-induced pulmonary fibrosis (RIPF) is a potentially serious and disabling late complication of radiation therapy. Monitoring RIPF progression is challenging due to the absence of early detection tools and the difficulty in distinguishing RIPF from other lung diseases using standard imaging methods. In the lungs, integrin αvβ6 is crucial in the development of RIPF, acting as a significant activator of transforming growth factor β after radiation injury. This study aimed to investigate integrin α<sub>v</sub>β<sub>6</sub>-targeted positron emission tomography (PET) imaging ([<sup>64</sup>Cu]Cu-α<sub>v</sub>β<sub>6</sub>-BP) to study RIPF development in vivo.</p><p><strong>Methods and materials: </strong>We used a focal RIPF model (70 Gy delivered focally to a 3 mm spot in the lung) and a whole lung RIPF model (14 Gy delivered to the whole lung) in adult C57BL/6J mice. Small animal PET/computed tomography images were acquired 1 hour postinjection of 11.1 MBq of [<sup>64</sup>Cu]Cu-α<sub>v</sub>β<sub>6</sub>-BP. Animals were imaged for 8 weeks in the focal RIPF model and 6 months in the whole lung RIPF model. Immunohistochemistry for integrin α<sub>v</sub>β<sub>6</sub> and trichrome staining were performed.</p><p><strong>Results: </strong>In the focal RIPF model, there was focal uptake of [<sup>64</sup>Cu]Cu-α<sub>v</sub>β<sub>6</sub>-BP in the irradiated region at week 4 that progressively increased at weeks 6 and 8. In the whole lung RIPF model, minimal uptake of the probe was observed at 4 months post-radiation therapy, which significantly increased at months 5 and 6. Expression of integrin α<sub>v</sub>β<sub>6</sub> was validated histologically by immunohistochemistry in both models.</p><p><strong>Conclusions: </strong>Integrin α<sub>v</sub>β<sub>6</sub>-targeted PET imaging using [<sup>64</sup>Cu]Cu-α<sub>v</sub>β<sub>6</sub>-BP can serve as a useful tool to identify RIPF in vivo.</p>","PeriodicalId":14215,"journal":{"name":"International Journal of Radiation Oncology Biology Physics","volume":" ","pages":"484-492"},"PeriodicalIF":6.4,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142287196","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Nalee Kim, Won Park, Haeyoung Kim, Won Kyung Cho, Sung Ja Ahn, Mi Young Kim, Shin-Hyung Park, Ik Jae Lee, Inbong Ha, Jin Hee Kim, Tae Hyun Kim, Kyu Chan Lee, Hyung-Sik Lee, Tae Gyu Kim, Kyung Hwan Shin, Jong Hoon Lee, Jinhong Jung, Oyeon Cho, Yong Bae Kim, Eun Seog Kim, In Young Jo, Taeryool Koo, Kyubo Kim, Hae Jin Park, Young-Joo Shin, Boram Ha, Jeanny Kwon, Ju Hye Lee, Sunrock Moon
{"title":"Patient-Reported Outcomes Between Whole-Breast Plus Regional Irradiation and Whole-Breast Irradiation Only in pN1 Breast Cancer After Breast-Conserving Surgery and Taxane-Based Chemotherapy: A Randomized Phase 3 Clinical Trial (KROG 17-01).","authors":"Nalee Kim, Won Park, Haeyoung Kim, Won Kyung Cho, Sung Ja Ahn, Mi Young Kim, Shin-Hyung Park, Ik Jae Lee, Inbong Ha, Jin Hee Kim, Tae Hyun Kim, Kyu Chan Lee, Hyung-Sik Lee, Tae Gyu Kim, Kyung Hwan Shin, Jong Hoon Lee, Jinhong Jung, Oyeon Cho, Yong Bae Kim, Eun Seog Kim, In Young Jo, Taeryool Koo, Kyubo Kim, Hae Jin Park, Young-Joo Shin, Boram Ha, Jeanny Kwon, Ju Hye Lee, Sunrock Moon","doi":"10.1016/j.ijrobp.2024.09.017","DOIUrl":"10.1016/j.ijrobp.2024.09.017","url":null,"abstract":"<p><strong>Purpose: </strong>The role of regional node irradiation (RNI) with whole-breast irradiation (WBI) in patients with pN1 breast cancer receiving taxane-based adjuvant chemotherapy is not well defined. The KROG 1701 trial, a phase 3, multicenter, noninferiority study, aimed to compare the disease-free survival between WBI+RNI and WBI alone in this patient cohort. Comprehensive patient-reported outcomes (PROs) collected at multiple timepoints are reported.</p><p><strong>Methods and materials: </strong>The trial (NCT03269981) enrolled patients with pN1 breast cancer after breast-conserving surgery and taxane-based adjuvant chemotherapy, allocating them to receive either WBI+RNI or WBI only. PROs were assessed using European Organization for Research and Treatment of Cancer Quality-of-Life Questionnaires Core 30and breast cancer-specific module 23 modules at baseline, during radiation therapy, and at subsequent follow-up intervals of 3 to 6 months, and annually up to 4 years.</p><p><strong>Results: </strong>From April 2017 to December 2021, 840 patients were enrolled; 777 received intervention as assigned, and 750 completed baseline PRO questionnaires (387 in WBI+RNI, 363 in WBI only). All PRO domains showed improvements over time (P < .001). During radiation therapy, the WBI+RNI group reported greater fatigue and nausea. Higher arm symptom scores were observed in the WBI+RNI group 3 months post-treatment (P = .030). No other significant PRO domain differences, including arm/breast symptoms, were observed between the 2 groups.</p><p><strong>Conclusions: </strong>In patients with pN1 breast cancer treated with taxane-based chemotherapy, adding RNI to WBI resulted in minor, temporary declines in specific PRO domains, but these differences were not clinically significant. This indicates that overall patient experience between WBI+RNI and WBI is comparable, supporting the safety and patient tolerability of both treatments.</p>","PeriodicalId":14215,"journal":{"name":"International Journal of Radiation Oncology Biology Physics","volume":" ","pages":"341-351"},"PeriodicalIF":6.4,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142346576","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}