scholarly journals The Risk Factors for Radiation Pneumonitis After Single-Fraction Carbon-Ion Radiotherapy for Lung Cancer or Metastasis

Cancers ◽  
2021 ◽  
Vol 13 (13) ◽  
pp. 3229
Author(s):  
Takashi Ono ◽  
Naoyoshi Yamamoto ◽  
Akihiro Nomoto ◽  
Mio Nakajima ◽  
Yuma Iwai ◽  
...  

There are no studies on the risk factors of radiation pneumonitis (RP) after carbon-ion radiotherapy at a dose of 50 Gy (relative biological effectiveness (RBE)) in a single fraction. The objective of this study was to identify factors associated with RP after radiotherapy, including dose–volume parameters. Ninety-eight patients without a history of thoracic radiotherapy who underwent treatment for solitary lung tumors between July 2013 and April 2016 were retrospectively analyzed. Treatment was planned using Xio-N. The median follow-up duration was 53 months, and the median clinical target volume was 32.3 mL. Three patients developed grade 2 RP, and one patient developed grade 3 interstitial pneumonitis. None of the patients developed grade 4 or 5 RP. The dose-volume parameters of the normal lung irradiated at least with 5–30 Gy (RBE), and the mean lung dose was significantly lower in patients with grade 0–1 RP than in those with grade 2–3 RP. Pretreatment with higher SP-D and interstitial pneumonitis were significant factors for the occurrence of symptomatic RP. The present study showed a certain standard for single-fraction carbon-ion radiotherapy that does not increase the risk of RP; however, further validation studies are needed.

2015 ◽  
Vol 55 (2) ◽  
pp. 163-166 ◽  
Author(s):  
Takanori Abe ◽  
Katsuyuki Shirai ◽  
Jun-Ichi Saitoh ◽  
Takeshi Ebara ◽  
Hirofumi Shimada ◽  
...  

2014 ◽  
Vol 9 (1) ◽  
pp. 92 ◽  
Author(s):  
Go Sasahara ◽  
Masashi Koto ◽  
Hiroaki Ikawa ◽  
Azusa Hasegawa ◽  
Ryo Takagi ◽  
...  

2017 ◽  
Vol 2017 ◽  
pp. 1-7 ◽  
Author(s):  
Yoshihiro Matsumoto ◽  
Makoto Shinoto ◽  
Makoto Endo ◽  
Nokitaka Setsu ◽  
Keiichiro Iida ◽  
...  

Background and Purpose. Carbon-ion radiotherapy (C-ion RT) was effective therapy for inoperable spinal and paraspinal sarcomas. However, a significant adverse event following radiotherapies is vertebral compression fractures (VCFs). In this study, we investigated the incidence of and risk factors for post-C-ion RT VCFs in patients with spinal or paraspinal sarcomas. Material and Methods. Thirty consecutive patients with spinal or paraspinal sarcomas treated with C-ion RT were retrospectively reviewed. Various clinical parameters and the Spinal Instability Neoplastic Score (SINS) were used to evaluate the risk factors for post-C-ion RT VCFs. Results. The overall incidence of VCFs was 23% (median time: 7 months). Patients with VCFs showed a markedly higher SINS score (median value, 9 points) than those without VCF (5 points). The area under the receiver operating characteristic curve for the SINS score was 0.88, and the optimum SINS cut-off score was 8 points. The cumulative incidence of VCFs at 1 year was 9% for patients with a SINS score under 8 points, versus 80% for those with a SINS score of 8 points or higher (p<0.0001). Conclusions. In patients with a SINS score of 8 points or higher, referral to a spine surgeon for stabilization and multidisciplinary discussion is appropriate.


2007 ◽  
Vol 213 (2) ◽  
pp. 149-156 ◽  
Author(s):  
Masashi Koto ◽  
Hirohiko Tsujii ◽  
Naoyoshi Yamamoto ◽  
Hideki Nishimura ◽  
Shogo Yamada ◽  
...  

2020 ◽  
Author(s):  
Liwen Zhang ◽  
Weiwei Wang ◽  
Jiyi Hu ◽  
Jiade Lu ◽  
Lin Kong

Abstract Background We sought to establish a conversion curve to convert the local effect model I (LEM) based RBE-weighted doses (LEM doses) in patients with locally recurrent nasopharyngeal carcinoma (rNPC) to the microdosimetric kinetic model (MKM) based RBE-weighted dose (MKM doses) model. We also converted the relevant organ at risk (OAR) constraints based on this curve. Methods Data from 13 patients with rNPC receiving carbon-ion radiotherapy (CIRT) in our hospital were collected. LEM in Raystation (V8A, Raystation, Sweden) was used to generate treatment plans. Clinical target volume CTV1(GTV+5mm)was given 63 Gy (RBE) in 21 fractions. Ninety-nine percent of target volumes should be covered by 95% of the prescriptions; the maximum doses of the brainstem and spinal cord were < 45 Gy (RBE) and < 30 Gy (RBE), respectively. The doses covering 20% volumes of optical nerves/chiasms D20 were < 30 Gy (RBE). Then physical doses of the LEM plans were recalculated by using MKM in Raystation to generate MKM plans. A series of the ratio of LEM dose to MKM dose was obtained as the conversion factor to obtain the conversion curve by using an isovolumetric dose method. Using prescriptions and OAR, constraints were converted to MKM doses with this curve. Results Conversion factors (LEM dose/MKM dose) from 1.37±0.02 to 3.09±0.09 corresponded to the LEM fractionated doses from 0.24 Gy (RBE) to 2.86 Gy (RBE), including the doses constraining upon OARs. LEM doses of 30 Gy (RBE) and 45 Gy (RBE) in 21 fractions were converted to MKM doses of 16.64 Gy (RBE) and 30.98 Gy (RBE) in 16 fractions. Conclusions This conversion curve could be used to convert LEM doses to MKM doses for patients with rNPC receiving CIRT, providing dose references for re-irradiation therapy.


Blood ◽  
2013 ◽  
Vol 122 (21) ◽  
pp. 5101-5101
Author(s):  
Anna Mesina ◽  
Surbhi Grover ◽  
Carmen Mesina ◽  
Sunita D. Nasta ◽  
Jakub Svoboda ◽  
...  

Abstract Introduction As volume-based radiotherapy planning has become a more standard part of combined modality therapy for lymphomas, dose-volume based constraints for organs-at-risk are needed for treatment planning. Conformal techniques such as intensity modulated radiation therapy and proton radiotherapy may achieve lower doses to certain organs like the heart, but may result in higher doses to other tissues like the lungs and breasts. We sought to define the dosimetric risk factors that are associated with development of radiation pneumonitis (RP). Methods This is a single-institution retrospective analysis of patients with thoracic lymphomas treated with combined modality therapy between 1999 and 2013 who had at least 4 months of follow-up after radiotherapy. Univariate analyses (UVA) were performed using Fisher exact and Wilcoxon rank-sum tests. Results Of the 89 patients analyzed, 13 (14.6%) were diagnosed with RP (at least Grade 1, Common Toxicity Criteria v4.0). Patients were predominantly female (62%) and never smoked (67%). Diagnoses were grouped as Hodgkin lymphoma (62.9%) or non-Hodgkin lymphoma (37.1%), and 18.5% were also treated with autologous stem cell transplants. UVA showed that RP was more commonly associated with a diagnosis of non-Hodgkin lymphoma (38%) than Hodgkin lymphoma (8%), despite exposure to bleomycin in the majority of patients with Hodgkin lymphoma. Higher lung doses were significantly associated with RP using multiple lung dose-volume parameters: mean lung dose (12.3 vs. 16.7 Gy, p=0.002), volume of lung receiving 20 Gy (27.3% vs. 39.1%, p=0.0009), and volume of lung receiving 5 Gy (51% vs. 66.8%, p=0.004). The majority (67%) of patients who developed RP had mean lung doses of over 15 Gy, whereas only 24% of those who did not develop RP had mean lung doses above 15 Gy, see Figure. Heart dosimetric parameters were also significantly associated with RP, including mean heart dose (13.3 vs. 21.5 Gy, p=0.004), volume of heart receiving 20 Gy (25.4% vs. 48.3%, p=0.003), and volume of heart receiving 5 Gy (57.6% vs. 81.1%, p=0.04). There were not enough events to determine if heart and lung parameters were independently associated with RP, but they were strongly correlated (R=0.75). Gender, smoking history, and autologous transplant were not significantly associated with RP. None of the 13 patients treated with proton radiotherapy developed RP. In general, patients treated with proton radiotherapy had lower mean heart doses (9.4 vs. 15.4 Gy) and mean lung doses (9.6 Gy vs. 13.5 Gy). Conclusions Higher doses to lung and heart are associated with increased risk of RP, and doses to these critical structures should be considered carefully during volume-based consolidative radiotherapy using advanced techniques. Disclosures: No relevant conflicts of interest to declare.


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