Skip to main content
Advertisement
Browse Subject Areas
?

Click through the PLOS taxonomy to find articles in your field.

For more information about PLOS Subject Areas, click here.

  • Loading metrics

Low-dose abdominopelvic computed tomography in patients with lymphoma: An image quality and radiation dose reduction study

  • Sungjin Yoon ,

    Roles Formal analysis, Methodology, Writing – original draft

    Current address: Department of Radiology, Chungju Medical Center, Chungju-si, Chungcheongbuk-do, Republic of Korea

    ‡ SY and KHY are contributed equally to this study and share the first authorship.

    Affiliation Department of Radiology, Gil Medical Center, Gachon University College of Medicine, Incheon, Republic of Korea

  • Kwai Han Yoo ,

    Roles Data curation, Formal analysis, Methodology

    ‡ SY and KHY are contributed equally to this study and share the first authorship.

    Affiliation Department of Internal Medicine, Gachon University Gil Medical Center, Gachon University College of Medicine, Incheon, Korea

  • So Hyun Park ,

    Roles Formal analysis, Funding acquisition, Methodology, Writing – review & editing

    nnoleeter@naver.com

    Affiliation Department of Radiology, Gil Medical Center, Gachon University College of Medicine, Incheon, Republic of Korea

  • Hawk Kim,

    Roles Data curation

    Affiliation Department of Internal Medicine, Gachon University Gil Medical Center, Gachon University College of Medicine, Incheon, Korea

  • Jae Hoon Lee,

    Roles Data curation

    Affiliation Department of Internal Medicine, Gachon University Gil Medical Center, Gachon University College of Medicine, Incheon, Korea

  • Jinny Park,

    Roles Data curation

    Affiliation Department of Internal Medicine, Gachon University Gil Medical Center, Gachon University College of Medicine, Incheon, Korea

  • Seong Ho Park,

    Roles Conceptualization, Methodology

    Affiliation Department of Radiology and Research Institute of Radiology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Korea

  • Hwa Jung Kim

    Roles Methodology, Writing – review & editing

    Affiliation Department of Clinical Epidemiology and Biostatistics, Asan Medical Center, Ulsan University College of Medicine, Seoul, Korea

Abstract

This study aimed to evaluate image quality, the detection rate of enlarged lymph nodes, and radiation dose exposure of ultralow-dose and low-dose abdominopelvic computed tomography (CT) in patients with lymphoma. Patients with lymphoma who underwent abdominopelvic CT using dual-source scanner were retrospectively recruited from a single center. CT images were obtained at 90 kVp dual-source mode reformatted in three data sets using the advanced modelled iterative reconstruction algorithm: 100% (standard-dose CT), 66.7% (low-dose CT), and 33.3% (ultralow-dose CT). Two radiologists analyzed subjective image quality and detection of abdominal enlarged lymph nodes on ultralow-dose, low-dose, and standard-dose CT blindly and independently. The results were compared with reference standards. Three readers (two radiologists and one hematologist) reviewed overall image quality and spleen size. In total, 128 consecutive CT scans (77 complete response, 44 partial response, 6 progressive disease, and 1 initial evaluation) from 86 patients (64 B-cell lymphoma, 14 T/NK-cell lymphoma, and 8 Hodgkin’s lymphoma cases) were assessed. The enlarged lymph node-based detection rates for two readers were 97.0% (96/99) and 94.0% (93/99) on standard-dose CT, 97.0% (96/99) and 94.0% (93/99) on low-dose CT, and 94.0% (93/99) and 89.9% (89/99) on ultralow-dose CT. Overall image quality was 3.8 ± 0.5, 3.9 ± 0.5, and 4.1 ± 0.5 on ultralow-dose CT; 4.7 ± 0.4, 4.6 ± 0.5, and 4.8 ± 0.3 on low-dose CT; and 4.8 ± 0.4, 4.7 ± 0.4, and 4.9 ± 0.2 on standard-dose CT, according to two radiologists and one hematologist, respectively. Intraclass correlation coefficients of spleen size were 0.90 (95% confidence interval [CI], 0.87–0.93), 0.91 (95% CI, 0.88–0.93), and 0.91 (95% CI, 0.88–0.93) on ultralow-dose, low-dose, and standard-dose CT, respectively. Mean effective radiation doses of standard-dose, low-dose, and ultralow-dose CT were 5.7 ±1.8 mSv, 3.8 ± 1.2 mSv, and 1.9 ± 0.6 mSv, respectively. Our findings suggest that ultralow-dose and low-dose CT, even with radiation doses reduced by 66.7% and 33.3%, respectively, maintained adequate image quality. These imaging modalities may be employed for follow-up lymphoma evaluation in consideration of the long surveillance periods.

Introduction

Lymphomas account for 3.4% of all malignancies worldwide and consist of heterogeneous subtypes (i.e., non-Hodgkin’s lymphomas and Hodgkin’s lymphoma) [1, 2]. The majority of lymphomas involve the lymph nodes and extralymphatic organs, and occur in young adults and pediatric patients. A proportion of lymphomas are considered potentially curable diseases due to improvements in treatment protocols [3]. The Lugano classification is used for lymphoma staging and response assessment, and imaging modalities such as positron emission tomography (PET)/CT and computed tomography (CT) play key roles in response assessment and surveillance to evaluate lymph nodes and spleen [47]. Due to their long life expectancy, patients with lymphoma require multiple CT examinations to evaluate treatment response and surveillance after treatment. The cumulative radiation exposure of repetitive CT examinations in pediatric and young adult patients may increase baseline cancer risk [8, 9]. Therefore, dose reduction techniques for CT can be useful for patients with lymphoma in consideration of the long surveillance periods.

Several studies have attempted low-dose CT to evaluate Hodgkin’s lymphoma in the thorax [10] and in patients undergoing staging or restaging of lymphoma [11, 12]. Generally, a reduction in radiation dose is related to increased image noise and decreased image quality, which may negatively impact diagnostic performance. However, in patients with lymphoma, particularly during follow-up after treatment, measurement of pre-existing lesions or improvements in lymphoma involvement constitute a major component of CT assessments. In this regard, low-dose CT with reduced image quality may be sufficient for follow-up evaluation.

Recent advances in CT techniques have contributed to a reduction in radiation dose, such as the implementation of automatic adjustment of tube potential, automated tube current modulation, and iterative reconstruction (IR) [13, 14]. A new third generation of IR was recently developed based on statistical-based to model-based IR [1416]. Advanced modelled IR (ADMIRE; Siemens Healthcare, Forchheim, Germany) [17] is a model-based IR that permits a large reduction in image noise in raw data and additional dose reduction with improved spatial resolution.

Dual-energy CT with dual-source scanners can be used to compare standard and low-dose CT images by separating and combining data from each tube without the need for additional examinations [18, 19]. In this study, we evaluated radiation dose exposure and image quality of low-dose and standard-dose CT to compare the detection rates of enlarged lymph nodes of low-dose and standard-dose CT for abdominal lymphoma evaluation and post-treatment follow-up in patients with lymphoma.

Materials and methods

Ethics approval

Approval for this retrospective study was obtained from the institutional review board (GAIRB2021-237) of the Gil Medical Center. All CT images were acquired using standard-dose CT scan, without additional radiation exposure. Thus, the informed consent was waived because of the retrospective nature of the study.

Study participants

In total, 197 consecutive patients who underwent dual-source CT scans for hematologic assessment at the hematologic department of Gil Medical Center from December 2018 to December 2020 were enrolled. All patients diagnosed with lymphoma were included. Patients underwent CT for lymphoma evaluation, chemotherapy response, or surveillance after treatment. Among 98 consecutive patients with 140 CT scans who were eligible, 12 patients were excluded due to a protocol change (n = 7) and lack of a reference standard (n = 5). A final total of 86 consecutive patients with 128 CT examinations were included in this study (Fig 1A). The study period, from December 2018 to March 2019, partially overlapped with that of a previous dual-energy study conducted in the same institution [20]. However, the previous study only included patients from the oncologic department. Therefore, there were no overlapping patients between the two studies.

thumbnail
Fig 1. Flow diagram of patients.

(a) Inclusion flow chart and (b) computed tomography (CT) examinations and reconstruction methods.

https://doi.org/10.1371/journal.pone.0272356.g001

CT technique

Contrast-enhanced abdominopelvic CT examination was acquired above the dome of the diaphragm and below the symphysis pubis. All patients received intravenous injection of 1.5 mL/kg of iopamidol (Pamiray 300; Dongkook Pharm., Korea), up to a maximum dose of 120 mL. The injection was delivered using a power injector at an injection rate of 4 mL/s and fixed injection duration of 75 s. CT scans were achieved at a fixed tube potential of 90 kVp using a third-generation dual-source CT scanner (SOMATOM Force, Siemens Healthcare, Forchheim, Germany) in dual-source mode with tube detector A (reference tube current: 100 mAs) and B (reference tube current: 200 mAs), using tube current dose modulation (CARE dose 4D; Siemens Healthcare) and the ADMIRE algorithm (Fig 1B and Table 1). We used the ADMIRE algorithm at a strength level of 2 out of 5, with an axial slice thickness of 5 mm and coronal slice thickness of 3 mm.

Qualitative visual image analysis

Two radiologists (S.J.Y and S.H.P, with 5 and 10 years of abdominal radiologic experience radiologists, respectively) reviewed the image analysis, and one hematologist (K.H.Y) reviewed the overall image quality and spleen size only. The images of 384 CT examinations were reviewed independently by three readers in a blinded manner. These interpretations were analyzed in three reading sessions, some of which included one-third of the three CT image sets. The images were reviewed anonymously, and the order of review was randomized with a 1-month washout period between sessions. Lymphoma involvement was evaluated based on the Lugano classification [4], with modifications: lymph nodes, spleen, liver, and other sites. An enlarged lymph node was regarded as a short-axis diameter > 1 cm, and splenomegaly was defined as the longest length of the spleen > 12 cm. Suspicious masses or nodules in the adrenal glands or liver were analyzed. Enlarged lymph nodes exhibiting a fatty hilum were considered to indicate a reactive change. We measured the average diameter of lymph nodes (short-axis diameter >0.5 cm in each data set) on standard-dose, low-dose, and ultralow-dose CT. The overall image quality score for assessing CT images was subjectively measured using a 5-point (Table 2).

Quantitative image noise analysis

To achieve objective image quality, regions of interest (ROI) were placed in four regions including psoas muscle, subcutaneous fat in the anterior abdominal wall, right hepatic lobe parenchyma, aorta lumen in L1 vertebral body level with same location in three image sets. The standard deviations (SDs) in Hounsfield units (HU) were measured by a 1–3 cm2 ROI by a single-blinded reader (S.J.Y.), as image noise. Mean attenuation values (HU) were measured for each ROI.

Radiation dose

The volume CT dose index (CTDIvol) and dose-length product were documented in the dose page of the scanner. In the calculation of effective dose, tissue-weighting factors for the abdomen was used in millisieverts (mSv) (male, k = 0.013; female, k = 0.017) and pelvis (male, k = 0.010; female, k = 0.016) using average values (male, k = 0.012; female, k = 0.017) [21, 22].

Reference standards

Reference standards comprised PET-CT or MRI within 3 months, interval changes of the lesion compared to serial CTs with patient’s symptoms, and clinician’s judgment based on electronic medical records (EMRs). Response assessment was based on EMRs and was categorized into complete, partial, stable, and progressive disease.

Statistical analysis

Radiation dose and objective image analyses were compared among the three CT scans using analysis of variance followed by post hoc Bonferroni correction. Subjective image evaluations of the three image analyses were compared using Kruskal-Wallis test adjusted with Monte Carlo simulation. In each image set, the detection rate for enlarged lymph nodes were compared with each other using Generalized Estimating Equations (GEE) with adjustment for multiple comparisons using Bonferroni correction. Interobserver agreement of enlarged lymph node detection among two readers was analyzed using kappa, and interobserver agreement of spleen size among three readers was assessed using intraclass correlation coefficients, defined as follows: 0.01–0.20, slight; 0.21–0.40, fair; 0.41–0.60, moderate; 0.61–0.80, substantial; and 0.81–1, excellent. Statistical significance was set at P < 0.05. After post hoc analysis, P-values < 0.01 were considered statistically significant. Statistical analyses were performed using SAS version 9.4 (SAS Institute Inc., Cary, NC, USA) for all data analyses.

Results

Patient characteristics

The clinical characteristics of the patients are summarized in Table 3. Of the 86 patients with 128 CT scans, 57 were men and 29 were women, with a mean age ± standard deviation of 58.4 ± 16.3 years. Of patients, 33 underwent two or more CT examinations during the study period (25 patients, 2 CT examinations; 8 patients, 3 CT examinations). Among patients, B-cell lymphoma was the most common disease (n = 63, 73.3%), followed by T/NK-cell lymphoma (n = 14, 16.3%) and Hodgkin’s lymphoma (n = 8, 9.3%).

Lesion detection analysis

Table 4 compares standard-dose, low-dose, and ultralow-dose CT for the detection of lesions in the aforementioned organs and enlarged lymph node analysis in patients with lymphoma. The number of enlarged lymph nodes detected by two readers was higher on standard-dose (n = 97 and 95) and low-dose CT (n = 97 and 95) than on ultralow-dose CT (n = 94 and n = 93). The enlarged lymph node-based detection rates (i.e., number of detected true enlarged lymph nodes/number of true enlarged lymph nodes) for two readers were 97.0% (96/99) and 94.0% (93/99) on standard-dose CT, 97.0% (96/99) and 94.0% (93/99) on low-dose CT, and 94.0% (93/99) and 89.9% (89/99) on ultralow-dose CT (Table 4A and Figs 2 and 3). After GEE with adjustment for multiple comparisons using Bonferroni correction, there was no statistical difference among three data sets by two readers (reader 1, Standard-dose CT vs. Ultralow-dose CT, P = 0.256; Low-dose CT vs. Ultralow-dose CT, P = 0.256; reader 2, Standard-dose CT vs. Ultralow-dose CT, P = 0.132; Low-dose CT vs. Ultralow-dose CT, P = 0.132). Pairwise comparisons revealed different numbers of enlarged lymph nodes in the common hepatic, paraaortic, aortocaval, and internal iliac areas (standard-dose CT vs. ultralow-dose CT and low-dose CT vs. ultralow-dose CT) among the three CT doses (Tables 4B and S1). The highest number of nodules in the adrenal glands was observed on standard-dose CT (n = 5, both), followed by low-dose CT (n = 3 and 4) and ultralow-dose CT (n = 3 and 2) by two readers.

thumbnail
Fig 2. Abdominopelvic computed tomography (CT) images of a 23-year-old woman with Hodgkin’s lymphoma, complete remission state (body mass index, 24.2 kg/m2; effective diameter, 24.0 cm).

The three different types of CT images, acquired according to the radiation dose (a-b: standard-dose CT, 5.6 mSv; c-d: low-dose CT, 3.7 mSv; e-f: ultralow-dose CT, 1.8 mSv), show the absence of enlarged lymph nodes and splenomegaly. Identical reports of the aforementioned features were also obtained from two radiologists. The overall image quality score was 4 for the ultralow-dose CT images and 5 for the low-dose and standard-dose CT images, according to three readers (two radiologists and one hematologist).

https://doi.org/10.1371/journal.pone.0272356.g002

thumbnail
Fig 3. Abdominopelvic computed tomography (CT) images of a 54-year-old man with follicular lymphoma, partial response state (body mass index, 29.4 kg/m2; effective diameter, 27.0 cm).

The three different types of CT images, acquired according to the radiation dose (a-c: standard-dose CT, 6.8 mSv; d-f: low-dose CT, 4.5 mSv; g-i: ultralow-dose CT, 2.3 mSv), show multiple enlarged paraaortic (white arrow), aortocaval (gray arrow), right common iliac, and bilateral external iliac lymph nodes (black arrows). Identical findings for the aforementioned lesions were reported by two radiologists. The overall image quality score was 4 for ultralow-dose CT images and 5 for low-dose and standard-dose CT images, according to two radiologists; the image quality score was 5 for all the three types of CT images according to one hematologist.

https://doi.org/10.1371/journal.pone.0272356.g003

thumbnail
Table 4.

Lesion detection in organs (a) and detailed enlarged lymph node (b) analysis.

https://doi.org/10.1371/journal.pone.0272356.t004

The number of patients with splenomegaly on ultralow-dose, low-dose, and standard-lose CT was determined to be 23, 22, and 23 for radiologist 1; 22, 24, and 24 for radiologist 2; and 16, 16, and 18 for the hematologist, respectively. Spleen size measured by three readers (radiologists and one hematologist was 10.7 ± 1.69, 10.6 ± 1.78, and 10.0 ± 0.28 cm on ultralow-dose CT; 10.7 ± 1.70, 10.7 ± 1.80, and 10.0 ± 0.14 on low-dose CT; and 10.7 ± 1.70, 10.7 ± 1.79, and 10.0 ± 0.28 cm on standard-dose CT, respectively). We measured the average diameter of lymph nodes (short-axis diameter >0.5 cm, a total of 170 lymph nodes in each data set) on standard-dose, low-dose, and ultralow-dose CT, with no significant differences in the mean lymph node diameter among them (0.7±0.3, 0.7±0.3, and 0.7±0.4, respectively).

Quantitative and qualitative image analysis

A comparison of objective CT image quality based on measurement of image noise in subcutaneous fat, psoas muscle, liver, and abdominal aorta is presented in Table 5. Standard-dose CT exhibited the lowest image noise (9.4–11.5 HU), followed by low-dose CT (11.0–14.3 HU) and ultralow-dose CT (12.2–15.8 HU; P-value < 0.001; all post-hoc analysis). With regard to subjective image quality assessed by all readers, ultralow-dose CT exhibited lower overall image quality (3.8–4.1; P < 0.001; Kruskal-Wallis test), while standard-dose CT (4.7–4.9) and low-dose CT (4.6–4.8) exhibited higher overall image quality. There was no significant difference in overall image quality between standard-dose and low-dose CT (P-value [adjusted with Monte Carlo simulation] = 0.167, 0.121, and 0.088 for each reader, respectively).

thumbnail
Table 5. Quantitative and qualitative image analysis of three CT image sets.

https://doi.org/10.1371/journal.pone.0272356.t005

Inter-observer agreement

S1 Table presents the inter-reader agreement of enlarged lymph node detection. Inter-reader agreement for enlarged lymph node detection by the two readers was excellent (κ = 0.83–1). Enlarged aortocaval lymph nodes on ultralow-dose CT exhibited the lowest inter-reader agreement score (κ = 0.83) in both common iliac areas. Intraclass correlation coefficient of spleen size was 0.90 (95% confidence interval [CI]), 0.87–0.93), 0.91 (95% CI, 0.88–0.94), and 0.91 (95% CI, 0.88–0.93) on ultralow-dose, low-dose, and standard-dose CT, respectively.

Radiation dose parameters

Table 6 summarizes the dose parameters of the three CT image sets. Mean CTDIvol of standard-dose, low-dose, and ultralow-dose CT was 5.6 ± 1.5 mGy, 3.7 ± 1.0 mGy, and 1.9 ± 0.5 mGy, respectively. Mean effective radiation dose of standard-dose, low-dose, and ultralow-dose CT was 5.7 ± 1.8 mSv, 3.8 ± 1.2 mSv, and 1.9 ± 0.6 mSv, respectively.

Discussion

This study compared the radiation dose exposure, the detection rate of enlarged lymph nodes, and image quality of standard-dose, low-dose, and ultralow-dose abdominopelvic CT using the ADMIRE algorithm in patients with lymphoma. The enlarged lymph node-based detection rate was 94.0−97.0% on standard-dose and low-dose CT, and 89.9−94.0% on ultralow-dose CT according to two readers, with excellent inter-reader agreement. Ultralow-dose and low-dose CT effectively reduced radiation dose by 66.7% and 33.3%, respectively, while maintaining adequate image quality. We observed the same rate of detection of enlarged lymph nodes (i.e., > 1 cm in diameter) by two readers between low-dose and standard-dose CT. Although the rate of detection of enlarged lymph nodes was slightly higher on standard-dose CT than on ultralow-dose CT, there was no statistically significant difference between standard-dose and ultralow-dose CT. We conjecture that the detection of enlarged abdominal lymph nodes can be achieved in a relatively simple and clear manner by radiologists. The development of CT techniques and image reconstruction algorithms, including ADMIRE, may facilitate higher detection rates, even on ultralow-dose CT.

Several studies have reported non-inferior or comparable diagnostic performance for a specific diagnosis (e.g., urinary stones or acute appendicitis) of a relatively simple disease or organ between low-dose abdominal CT and standard-dose CT [2325]. However, the diagnostic performance of low-dose CT for small or inconspicuous abdominal structures has been unsatisfactory, even with the use of model-based IR [26, 27]. Due to high image noise in the abdomen, low-dose CT has limitations in the evaluation of small lesions in neoplastic conditions (e.g., liver metastasis and pancreatic cancer) and inflammatory diseases [18, 27, 28]. Small lesions with high image noise may obscure lesion detection due to similar attenuation as the background [27, 29]. Compared to standard-dose CT, ultralow-dose CT exhibited a similar rate of detection of enlarged lymph nodes in this study, while reducing the radiation dose by 33.3%. The high rate of detection of enlarged lymph nodes on ultralow-dose CT could be underpinned by the abdominal lymph nodes being less affected by image noise due to definite contrast differences between retroperitoneal or peritoneal fat and surrounding lymph nodes with a clear margin (i.e., background and lesion sharpness). These findings suggest that ultralow-dose CT may be employed instead of standard-dose CT during follow-up of patients with lymphoma. Notably, the interobserver agreement for abdominal lymph nodes was excellent in our study. This could be due to the sparsity of other anatomical structures surrounding the abdominal lymph nodes; as such, the diagnosis of enlarged lymph nodes exhibited small differences between the two readers despite the presence of image noise.

With regard to lymph node evaluation using low-dose CT, Paolini et al. reported that there was no significant difference in the delineation of thoracic lymph nodes between contrast-enhanced low-dose and standard-dose CT [30]. Mueller‑Lisse et al. also reported that contrast-enhanced low-dose CT with approximately 1 mSv revealed equivalent delineation of thoracic lymph nodes compared to standard-dose CT [31]. In line with prior studies on thoracic lymph nodes, our study revealed similar results regarding abdominal lymph node evaluation using low-dose and ultralow-dose CT in patients with lymphoma.

Hérin et al. reported that reduced-dose CT with model-based IR could reduce the amount of radiation delivered to patients with lymphoma while maintaining image quality comparable to that of standard-dose CT with filtered-back projection [12]. Herein, we compared three CT image sets using ADMIRE (i.e., without using a filtered-back projection comparison). We implemented ADMIRE in actual practice and focused on the number of radiation doses to be reduced in patients with lymphoma while maintaining image quality. Quantitative image noise increased with a decrease in radiation dose. However, we observed that subjective visual image quality was comparable between standard-dose and low-dose CT, and there were no significant differences in the results of lymph node evaluation between these image sets. Although low-dose CT exhibited slightly increased objective image noise and comparable subjective image quality compared to standard-dose CT, this may not affect the diagnosis of lymph node detection. Nevertheless, ultralow-dose CT resulted in degradation of both qualitative visual image quality and quantitative image noise analysis.

A blind image analysis was performed in this study for the independent evaluation of lymph node enlargement in each image reading session. The use of low-dose CT as an imaging modality for follow-up evaluation of lymphoma permits the use of initial standard-dose CT as a reference and comparative examinations in actual practice. We predict better diagnostic performance of enlarged lymph node detection, even using ultralow-dose CT, compared to the current results. In consideration of the long-term follow-up period, low-dose and/or ultralow-dose CT offers a safe and accurate alternative imaging modality to replace current standard-dose CT.

Our study has a few limitations. First, we only assessed changes in tube load (mAs) and a single image reconstruction using ADMIRE, and we did not consider filtered-back projection. Thus, the study protocol differs from clinical protocols, as a fixed kVp was used for both detection tubes without automatic tube voltage adjustment (Care kV). As various image acquisition parameters can affect image quality in CT, our results may have limited generalizability. Second, as images reconstructed with ADMIRE have different appearances, it is difficult to achieve a true blinded analysis of subjective criteria. Third, because most of the patients who underwent dual energy CT examination at our hospital were outpatients, most of the patients with lymphoma included in the study were outpatients, and we predominantly focused on treatment response. Therefore, our results may be applicable to surveillance of patients after lymphoma treatment but not for patients with initial lymphoma evaluation, relapse, or suspected progressive disease. Finally, we analyzed CT images with a slice thickness of 5 mm in the axial direction and 3 mm in the coronal direction. Although these parameters can reflect readings in actual practice, it may also lead to partial volume effect when measuring lymph nodes since thin slices (e.g., 2 mm) were not analyzed.

In conclusion, our findings suggest that ultralow-dose and low-dose CT effectively reduce radiation dose by 66.7% and 33.3%, respectively, while maintaining acceptable image quality and can be used as an imaging modality for follow-up evaluation of lymphoma, in consideration of the long-term follow-up period.

Supporting information

S1 Table. The number of enlarged lymph nodes and each interobserver agreement.

https://doi.org/10.1371/journal.pone.0272356.s001

(DOCX)

S2 Appendix. Statistical analysis of subjective image quality comparisons.

https://doi.org/10.1371/journal.pone.0272356.s003

(DOCX)

Acknowledgments

The authors thank Seong Yong Pak, for his help in reconstructing the image data.

References

  1. 1. Jiang M, Bennani NN, Feldman AL. Lymphoma classification update: T-cell lymphomas, Hodgkin lymphomas, and histiocytic/dendritic cell neoplasms. Exp Rev Hematol. 2017;10(3): 239–249.
  2. 2. Huh J. Epidemiologic overview of malignant lymphoma. Korean J Hematol. 2012;47(2): 92–104. pmid:22783355
  3. 3. Siegel RL, Miller KD, Jemal A. Cancer statistics, 2018. CA Cancer J Clin. 2018;68(1): 7–30. pmid:29313949
  4. 4. Cheson BD, Fisher RI, Barrington SF, Cavalli F, Schwartz LH, Zucca E, et al. Recommendations for initial evaluation, staging, and response assessment of Hodgkin and non-Hodgkin lymphoma: the Lugano classification. J Clin Oncol. 2014;32(27): 3059–3068. pmid:25113753
  5. 5. Johnson SA, Kumar A, Matasar MJ, Schoeder H, Rademaker J. Imaging for staging and response assessment in lymphoma. Radiology. 2015;276(2): 323–338. pmid:26203705
  6. 6. Horwitz SM, Zelenetz AD, Gordon LI, Wierda WG, Abramson JS, Advani RH, et al. NCCN guidelines insights: non-Hodgkin’s lymphomas, version 3.2016. J Natl Compr Cancer Netw. 2016;14(9): 1067–1079. pmid:27587620
  7. 7. Nabhan C, Smith SM, Cifu AS. Surveillance imaging in patients in remission from Hodgkin and diffuse large B-cell lymphoma. JAMA. 2016;315(19): 2115–2116. pmid:27187305
  8. 8. Fabritius G, Brix G, Nekolla E, Klein S, Popp HD, Meyer M, et al. Cumulative radiation exposure from imaging procedures and associated lifetime cancer risk for patients with lymphoma. Sci Rep. 2016;6: 35181. pmid:27748377
  9. 9. Sodickson A, Baeyens PF, Andriole KP, Prevedello LM, Nawfel RD, Hanson R, et al. Recurrent CT, cumulative radiation exposure, and associated radiation-induced cancer risks from CT of adults. Radiology. 2009;251(1): 175–184. pmid:19332852
  10. 10. Wattson DA, Hunink MG, DiPiro PJ, Das P, Hodgson DC, Mauch PM, et al. Low-dose chest computed tomography for lung cancer screening among Hodgkin lymphoma survivors: a cost-effectiveness analysis. Int J Radiat Oncol Biol Phys. 2014;90(2): 344–353. pmid:25104066
  11. 11. Elstrom RL, Leonard JP, Coleman M, Brown RK. Combined PET and low-dose, noncontrast CT scanning obviates the need for additional diagnostic contrast-enhanced CT scans in patients undergoing staging or restaging for lymphoma. Ann Oncol. 2008;19(10): 1770–1773. pmid:18550578
  12. 12. Hérin E, Gardavaud F, Chiaradia M, Beaussart P, Richard P, Cavet M, et al. Use of Model-Based Iterative Reconstruction (MBIR) in reduced-dose CT for routine follow-up of patients with malignant lymphoma: dose savings, image quality and phantom study. Eur Radiol. 2015;25(8): 2362–2370. pmid:25749813
  13. 13. McCollough CH, Primak AN, Braun N, Kofler J, Yu L, Christner J. Strategies for reducing radiation dose in CT. Radiol Clin North Am. 2009;47(1): 27–40. pmid:19195532
  14. 14. Higaki T, Nakamura Y, Fukumoto W, Honda Y, Tatsugami F, Awai K. Clinical application of radiation dose reduction at abdominal CT. Eur J Radiol. 2019;111: 68–75. pmid:30691668
  15. 15. Padole A, Ali Khawaja RD, Kalra MK, Singh S. CT radiation dose and iterative reconstruction techniques. Am J Roentgenol. 2015;204(4): W384–W392. pmid:25794087
  16. 16. Mohammadinejad P, Mileto A, Yu L, Leng S, Guimaraes LS, Missert AD, et al. CT noise-reduction methods for lower-dose scanning: strengths and weaknesses of iterative reconstruction algorithms and new techniques. RadioGraphics. 2021;41(5): 1493–1508. pmid:34469209
  17. 17. Nuyts J, De Man B, Fessler JA, Zbijewski W, Beekman FJ. Modelling the physics in the iterative reconstruction for transmission computed tomography. Phys Med Biol. 2013;58(12): R63–96. pmid:23739261
  18. 18. Lee KH, Shim YS, Park SH, Park SH, Choi SJ, Pak SY, et al. Comparison of standard-dose and half-dose dual-source abdominopelvic CT scans for evaluation of acute abdominal pain. Acta Radiol. 2019;60(8): 946–954. pmid:30376718
  19. 19. Lee SJ, Park SH, Kim AY, Yang S-K, Yun S-C, Lee SS, et al. A prospective comparison of standard-dose CT enterography and 50% reduced-dose CT enterography with and without noise reduction for evaluating Crohn disease. Am J Roentgenol. 2011;197(1): 50–57.
  20. 20. Choi SJ, Ahn SJ, Park SH, Park SH, Pak SY, Choi JW, et al. Dual-source abdominopelvic computed tomography: Comparison of image quality and radiation dose of 80 kVp and 80/150 kVp with tin filter. PLoS One. 2020 Sep 3;15(9):e0231431. pmid:32881876
  21. 21. Goo HW. CT radiation dose optimization and estimation: an update for radiologists. Korean J Radiol. 2012;13(1): 1–11. pmid:22247630
  22. 22. International Commission on Radiation Protection. The 2007 Recommendations of the International Commission on Radiological Protection: ICRP Publication 103. Ann ICRP 2007;37(2–4):1–321. pmid:18082557
  23. 23. Kim K, Kim YH, Kim SY, Kim S, Lee YJ, Kim KP, et al. Low-dose abdominal CT for evaluating suspected appendicitis. N Engl J Med. 2012;366(17): 1596–1605. pmid:22533576
  24. 24. Rodger F, Roditi G, Aboumarzouk OM. Diagnostic accuracy of low and ultra-low dose CT for identification of urinary tract stones: a systematic review. Urol Int. 2018;100(4): 375–385. pmid:29649823
  25. 25. Weinrich JM, Bannas P, Regier M, Keller S, Kluth L, Adam G, et al. Low-dose CT for evaluation of suspected urolithiasis: diagnostic yield for assessment of alternative diagnoses. AJR Am J Roentgenol. 2018;210(3): 557–563. pmid:29364722
  26. 26. Padole A, Singh S, Lira D, Blake MA, Pourjabbar S, Khawaja RD, et al. Assessment of filtered back projection, adaptive statistical, and model-based iterative reconstruction for reduced dose abdominal computed tomography. J Comput Assist Tomogr. 2015;39(4): 462–467. pmid:25734468
  27. 27. Jensen CT, Wagner-Bartak NA, Vu LN, Liu X, Raval B, Martinez D, et al. Detection of colorectal hepatic metastases is superior at standard radiation dose CT versus reduced dose CT. Radiology. 2019;290(2): 400–409. pmid:30480489
  28. 28. Fletcher JG, Fidler JL, Venkatesh SK, Hough DM, Takahashi N, Yu L, et al. Observer performance with varying radiation dose and reconstruction methods for detection of hepatic metastases. Radiology. 2018;289(2): 455–464. pmid:30204077
  29. 29. Dobeli KL, Lewis SJ, Meikle SR, Thiele DL, Brennan PC. Noise-reducing algorithms do not necessarily provide superior dose optimisation for hepatic lesion detection with multidetector CT. Br J Radiol. 2013;86(1023): 20120500. pmid:23392194
  30. 30. Paolini M, Wirth K, Tufman A, Reiser M, Huber RM, Mueller-Lisse UG. Thoracic lymph node delineation at dose-reduced (1 mSv) dose-modulated contrast enhanced MDCT: a retrospective pilot study. Radiol Med. 2016;121(8): 644–651. pmid:27154525
  31. 31. Mueller-Lisse UG, Marwitz L, Tufman A, Huber RM, Zimmermann HA, Walterham A, et al. Less radiation, same quality: contrast-enhanced multi-detector computed tomography investigation of thoracic lymph nodes with one milli-sievert. Radiol Med. 2018;123(11): 818–826. pmid:29961228