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Article ; Online: Diagnostic accuracy of fine needle aspiration cytology and core needle biopsy in bone and soft tissue tumor: A comparative study of the image-guided and blindly performed procedure.

Ariizumi, Takashi / Kawashima, Hiroyuki / Yamagishi, Tetsuro / Oike, Naoki / Murayama, Yudai / Umezu, Hajime / Endo, Naoto / Ogose, Akira

Annals of diagnostic pathology

2022 Volume 59, Page(s) 151936

Abstract: Introduction: Fine needle aspiration cytology (FNAC) and core needle biopsy (CNB) can provide tissue samples for the diagnoses of bone and soft tissue tumors. We evaluated the diagnostic accuracy of FNAC and CNB, the usefulness of the image-guided ... ...

Abstract	Introduction: Fine needle aspiration cytology (FNAC) and core needle biopsy (CNB) can provide tissue samples for the diagnoses of bone and soft tissue tumors. We evaluated the diagnostic accuracy of FNAC and CNB, the usefulness of the image-guided needle procedures, and assessed whether a discordance can influence the prognosis. Patients and methods: We retrospectively examined the accuracy rates of FNAC and CNB procedures by analyzing results of 405 specimens of 389 patients. We evaluated the diagnostic accuracy of FNAC and CNB, compared the clinical effectiveness between the image-guided procedures and the blind procedures, and also compared survival rates between the true positive and the false negative cases for patients with high-grade malignant tumors. Results: The accuracy rates of FNAC were 86.6% and 93.8% for CNB. In cases with non-palpable masses, there were significantly low sampling error rates in the image-guided procedure. There were no significant differences in progression-free-survival and overall survival rates in patients between the false negative and true positive cases. Conclusion: Both FNAC and CNB procedures had high accuracy rates. Limited to cases with no palpable masses, the image-guided procedure had a low sampling error rate and was an effective method for obtaining tissue samples.
MeSH term(s)	Biopsy, Fine-Needle/methods ; Biopsy, Large-Core Needle ; Humans ; Prognosis ; Retrospective Studies ; Sensitivity and Specificity ; Soft Tissue Neoplasms/diagnosis
Language	English
Publishing date	2022-03-18
Publishing country	United States
Document type	Journal Article
ZDB-ID	1440011-x
ISSN	1532-8198 ; 1092-9134
ISSN (online)	1532-8198
ISSN	1092-9134
DOI	10.1016/j.anndiagpath.2022.151936
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Article: Single cell RNA-sequencing of Ewing sarcoma tumors demonstrates transcriptional heterogeneity and clonal evolution.

Goodspeed, Andrew / Bodlak, Avery / Nelson-Taylor, Sarah / Oike, Naoki / Porfilio, Timothy / Shirai, Ryota / Walker, Deandra / Treece, Amy / Black, Jennifer / Donaldson, Nathan / Cost, Carrye / Garrington, Tim / Greffe, Brian / Luna-Fineman, Sandra / Demedis, Jenna / Lake, Jessica / Danis, Etienne / Verneris, Michael / Hayashi, Masanori

bioRxiv : the preprint server for biology

2024

Abstract: Ewing sarcoma is the second most common bone cancer in children, accounting for 2% of pediatric cancer diagnoses. Patients who present with metastatic disease at the time of diagnosis have a dismal prognosis, compared to the >70% 5-year survival of those ...

Abstract	Ewing sarcoma is the second most common bone cancer in children, accounting for 2% of pediatric cancer diagnoses. Patients who present with metastatic disease at the time of diagnosis have a dismal prognosis, compared to the >70% 5-year survival of those with localized disease. Here, we utilized single cell RNA-sequencing to characterize the transcriptional landscape of primary Ewing sarcoma tumors and surrounding tumor microenvironment (TME). Copy-number analysis identified subclonal evolution within patients even prior to treatment. Primary tumor samples demonstrate a heterogenous transcriptional landscape with several conserved gene expression programs, including those composed of genes related to proliferation and EWS targets. We also were able to identify the composition of the TME and molecularly dissect the transcriptional profile of circulating tumor cells in peripheral blood at the time of diagnosis.
Language	English
Publishing date	2024-01-20
Publishing country	United States
Document type	Preprint
DOI	10.1101/2024.01.18.576251
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Article ; Online: Deep dermatophytosis caused by Trichophyton rubrum in an elderly patient with CARD9 deficiency: A case report and literature review.

Ansai, Osamu / Hayashi, Ryota / Nakamura, Anna / Sasaki, Jin / Hasegawa, Akito / Deguchi, Tokiko / Yuki, Akihiko / Oike, Naoki / Ariizumi, Takashi / Abe, Masahiro / Miyazaki, Yoshitsugu / Takenouchi, Tatsuya / Kawashima, Hiroyuki / Abe, Riichiro

The Journal of dermatology

2023 Volume 51, Issue 2, Page(s) 294–300

Abstract: Deep dermatophytosis is an invasive and sometimes life-threatening fungal infection mainly reported in immunocompromised patients. However, a caspase recruitment domain-containing protein 9 (CARD9) deficiency has recently been reported to cause deep ... ...

Abstract	Deep dermatophytosis is an invasive and sometimes life-threatening fungal infection mainly reported in immunocompromised patients. However, a caspase recruitment domain-containing protein 9 (CARD9) deficiency has recently been reported to cause deep dermatophytosis. Herein, we report the first Japanese case of deep dermatophytosis associated with CARD9 deficiency. An 80-year-old Japanese man with tinea corporis presented with subcutaneous nodules on his left sole. Histopathological findings revealed marked epithelioid cell granulomas with filamentous fungal structures in the deep dermis and subcutis, and the patient was diagnosed with deep dermatophytosis. Despite antifungal therapy, the subcutaneous nodule on his left sole gradually enlarged, his left calcaneal bone was invaded, and the patient finally underwent amputation of his left leg. Genetic analysis revealed a homozygous CARD9 c.586 A > G (p. Lys196Glu) variant, suggesting a CARD9 deficiency. Here, we discuss the clinical features of CARD9 deficiency-associated deep dermatophytosis with a case report and review of the literature.
MeSH term(s)	Male ; Humans ; Aged ; Aged, 80 and over ; Candidiasis, Chronic Mucocutaneous/genetics ; Candidiasis, Chronic Mucocutaneous/pathology ; Candidiasis, Chronic Mucocutaneous/therapy ; Tinea/microbiology ; Trichophyton/genetics ; CARD Signaling Adaptor Proteins ; Arthrodermataceae
Chemical Substances	CARD9 protein, human ; CARD Signaling Adaptor Proteins
Language	English
Publishing date	2023-10-07
Publishing country	England
Document type	Review ; Case Reports ; Journal Article
ZDB-ID	800103-0
ISSN	1346-8138 ; 0385-2407
ISSN (online)	1346-8138
ISSN	0385-2407
DOI	10.1111/1346-8138.16995
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Article ; Online: Aortic mural leiomyosarcoma with spinal involvement.

Kawashima, Hiroyuki / Ariizumi, Takashi / Ogose, Akira / Umezu, Hajime / Okamoto, Takeshi / Oike, Naoki / Endo, Naoto

The Journal of thoracic and cardiovascular surgery

2019 Volume 159, Issue 4, Page(s) e249–e254

MeSH term(s)	Aorta ; Humans ; Leiomyosarcoma/pathology ; Leiomyosarcoma/surgery ; Male ; Middle Aged ; Neoplasm Invasiveness ; Spinal Cord Compression/diagnostic imaging ; Spinal Cord Compression/etiology ; Spinal Cord Compression/surgery ; Thoracic Vertebrae ; Vascular Neoplasms/pathology ; Vascular Neoplasms/surgery
Language	English
Publishing date	2019-04-24
Publishing country	United States
Document type	Case Reports ; Journal Article
ZDB-ID	3104-5
ISSN	1097-685X ; 0022-5223
ISSN (online)	1097-685X
ISSN	0022-5223
DOI	10.1016/j.jtcvs.2019.04.015
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Article ; Online: ＜Editors' Choice＞

Yamagishi, Tetsuro / Kawashima, Hiroyuki / Ogose, Akira / Ariizumi, Takashi / Oike, Naoki / Sasaki, Taro / Hatano, Hiroshi / Endo, Naoto

Nagoya journal of medical science

2020 Volume 82, Issue 1, Page(s) 85–92

Abstract: Stanniocalcin-1 ( ...

Abstract	Stanniocalcin-1 (
MeSH term(s)	Biomarkers, Tumor/genetics ; Biomarkers, Tumor/metabolism ; Cell Line, Tumor ; Gene Expression Regulation, Neoplastic ; Glycoproteins/genetics ; Glycoproteins/metabolism ; Humans ; Neoplasm Grading ; RNA, Messenger/genetics ; RNA, Messenger/metabolism ; Soft Tissue Neoplasms/genetics ; Soft Tissue Neoplasms/metabolism ; Soft Tissue Neoplasms/pathology
Chemical Substances	Biomarkers, Tumor ; Glycoproteins ; RNA, Messenger ; teleocalcin (76687-96-2)
Language	English
Publishing date	2020-03-31
Publishing country	Japan
Document type	Journal Article
ZDB-ID	193148-9
ISSN	2186-3326 ; 0027-7622
ISSN (online)	2186-3326
ISSN	0027-7622
DOI	10.18999/nagjms.82.1.85
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Article ; Online: Intravertebral cleft in pathological vertebral collapse resulting from cancer metastasis: report of three cases.

Hatano, Hiroshi / Oike, Naoki / Ariizumi, Takashi / Sasaki, Taro / Kawashima, Hiroyuki

Skeletal radiology

2016 Volume 45, Issue 12, Page(s) 1747–1750

Abstract: Intravertebral cleft (IVC) is a common finding in osteoporotic compression fracture. However, since the vertebral collapse attributable to cancer metastasis is rarely associated with IVC, the phenomenon is generally considered as a sign of a benign ... ...

Abstract	Intravertebral cleft (IVC) is a common finding in osteoporotic compression fracture. However, since the vertebral collapse attributable to cancer metastasis is rarely associated with IVC, the phenomenon is generally considered as a sign of a benign lesion. In this study, we retrospectively reviewed the radiographs, computed tomography scans, and magnetic resonance images of 111 patients with spinal metastasis. Three cases (2.7 %) had IVC in the collapsed thoracic vertebral bodies (T7, T8, and T11) attributable to cancer metastasis. IVC alone is not necessarily an indicator of a benign vertebral collapse.
Language	English
Publishing date	2016-12
Publishing country	Germany
Document type	Journal Article
ZDB-ID	527592-1
ISSN	1432-2161 ; 0364-2348
ISSN (online)	1432-2161
ISSN	0364-2348
DOI	10.1007/s00256-016-2505-5
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Article: NKp44-based chimeric antigen receptor effectively redirects primary T cells against synovial sarcoma.

Murayama, Yudai / Kasahara, Yasushi / Kubo, Nobuhiro / Shin, Chansu / Imamura, Masaru / Oike, Naoki / Ariizumi, Takashi / Saitoh, Akihiko / Baba, Minori / Miyazaki, Tomohiro / Suzuki, Yuko / Ling, Yiwei / Okuda, Shujiro / Mihara, Keichiro / Ogose, Akira / Kawashima, Hiroyuki / Imai, Chihaya

Translational oncology

2022 Volume 25, Page(s) 101521

Abstract: Background: T-cell receptor-engineered T-cell therapies have achieved promising response rates against synovial sarcoma in clinical trials, but their applicability is limited owing to the HLA matching requirement. Chimeric antigen receptor (CAR) can ... ...

Abstract	Background: T-cell receptor-engineered T-cell therapies have achieved promising response rates against synovial sarcoma in clinical trials, but their applicability is limited owing to the HLA matching requirement. Chimeric antigen receptor (CAR) can redirect primary T cells to tumor-associated antigens without requiring HLA matching. However, various obstacles, including the paucity of targetable antigens, must be addressed for synovial sarcoma. Ligands for natural killer (NK) cell-activating receptors are highly expressed by tumor cells. Methods: The surface expression of ligands for NK cell-activating receptors in synovial sarcoma cell lines was analyzed. We analyzed RNA sequencing data deposited in a public database to evaluate NKp44-ligand expression. Primary T cells retrovirally transduced with CAR targeting NKp44 ligands were evaluated for their functions in synovial sarcoma cells. Alterations induced by various stimuli, including a histone deacetylase inhibitor, a hypomethylating agent, inflammatory cytokines, and ionizing radiation, in the expression levels of NKp44 ligands were investigated. Results: Ligands for NKp44 and NKp30 were expressed in all cell lines. NKG2D ligands were barely expressed in a single cell line. None of the cell lines expressed NKp46 ligand. Primary synovial sarcoma cells expressed the mRNA of the truncated isoform of MLL5, a known cellular ligand for NKp44. NKp44-based CAR T cells specifically recognize synovial sarcoma cells, secrete interferon-γ, and exert suppressive effects on tumor cell growth. No stimulus altered the expression of NKp44 ligands. Conclusion: NKp44-based CAR T cells can redirect primary human T cells to synovial sarcoma cells. CAR-based cell therapies may be an option for treating synovial sarcomas.
Language	English
Publishing date	2022-08-20
Publishing country	United States
Document type	Journal Article
ZDB-ID	2443840-6
ISSN	1936-5233
ISSN	1936-5233
DOI	10.1016/j.tranon.2022.101521
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Article: Effectiveness of 4-1BB-costimulated HER2-targeted chimeric antigen receptor T cell therapy for synovial sarcoma.

Murayama, Yudai / Kawashima, Hiroyuki / Kubo, Nobuhiro / Shin, Chansu / Kasahara, Yasushi / Imamura, Masaru / Oike, Naoki / Ariizumi, Takashi / Saitoh, Akihiko / Mihara, Keichiro / Umezu, Hajime / Ogose, Akira / Imai, Chihaya

Translational oncology

2021 Volume 14, Issue 12, Page(s) 101227

Abstract: Background: Synovial sarcoma is a rare malignant soft-tissue tumor that is prevalent in adolescents and young adults, and poor prognosis has been reported in patients with metastatic lesions. Chimeric antigen receptor (CAR) T-cell therapy is an emerging ...

Abstract	Background: Synovial sarcoma is a rare malignant soft-tissue tumor that is prevalent in adolescents and young adults, and poor prognosis has been reported in patients with metastatic lesions. Chimeric antigen receptor (CAR) T-cell therapy is an emerging novel therapy for solid tumors; however, its application in synovial sarcoma has not yet been explored. Methods: A novel human epidermal growth factor receptor 2 (HER2)-targeted CAR containing scFv-FRP5, CD8α hinge and transmembrane domains as well as 4-1BB costimulatory and CD3ζ signaling domains was developed. Three synovial sarcoma cell lines that expressed the fusion transcript SS18-SSX1/2/4 were used in the study. Cytokine secretion assay, cytotoxicity assay, and real-time cell analysis experiments were conducted to confirm the function of T cells transduced with the CAR gene. Results: High cell-surface expression of HER2 was observed in all the cell lines. HER2-targeted/4-1BB-costimulated CAR T cells specifically recognized the synovial sarcoma cells, secreted interferon gamma and tumor necrosis factor alpha, and exerted cytotoxic effects in these cells. Conclusion: To the best of our knowledge, this is the first study to indicate that HER2-targeted CAR T cells are directly effective against molecularly defined synovial sarcoma cells. Furthermore, our findings might set the basis for developing improved CAR T cell-based therapies for chemo-refractory or relapsed synovial sarcoma.
Language	English
Publishing date	2021-09-21
Publishing country	United States
Document type	Journal Article
ZDB-ID	2443840-6
ISSN	1936-5233
ISSN	1936-5233
DOI	10.1016/j.tranon.2021.101227
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Article ; Online: The natural history of incidental retroperitoneal schwannomas.

Ogose, Akira / Kawashima, Hiroyuki / Hatano, Hiroshi / Ariizumi, Takashi / Sasaki, Taro / Yamagishi, Tetsuro / Oike, Naoki / Inagawa, Syoichi / Endo, Naoto

PloS one

2019 Volume 14, Issue 4, Page(s) e0215336

Abstract: The natural history of asymptomatic retroperitoneal schwannomas is poorly understood. This study aimed at investigating the natural history of incidental retroperitoneal schwannomas. The medical charts and imaging studies of 22 asymptomatic patients ... ...

Abstract	The natural history of asymptomatic retroperitoneal schwannomas is poorly understood. This study aimed at investigating the natural history of incidental retroperitoneal schwannomas. The medical charts and imaging studies of 22 asymptomatic patients under observation for at least 12 months for retroperitoneal schwannomas were reviewed. The duration of follow-up ranged between 13 and 176 months (mean 48 months). In the 22 patients managed by the "wait and see" approach, the average tumor size at initial presentation was 51 mm, which increased to 57 mm at final follow-up. During the final follow-up, 2 patients required surgical treatment for tumor enlargement, while the remaining patients remained asymptomatic without surgery. The average growth rate of the tumors was 1.9 mm/year (range: -1.9 to 8.7 mm/year). The majority of asymptomatic retroperitoneal schwannomas demonstrate minimal growth and may be suitable for management with the "wait and see" approach.
MeSH term(s)	Adult ; Aged ; Biopsy, Needle ; Female ; Follow-Up Studies ; Humans ; Male ; Middle Aged ; Neurilemmoma/diagnostic imaging ; Neurilemmoma/pathology ; Neurilemmoma/physiopathology ; Neurilemmoma/surgery ; Retroperitoneal Neoplasms/diagnostic imaging ; Retroperitoneal Neoplasms/pathology ; Retroperitoneal Neoplasms/physiopathology ; Retroperitoneal Neoplasms/surgery ; Tomography, X-Ray Computed
Language	English
Publishing date	2019-04-15
Publishing country	United States
Document type	Clinical Trial ; Journal Article
ISSN	1932-6203
ISSN (online)	1932-6203
DOI	10.1371/journal.pone.0215336
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Article ; Online: Reconstruction of knee extensor with patellar tendon autograft following intraoperative radiotherapy.

Kawashima, Hiroyuki / Ogose, Akira / Ariizumi, Takashi / Yamagishi, Tetsuro / Oike, Naoki / Aoyama, Hidefumi / Hatano, Hiroshi / Endo, Naoto

The Knee

2019 Volume 27, Issue 1, Page(s) 257–262

Abstract: Background: Patellar tendon autograft after intraoperative extracorporeal radiotherapy has been used for reconstruction of the extensor mechanism following limb-sparing wide tumor resection around the knee. The purpose of this study was to determine the ...

Abstract	Background: Patellar tendon autograft after intraoperative extracorporeal radiotherapy has been used for reconstruction of the extensor mechanism following limb-sparing wide tumor resection around the knee. The purpose of this study was to determine the clinical outcome of this reconstruction technique. Methods: We retrospectively reviewed six consecutive patients with peripatellar tendon and proximal tibial sarcoma who underwent reconstruction of the knee extensor mechanism. The resection area was planned to be contained with the patellar tendon in order to obtain a wide margin. First, the patella was osteotomized at the midline, and the inferior half of patella, patellar tendon, and tibial tuberosity were excised en bloc. The resected segments were devitalized with intraoperative extracorporeal radiotherapy and reimplanted into the original site. A follow-up evaluation included an assessment of the range of motion, extensor lag, the International Society of Limb Salvage score, and complications. Results: Six patients were followed up for 121-270 months. One patient underwent an additional reconstruction with total knee arthroplasty due to a collapse of the tibial subchondral bone. A supracondylar fracture of the femur occurred in two patients, and a delayed union of the osteosynthesis site of the tibial shaft was observed in one patient. At the latest follow up, extensor lag had a median of five degrees, and International Society of Limb Salvage scores had a median of 83%. No local recurrence or rupture of the patellar tendon was observed. Conclusions: Reconstruction of the knee extensor mechanism using a patellar tendon treated with intraoperative radiotherapy is a reliable and successful method.
MeSH term(s)	Adolescent ; Adult ; Arthroplasty/methods ; Bone Neoplasms/radiotherapy ; Bone Neoplasms/surgery ; Child ; Female ; Femur/surgery ; Humans ; Knee Joint/surgery ; Limb Salvage ; Male ; Patellar Ligament/transplantation ; Range of Motion, Articular ; Retrospective Studies ; Rupture/surgery ; Sarcoma/radiotherapy ; Sarcoma/surgery ; Tibia/surgery ; Transplantation, Autologous ; Treatment Outcome
Language	English
Publishing date	2019-12-05
Publishing country	Netherlands
Document type	Case Reports ; Journal Article
ZDB-ID	1200476-5
ISSN	1873-5800 ; 0968-0160
ISSN (online)	1873-5800
ISSN	0968-0160
DOI	10.1016/j.knee.2019.10.008
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