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Case Report
Severe Hepatic Sinusoidal Obstruction Syndrome in a Child Receiving Vincristine, Actinomycin-D, and Cyclophosphamide for Rhabdomyosarcoma: Successful Treatment with Defibrotide
Aery Choi, Young Kyung Kang, Sewon Lim, Dong Ho Kim, Jung Sub Lim, Jun Ah Lee
Cancer Res Treat. 2016;48(4):1443-1447.   Published online March 30, 2016
DOI: https://doi.org/10.4143/crt.2016.096
AbstractAbstract PDFPubReaderePub
Hepatic sinusoidal obstruction syndrome (SOS) is a life-threatening syndrome that generally occurs as a complication after hematopoietic stem cell transplantation or, less commonly, after conventional chemotherapy. Regarding SOS in rhabdomyosarcoma patients who received conventional chemotherapy, the doses of chemotherapeutic agents are associated with the development of SOS. Several cases of SOS in rhabdomyosarcoma patients after receiving chemotherapy with escalated doses of cyclophosphamide have been reported. Here, we report on a 9-year-old female with rhabdomyosarcoma who developed severe SOS after receiving chemotherapy consisting of vincristine, actinomycin-D, and a moderate dose of cyclophosphamide. She was treated successfully with defibrotide without sequelae to the liver.

Citations

Citations to this article as recorded by  
  • Drug-induced hepatic sinusoidal obstruction syndrome: current advances and future perspectives
    Zaoqin Yu, Wei Li, Cheng Tian, Yan Cao, Chengliang Zhang
    Archives of Toxicology.2024;[Epub]     CrossRef
  • Treatment of Sinusoidal Obstruction Syndrome With Defibrotide in Pediatric Cancer Patients Following Nontransplant-associated Chemotherapy: A Case Report and Review of the Literature
    Marc R. Lawrence, Mylène Bassal, Raveena Ramphal, Donna L. Johnston
    Journal of Pediatric Hematology/Oncology.2022; 44(3): e788.     CrossRef
  • Indispensable role of microbes in anticancer drugs and discovery trends
    Ridam Kapoor, Anamika Saini, Deepika Sharma
    Applied Microbiology and Biotechnology.2022; 106(13-16): 4885.     CrossRef
  • Caspase inhibitor z-VAD-FMK increases the survival of hair cells after Actinomycin-D-induced damage in vitro
    Huimin Chang, Fei Sun, Keyong Tian, Weilong Wang, Ke Zhou, Dingjun Zha, Jianhua Qiu
    Neuroscience Letters.2020; 732: 135089.     CrossRef
  • Adjuvant recombinant thrombomodulin therapy for hepatopathy induced by vincristine, actinomycin D, and cyclophosphamide in pediatric rhabdomyosarcoma: A case report
    Tetsuko Kobayashi, Maiko Noguchi, Hideki Nakayama, Reiji Fukano, Shouichi Ohga
    Molecular and Clinical Oncology.2019;[Epub]     CrossRef
  • “Pre‐emptive strike”—the case for early treatment of hepatic sinusoidal obstruction syndrome with defibrotide
    Revathi Rajagopal, Marianne B. Phillips, Nicholas G. Gottardo
    Pediatric Blood & Cancer.2018;[Epub]     CrossRef
  • Cyclophosphamide/dactinomycin/vincristine

    Reactions Weekly.2017; 1637(1): 75.     CrossRef
  • 10,609 View
  • 207 Download
  • 7 Web of Science
  • 7 Crossref
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Original Articles
Immunogenicity of Influenza Vaccine in Colorectal Cancer Patients
Dong Ho Kim, Yun Yong Lee, Ui Sup Shin, Sun Mi Moon
Cancer Res Treat. 2013;45(4):303-312.   Published online December 31, 2013
DOI: https://doi.org/10.4143/crt.2013.45.4.303
AbstractAbstract PDFPubReaderePub
PURPOSE
Although influenza is regarded as a major cause of morbidity and mortality in immunocompromised patients, vaccine coverage remains poor. We evaluated the immunogenicity of influenza vaccines in colorectal cancer patients.
MATERIALS AND METHODS
In this study, 40 colorectal cancer patients who received an influenza vaccine at the Korea Cancer Center Hospital during the 2009-2010 and 2010-2011 influenza seasons were analyzed. The blood samples were collected at prevaccination and 30 days post vaccination, and antibody titers were measured using the hemagglutination-inhibition tests.
RESULTS
In the 2009-2011 season, the seroprotection rate for H1N1 (94.7%) was significantly higher than that for H3N2 (42.1%) and B (47.3%). The seroconversion rate was 52.6%, 26.3%, and 36.8% for H1N1, H3N2, and B, respectively. Fold increase of geometric mean titer (MFI) was 3.86, 1.49, and 3.33 for H1N1, H3N2, and B, respectively. In the 2010-2011 season, the seroprotection rate for H1N1 (57.1%) was significantly higher than that for H3N2 (52.4%) and B (38.1%). The seroconversion rate was 52.4%, 47.6% and 33.3% for H1N1, H3N2, and B, respectively. MFI was 12.29, 3.62 and 4.27 for H1N1, H3N2, and B, respectively.
CONCLUSION
Our study cohort showed an acceptable immune response to an influenza vaccine without significant adverse effects, supporting the recommendation for annual influenza vaccination in colorectal cancer patients.

Citations

Citations to this article as recorded by  
  • Therapeutic vaccines for colorectal cancer: The progress and future prospect
    Mina Shahnazari, Pouria Samadi, Mona Pourjafar, Akram Jalali
    International Immunopharmacology.2020; 88: 106944.     CrossRef
  • Vaccines for colorectal cancer: an update
    Mostafa Sarvizadeh, Faezeh Ghasemi, Fatemeh Tavakoli, Sara Sadat Khatami, Ebrahim Razi, Hossein Sharifi, Nousin Moussavi Biouki, Mohsen Taghizadeh
    Journal of Cellular Biochemistry.2019; 120(6): 8815.     CrossRef
  • Quadrivalent Influenza Vaccine-Induced Antibody Response and Influencing Determinants in Patients ≥ 55 Years of Age in the 2018/2019 Season
    Maria Ganczak, Paulina Dubiel, Marzena Drozd-Dąbrowska, Ewelina Hallmann-Szelińska, Karol Szymański, Lidia B. Brydak
    International Journal of Environmental Research and Public Health.2019; 16(22): 4489.     CrossRef
  • Immunogenicity of Influenza Vaccination in Patients With Cancer
    Saiama N. Waqar, Leigh Boehmer, Daniel Morgensztern, Andrea Wang-Gillam, Steven Sorscher, Steven Lawrence, Feng Gao, Kalin Guebert, Kristina Williams, Ramaswamy Govindan
    American Journal of Clinical Oncology.2018; 41(3): 248.     CrossRef
  • Immunogenicity of trivalent influenza vaccine in patients with lung cancer undergoing anticancer chemotherapy
    Kei Nakashima, Masahiro Aoshima, Satoko Ohfuji, Kanzo Suzuki, Masahiro Katsurada, Naoko Katsurada, Masafumi Misawa, Yoshihito Otsuka, Kyoko Kondo, Yoshio Hirota
    Human Vaccines & Immunotherapeutics.2017; 13(3): 543.     CrossRef
  • Influenza vaccination in adult patients with solid tumours treated with chemotherapy
    Albert Vollaard, Imke Schreuder, Lizzy Slok-Raijmakers, Wim Opstelten, Guus Rimmelzwaan, Hans Gelderblom
    European Journal of Cancer.2017; 76: 134.     CrossRef
  • Vaccination in Patients with Primary Immune Deficiency, Secondary Immune Deficiency and Autoimmunity with Immune Regulatory Abnormalities
    Martha M Eibl, Hermann M Wolf
    Immunotherapy.2015; 7(12): 1273.     CrossRef
  • 44,736 View
  • 59 Download
  • 7 Crossref
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Epidermal Growth Factor Receptor: Is It a Feasible Target for the Treatment of Osteosarcoma?
Jun Ah Lee, Yunmi Ko, Dong Ho Kim, Jung Sub Lim, Chang-Bae Kong, Wan Hyeong Cho, Dae-Geun Jeon, Soo-Yong Lee, Jae-Soo Koh
Cancer Res Treat. 2012;44(3):202-209.   Published online September 30, 2012
DOI: https://doi.org/10.4143/crt.2012.44.3.202
AbstractAbstract PDFPubReaderePub
PURPOSE
Features of epidermal growth factor receptor (EGFR) expression in osteosarcoma and in vitro efficacies of EGFR inhibitors against osteosarcoma cells were evaluated.
MATERIALS AND METHODS
Thirty biopsy samples of osteosarcoma patients were retrospectively analyzed for EGFR protein expression by immunohistochemistry. Relationships between EGFR expression and clinicopathologic characteristics and treatment outcomes were evaluated. Four osteosarcoma cell lines were analyzed for EGFR and p-EGFR expression by western blotting. Efficacies of gefitinib and BIBW2992 on osteosarcoma cells were evaluated using a 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay. Tyrosine kinase domains in exons 18 to 21 were sequenced and gene expression analyses of EGFR and PTEN were performed in four osteosarcoma cell lines.
RESULTS
EGFR protein was expressed in 27 (90%) samples (6 low, 12 intermediate, 9 high) and in three cell lines. Intermediate or high staining for EGFR was related to a tumor volume<150 mL (p<0.001) and histologic subtype other than osteoblastic type (p=0.03). However, EGFR expression was not associated with histologic response to preoperative chemotherapy or survival. Gefitinib and BIBW 2992 did not have any significant inhibitory effect on cell viabilities. DNA sequencing analysis revealed three osteosarcoma cell lines have single base changes at codon 2361 of exon 20 (G to A), without affecting translation results. Furthermore, no mutation was found to be associated with constitutive EGFR activation.
CONCLUSION
In the present study, gefitinib and BIBW2992 were not effective against osteosarcoma cells. However, as osteosarcoma cells express EGFR, further studies are necessary to explore the potential of other therapeutic agents targeting EGFR.

Citations

Citations to this article as recorded by  
  • PD-L1, STAT3, IL6, and EGFR Immunoexpressions in High-Grade Osteosarcoma
    Nayla Rahmadiani, Eviana Norahmawati, Agustina Tri Endharti, Ailen Oktaviana Hambalie, Satria Pandu Persada Isma, Raffaele Vitiello
    Advances in Orthopedics.2024; 2024: 1.     CrossRef
  • Optimizing near infrared laser irradiation and photosensitizer accumulation period for indocyanine green-mediated photodynamic therapy in breast cancer xenografts: a focus on treatment and characterization
    Hasim Ozgur Tabakoglu, Tuğba Kiriş Aydoğan, Ayşenur Kiriş, Saadet Akbulut
    Lasers in Medical Science.2024;[Epub]     CrossRef
  • EGFR-targeting peptide conjugated polymer–lipid hybrid nanoparticles for delivery of salinomycin to osteosarcoma
    Longhai Du, Yanlong Xu, Binxu Han, Yu Wang, Qingmin Zeng, Minghao Shao, Zuochong Yu
    Journal of Cancer Research and Therapeutics.2023; 19(6): 1544.     CrossRef
  • Epidermal growth factor signalling pathway in endochondral ossification: an evidence-based narrative review
    L. Mangiavini, G. M. Peretti, B. Canciani, N. Maffulli
    Annals of Medicine.2022; 54(1): 37.     CrossRef
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    Zuochong Yu, Yanlong Xu, Longhai Du, Fan Zhang, Minghao Shao, Lin Xie, Guoping Cai, Feizhou Lyu
    Journal of Cancer Research and Therapeutics.2022; 18(2): 352.     CrossRef
  • Stattic sensitizes osteosarcoma cells to epidermal growth factor receptor inhibitors via blocking the interleukin 6-induced STAT3 pathway
    Shenglin Wang, Yunqing Wang, Zhen Huang, Hongxiang Wei, Xinwen Wang, Rongkai Shen, Wenbin Lan, Guangxian Zhong, Jianhua Lin
    Acta Biochimica et Biophysica Sinica.2021; 53(12): 1670.     CrossRef
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    Marlid Cruz-Ramos, Yessica Zamudio-Cuevas, Daniel Medina-Luna, Karina Martínez-Flores, Gabriela Martínez-Nava, Javier Fernández-Torres, Alberto López-Reyes, Flavio Solca
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    Oncotarget.2020; 11(1): 46.     CrossRef
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    International Journal of Molecular Sciences.2020; 21(18): 6885.     CrossRef
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    Investigational New Drugs.2019; 37(1): 175.     CrossRef
  • The TGFβ-miR-499a-SHKBP1 pathway induces resistance to EGFR inhibitors in osteosarcoma cancer stem cell-like cells
    Tian Wang, Dexing Wang, Lian Zhang, Ping Yang, Jing Wang, Qi Liu, Fei Yan, Feng Lin
    Journal of Experimental & Clinical Cancer Research.2019;[Epub]     CrossRef
  • Interpretation of Tongue Squamous Cell Carcinoma via Protein-Protein Interaction Network Construction and Analysis
    Mona Zamanian Azodi, Mostafa Rezaei-Tavirani, Majid Rezaei-Tavirani, Vahid Mansouri, Reza Vafaee
    International Journal of Cancer Management.2018;[Epub]     CrossRef
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    Pierre J. Marie
    Cellular and Molecular Life Sciences.2015; 72(7): 1347.     CrossRef
  • Receptor tyrosine kinases: Characterisation, mechanism of action and therapeutic interests for bone cancers
    Aude I. Ségaliny, Marta Tellez-Gabriel, Marie-Françoise Heymann, Dominique Heymann
    Journal of Bone Oncology.2015; 4(1): 1.     CrossRef
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    Bérengère Gobin, Gatien Moriceau, Benjamin Ory, Céline Charrier, Régis Brion, Frederic Blanchard, Françoise Redini, Dominique Heymann, Gerard Roel Rutteman
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  • 11,595 View
  • 79 Download
  • 28 Crossref
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Assessment of Chemotherapy Response Using FDG-PET in Pediatric Bone Tumors: A Single Institution Experience
Dong Hwan Kim, Seung Yeon Kim, Hyeon Jeong Lee, Bong Sup Song, Dong Ho Kim, Joong Bum Cho, Jung Sub Lim, Jun Ah Lee
Cancer Res Treat. 2011;43(3):170-175.   Published online September 30, 2011
DOI: https://doi.org/10.4143/crt.2011.43.3.170
AbstractAbstract PDFPubReaderePub
PURPOSE
Response to neo-adjuvant chemotherapy is an important prognostic factor for osteosarcoma (OS) and the Ewing sarcoma family of tumors (ESFT). [F-18]-fluorodeoxy-D-glucose (FDG)-positron emission tomography (PET) is a non-invasive imaging modality that predicts histologic response to chemotherapy of various malignancies; however, limited data exist about the usefulness of FDG-PET in predicting the histologic response of pediatric bone tumors to chemotherapy. We analyzed the FDG-PET imaging characteristics of pediatric bone tumors and determined the association with response to chemotherapy.
MATERIALS AND METHODS
Pediatric patients with OS (n=19) or ESFT (n=17) were evaluated for FDG-PET standard uptake values before (SUV1) and after (SUV2) chemotherapy. The relationship to the chemotherapy response was assessed by histopathology in surgically-excised tumors. A complete data set (SUV1, SUV2, and histologic response) was available in 23 patients.
RESULTS
While the mean SUV1s were not different between patients with OSs and ESFTs (9.44 vs. 6.07, p=0.24), the SUV2s were greater in the patients with OSs than ESFTs (4.55 vs. 1.66, p=0.01). The ratios of SUV2-to-SUV1 (SUV2 : SUV1) were 0.65 and 0.35 for OS and ESFT, respectively (p=0.08). All of the patients with ESFTs and 47% of the patients with OS had a favorable histologic response to chemotherapy. The SUV2 : 1 [(SUV1-SUV2)/SUV1]> or =0.5 and SUV2< or =2.5 were related to favorable histologic responses to chemotherapy; the sensitivity and specificity of SUV2 : 1 at 0.5 and SUV2 at 2.5 were 93% and 88%, and 88% and 78%, respectively.
CONCLUSION
FDG-PET can be used as a non-invasive surrogate to predict response to chemotherapy in children with bone tumors.

Citations

Citations to this article as recorded by  
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    Chiwoo Oh, Michael W. Bishop, Steve Y. Cho, Hyung-Jun Im, Barry L. Shulkin
    Journal of Nuclear Medicine.2023; 64(6): 842.     CrossRef
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    European Radiology.2021; 31(9): 7012.     CrossRef
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  • 21 Crossref
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Case Report
Two Pediatric Osteosarcoma Cases with Delayed Methotrexate Excretion: Its Clinical Course and Management
Kang Min Lee, Hee Woo Lee, Seung Yeon Kim, Hyeon Jeong Lee, Dong Hwan Kim, Joongbum Cho, Dong Ho Kim, Jung Sub Lim, Jin Kyung Lee, Jun Ah Lee
Cancer Res Treat. 2011;43(1):67-70.   Published online March 31, 2011
DOI: https://doi.org/10.4143/crt.2011.43.1.67
AbstractAbstract PDFPubReaderePub
High-dose methotrexate (MTX) chemotherapy extends the duration of hospitalization and introduces the risks of serious complications related to delayed MTX excretion. The treatment of delayed MTX excretion is largely dependent on invasive measures such as hemodialysis because the clinical data regarding the efficacy or safety of carboxypetidase G2 is limited. We report here on the cases of two pediatric osteosarcoma patients with delayed MTX excretion and who were successfully managed using supportive measures. Potential life-threatening complications were prevented by administering high doses of leucovorin.

Citations

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  • 3 Crossref
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Original Article
The Survival of Osteosarcoma Patients 10 Years Old or Younger Is Not Worse than the Survival of Older Patients: A Retrospective Analysis
Jun Ah Lee, Dong Ho Kim, Jung Sub Lim, Kyung Duk Park, Won Seok Song, Soo-Yong Lee, Dae-Geun Jeon
Cancer Res Treat. 2007;39(4):160-164.   Published online December 31, 2007
DOI: https://doi.org/10.4143/crt.2007.39.4.160
AbstractAbstract PDFPubReaderePub
Purpose

This study aimed to assess whether a young age at the time of diagnosis with osteosarcoma has value to predict the prognosis.

Materials and Methods

Sixty-seven children with stage II osteosarcoma were stratified according to the age of 10. There were 32 preadolescents (≤10 years) and 35 adolescents (10<age≤15 years). The patients were analyzed for their clinical characteristics, the histologic response to preoperative chemotherapy, event-free survival (EFS) and the patterns of relapse.

Results

After a median follow-up of 54 months (range: 6~153 months), the 5-year EFS of the preadolescent and adolescent groups was 64.5±9.3% and 58.2±9.1%, respectively, and age did not have any statistical significance for survival (p=0.55). Cox regression analysis revealed that both the serum level of alkaline phosphatase and the histologic response to preoperative chemotherapy were significantly related to survival of the 67 patients. Those patients aged less than 7 years responded poorly to preoperative chemotherapy and their rate of amputation was 43%. However, their 5-year EFS was not statistically different from the older patients (57.1±18.7 vs 67.7±6.3%, respectively, p=0.58).

Conclusions

We could not find any statistical difference in the clinical characteristics and survival from osteosarcoma for the preadolescents and adolescents, so the current approach of having the same protocol for both groups of patients seems to be reasonable.

Citations

Citations to this article as recorded by  
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