<?xml version="1.0"?>
<Articles JournalTitle="International Journal of Hematology-Oncology and Stem Cell Research">
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>International Journal of Hematology-Oncology and Stem Cell Research</JournalTitle>
      <Issn>2008-2207</Issn>
      <Volume>14</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="epublish">
        <Year>2020</Year>
        <Month>07</Month>
        <Day>02</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Safety and Feasibility of Outpatient High Dose Cytarabine for Acute Myeloid Leukemia in the Brazilian Amazon</title>
    <FirstPage>151</FirstPage>
    <LastPage>156</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Amanda</FirstName>
        <LastName>Rodrigues</LastName>
        <affiliation locale="en_US">School of Medical Sciences, Par&#xE1; State University, Bel&#xE9;m &#x2013; PA, Brazil</affiliation>
      </Author>
      <Author>
        <FirstName>Daniel</FirstName>
        <LastName>do Nascimento</LastName>
        <affiliation locale="en_US">School of Medical Sciences, Par&#xE1; State University, Bel&#xE9;m &#x2013; PA, Brazil</affiliation>
      </Author>
      <Author>
        <FirstName>Josy</FirstName>
        <LastName>de Lima</LastName>
        <affiliation locale="en_US">Division of Hematology-Oncology and Stem Cell Transplantation, Ophir Loyola Hospital, Bel&#xE9;m &#x2013; PA, Brazil</affiliation>
      </Author>
      <Author>
        <FirstName>Marcos La&#xE9;rcio</FirstName>
        <LastName>Reis</LastName>
        <affiliation locale="en_US">Division of Hematology-Oncology and Stem Cell Transplantation, Ophir Loyola Hospital, Bel&#xE9;m &#x2013; PA, Brazil</affiliation>
      </Author>
      <Author>
        <FirstName>Lucyana</FirstName>
        <LastName>Le&#xE3;o</LastName>
        <affiliation locale="en_US">Division of Hematology-Oncology and Stem Cell Transplantation, Ophir Loyola Hospital, Bel&#xE9;m &#x2013; PA, Brazil</affiliation>
      </Author>
      <Author>
        <FirstName>Murilo</FirstName>
        <LastName>Azavedo</LastName>
        <affiliation locale="en_US">School of Medical Sciences, Federal University of Par&#xE1;, Bel&#xE9;m &#x2013; PA, Brazil</affiliation>
      </Author>
      <Author>
        <FirstName>Samanta</FirstName>
        <LastName>Muccini</LastName>
        <affiliation locale="en_US">School of Medical Sciences, Federal University of Par&#xE1;, Bel&#xE9;m &#x2013; PA, Brazil</affiliation>
      </Author>
      <Author>
        <FirstName>Polyana</FirstName>
        <LastName>da Silva</LastName>
        <affiliation locale="en_US">School of Medical Sciences, Federal University of Par&#xE1;, Bel&#xE9;m &#x2013; PA, Brazil</affiliation>
      </Author>
      <Author>
        <FirstName>Thiago</FirstName>
        <LastName>Carneiro</LastName>
        <affiliation locale="en_US">Division of Hematology-Oncology and Stem Cell Transplantation, Ophir Loyola Hospital, Bel&#xE9;m &#x2013; PA, Brazil</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2019</Year>
        <Month>09</Month>
        <Day>07</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2020</Year>
        <Month>03</Month>
        <Day>26</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background: The attempt to manage patients with acute myeloid leukemia as outpatients has become increasingly common due to high hospitalization costs, low availability for beds and patient preference. Publications on the subject are scarce, especially in low-income regions and the safety in this population remains to be determined. The present study aims to assess the safety of consolidation with high dose cytarabine in the outpatient setting.
Materials and Methods: We retrospectively analyzed 39 patients who underwent consolidation with high-dose cytarabine, between 2009 and 2018, at Ophir Loyola Hospital, in Bel&#xE9;m, Brazil. Patients treated after 2015 were given high-dose cytarabine as outpatients due to the decision of medical staff.
Results: 27 patients received 76 cycles of cytarabine as outpatients; males were 48.14% of the total population, with a median age of approximately 45 years. The occurrence of delay between cycles was significantly lower among outpatients (48.14% vs. 83.33%, p = 0.04). There was no difference between relapse rates, transfusion requirements and non-relapse mortality between both groups. Hospitalization was required in 40.74% of patients during outpatient cycles and 18.51% of blood cultures were positive for pathogens. Non-relapse mortality was significantly higher among patients above 50 years old and treated on an outpatient basis (44.4% vs. 5.60%, p = 0.03).
Conclusion: High-dose cytarabine administration on an outpatient basis appears to be safe and effective in a low-income population at the Brazilian Amazon region, but toxicity seems to be increased for patients older than 50 years.</abstract>
    <web_url>https://ijhoscr.tums.ac.ir/index.php/ijhoscr/article/view/1179</web_url>
    <pdf_url>https://ijhoscr.tums.ac.ir/index.php/ijhoscr/article/download/1179/835</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>International Journal of Hematology-Oncology and Stem Cell Research</JournalTitle>
      <Issn>2008-2207</Issn>
      <Volume>14</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="epublish">
        <Year>2020</Year>
        <Month>07</Month>
        <Day>02</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Serum Cystatin C as a Potential Marker for Glomerular Filtration Rate in Patients with Cholangiocarcinoma</title>
    <FirstPage>157</FirstPage>
    <LastPage>166</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Mang Ngaih</FirstName>
        <LastName>Ciin</LastName>
        <affiliation locale="en_US">Centre of Research and Development of Medical Diagnostic Laboratories (CMDL), Faculty of Associated Medical Sciences, Khon Kaen University, Khon Kaen 40002, Thailand</affiliation>
      </Author>
      <Author>
        <FirstName>Tanakorn</FirstName>
        <LastName>Proungvitaya</LastName>
        <affiliation locale="en_US">Centre of Research and Development of Medical Diagnostic Laboratories (CMDL), Faculty of Associated Medical Sciences, Khon Kaen University, Khon Kaen 40002, Thailand</affiliation>
      </Author>
      <Author>
        <FirstName>Temduang</FirstName>
        <LastName>Limpaiboon</LastName>
        <affiliation locale="en_US">Centre of Research and Development of Medical Diagnostic Laboratories (CMDL), Faculty of Associated Medical Sciences, Khon Kaen University, Khon Kaen 40002, Thailand. AND Cholangiocarcinoma Research Institute (CARI), Faculty of Medicine, Khon Kaen University, Khon Kaen 40002, Thailand</affiliation>
      </Author>
      <Author>
        <FirstName>Ubon</FirstName>
        <LastName>Cha&#x2019;on</LastName>
        <affiliation locale="en_US">Department of Biochemistry, Faculty of Medicine, Khon Kaen University, Khon Kaen 40002, Thailand</affiliation>
      </Author>
      <Author>
        <FirstName>Sittiruk</FirstName>
        <LastName>Roytrakul</LastName>
        <affiliation locale="en_US">National Center for Genetic Engineering and Biotechnology, National Science and Technology Development Agency, Pathumthani 12120, Thailand</affiliation>
      </Author>
      <Author>
        <FirstName>Siriporn</FirstName>
        <LastName>Proungvitaya</LastName>
        <affiliation locale="en_US">Centre of Research and Development of Medical Diagnostic Laboratories (CMDL), Faculty of Associated Medical Sciences, Khon Kaen University, Khon Kaen 40002, Thailand. AND Cholangiocarcinoma Research Institute (CARI), Faculty of Medicine, Khon Kaen University, Khon Kaen 40002, Thailand</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2019</Year>
        <Month>08</Month>
        <Day>30</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2020</Year>
        <Month>01</Month>
        <Day>26</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background: Cholangiocarcinoma (CCA) is the second most common primary hepatobiliary cancer. These patients have meager prognosis and short-term survival. Precise assessment of glomerular filtration rate is a fundamental aspect of clinical care in cancer patients. Cystatin C has been proposed to be superior to creatinine, a well-known marker of renal function. This study aimed to evaluate cystatin C as a marker of GFR calculation in CCA patients.
Materials and Methods: One hundred thirty serum samples from CCA patients and 32 from controls were included in this study. Serum cystatin C was measured using immunoturbidity assay. Estimated glomerular filtration rate was calculated by three equations established by chronic kidney disease epidemiology collaboration (based on creatinine and/or cystatin C).
Results: Serum cystatin C in CCA patients was higher than that of controls (p=0.0002). Cystatin C was positively correlated with BUN in CCA group (p=0.019). eGFR based on cystatin C and based on both cystatin C and creatinine in CCA was low with significantly different from those of control (p&lt;0.001). Although there was no difference in eGFR using three equations in control, creatinine based eGFR was high with significantly different from eGFR based on cystatin C and on both creatinine and cystatin C in CCA (P=0.000). &#xA0;Proportion in each eGFR stage by three equations showed a high sensitivity with significantly different in CCA (p&lt;0.05).
Conclusion: There was a high sensitivity of cys C with significant difference between creatinine and/or cystatin C based eGFR in CCA patients. It should take account into consideration of mild changes in eGFR by cystatin C which is important in managing drug dosage for CCA patients.</abstract>
    <web_url>https://ijhoscr.tums.ac.ir/index.php/ijhoscr/article/view/1174</web_url>
    <pdf_url>https://ijhoscr.tums.ac.ir/index.php/ijhoscr/article/download/1174/834</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>International Journal of Hematology-Oncology and Stem Cell Research</JournalTitle>
      <Issn>2008-2207</Issn>
      <Volume>14</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="epublish">
        <Year>2020</Year>
        <Month>07</Month>
        <Day>02</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Evaluation of Reversed Administration Order of Busulfan (BU) and Cyclophosphamide (CY) as Conditioning on Liver Toxicity in Allogenic Hematopoietic Stem Cell Transplantation (ALL-HSCT)</title>
    <FirstPage>171</FirstPage>
    <LastPage>176</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Mani</FirstName>
        <LastName>Ramzi</LastName>
        <affiliation locale="en_US">Hematology and Bone Marrow Transplant Research Center, Shiraz University of Medical Sciences, Shiraz, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Nasrin</FirstName>
        <LastName>Namdari</LastName>
        <affiliation locale="en_US">Department of Hematology and Medical Oncology, Shiraz University of Medical Sciences, Shiraz, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Shirin</FirstName>
        <LastName>Haghighat</LastName>
        <affiliation locale="en_US">Department of Hematology, Hematology Research Center, Medical Oncology and Stem Cell Transplantation, Shiraz University of Medical Sciences, Shiraz, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Hourvash</FirstName>
        <LastName>Haghighinejad</LastName>
        <affiliation locale="en_US">Department of Family Medicine, Shiraz University of Medical Sciences, Shiraz, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2019</Year>
        <Month>06</Month>
        <Day>29</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2020</Year>
        <Month>02</Month>
        <Day>15</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background: Busulfan (BU) in combination with cyclophosphamide (CY) is used as an effective conditioning regimen in hematopoietic SCT. Busulfan, depletes glutathione level in liver and causes elevated levels of CY metabolites. Cyclophosphamide metabolites are highly toxic for sinusoidal endothelial cells and cause VOD/ SOS with high mortality rate.
Materials and Methods: All adult patients with acute leukemia, who were candidates for myeloablative allogenic SCT admitted in Stem Cell Transplantation center of our center were enrolled in this prospective randomized clinical trial during 2 years. We tested the hypothesis that reverse administration from BU-CY (28 patients) to CY-BU group (27 patients) would reduce liver toxicity.
Results: Liver function tests were significantly higher in BU-CY group between day -1 and +4 (p&lt;0.05), but we do not have VOD/SOS in both groups. The incidence and severity of acute GVHD was higher in BU-CY group, but not statistically significant. Engraftment and mortality rate were not different.
Conclusion: These data support the concept that CY-BU is associated with less liver toxicity, suggesting CY-BU is superior to BU-CY as conditioning.</abstract>
    <web_url>https://ijhoscr.tums.ac.ir/index.php/ijhoscr/article/view/1152</web_url>
    <pdf_url>https://ijhoscr.tums.ac.ir/index.php/ijhoscr/article/download/1152/829</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>International Journal of Hematology-Oncology and Stem Cell Research</JournalTitle>
      <Issn>2008-2207</Issn>
      <Volume>14</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="epublish">
        <Year>2020</Year>
        <Month>07</Month>
        <Day>02</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Relationship between the Expression of the Thymidylate Synthase and the Prognosis of Gastric Cancer Patients Treated with Combinational Chemotherapy Regimen Including Fluorouracil, Docetaxel and Cisplatin</title>
    <FirstPage>181</FirstPage>
    <LastPage>187</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Mozaffar</FirstName>
        <LastName>Aznab</LastName>
        <affiliation locale="en_US">Department of Internal Medicine, Taleghani Hospital, Kermanshah University of Medical Sciences, Kermanshah, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Seyed Majid</FirstName>
        <LastName>Ahmadi</LastName>
        <affiliation locale="en_US">School of Medicine, , Yasuj University of Medical Sciences, Yasuj, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Sedigheh</FirstName>
        <LastName>Khazaei</LastName>
        <affiliation locale="en_US">Molecular Pathology Research Center, Imam Reza University Hospital, Kermanshah University of Medical Sciences, Kermanshah, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Seyed Mojtaba</FirstName>
        <LastName>Ahmadi</LastName>
        <affiliation locale="en_US">Department of Clinical Psychology, School of Medicine, Kermanshah University of Medical Sciences, Kermanshah, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mansour</FirstName>
        <LastName>Khazaei</LastName>
        <affiliation locale="en_US">Taleghani University Hospital, Kermanshah University of Medical Sciences, Kermanshah, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Hamid</FirstName>
        <LastName>Hamdi</LastName>
        <affiliation locale="en_US">Armi Hospital, Sanandaj, Kurdistan</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2019</Year>
        <Month>05</Month>
        <Day>15</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2020</Year>
        <Month>02</Month>
        <Day>12</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background: Thymidylate synthase is one of the target enzymes of 5-fluorouracil. However, the clinical and prognostic significance of TS expression in gastric cancer has remained controversial. In this study, the expression of thymidylate synthase was evaluated in gastric cancer patients treated with combinational chemotherapy; moreover, the association between TS expression and clinicopathologic characteristics and overall survival of the patients were also assessed.
Materials and Methods: In this descriptive study, 89 pathological samples were gathered from patients at Kermanshah hospitals during 2008-2017. The survival status of patients was recorded and their overall survival was evaluated individually.
Results: The average survival period for low and high thymidylate synthase groups was 54 and 50 months, respectively, meaning higher survival time in the lower thymidylate group. But this difference was not statistically significant (log Rank=0.88). In addition, sex, stage, recurrence, and survival had no significant difference between the low and high expression of thymidylate synthase groups (p=0.89).
Conclusion: The results clearly indicated that the level of thymidylate synthase is not a significant modulator of 5- fluorouracil in gastric cancer patients. Nevertheless, evaluation of the level of the enzymes and markers, as well as their effects, is highly recommended for accurate selection of chemotherapeutical strategies.</abstract>
    <web_url>https://ijhoscr.tums.ac.ir/index.php/ijhoscr/article/view/1133</web_url>
    <pdf_url>https://ijhoscr.tums.ac.ir/index.php/ijhoscr/article/download/1133/833</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>International Journal of Hematology-Oncology and Stem Cell Research</JournalTitle>
      <Issn>2008-2207</Issn>
      <Volume>14</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="epublish">
        <Year>2020</Year>
        <Month>07</Month>
        <Day>02</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Short Dysfunctional Telomere is Highly Predictive of Dismal Outcome in MDS but Not in AML Patients</title>
    <FirstPage>188</FirstPage>
    <LastPage>199</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Nadia</FirstName>
        <LastName>Menshawy</LastName>
        <affiliation locale="en_US">Clinical Pathology, Hematology Unit, Faculty of Medicine, Mansoura University, Mansoura, Egypt</affiliation>
      </Author>
      <Author>
        <FirstName>Shaimaa</FirstName>
        <LastName>Ashwah</LastName>
        <affiliation locale="en_US">Clinical Hematology Unit, Internal Medicine Department, Faculty of Medicine, Mansoura University, Mansoura, Egypt</affiliation>
      </Author>
      <Author>
        <FirstName>Mohamed</FirstName>
        <LastName>Ebrahim</LastName>
        <affiliation locale="en_US">Medical Oncology Unit, Internal Medicine Department, Faculty of Medicine, Mansoura University, Mansoura, Egypt</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2019</Year>
        <Month>04</Month>
        <Day>27</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2020</Year>
        <Month>05</Month>
        <Day>07</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background: A trigger for initiation the clonal hematopoietic stem cells disorders could be short telomere length, probably due to chromosomal instability. The relationship between relative telomere length (RTL) and the two linked hematological stem cell disorders, myelodysplastic syndromes (MDS) and acute myeloid leukemia (AML), is still unclear.
Material and Methods: We evaluated the role of RTL in MDS (n=96) and AML (n=130) at the time of diagnosis using a real time quantitative polymerase chain reaction (RT-PCR) technique. The median value of RTL (1) was set as the cutoff for statistical comparison. Overall survival (OS) is defined as the time from diagnosis to death or last follow-up.
Results: RTL was significantly longer in both MDS and AML cases versus control (p&lt;0.0001) and was significantly longer in MDS versus AML cases (p =0.03). RTL correlated negatively with age in MDS (p &lt;0.0001) but not in AML cases. RTL was also significantly shorter in MDS cases with pancytopenia and poor risk cytogenetics (p &lt; 0.0001 for each) and short RTL was significantly associated with inferior survival (p = 0.007), while RTL showed no significant impact on OS in AML cases. Moreover, short RTL retained independent prognostic value in multivariate analysis (HR= 3.42 [95% CI, 8.97-19.35], p = 0.004).
Conclusion: RTL showed an association with both AML and MDS; however, short RTL was an independent poor prognostic factor in MDS patients only.</abstract>
    <web_url>https://ijhoscr.tums.ac.ir/index.php/ijhoscr/article/view/1124</web_url>
    <pdf_url>https://ijhoscr.tums.ac.ir/index.php/ijhoscr/article/download/1124/832</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>International Journal of Hematology-Oncology and Stem Cell Research</JournalTitle>
      <Issn>2008-2207</Issn>
      <Volume>14</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="epublish">
        <Year>2020</Year>
        <Month>07</Month>
        <Day>02</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Application of Chromosome Conformation Capture Method for Detection MYC/TRD Chromosomal Translocation in Leukemia Cell Line</title>
    <FirstPage>200</FirstPage>
    <LastPage>212</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Moloud</FirstName>
        <LastName>Absalan</LastName>
        <affiliation locale="en_US">Department of Molecular Medicine, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mohammad Hossein</FirstName>
        <LastName>Ghahremani</LastName>
        <affiliation locale="en_US">Department of Pharmacology and Toxicology, School of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Zahra</FirstName>
        <LastName>Jabbarpour</LastName>
        <affiliation locale="en_US">Department of Molecular Medicine, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Roya</FirstName>
        <LastName>Karimi</LastName>
        <affiliation locale="en_US">Department of Tissue Engineering and Applied Cell Sciences, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Shilan</FirstName>
        <LastName>Shafei</LastName>
        <affiliation locale="en_US">Department of Molecular Medicine, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Reza</FirstName>
        <LastName>Heidari</LastName>
        <affiliation locale="en_US">Department of Molecular Medicine, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mostafa</FirstName>
        <LastName>Akbariqomi</LastName>
        <affiliation locale="en_US">Department of Molecular Medicine, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Gholamreza</FirstName>
        <LastName>Tavoosidana</LastName>
        <affiliation locale="en_US">Department of Molecular Medicine, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
     Shariati Hospital, Tehran University of Medical Sciences,&#xD;
Tehran, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>01</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background: Osteosarcoma is the most common bone sarcoma, and the third most common malignancy in children and adolescents. Before 1970, amputation was the sole treatment. Eighty percent of patients died from metastatic diseases, most commonly in the lungs. Over the past three decades, effective neoadjuvant (preoperative) and adjuvant (postoperative) chemotherapy protocols have improved the ability to perform limb salvage resections, disease free survival and overall survival rates.
Patients and Methods: The study was conducted on 28 patients (15 male and 13 female) whose diagnoses were confirmed by excisional biopsy without any proof of metastasis in clinical and radiological assessments from September 2001 to November 2002. All patients were treated with three-drug regimen consisting of Adriamycin, Ifosfamide and Cisplatin. The neoadjuvant chemotherapy was administered in three courses. The first course, Ifosfamide (2gr/IV) and Adriamycin (75mg/m&#xB2;, IV infusion) were given on the first day and Ifosfamide (1.5 gr/m&#xB2; by continuous infusion) alone for 6 days. The second course consisted of Adriamycin (75mg/m&#xB2;, IV infusion) and Cisplatin (100mg/m&#xB2;, IV infusion) for one day. The third course was the same as the first. After surgery, all patients received adjuvant therapy similar to the neoadjuvant protocol mentioned above. Limb salvage was the most common surgical method. The treatment outcome particularly depended on the percentage of tumor necrosis. Overall and disease-free survival were also measured.
Results: According to the tumor necrosis percentage, the tumor response to chemotherapy was classified from good to poor response. In this study, 63.6% of patients showed good response and 36.4% indicated poor or no response to chemotherapy. The tumor necrosis percentage was significantly correlated with age&#x2264; 20 years (P= 0.01), tumor size &#x2264;84 cm&#xB3; (P= 0.03) and the site of tumors in femurs (P= 0.03). The average follow-up time was 132 days, ranging from 15 to 618 days. The first year survival rate was 100%, and the disease-free survival (DFS) was 70.8% for the same time period. Disease-free survival was significantly correlated with the chemotherapy response (P= 0.03), which was 100% in the good response group in the first year.
Conclusion: Although we had utilized bone grafts for substantially resected bones, local relapses were remarkably low (2 cases), so we suggest that this surgical method can be a proper alternative treatment for different types of expensive prosthesis in countries with low socioeconomic status.</abstract>
    <web_url>https://ijhoscr.tums.ac.ir/index.php/ijhoscr/article/view/162</web_url>
    <pdf_url>https://ijhoscr.tums.ac.ir/index.php/ijhoscr/article/download/162/155</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>International Journal of Hematology-Oncology and Stem Cell Research</JournalTitle>
      <Issn>2008-2207</Issn>
      <Volume>1</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2004</Year>
        <Month>03</Month>
        <Day>10</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Chronic Graft versus Host Disease after Allogeneic Bone Marrow Transplantation; An Analysis of Incidence and Risk Factors.</title>
    <FirstPage>16</FirstPage>
    <LastPage>19</LastPage>
    <AuthorList>
      <Author>
        <FirstName>A</FirstName>
        <LastName>Ghavamzadeh</LastName>
        <affiliation locale="en_US">Hematology- Oncology and BMT Research Center, Shariati Hospital, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>K</FirstName>
        <LastName>Alimoghaddam</LastName>
        <affiliation locale="en_US">Hematology- Oncology and BMT Research Center, Shariati Hospital, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>B</FirstName>
        <LastName>Bahar</LastName>
        <affiliation locale="en_US">Hematology- Oncology and BMT Research Center, Shariati Hospital, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>F</FirstName>
        <LastName>Foroughi</LastName>
        <affiliation locale="en_US">Hematology- Oncology and BMT Research Center, Shariati Hospital, Tehran, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>01</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background: Chronic graft versus host disease (cGVHD) is one of the most serious potential complications of allogeneic bone marrow transplantation.
 Study design and method: We analyzed the incidence of cGVHD and its associated risk factors in a group of 161 Iranian recipients of HLA-identical sibling transplants, with at least 90 days post-transplantation survival. In the majority of cases (n=73), cGVHD occurred in the first year after the transplant (median 273 days). The actual probability of cGVHD within 1 year was 45.3&#xB1;7% (CI 95%). 
Results: In a univariate analysis, the most important risk factor was the type of transplant. Peripheral blood stem cell transplants (PBSCT) showed a significant increase in cGVHD compared with bone marrow transplants (BMT) (RR=2.34, p&lt;0.001). In addition, male recipients were at a greater risk than female recipients (RR=2.08, p=0.004). Other risk factors were the presence of prior acute GVHD (RR=2.37, p=0.04) and the previous acute GVHD grade (p=0.03); The probabilities of cGV D in patients with grade 0, &#x399;, &#x399;&#x406;, &#x399;&#x399;&#x399;, &#x399;V acute GVHD were 24%, 44.7%, 42.6%, 56.8%, 64.3%, respectively. 
Conclusion: In a multivariate analysis, the only independent predictive factors for the development of cGVHD were the type of transplant (PBSC&gt;BM, p&lt;0.001) and male recipient (p=0.005). The survival rate was 88.8% and there was no significant difference in the probability of survival between BPSCT vs BMT (93.8% vs 86.6%, p=0.5).</abstract>
    <web_url>https://ijhoscr.tums.ac.ir/index.php/ijhoscr/article/view/163</web_url>
    <pdf_url>https://ijhoscr.tums.ac.ir/index.php/ijhoscr/article/download/163/156</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>International Journal of Hematology-Oncology and Stem Cell Research</JournalTitle>
      <Issn>2008-2207</Issn>
      <Volume>1</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2004</Year>
        <Month>03</Month>
        <Day>10</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Evaluation of the Affect of Maternal and Neonatal Factors on Cord Blood Parameters?</title>
    <FirstPage>20</FirstPage>
    <LastPage>23</LastPage>
    <AuthorList>
      <Author>
        <FirstName>M</FirstName>
        <LastName>Mohyeddin Bonab</LastName>
        <affiliation locale="en_US">Heamatology, Oncology &amp; BMT Research center, Shariati hospital, Tehran University of Medical Sciences; Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Z</FirstName>
        <LastName>Goliaei</LastName>
        <affiliation locale="en_US">Heamatology, Oncology &amp; BMT Research center, Shariati hospital, Tehran University of Medical Sciences; Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>K</FirstName>
        <LastName>Alimoghaddam</LastName>
        <affiliation locale="en_US">Heamatology, Oncology &amp; BMT Research center, Shariati hospital, Tehran University of Medical Sciences; Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>A</FirstName>
        <LastName>Ghavamzadeh</LastName>
        <affiliation locale="en_US">Heamatology, Oncolo