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Featured researches published by Manal Zamzam.


Nuclear Medicine Communications | 2010

False-positive F-18 FDG uptake in PET/CT studies in pediatric patients with abdominal Burkittʼs lymphoma

Raef Riad; Walid S. Omar; Iman Sidhom; Manal Zamzam; Iman Zaky; Magdy Hafez; Hussein M. Abdel-Dayem

IntroductionIn pediatric patients with abdominal Burkitts lymphoma, the involvement of the gastrointestinal tract and abdominal lymph nodes are the main presenting feature of the disease. Chemotherapy is the main treatment modality and could be preceded by surgical excision of the abdominal masses. To achieve cure or long-term disease-free survival a balance has to be struck between aggressive chemotherapy and the probability of tumor necrosis secondary to treatment complicated by acute infections, perforation or intestinal bleeding. F-18 fluorodeoxyglucose-positron emission tomography/computed tomography (F-18 FDG-PET/CT) has been recommended over conventional imaging modalities for the follow-up of these patients and for monitoring treatment response. As the incidences of postchemotherapy complications are high, the positive predictive value of PET/CT studies in these patients is very low and the false-positive rate is high from acute infections and tumor necrosis. Accordingly, histopathological confirmation of positive lesions on F-18 FDG-PET/CT studies is essential. This is especially important as post-therapy complications might present with nonspecific and nonurgent symptoms. At the same time initiating a second course of salvage chemotherapy is risky. Aim of studyRetrospectively reviewed F-18 FDG-PET/CT studies for 28 pediatric patients with abdominal Burkitts lymphoma and diffuse large B-cell lymphoma after their treatment with chemotherapy or surgery. ResultsFour positive studies were found. All had pathological verification and were because of acute inflammation and tumor necrosis and there was no evidence of viable tumor cells. One patient had multiple recurrent lesions in the abdomen after the initial surgical excision and before starting chemotherapy. The incidence of acute complications in this series is 10.7%. ConclusionThis study confirms the high incidence of tumor necrosis and inflammation after chemotherapy for the abdominal Burkitts lymphoma and consequently, the incidence of true-positive F-18 FDG studies is low. This necessitates the need for histopathological confirmation of positive studies.


Clinical sarcoma research | 2014

Workshop report on the 2nd Joint ENCCA/EuroSARC European bone sarcoma network meeting: integration of clinical trials with tumour biology

Jakob K. Anninga; Anne-Marie Cleton-Jansen; Bass Hassan; M Fernanda Amary; Daniel Baumhoer; Jean-Yves Blay; Laurence Brugières; Stefano Ferrari; Heribert Jürgens; Beate Kempf-Bielack; Heinrich Kovar; Ola Myklebost; Michaela Nathrath; Piero Picci; Peter Riegman; Marco W. Schilham; Ranin Soliman; Dan Stark; Sandra J. Strauss; Matthew R. Sydes; Patrick Tarpey; David Thomas; Jeremy Whelan; Miriam Wilhelm; Manal Zamzam; Hans Gelderblom; Stefan S. Bielack

This is the report of the 2nd Joint ENCCA/EuroSARC European Bone Sarcoma Network Meeting held in Leiden, The Netherlands, on 26-27 September 2013, bringing together preclinical and clinical investigators on bone sarcoma. The purpose of this workshop was to present the achievements of biological research and clinical trials in bone sarcomas and to stimulate crosstalk.


Journal of Pediatric Surgery | 2018

Effect of timing of pulmonary metastasis occurrence on the outcome of metastasectomy in osteosarcoma patients

Gehad Ahmed; Manal Zamzam; Ahmed Kamel; Sonia Ahmed; Asmaa Salama; Iman Zaki; Nehal Kamal; Maged M. Elshafiey

BACKGROUND Complete metastasectomy is the best predictor of survival in patients with osteosarcoma pulmonary metastases. There has been some controversy in the literature regarding the prognostic significance of the timing of occurrence of lung metastasis. METHODS We reviewed the clinical course of all osteosarcoma patients with pulmonary metastases treated by metastasectomy in our hospital from January 2008 through December 2016. Each patient who underwent metastasectomy was placed into one of three groups based on whether lung metastases were present at initial presentation (Group 1), developed during chemotherapy (Group 2), or appeared after completion of chemotherapy (Group 3). Data were obtained retrospectively and follow-up was obtained until the end of June 2017. RESULTS We identified 170 patients with pulmonary nodules of whom 99 (58.2%) underwent at least one metastasectomy (149 thoracotomies). Eleven patients had benign pulmonary nodules and were excluded. The other 88 patients were classified as Group 1 (37), Group 2 (18) or Group 3 (33). The median follow-up was 35 months (range 8 to 99). Postmetastasis 5-year overall survival (OS) was 38.1 ± 6.4%; event-free survival (EFS) was 25 ± 5.3%. By group, postmetastasis 5-year OS and EFS were 34.3 ± 13% and 18 ± 9.3% in Group 1, 8 ± 6.5% and 6.5 ± 5% in Group 2, and 52 ± 11.4% and 25 ± 9% in Group 3 (P < 0.001). In univariate analysis, the only significant factors associated with survival were timing of occurrence of lung metastasis and the number of lung nodules found. CONCLUSION The timing of occurrence of lung metastasis is an important prognostic factor among osteosarcoma patients eligible for metastasectomy. Patients whose metastases occurred during chemotherapy had the worst survival. LEVEL OF EVIDENCE Level II.


Journal of the Egyptian National Cancer Institute | 2017

Corrigendum to "Risk stratification and pattern of cardiotoxicity in pediatric Ewing sarcoma" [J. Egypt Natl. Cancer Instit. 29 (2017) 53-56].

Emad Moussa; Manal Zamzam; Ahmed Kamel; Zeinab Salah; Iman Attia; Lina Gaber; Ranin Soliman; Sameera Ezzat

http://dx.doi.org/10.1016/j.jnci.2017.06.001 1110-0362/ 2017 National Cancer Institute, Cairo University. Production and hosting by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). DOI of original article: http://dx.doi.org/10.1016/j.jnci.2016.12.001 Peer review under responsibility of The National Cancer Institute, Cairo University. ⇑ Corresponding author. E-mail address: [email protected] (R. Soliman).


Journal of the Egyptian National Cancer Institute | 2017

Outcome of resectable pediatric Ewing sarcoma of the ribs

Gehad Ahmed; Manal Zamzam; Mohamed S. Zaghloul; Ahmed Kamel; Ranin Soliman; Iman Zaky; Asmaa Salama; Nehal Kamal; Maged M. Elshafiey

PURPOSE Was to evaluate the outcome of multimodality treatment in resectable primary Ewing sarcoma/primitive neuroectodermal tumor ES/PNET of the ribs and role of thoracoscopy in facilitating resection of these tumors. PATIENTS AND METHODS This was a retrospective study including 22 patients with primary ES/PNET of the ribs surgically treated at Childrens Cancer Hospital Egypt (CCHE) between January 2008 until the end of December 2014. RESULTS Median age was 8.5years (range 5months to 16years.). All patients received neoadjuvant chemotherapy. Thoracoscopic exploration was performed in 15 (68%) patients. Resection included 1,2,3 and 4 ribs in (7,4,8 and 3 patients) respectively, parts of the diaphragm (3 patients), wedge resection of the lung (10 patients) and pleural nodules (2 patients). Primary closure was feasible in 11 patients and rib transposition was done in one patient. Reconstruction by proline mesh covered by muscle flap was done in 10 patients. Margins were microscopically positive in 3 patients and close in 2 patients. Postoperative radiotherapy was given in 8 patients. With a median follow-up of 38.5months, the 3-year event -free survival (EFS) and overall survival(OS) rates were 31.6% and 55.6%, respectively. CONCLUSION Multimodality treatment is essential in the management of ES-PNET of the ribs. Neoadjuvant chemotherapy facilitates adequate resection. The role of thoracoscopy and the indications of postoperative radiotherapy need further evaluation.


Journal of the Egyptian National Cancer Institute | 2017

Risk stratification and pattern of cardiotoxicity in pediatric Ewing sarcoma

Emad Moussa; Manal Zamzam; Ahmed Kamel; Zeinab Salah; Iman Attia; Lina Gaber; Ranin Soliman; Sameera Ezzat

INTRODUCTION Anthracycline chemotherapy contributes to improved outcomes in Ewing sarcoma; however, the most feared complication is cardiotoxicity. Echocardiograms were routinely used to monitor cardiac function after anthracycline treatment. Nevertheless, indices chosen to assess cardiac toxicity vary significantly among different centers, and no uniform protocol has been accepted as ideal. METHODS This retrospective study included children with Ewing sarcoma treated at Childrens Cancer Hospital Egypt over 4years. All echocardiograms and related clinical assessments were reviewed. RESULTS In total, 149 patients (median age 11years; range 1-18years) were included. Although all patients had a reduced ejection fraction compared with their baseline echocardiogram, only 39 patients developed cardiotoxicity (26%): 43% acute-onset, 36% chronic early-onset, and 21% chronic late-onset. There were no statistically significant association between the frequency of myocardial dysfunction and risk factors, including age, sex, follow-up duration, cumulative doxorubicin dose, and mediastinal irradiation. Over one-third (39%) of the patients with cardiac toxicity regained normal cardiac parameters, whereas seven patients died of acute cardiac toxicity. CONCLUSION The routine use of echocardiography to screen for anthracycline-induced cardiac toxicity before and during chemotherapy identified myocardial dysfunction. Early medical intervention can improve cardiac parameters. Improved screening techniques with better sensitivity and predictability are needed.


European Journal of Nuclear Medicine and Molecular Imaging | 2010

Role of PET/CT in malignant pediatric lymphoma

Raef Riad; Walid Omar; Magdy Kotb; Magdy Hafez; Iman Sidhom; Manal Zamzam; Iman Zaky; Hussein M. Abdel-Dayem


International Journal of Infectious Diseases | 2005

Clinical and microbiologic determinants of serious bloodstream infections in Egyptian pediatric cancer patients: a one-year study.

H. El-Mahallawy; Iman Sidhom; N.H. Ali El-Din; Manal Zamzam; M.M. El-Lamie


Archive | 2003

Blood Stream Infections in Pediatric Cancer Patients, Epidemiology and Outcome Analysis

Nelly H. Ali El-Din; Iman Sidhom; Manal Zamzam; Hadir A. El-Mahalaway


Journal of the Egyptian National Cancer Institute | 2004

Multidisciplinary treatment in children with non-metastatic hepatoblastoma: treatment results at the National Cancer Institute, Cairo University.

Manal Zamzam; Elmalt O; Aboul Kassem H; Nouh A; Elbasmy Aa

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Hussein M. Abdel-Dayem

Memorial Sloan Kettering Cancer Center

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