To study the epidemiology, etiologies, and complications of playtime open globe injuries in children at the Assiut University Hospital, Egypt.
This prospective cross-sectional study enrolled children with open globe injury who were admitted to Assiut University Hospital during a 6-month period (January to July 2016). All causes of trauma that occurred during playtime (at home, outside home, at the club, or at school) were recorded and analyzed.
Eighty-one children (age = 18 years and younger; mean ± standard deviation age = 8.35 ± 4.84 years) were admitted with open globe injury, and 32 of them (39.51%) sustained ocular trauma during playtime. The majority of children were boys (n = 23, 71.88%). The causes of trauma during playtime were: playing with sharp objects (n = 11; 34.38%), playing with a wooden stick (n = 7; 21.88%), falling on the ground (n = 5; 15.63%), trauma by a stone (n = 2; 6.25%), trauma during running (n = 1; 3.13%), playing with a plastic toy (n = 1; 3.13%), and unknown causes (n = 5; 15.63%). The sites of globe perforation were corneal (n = 23; 71.88%), corneoscleral (n = 8; 25%), and scleral (n = 1; 3.13%).
Playtime trauma that causes open globe injury and visual disability is avoidable and constituted approximately half of the open globe injuries in this study population. Corneal involvement occurred in almost all open globe injuries. Parental supervision for children during playtime is crucial to injury prevention. Children should avoid playing with sharp, dangerous objects and desist from playing or running on unsafe ground.
Checkpoint inhibitors (CPIs), such as nivolumab, have transformed the treatment paradigm for patients with metastatic non‑small cell lung cancer (mNSCLC) and metastatic renal cell carcinoma (mRCC). The combination of CPIs and radiotherapy (RT) constitutes a multimodal treatment approach that may work synergistically and facilitate augmented systemic responses. The aim of the present retrospective study was to assess the efficacy and safety of continuation of nivolumab treatment with the addition of RT in patients with mNSCLC and mRCC who develop oligometastatic disease progression on single‑agent nivolumab. All patients with mNSCLC and mRCC who received nivolumab at the Department of Oncology, Prince Sultan Military Medical City (Riyadh, Saudi Arabia) between November 2016 and April 2018 were identified. The records of patients who developed oligometastatic disease progression during nivolumab treatment and were subsequently treated with RT, with nivolumab continued beyond disease progression, were retrospectively reviewed. Details of RT, clinical outcomes and toxicity data were collected. Of the 96 patients who received nivolumab, 22 received multiple courses of RT. A total of 39 sites were irradiated: Bone (n=15), lung (n=9), brain (n=8), adrenal gland (n=2), renal bed (n=2), skin (n=1), ethmoid sinus (n=1) and scalp (n=1). Partial response and complete response were noted at 25 (64%) and 3 (8%) sites, respectively. Stable disease was noted at 6 sites (15%) and disease progression was noted at 5 sites (13%). The median time on nivolumab from the date of the first fraction of RT was 4.5 months (range, 1.5‑29 months) for patients with mNSCLC and 5 months (range, 1‑38.5 months) for patients with mRCC. No patients developed grade 3‑4 toxicities. Grade 2 pneumonitis was noted in 3 patients receiving lung RT. The addition of RT appeared to initiate a response and prolong the duration of nivolumab treatment. Therefore, the combination of nivolumab and RT was found to be well tolerated, with response rates exceeding those in published studies of nivolumab monotherapy.
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Background: Checkpoint inhibitors (CPIs) such as nivolumab have transformed the treatment paradigm for patients (pts) with metastatic non-small cell lung cancer (mNSCLC) and renal cell carcinoma (mRCC). Low response rates (20%) with CPIs has prompted novel immunotherapy combination trials. Radiotherapy (RT) causes direct tumor cell death and in addition also effectively stimulates T-cell immunity. RT is a highly cost-effective anti-cancer treatment and its combination with CPIs may herald a new potent therapeutic tool. This study reports on the efficacy and toxicity of concurrent nivolumab and RT administration. Methods: Pts with mNSCLC and mRCC receiving concurrent nivolumab and RT were assessed retrospectively for radiological response (RECIST 1.1), toxicity and symptom benefit (pain score). Results: Of the 63 pts that received nivolumab at our institution, 15 pts received concurrent RT for 32 courses; mNSCLC (n = 8), mRCC (n = 7). Median age 59 years (range 39-71); M:F ratio (4:1). Stereotactic and conformal RT was delivered to 5 and 27 sites, respectively. Most common indication for RT was oligometastatic disease progression (PD): 59%. Treatment sites included: bones (n = 13), lung (n = 7), brain (n = 5), adrenal, renal bed, skin, ethmoid and scalp. The gap between RT & nivolumab did not exceed 2 weeks for all patients. No grade 3-4 toxicities were observed; grade 2 pneumonitis noted in 2 pts. Fractionation schedules included 20Gy/5 fractions (#) (most common-47%), 48Gy/4#, 40Gy/10#, 40Gy/4#, 34Gy/4#, 30Gy/10#, 25Gy/5#, 20Gy/4#, 16Gy/4#, 22Gy/1# and 8Gy/1#. Of the 23 measurable sites, 70% had excellent response including complete response at 3 sites. Pain scores improved in 6 out of 9 sites (67%). Conclusions:The combination of nivolumab and RT appears to be well tolerated in pts with mNSCLC and mRCC with response rates exceeding published studies of nivolumab monotherapy. For patients with oligometastatic PD during nivolumab therapy, addition of RT appears to initiate a response and prolong time spent on nivolumab. Future clinical trials may better define whether RT during nivolumab treatment should be used as induction therapy, consolidative therapy or should be used for pts with oligometastatic PD.
© 2018 by American Society of Clinical OncologyIntracardiac metastases in the absence of inferior vena cava involvement is a rare occurrence in patients with metastatic renal cell carcinoma (mRCC). There is limited evidence regarding the efficacy and safety of standard treatment modalities for mRCC patients with intracardiac metastases. Presence of intracardiac metastases is known to indicate poor prognosis and may potentially increase risk of treatment-related complications. Recent advances in RCC management have integrated nivolumab, a programmed death-1 (PD-1) receptor inhibitor, as a preferred treatment option in the second-line setting after failure of prior anti-angiogenic therapy; or in combination with ipilimumab, an anti-Cytotoxic T-lymphocyte antigen-4 antibody as first-line therapy for intermediate to poor risk patients with mRCC. The efficacy and toxicity of nivolumab in patients with mRCC and intracardiac metastases has never been reported previously. We herein present the first reported case of mRCC with intracardiac metastasis and a resultant excellent response to nivolumab treatment and discuss the imaging techniques and treatment options for this rare presentation.
© 2018 The Author(s). Published by S. Karger AG, Basel
Abstract Background: Lung cancer is the main cause of cancer deaths worldwide. It is important to identify the prognostic factors of this disease which leads to low survival times despite the advancing treatment modalities. Aim: To investigate the role of clincopathological parameters and treatment modality as a prognostic factors affecting survival of patients with advanced non-small cell lung cancer (NSCLC). Methods: We retrospectively reviewed the clinical records of patients with inoperable stage III/IV NSCLC, who were treated at the department of Clinical Oncology, Assiut University Hospital between 2009 and 2014. The association between the demographic and clinical characteristics and survival of these patients was analyzed. Results: A total of 69 patients (32 stage III& 39 stage IV) were identified and included in this study. Sex (males vs. females, p=0.04), Eastern cooperative Oncology group performance status (0 vs. 1 vs. 2, p=0.001), smoking habit (never vs. current vs. former, p=0.001), stage (IIIA vs. IIIB vs. IV, p=0.008) and the initial treatment (no vs. chemotherapy vs. concurrent chemoradiotherapy, p=0.001) were found to be factors affecting survival in univariate analyses. Sex and histological subtype did not affect survival. Performance status, stage and initial treatment were determined as the independent prognostic factors affecting survival in multivariate analyses. Conclusion: Performance status, stage and initial treatment with concurrent chemoradiotherapy in eligible patients were prognostic factors affecting overall survival of patients with advanced NSCLC. Keywords: non-small cell lung cancer, prognostic factors, survival
Double primary malignancies could be divided into two categories, depending on the interval between tumor diagnoses. A secondary malignancy could be defined as a new cancer that has occurred as a result of previous treatment with radiation or chemotherapy. Second primary malignancy can occur at any age but it’s commonly at old age. A 46 premenopausal female patient presented to our outpatient clinic complaining from a mass in her right breast, routine metastatic work-up for distant metastasis declared multiple hepatic metastases, RT renal mass, and bone metastases. Palliative radiotherapy to tender and weight bearing sites followed by 4 cycles of systemic chemotherapy FEC regimen were received. Tru-cut needle biopsy from renal mass detected renal cell carcinoma of clear cell type, the patient started sunitinib and tamoxifen with bisphosphonate (Zoledronic acid), assessment of the response revealed reduction of the size and number of HFLs, and the size of renal mass, so the patient was decided to do cytoreductive nephrectomy and then continued on TAM and sunitinib. Collectively, due to the rising incidence of multiple primary malignancies, further studies should be done not only for better clinical evaluation and treatments but also for accurate determination of possible causes, pathogenesis, effective managements and screening programs.
Keywords:
Renal Cell Carcinoma, Breast Cancer, PET/CT, Double Malignancies
Triple-negative breast cancer (TNBC) has a very high rate of recurrence and till now there is no standard of care. Because of the sensitivity of TNBC to platinum compounds and the synergistic effect between bevacizumab and paclitaxel according to many studies, our aim was to combine all these agents to evaluate the efficacy of bevacizumab in combination with carboplatin and paclitaxel as first-line treatment in metastatic TNBC (mTNBC) and to predict whom can benefit from this combination.
This prospective phase two study included 54 female patients diagnosed with mTNBC at the Clinical Oncology Department, Assuit University Hospital, Egypt from 2017- 2019, 40 of them diagnosed after adjuvant treatment and 14 as denovo. They received bevacizumab 15 mg/ kg + carboplatin AUC 6 + paclitaxel 175m.g/m2 every 21 day for 8 cycles then followed up till data cut off in February 2021. Primary end point was progression-free survival (PFS) at 2 years. Secondary end points were overall survival (OS) at 2 years. Kaplan Meier curve and regression tests were used.
Evaluation was done Feb 2021; 32 patients were alive and only 26 out of them remained in the study. 15 (57.7%) still in CR, 2 (7.7%) were PD and 9 (34.6 %) SD and ORR was 57.7 %, DCR was 92.3 %. Median PFS at 2 years was 27 months with (95 % CI 17.019 - 36.981). By Cox regression both viseral only disease and performance status (PS) 0 had longer PFS (HR 0.23, P value = 0.05) and (HR = 0.16, P value = 0.02) respectively with C index 0.77. The 2 year median OS was 55 months (95 % CI 38.973 - 71.027). Both type of presentation either denovo or after adjuvant treatment and also PS conistentaly affect OS with C index 0.73; (HR = 7.91, P value = 0.02) for denovo patients and (HR=0.12 - P value = 0.01) in patients with PS 0. Three factors affecting final response to gain either SD or CR; patients with visceral only disease OR was 13.20 (P value 0.001), patients with PS 0 had the highest OR 19.5 (P value 0.001) with prediction value 70.4 % and having ≤ 3 sites of metastasis (OR 3.92 P value = 0.02) and 64.8% as percentage of prediction.
TNBC became a challenging area of research to improve the patients’ survival and quality of life. We concluded that tumor burden and PS significantly can be useful in predicting efficacy and tolerability of bevacizumab in metastatic stage in terms of response, PFS and OS.
NCT03577743, ID: BMTN.
Assuit University Hospitals Faculty of Medicine.
Has not received any funding.
Triple-negative breast cancer (TNBC) has a very high rate of recurrence. Our aim is to investigate the efficacy of bevacizumab, platinum and paclitaxel as first-line in metastatic TNBC (mTNBC). This study included 54 female patients with mTNBC. They received bevacizumab, carboplatin and paclitaxel every 21 day for six cycles then who progressed shifted to second-line chemotherapy and the responders continue another two cycles. The median progression-free survival (PFS) was 27 months [95% confidence interval (CI), 17.019-36.981]. There were two factors that affect PFS; visceral only metastasis (hazard ratio, 0.23; P = 0.05) and performance status 0 (hazard ratio = 0.16; P = 0.02) with C-index 0.77. The median overall survival (OS) was 55 months (95% CI, 38.973-71.027). There were two factors that affect OS; type of presentation (hazard ratio = 7.91; P = 0.02) and performance status 0 (hazard ratio = 0.12; P = 0.01) with C-index 0.73. In the final evaluation, three factors have their print on achieving either stable disease (SD) or complete response (CR). Patients having ≤3 sites of metastasis odds ratio (OR) 3.92 (P = 0.02), patients with visceral only metastasis OR was 13.20 (P = 0.001), those with performance status 0 had the highest OR 19.5 (P = 0.001) and the percentage of this prediction was 64.8, 70.4 and 70.4%, respectively. Bevacizumab, carboplatin and paclitaxel were well tolerated, continuation of bevacizumab is recommended as long as SD or CR responses are obtained and tolerated.