Tanzina Chowdhury
Great Ormond Street Hospital
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Publication
Featured researches published by Tanzina Chowdhury.
Journal of Pediatric Hematology Oncology | 2013
Tanzina Chowdhury; K Prichard-Jones; Nj Sebire; Nelly Bier; A Cherian; Mo Sullivan; A O'Meara; John R. Anderson
Forty percent of renal cell carcinomas (RCCs) in childhood are characterized by translocation involving transcription factor E3 (TFE3) family members. Here, we describe a case of TFE3-positive RCC in which metastatic relapse to the mediastinal lymph nodes and pulmonary nodules was treated with single-agent sunitinib, a multitargeted tyrosine inhibitor. Complete radiologic remission was achieved after only 3 courses of treatment, and surgical exploration of metastases failed to identify any residual viable disease. The published experience of sunitinib in TFE-RCC is limited, and prospective evaluation of its activity in a larger number of patients is warranted.
Pediatric Blood & Cancer | 2009
Tanzina Chowdhury; Alex M. Barnacle; Saira Haque; Nj Sebire; Sian Gibson; John Anderson; Derek J. Roebuck
Most commonly a tissue diagnosis of rhabdomyosarcoma (RMS) in children is made by biopsy as opposed to primary resection. Open surgical procedures are often recommended to obtain sufficient material for accurate and complete diagnostic work up. Our institution has routinely used image‐guided needle biopsies for soft tissue tumour diagnosis. We therefore sought to assess diagnostic accuracy and completeness, and procedure safety of consecutive patients diagnosed by needle biopsies in a single institution.
Journal of Pediatric Hematology Oncology | 2014
Martine van Grotel; Esther Blanco; Nj Sebire; Olga Slater; Tanzina Chowdhury; John Anderson
Infantile fibrosarcoma (IFS) is a malignant neoplasm, arising in children younger than 2 years of age and with a hallmark chromosomal translocation t(12;15)(p13;q26) encoding an ETV6-NTRK3 fusion oncoprotein. A review of the world literature found no reported cases of molecularly proven IFS with distant metastatic spread at presentation. We report the case of a 2-month-old infant girl presenting with a chest wall primary IFS bearing and expressing the ETV6-NTRK3 fusion, who had several pulmonary metastatic deposits at diagnosis. She achieved complete remission with chemotherapy and surgery. To our knowledge, this is the first reported case of molecularly proven IFS with distant metastatic spread.
Oncogene | 2018
Ido D. Fabian; Zerrin Onadim; Esin Karaa; Catriona Duncan; Tanzina Chowdhury; Irene Scheimberg; Shin-ichi Ohnuma; M. Ashwin Reddy; Mandeep S. Sagoo
Retinoblastoma (Rb) is the most common primary intraocular malignancy of childhood, but an uncommon paediatric cancer, with a constant incidence worldwide of 1:15,000–1:20,000 live births. Despite its rarity, Rb has served as a cornerstone in the field of oncology in many of the aspects that comprise cancer management, including classification schemes, treatment modalities, genetic testing and screening. Until just over half a century ago, the major treatment for Rb was eye removal, and prognosis was poor with outcome fatal for most children. The dramatic evolution, in a short period of time across all fields of Rb management, as well as the development of specialized centres, better infrastructure and introduction of awareness campaigns, has resulted in nearly 100% survival in developed countries and allowed eye salvage in many of the cases. External beam radiotherapy was used as the main treatment choice for four decades, but replaced by chemotherapy at the turn of the century. Initially, and still in many centres, chemotherapy is administered intravenously, but recently is targeted directly into the eye by means of intra-ophthalmic artery and intravitreal chemotherapy. To date, a range of treatments is available to the Rb expert, including enucleation, but there is lack of consensus in a number of scenarios as to what to use and when. In such a rare cancer, treatment outcomes are reported usually via retrospective analyses, with few prospective randomized controlled trials. Classification schemes have also evolved following the introduction of new treatment modalities, but discrepancies exist among centres with respect to the preferred schema and its interpretation. Retinoblastoma management is a remarkable success story, but the future will require a collaborative effort in the form of multicentre randomized controlled trials in order to further improve the quality of care for this subset of young children with ocular cancer.
British Journal of Ophthalmology | 2018
Ido Didi Fabian; Andrew W. Stacey; Kenneth C Johnson; Tanzina Chowdhury; Catriona Duncan; M. Ashwin Reddy; Mandeep S. Sagoo
Background Chemotherapy is increasingly used as primary treatment for group D retinoblastoma, whereas primary enucleation is considered to have a diminishing role. This study aimed to compare the management course, including number of examinations under anaesthesia (EUAs), of group D patients treated by enucleation versus chemotherapy. Methods A retrospective analysis of 92 group D patients, of which 40 (37 unilateral) underwent primary enucleation and 52 (17 unilateral) were treated with intravenous chemotherapy. Number of EUAs was compared between the treatment groups with respect to the whole cohort, using univariate and multivariate analysis, and to unilateral cases only. Results Patients were followed up for a median of 61 months (mean: 66, range: 14–156), in which time primary enucleated patients had on average seven EUAs and chemotherapy-treated patients 21 EUAs (p<0.001). Chemotherapy, young age, bilateral disease, multifocal tumours, familial and germline retinoblastoma were found on univariate analysis to correlate with increased number of EUAs (p≤0.019). On multivariate analysis, however, only treatment type and presentation age were found significant (p≤0.001). On subanalysis of the unilateral cases, patients undergoing primary enucleation had in average seven EUAs, as compared with 16 in the chemotherapy group (p<0.001). Of the 55 unilateral-presenting patients, a new tumour developed in the fellow eye only in a single familial case. Conclusion Group D patients’ families should be counselled regarding the significant difference in number of EUAs following primary enucleation versus chemotherapy when deciding on a treatment strategy. In this regard, primary enucleation would be most beneficial for older patients with unilateral disease.
Cancer Chemotherapy and Pharmacology | 2016
Gareth J. Veal; Julie Errington; Jairam Sastry; Julia Chisholm; Penelope Brock; Daniel A. Morgenstern; Kathy Pritchard-Jones; Tanzina Chowdhury
Ophthalmology | 2017
Ido D. Fabian; Andrew W. Stacey; Tanzina Chowdhury; Catriona Duncan; Esin Karaa; Irene Scheimberg; M. Ashwin Reddy; Mandeep S. Sagoo
British Journal of Ophthalmology | 2017
Ido D. Fabian; Andrew W. Stacey; Johnson Kp; Zerrin Onadim; Tanzina Chowdhury; Catriona Duncan; Reddy Ma; Mandeep S. Sagoo
American Journal of Ophthalmology | 2017
Ido D. Fabian; Zishan Naeem; Andrew W. Stacey; Tanzina Chowdhury; Catriona Duncan; M. Ashwin Reddy; Mandeep S. Sagoo
Journal of Aapos | 2018
Ido D. Fabian; Andrew W. Stacey; Zishan Naeem; Zerrin Onadim; Tanzina Chowdhury; Catriona Duncan; Mandeep S. Sagoo; M. Ashwin Reddy