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    Saroj Gupta Cancer Centre and Research Institute

    115论文总数
    1,710引用总数

    Saroj Gupta Cancer Centre and Research Institute, formerly known as "Cancer Centre Welfare Home & Research Institute" is a hospital that is spread over an area of 16 acres of land. It is a fully comprehensive, dedicated cancer hospital with 311 beds and over 850 staff members. This is a nonprofit organization. The SGCC&RI is located in Thakurpukur, on the outskirts of the city of Kolkata, West Bengal.

    论文量&引用量时间轴

    机构学者

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    Susanta Roychoudhury
    Susanta Roychoudhury
    Biophysics Division;Indian Institute of Chemical Biology;Biophysics Division, Indian Institute of Chemical Biology
    论文:32引用:0H-index:0
    Roy Shravasti
    Roy Shravasti
    Dept. of Pathology and Paediatric Oncology, Saroj Gupta Cancer Centre and Research Institute
    论文:12引用:0H-index:0
    Nath Somsubhra
    Nath Somsubhra
    Indian Institute of Chemical Biology, Council of Scientific and Industrial Research
    论文:12引用:0H-index:0
    Arnab Gupta
    Arnab Gupta
    Dept. of Surgical Oncology, Saroj Gupta Cancer Centre and Research Institute Kolkata
    论文:12引用:0H-index:0
    Roy Anup
    Roy Anup
    Department of Pathology, Nil Ratan Sircar Medical College and Hospital
    论文:11引用:0H-index:0
    Chinmay Panda
    Chinmay Panda
    Chittaranjan National Cancer Institute
    论文:11引用:0H-index:0
    Roy Chowdhury Rahul
    Roy Chowdhury Rahul
    Department of Gynecology, Saroj Gupta Cancer Centre and Research Institute
    论文:10引用:0H-index:0
    Mandal Palash Kumar
    Mandal Palash Kumar
    Department of Pathology, Sagar Dutta Medical College
    论文:9引用:0H-index:0
    Gautam Bhattacharjee
    Gautam Bhattacharjee
    Department of Zoology, M.B.B. College
    论文:8引用:0H-index:0

    论文(115)

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    1Clinical Impact of Integrating RNA-Based Next-Generation Sequencing into the Diagnostic Evaluation of Soft Tissue Sarcomas: Insights from a Single-Center Multidisciplinary Workflow
    Nihanthy D Sreenath, Kinjal Singh,Sameer Rastogi, Niranjan Biswal, Akash Singh,Adarsh Barwad,Asit Ranjan Mridha,Shivanand Gamanagatti,Shamim Ahmed Shamim, Yamini Dharmashaktu, Charu Bahl, Aparna Natrajan,

    PURPOSESarcomas exhibit clinicopathologic heterogeneity, leading to diagnostic and therapeutic uncertainty. This study assesses the clinical value of integrating targeted RNA-based next-generation sequencing (NGS) into a multidisciplinary sarcoma workflow to improve diagnosis, enable comprehensive molecular characterization, and inform personalized treatment strategies.METHODSIn this prospective single-center study, 68 patients with suspected or confirmed soft tissue sarcoma underwent RNA-based NGS using a 138-gene fusion panel, integrated within a multidisciplinary sarcoma framework. Genomic findings integrated with histopathology and immunohistochemistry for diagnostic reclassification and treatment changes.RESULTSOf 70 patients advised RNA-based NGS, 68 (97.1%) were evaluable (median age, 38.5 years). Soft tissue sarcomas predominated (77.1%), with 67.1% presenting with advanced disease. Initial histology included 17 round cell sarcomas (RC), 19 undifferentiated sarcomas (US), and 34 other subtypes. Among evaluable RC cases (n = 16), NGS identified diagnostic fusions in 87.5%, enabling reclassification in 68.7% and treatment change in 18.7%. In US, fusions were detected in 21.1%, all reclassified, with treatment altered in 75%. In other subtypes, fusions were found in 48.4%, enabling reclassification in 39.3% and treatment impact in 21.2%. Nondiagnostic mutations (eg, TP53, SLX4, NF1) were observed in 47.4% of US and 18.2% of other subtypes. Potentially actionable variants (KIT, PIK3CA) were seen in 5.8%. Overall, RNA-NGS was clinically informative in 50%, refined diagnosis in 41.1%, and influenced treatment in 26.4% of patients.CONCLUSIONTo our knowledge, this first-of-its-kind study highlights the clinical utility of integrating targeted RNA-based NGS into multidisciplinary sarcoma care, enabling diagnostic reclassification in 41.1% of cases most notably in round cell sarcomas with atypical morphology. Both canonical and rare fusions informed individualized therapy, reinforcing RNA-NGS as a pivotal tool for diagnostic refinement and precision oncology in sarcoma management.

    2026JCO global oncology(2026)引用:1
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    2Bold Brushstrokes, Bravery, and the Bat-Fan: the Girl Who Laughed in Color
    Nihanthy D Sreenath, Akhil Santhosh
    2026JCO global oncology(2026)
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    3Distribution, Socioeconomic Inequalities and Contributing Factors of Anaemia Prevalence Across Wealth Index among Indian Adolescent Girls: Multivariate Decomposition Analysis of Nationally Representative Survey
    Arnab Ghorui, Sushanta Sarkar, Anamika Das, Chandramohan Kumar, Ravneet Kaur, Esha Das, Pritam Halder, Indra Shekhar Prasad, Anshul Mamgai, Shivani Rathor, Kathirvel Srinath, Manish Chandra Prabhakar

    Background Anaemia among adolescent girls aged 15–19 years can adversely affect educational, vocational and reproductive outcomes. Amid rapid urbanisation, understanding its prevalence, determinants and urban–rural inequities is essential. Using National Family Health Survey (NFHS)-5 data in India, this study comprehensively assessed anaemia epidemiology and quantified urban–rural disparities and their contributing factors through multivariate decomposition analysis.Methodology NFHS-5 data from 113 606 adolescent girls aged 15–19 years were analysed. Socio-demographic, health, and behavioural factors were assessed through standardised interviews. Haemoglobin was measured using HemoCue Hb 201+, with anaemia defined as <12 g/dL. Decomposition and concentration indices assessed disparities inequities.Results Anaemia was more prevalent among adolescent girls from rural areas (60.2%, 95% CI 59.9 to 60.5%) compared with those from urban areas (56.6%, 95% CI 56.0 to 57.3%). Multivariate decomposition analysis showed that the largest variable-level contribution to the explained urban–rural disparity in anaemia prevalence was from wealth index (52.4%; richest: −1.497, 95% CI−1.501 to −1.493), followed by region (21.7%; East: −0.750, 95% CI−0.753 to −0.748), caste (17.3%; schedule tribe: −0.406, 95% CI −0.408 to −0.403), accessibility of healthcare centre (12.6%; not accessible: −0.319, 95% CI −0.323 to −0.315) and fruit intake (8.2%; daily: −0.834, 95% CI −0.839 to −0.829). In contrast, media exposure showed a negative contribution (−13.1%; 0.452, 95% CI 0.450 to 0.455), indicating that differences in media exposure reduced the observed urban–rural disparity. The concentration indices were comparable between urban (−0.075, 95% CI −0.089 to −0.061) and rural (−0.071, 95% CI −0.078 to −0.064) populations, indicating modest wealth-related inequality in both settings.Conclusion Anaemia burden was high among Indian adolescent girls, with urban–rural disparities driven by socioeconomic status, dietary patterns and media exposure, requiring comprehensive, multifaceted nationwide interventions.

    2026BMJ Paediatrics Open(2026)
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    4Impact of Structured Psychosocial Intervention on Distress in Adolescent and Young Adult Cancer Patients: A Randomized Controlled Trial from India
    Dr Nihanthy Sreenath, Mahadev P
    2026International Journal of Cancer Care and Delivery(2026)
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    5Glioblastoma Arising in an Immature Teratoma: A Rare Somatic Malignancy in a Germ Cell Tumor
    Sagarika Pahwa, Sunipa Ghosh Pradhan, Soumendra Mishra, Sudipta Roy, Sandipan Chowdhuri

    Mature cystic teratomas constitute the most common ovarian neoplasm occurring in childhood. All the components present in mature cystic teratoma are, by definition, mature. Immature teratomas, on the other hand, are malignant, and they constitute a mixture of embryonal and adult tissues derived from all three germ layers. Commonly, the main component is neuroepithelium. The treatment of immature teratoma is surgery and multidrug chemotherapy for grade 2 and 3 tumours. Sometimes only mature components persist in metastatic sites, which may continue to grow (growing teratoma syndrome) following chemotherapy. Emergence of benign or malignant neoplasm with somatic-type features is an uncommon event in mature cystic teratomas. The most common malignant change is squamous cell carcinoma, followed by carcinoid tumour and adenocarcinoma. Other types include melanomas, sarcomas of various types, carcinosarcomas, glioblastoma, etc. Glioblastomas are among extremely rare somatic malignancies arising from mature or immature teratomas. Their etiology is not well understood, and it is still a matter of research whether they share the same genetic alteration as the tumours occurring in the central nervous system. We present a rare case of glioblastoma arising in an immature teratoma in a young female in her early 20s.

    2026Cureus(2026)
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    合作机构(78)

    加尔各答大学合作论文 8
    Nil Ratan Sircar Medical College and Hospital,West Bengal University of Health Sciences合作论文 6
    All India Institute of Medical Sciences合作论文 5
    North Bengal Medical College and Hospital合作论文 5
    印度化学生物学研究所合作论文 3
    West Bengal University of Health Sciences合作论文 3
    Presidency University合作论文 3
    Chittaranjan National Cancer Institute合作论文 3
    塔塔纪念医院合作论文 3
    贾达普大学合作论文 3

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