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Dive into the research topics where Arnie Purushotham is active.

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Featured researches published by Arnie Purushotham.


Nature | 2012

The genomic and transcriptomic architecture of 2,000 breast tumours reveals novel subgroups

Christina Curtis; Sohrab P. Shah; Suet-Feung Chin; Gulisa Turashvili; Oscar M. Rueda; Mark J. Dunning; Doug Speed; Andy G. Lynch; Shamith Samarajiwa; Yinyin Yuan; Stefan Gräf; Gavin Ha; Gholamreza Haffari; Ali Bashashati; Roslin Russell; Steven McKinney; Anita Langerød; Andrew T. Green; Elena Provenzano; G.C. Wishart; Sarah Pinder; Peter H. Watson; Florian Markowetz; Leigh Murphy; Ian O. Ellis; Arnie Purushotham; Anne Lise Børresen-Dale; James D. Brenton; Simon Tavaré; Carlos Caldas

The elucidation of breast cancer subgroups and their molecular drivers requires integrated views of the genome and transcriptome from representative numbers of patients. We present an integrated analysis of copy number and gene expression in a discovery and validation set of 997 and 995 primary breast tumours, respectively, with long-term clinical follow-up. Inherited variants (copy number variants and single nucleotide polymorphisms) and acquired somatic copy number aberrations (CNAs) were associated with expression in ∼40% of genes, with the landscape dominated by cis- and trans-acting CNAs. By delineating expression outlier genes driven in cis by CNAs, we identified putative cancer genes, including deletions in PPP2R2A, MTAP and MAP2K4. Unsupervised analysis of paired DNA–RNA profiles revealed novel subgroups with distinct clinical outcomes, which reproduced in the validation cohort. These include a high-risk, oestrogen-receptor-positive 11q13/14 cis-acting subgroup and a favourable prognosis subgroup devoid of CNAs. Trans-acting aberration hotspots were found to modulate subgroup-specific gene networks, including a TCR deletion-mediated adaptive immune response in the ‘CNA-devoid’ subgroup and a basal-specific chromosome 5 deletion-associated mitotic network. Our results provide a novel molecular stratification of the breast cancer population, derived from the impact of somatic CNAs on the transcriptome.


European Journal of Cancer | 2010

Magnetic resonance imaging of the breast: Recommendations from the EUSOMA working group

Francesco Sardanelli; Carla Boetes; Bettina Borisch; Thomas Decker; Massimo Federico; Fiona J. Gilbert; Thomas H. Helbich; Sylvia H. Heywang-Köbrunner; Werner A. Kaiser; Michael J. Kerin; Robert E. Mansel; Lorenza Marotti; L. Martincich; L. Mauriac; Hanne Meijers-Heijboer; Roberto Orecchia; Pietro Panizza; Antonio Ponti; Arnie Purushotham; Peter Regitnig; Marco Rosselli Del Turco; F. Thibault; R Wilson

The use of breast magnetic resonance imaging (MRI) is rapidly increasing. EUSOMA organised a workshop in Milan on 20-21st October 2008 to evaluate the evidence currently available on clinical value and indications for breast MRI. Twenty-three experts from the disciplines involved in breast disease management - including epidemiologists, geneticists, oncologists, radiologists, radiation oncologists, and surgeons - discussed the evidence for the use of this technology in plenary and focused sessions. This paper presents the consensus reached by this working group. General recommendations, technical requirements, methodology, and interpretation were firstly considered. For the following ten indications, an overview of the evidence, a list of recommendations, and a number of research issues were defined: staging before treatment planning; screening of high-risk women; evaluation of response to neoadjuvant chemotherapy; patients with breast augmentation or reconstruction; occult primary breast cancer; breast cancer recurrence; nipple discharge; characterisation of equivocal findings at conventional imaging; inflammatory breast cancer; and male breast. The working group strongly suggests that all breast cancer specialists cooperate for an optimal clinical use of this emerging technology and for future research, focusing on patient outcome as primary end-point.


Lancet Oncology | 2011

Delivering affordable cancer care in high-income countries

Richard Sullivan; Jeff rey Peppercorn; Karol Sikora; John Zalcberg; Neal J. Meropol; Eitan Amir; David Khayat; Peter Boyle; Philippe Autier; Ian F. Tannock; Tito Fojo; Jim Siderov; Steve Williamson; Silvia Camporesi; J. Gordon McVie; Arnie Purushotham; Peter Naredi; Alexander Eggermont; Murray F. Brennan; Michael L. Steinberg; Mark De Ridder; Susan A. McCloskey; Dirk Verellen; Terence Roberts; Guy Storme; Rodney J. Hicks; Peter J. Ell; Bradford R. Hirsch; David P. Carbone; Kevin A. Schulman

The burden of cancer is growing, and the disease is becoming a major economic expenditure for all developed countries. In 2008, the worldwide cost of cancer due to premature death and disability (not including direct medical costs) was estimated to be US


Nature Communications | 2016

The somatic mutation profiles of 2,433 breast cancers refines their genomic and transcriptomic landscapes

Bernard Pereira; Suet Feung Chin; Oscar M. Rueda; Hans Kristian Moen Vollan; Elena Provenzano; Helen Bardwell; Michelle Pugh; Linda Jones; Roslin Russell; Stephen John Sammut; Dana W.Y. Tsui; Bin Liu; Sarah-Jane Dawson; Jean Abraham; Helen Northen; John F. Peden; Abhik Mukherjee; Gulisa Turashvili; Andrew R. Green; Steve McKinney; Arusha Oloumi; Sohrab P. Shah; Nitzan Rosenfeld; Leigh C. Murphy; David R. Bentley; Ian O. Ellis; Arnie Purushotham; Sarah Pinder; Anne Lise Børresen-Dale; Helena M. Earl

895 billion. This is not simply due to an increase in absolute numbers, but also the rate of increase of expenditure on cancer. What are the drivers and solutions to the so-called cancer-cost curve in developed countries? How are we going to afford to deliver high quality and equitable care? Here, expert opinion from health-care professionals, policy makers, and cancer survivors has been gathered to address the barriers and solutions to delivering affordable cancer care. Although many of the drivers and themes are specific to a particular field-eg, the huge development costs for cancer medicines-there is strong concordance running through each contribution. Several drivers of cost, such as over-use, rapid expansion, and shortening life cycles of cancer technologies (such as medicines and imaging modalities), and the lack of suitable clinical research and integrated health economic studies, have converged with more defensive medical practice, a less informed regulatory system, a lack of evidence-based sociopolitical debate, and a declining degree of fairness for all patients with cancer. Urgent solutions range from re-engineering of the macroeconomic basis of cancer costs (eg, value-based approaches to bend the cost curve and allow cost-saving technologies), greater education of policy makers, and an informed and transparent regulatory system. A radical shift in cancer policy is also required. Political toleration of unfairness in access to affordable cancer treatment is unacceptable. The cancer profession and industry should take responsibility and not accept a substandard evidence base and an ethos of very small benefit at whatever cost; rather, we need delivery of fair prices and real value from new technologies.


British Journal of Surgery | 2008

A model for predicting non-sentinel lymph node metastatic disease when the sentinel lymph node is positive

A Pal; Elena Provenzano; Stephen W. Duffy; Sarah Pinder; Arnie Purushotham

The genomic landscape of breast cancer is complex, and inter- and intra-tumour heterogeneity are important challenges in treating the disease. In this study, we sequence 173 genes in 2,433 primary breast tumours that have copy number aberration (CNA), gene expression and long-term clinical follow-up data. We identify 40 mutation-driver (Mut-driver) genes, and determine associations between mutations, driver CNA profiles, clinical-pathological parameters and survival. We assess the clonal states of Mut-driver mutations, and estimate levels of intra-tumour heterogeneity using mutant-allele fractions. Associations between PIK3CA mutations and reduced survival are identified in three subgroups of ER-positive cancer (defined by amplification of 17q23, 11q13–14 or 8q24). High levels of intra-tumour heterogeneity are in general associated with a worse outcome, but highly aggressive tumours with 11q13–14 amplification have low levels of intra-tumour heterogeneity. These results emphasize the importance of genome-based stratification of breast cancer, and have important implications for designing therapeutic strategies.


Lancet Oncology | 2014

Challenges to effective cancer control in China, India, and Russia

Paul E. Goss; Kathrin Strasser-Weippl; Brittany L. Lee-Bychkovsky; Lei Fan; Junjie Li; Yanin Chavarri-Guerra; Pedro E.R. Liedke; C.S. Pramesh; Tanja Badovinac-Crnjevic; Yuri Sheikine; Zhu Chen; You-Lin Qiao; Zhiming Shao; Yi-Long Wu; Daiming Fan; Louis W.C. Chow; Jun Wang; Qiong Zhang; Shiying Yu; Gordon Shen; Jie He; Arnie Purushotham; Richard Sullivan; Rajendra A. Badwe; Shripad Banavali; Reena Nair; Lalit Kumar; Purvish M. Parikh; Somasundarum Subramanian; Pankaj Chaturvedi

Women with axillary sentinel lymph node (SLN)‐positive breast cancer usually undergo completion axillary lymph node dissection (ALND). However, not all patients with positive SLNs have further axillary nodal disease. Therefore, in the patients with low risk of further disease, completion ALND could be avoided. The Memorial Sloan‐Kettering Cancer Center (MSKCC) developed a nomogram to estimate the risk of non‐SLN disease. This study critically appraised the nomogram and refined the model to improve predictive accuracy.


Lancet Oncology | 2015

Global cancer surgery: delivering safe, affordable, and timely cancer surgery

Richard Sullivan; Olusegun I. Alatise; Benjamin O. Anderson; Riccardo A. Audisio; Philippe Autier; Ajay Aggarwal; Charles M. Balch; Murray F. Brennan; Anna J. Dare; Anil D'Cruz; Alexander M.M. Eggermont; Kenneth A. Fleming; Serigne Magueye Gueye; Lars Hagander; Cristian A Herrera; Hampus Holmer; André M. Ilbawi; Anton Jarnheimer; Jiafu Ji; T. Peter Kingham; Jonathan Liberman; Andrew J M Leather; John G. Meara; Swagoto Mukhopadhyay; Ss Murthy; Sherif Omar; Groesbeck P. Parham; Cs Pramesh; Robert Riviello; Danielle Rodin

Cancer is one of the major non-communicable diseases posing a threat to world health. Unfortunately, improvements in socioeconomic conditions are usually associated with increased cancer incidence. In this Commission, we focus on China, India, and Russia, which share rapidly rising cancer incidence and have cancer mortality rates that are nearly twice as high as in the UK or the USA, vast geographies, growing economies, ageing populations, increasingly westernised lifestyles, relatively disenfranchised subpopulations, serious contamination of the environment, and uncontrolled cancer-causing communicable infections. We describe the overall state of health and cancer control in each country and additional specific issues for consideration: for China, access to care, contamination of the environment, and cancer fatalism and traditional medicine; for India, affordability of care, provision of adequate health personnel, and sociocultural barriers to cancer control; and for Russia, monitoring of the burden of cancer, societal attitudes towards cancer prevention, effects of inequitable treatment and access to medicine, and a need for improved international engagement.


British Journal of Surgery | 2005

Neoadjuvant chemotherapy in breast cancer

H. Charfare; S. Limongelli; Arnie Purushotham

Surgery is essential for global cancer care in all resource settings. Of the 15.2 million new cases of cancer in 2015, over 80% of cases will need surgery, some several times. By 2030, we estimate that annually 45 million surgical procedures will be needed worldwide. Yet, less than 25% of patients with cancer worldwide actually get safe, affordable, or timely surgery. This Commission on global cancer surgery, building on Global Surgery 2030, has examined the state of global cancer surgery through an analysis of the burden of surgical disease and breadth of cancer surgery, economics and financing, factors for strengthening surgical systems for cancer with multiple-country studies, the research agenda, and the political factors that frame policy making in this area. We found wide equity and economic gaps in global cancer surgery. Many patients throughout the world do not have access to cancer surgery, and the failure to train more cancer surgeons and strengthen systems could result in as much as US


Lancet Oncology | 2014

The growing burden of cancer in India: epidemiology and social context.

Mohandas K. Mallath; David G Taylor; Rajendra A. Badwe; Goura K. Rath; Viswanathan Shanta; C.S. Pramesh; Raghunadharao Digumarti; Paul Sebastian; Bibhuti B Borthakur; Ashok Kalwar; Sanjay Kapoor; Shaleen Kumar; Jennifer L. Gill; Moni Abraham Kuriakose; Hemant Malhotra; Suresh C. Sharma; Shilin Shukla; Lokesh Viswanath; Raju Titus Chacko; Jeremy Pautu; Kenipakapatnam S Reddy; Kailash S Sharma; Arnie Purushotham; Richard Sullivan

6.2 trillion in lost cumulative gross domestic product by 2030. Many of the key adjunct treatment modalities for cancer surgery--e.g., pathology and imaging--are also inadequate. Our analysis identified substantial issues, but also highlights solutions and innovations. Issues of access, a paucity of investment in public surgical systems, low investment in research, and training and education gaps are remarkably widespread. Solutions include better regulated public systems, international partnerships, super-centralisation of surgical services, novel surgical clinical trials, and new approaches to improve quality and scale up cancer surgical systems through education and training. Our key messages are directed at many global stakeholders, but the central message is that to deliver safe, affordable, and timely cancer surgery to all, surgery must be at the heart of global and national cancer control planning.


British Journal of Cancer | 2004

Can breast MRI help in the management of women with breast cancer treated by neoadjuvant chemotherapy

Ruth Warren; L G Bobrow; Helena M. Earl; P.D. Britton; D Gopalan; Arnie Purushotham; Gordon Wishart; John R Benson; William Hollingworth

Neoadjuvant chemotherapy for breast cancer was originally used in locally advanced inoperable disease in order to achieve surgical resection. It was then extended to operable breast cancer with a view to downstaging tumours to facilitate breast‐conserving surgery. Increasingly, it is being considered as a treatment for earlier‐stage disease.

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G.C. Wishart

Cambridge University Hospitals NHS Foundation Trust

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A. Michael Peters

Brighton and Sussex Medical School

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Chandra K. Solanki

Cambridge University Hospitals NHS Foundation Trust

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