A. J. Norton
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Publications of the Astronomical Society of the Pacific | 2006
Don Pollacco; I. Skillen; A. Collier Cameron; D. J. Christian; C. Hellier; J. Irwin; T. A. Lister; R. A. Street; Richard G. West; D. R. Anderson; W. I. Clarkson; H. J. Deeg; B. Enoch; A. Evans; A. Fitzsimmons; C. A. Haswell; Simon T. Hodgkin; K. Horne; Stephen R. Kane; F. P. Keenan; P. F. L. Maxted; A. J. Norton; Julian P. Osborne; N. Parley; R. Ryans; B. Smalley; P. J. Wheatley; D. M. Wilson
ABSTRACT The SuperWASP cameras are wide‐field imaging systems at the Observatorio del Roque de los Muchachos on the island of La Palma in the Canary Islands, and at the Sutherland Station of the South African Astronomical Observatory. Each instrument has a field of view of some 482 deg2 with an angular scale of 13 \documentclass{aastex} \usepackage{amsbsy} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{bm} \usepackage{mathrsfs} \usepackage{pifont} \usepackage{stmaryrd} \usepackage{textcomp} \usepackage{portland,xspace} \usepackage{amsmath,amsxtra} \usepackage[OT2,OT1]{fontenc} \newcommand\cyr{ \renewcommand\rmdefault{wncyr} \renewcommand\sfdefault{wncyss} \renewcommand\encodingdefault{OT2} \normalfont \selectfont} \DeclareTextFontCommand{\textcyr}{\cyr} \pagestyle{empty} \DeclareMathSizes{10}{9}{7}{6} \begin{document} \landscape
Journal of Clinical Oncology | 2007
Daphne de Jong; Andreas Rosenwald; Mukesh Chhanabhai; Philippe Gaulard; Wolfram Klapper; Abigail Lee; Birgitta Sander; Christoph Thorns; Elias Campo; Thierry Molina; A. J. Norton; Anton Hagenbeek; Sandra J. Horning; Andrew Lister; John Raemaekers; Randy D. Gascoyne; Gilles Salles; Edie Weller
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Journal of Clinical Oncology | 2007
Silvia Montoto; Andrew Davies; Janet Matthews; Maria Calaminici; A. J. Norton; J. Amess; Sarah Vinnicombe; Rachel Waters; A. Z. S. Rohatiner; T. Andrew Lister
\end{document} 7 pixel−1, and is capable of delivering photometry with accuracy better than 1% for objects having \documentclass{aastex} \usepackage{amsbsy} \usepa...
The Astrophysical Journal | 2009
L. Hebb; Andrew Collier-Cameron; B. Loeillet; Don Pollacco; G. Hébrard; R. A. Street; F. Bouchy; H. C. Stempels; C. Moutou; E. K. Simpson; S. Udry; Y. C. Joshi; Richard G. West; I. Skillen; D. M. Wilson; I. McDonald; N. P. Gibson; S. Aigrain; D. R. Anderson; Chris R. Benn; D. J. Christian; B. Enoch; C. A. Haswell; C. Hellier; K. Horne; J. Irwin; T. A. Lister; P. F. L. Maxted; Michel Mayor; A. J. Norton
PURPOSE The results of immunohistochemical class prediction and prognostic stratification of diffuse large B-cell lymphoma (DLBCL) have been remarkably various thus far. Apart from biologic variations, this may be caused by differences in laboratory techniques, scoring definitions, and inter- and intraobserver variations. In this study, an international collaboration of clinical lymphoma research groups from Europe, United States, and Canada concentrated on validation and standardization of immunohistochemistry of the currently potentially interesting prognostic markers in DLBCL. PATIENTS AND METHODS Sections of a tissue microarray from 36 patients with DLBCL were stained in eight laboratories with antibodies to CD20, CD5, bcl-2, bcl-6, CD10, HLA-DR, MUM1, and MIB-1 according to local methods. The study was performed in two rounds firstly focused on the evaluation of laboratory staining variation and secondly on the scoring variation. RESULTS Different laboratory staining techniques resulted in unexpectedly highly variable results and very poor reproducibility in scoring for almost all markers. No single laboratory stood out as uniformly poor or excellent. With elimination of variation due to staining, high agreement was found for CD20, HLA-DR, and CD10. Poor agreement was found for bcl-6 and Ki-67. Optimization of techniques and uniformly agreed on scoring criteria improved reproducibility. CONCLUSION This study shows that semiquantitative immunohistochemistry for subclassification of DLBCL is feasible and reproducible, but exhibits varying rates of concordance for different markers. These findings may explain the wide variation of biomarker prognostic impact reported in the literature. Harmonization of techniques and centralized consensus review appears mandatory when using immunohistochemical biomarkers for treatment stratification.
Journal of Clinical Oncology | 2006
Abigail Lee; Andrew Clear; Maria Calaminici; Andrew Davies; Suzanne Jordan; Finlay MacDougall; Janet Matthews; A. J. Norton; John G. Gribben; T. Andrew Lister; Lindsey K. Goff
PURPOSE To study the clinical significance of transformation to diffuse large B-cell lymphoma (DLBCL) in patients with follicular lymphoma (FL). PATIENTS AND METHODS From 1972 to 1999, 325 patients were diagnosed with FL at St Bartholomews Hospital (London, United Kingdom). With a median follow-up of 15 years, progression occurred in 186 patients and biopsy-proven transformation in 88 of the 325. The overall repeat biopsy rate was 70%. RESULTS The risk of histologic transformation (HT) by 10 years was 28%, HT not yet having been observed after 16.2 years. The risk was higher in patients with advanced stage (P = .02), high-risk Follicular Lymphoma International Prognostic Index (FLIPI; P = .01), and International Prognostic Index (IPI; P = .04) scores at diagnosis. Expectant management (as opposed to treatment being initiated at diagnosis) also predicted for a higher risk of HT (P = .008). Older age (P = .005), low hemoglobin level (P = .03), high lactate dehydrogenase (P < .0001), and high-risk FLIPI (P = .01) or IPI (P = .003) score at the time of first recurrence were associated with the diagnosis of HT in a biopsy performed at that time. The median survival from transformation was 1.2 years. Patients with HT had a shorter overall survival (P < .0001) and a shorter survival from progression (P < .0001) than did those in whom it was not diagnosed. CONCLUSION Advanced stage and high-risk FLIPI and IPI scores at diagnosis correlate with an increased risk of HT. This event strongly influences the outcome of patients with FL by shortening their survival. There may be a subgroup of patients in whom HT does not occur.
Monthly Notices of the Royal Astronomical Society | 2007
A. Collier Cameron; F. Bouchy; G. Hébrard; P. F. L. Maxted; Don Pollacco; Frederic Pont; I. Skillen; B. Smalley; R. A. Street; Richard G. West; D. M. Wilson; Suzanne Aigrain; D. J. Christian; W. I. Clarkson; B. Enoch; A. Evans; A. Fitzsimmons; M. Fleenor; Michaël Gillon; C. A. Haswell; L. Hebb; C. Hellier; Simon T. Hodgkin; K. Horne; J. Irwin; S. R. Kane; F. P. Keenan; B. Loeillet; Tim Lister; Michel Mayor
We report on the discovery of WASP-12b, a new transiting extrasolar planet with R pl = 1.79+0.09 –0.09 RJ and M pl = 1.41+0.10 –0.10 M J. The planet and host star properties were derived from a Monte Carlo Markov Chain analysis of the transit photometry and radial velocity data. Furthermore, by comparing the stellar spectrum with theoretical spectra and stellar evolution models, we determined that the host star is a supersolar metallicity ([M/H] = 0.3+0.05 –0.15), late-F (T eff = 6300+200 –100 K) star which is evolving off the zero-age main sequence. The planet has an equilibrium temperature of T eq = 2516 K caused by its very short period orbit (P = 1.09 days) around the hot, twelfth magnitude host star. WASP-12b has the largest radius of any transiting planet yet detected. It is also the most heavily irradiated and the shortest period planet in the literature.
Journal of Clinical Oncology | 1999
James M. Foran; A. Z. S. Rohatiner; Bertrand Coiffier; Tiziano Barbui; Stephen A. Johnson; Wolfgang Hiddemann; John Radford; A. J. Norton; Susan M. Tollerfield; Martin P. Wilson; T. Andrew Lister
PURPOSE To examine the immune microenvironment in diagnostic follicular lymphoma (FL) biopsies and evaluate its prognostic significance. PATIENTS AND METHODS Immunohistochemistry was used to study numbers and location of cells staining positive for immune cell markers CD4, CD7, CD8, CD25, CD68, forkhead box protein P3 (FOXP3), T-cell intracellular antigen-1, and Granzyme B in tissue microarrays of paraffin-embedded, diagnostic lymph node biopsies taken from 59 FL patients who lived less than 5 years (short-survival group; n = 34) and more than 15 years (long-survival group; n = 25). RESULTS CD4 and FOXP3 expression were significantly different between the two groups. Samples from the long-survival group were more likely than those from the short-survival group to have CD4+ staining cells and to have FOXP3-positive cells in a perifollicular location. CONCLUSION This study has identified differences in immune cell composition of the diagnostic FL lymph node immune microenvironment and these have the potential for use as prognostic biomarkers in a routine histopathology setting.
Monthly Notices of the Royal Astronomical Society | 2008
Don Pollacco; I. Skillen; A. Collier Cameron; B. Loeillet; H. C. Stempels; F. Bouchy; N. P. Gibson; L. Hebb; G. Hébrard; Y. C. Joshi; I. McDonald; B. Smalley; A. M. S. Smith; R. A. Street; S. Udry; Richard G. West; D. M. Wilson; P. J. Wheatley; Suzanne Aigrain; K. Alsubai; Chris R. Benn; V. A. Bruce; D. J. Christian; W. I. Clarkson; B. Enoch; A. Evans; A. Fitzsimmons; C. A. Haswell; C. Hellier; Samantha Hickey
We have detected low-amplitude radial-velocity variations in two stars, USNO-B1.0 1219‐ 0005465 (GSC 02265‐00107 = WASP‐1) and USNO-B1.0 0964‐0543604 (GSC 00522‐ 01199 = WASP‐2). Both stars were identified as being likely host stars of transiting exoplanets in the 2004 SuperWASP wide-field transit survey. Using the newly commissioned radial-velocity spectrograph SOPHIE at the Observatoire de Haute-Provence, we found that both objects exhibit reflex orbital radial-velocity variations with amplitudes characteristic of planetary-mass companions and in-phase with the photometric orbits. Line-bisector studies rule out faint blended binaries as the cause of either the radial-velocity variations or the transits. We perform preliminary spectral analyses of the host stars, which together with their radialvelocity variations and fits to the transit light curves yield estimates of the planetary masses and radii. WASP-1b and WASP-2b have orbital periods of 2.52 and 2.15 d, respectively. Given mass estimates for their F7V and K1V primaries, we derive planet masses 0.80‐0.98 and 0.81‐ 0.95 times that of Jupiter, respectively. WASP-1b appears to have an inflated radius of at least 1.33 RJup, whereas WASP-2b has a radius in the range 0.65‐1.26 RJup.
Scopus | 2009
L. Hebb; Andrew Collier-Cameron; H. C. Stempels; B. Enoch; K. Horne; N. Parley; B. Loeillet; C. Moutou; Don Pollacco; E. K. Simpson; Y. C. Joshi; N. P. Gibson; D. J. Christian; G. Hébrard; Francois Bouchy; R. A. Street; T. A. Lister; S. Udry; M. Mayor; D. Queloz; Richard G. West; I. Skillen; Chris R. Benn; D. M. Wilson; I. McDonald; Anderson; C. Hellier; P. F. L. Maxted; B. Smalley; S. Aigrain
PURPOSE Fludarabine phosphate (F-AMP) has significant activity in follicular lymphoma and in B-cell chronic lymphatic leukemia, where it has demonstrated high complete response (CR) rates. Lymphoplasmacytoid (LPC) lymphoma, Waldenstroms macroglobulinemia (WM), and mantle-cell lymphoma (MCL) also present with advanced-stage disease and are incurable with standard alkylator-based chemotherapy. A phase II trial was undertaken to determine the activity of F-AMP in patients newly diagnosed with these diseases. PATIENTS AND METHODS Between 1992 and 1996, 78 patients (aged 18 to 75 years) received intravenous F-AMP (25 mg/m2/d for 5 days, every 4 weeks) until maximum response, plus two further cycles as consolidation. The primary end point was response rate; secondary end points included time to progression (TTP), duration of response, and overall survival (OS). RESULTS Forty-four (62%) of 71 assessable patients had a response to F-AMP (LPC lymphoma, 63%; WM, 79%; MCL, 41%); the CR rate was 15%. At a median follow-up of 1.5 years, 19 of 44 responding patients have had progression of lymphoma; the median duration of response was 2.5 years. The median survival has not yet been reached. There was no significant difference in the duration of response or OS between patients with different histologies; TTP was shorter in patients with MCL (P = .015). Myelosuppression was relatively common, and the treatment-related mortality (TRM) was 5%, mostly associated with pancytopenia and infection. CONCLUSION Single-agent fludarabine phosphate is active in previously untreated LPC lymphoma and WM, with only moderate activity in MCL. However, the CR rate is low, and the TRM is relatively high. Its role in combination chemotherapy remains to be demonstrated.
Monthly Notices of the Royal Astronomical Society | 2006
A. Collier Cameron; Don Pollacco; R. A. Street; Tim Lister; Richard G. West; D. M. Wilson; F. Pont; D. J. Christian; W. I. Clarkson; B. Enoch; A. Evans; A. Fitzsimmons; C. A. Haswell; C. Hellier; Simon T. Hodgkin; K. Horne; J. Irwin; S. R. Kane; F. P. Keenan; A. J. Norton; N. Parley; J. P. Osborne; R. Ryans; I. Skillen; P. J. Wheatley
We report the discovery of WASP-3b, the third transiting exoplanet to be discovered by the WASP and SOPHIE collaboration. WASP-3b transits its host star USNO-B1.0 1256−0285133 every 1.846 834 ± 0.000 002 d. Our high-precision radial velocity measurements present a variation with amplitude characteristic of a planetary-mass companion and in phase with the light curve. Adaptive optics imaging shows no evidence for nearby stellar companions, and line-bisector analysis excludes faint, unresolved binarity and stellar activity as the cause of the radial velocity variations. We make a preliminary spectroscopic analysis of the host star and find it to have T eff = 6400 ± 100 K and log g = 4.25 ± 0.05 which suggests it is most likely an unevolved main-sequence star of spectral type F7-8V. Our simultaneous modelling of the transit photometry and reflex motion of the host leads us to derive a mass of 1.76 +0.08 −0.14 MJ and radius 1.31 +0.07 −0.14 RJ for WASP-3b. The proximity and relative temperature of the host star suggests that WASP-3b is one of the hottest exoplanets known, and thus has the potential to place stringent constraints on exoplanet atmospheric models.