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Anne-Marie Martin
Researcher at GlaxoSmithKline
Publications - 60
Citations - 12717
Anne-Marie Martin is an academic researcher from GlaxoSmithKline. The author has contributed to research in topics: Dabrafenib & Lapatinib. The author has an hindex of 30, co-authored 60 publications receiving 11395 citations. Previous affiliations of Anne-Marie Martin include University of Pennsylvania & Mount Vernon Hospital.
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Journal ArticleDOI
Dabrafenib in BRAF-mutated metastatic melanoma: a multicentre, open-label, phase 3 randomised controlled trial
Axel Hauschild,Jean-Jacques Grob,Lev V. Demidov,Thomas Jouary,Ralf Gutzmer,Michael Millward,Piotr Rutkowski,Christian U. Blank,Wilson H. Miller,Eckhart Kaempgen,Salvador Martín-Algarra,Boguslawa Karaszewska,Cornelia Mauch,Vanna Chiarion-Sileni,Anne-Marie Martin,Suzanne Swann,Patricia Haney,Beloo Mirakhur,Mary E. Guckert,Vicki L. Goodman,Paul B. Chapman +20 more
TL;DR: Dabrafenib significantly improved progression-free survival compared with dacarbazine, and skin-related toxic effects, fever, fatigue, arthralgia, and headache were uncommon in both groups.
Journal ArticleDOI
Improved Overall Survival in Melanoma with Combined Dabrafenib and Trametinib
Caroline Robert,Boguslawa Karaszewska,Jacob Schachter,Piotr Rutkowski,Andrzej Mackiewicz,Daniil Stroiakovski,Michael Lichinitser,Reinhard Dummer,Florent Grange,Laurent Mortier,Vanna Chiarion-Sileni,Kamil Drucis,Ivana Krajsová,Axel Hauschild,Paul Lorigan,Pascal Wolter,Georgina V. Long,Keith T. Flaherty,Paul Nathan,Antoni Ribas,Antoni Ribas,Anne-Marie Martin,Peng Sun,Wendy A. Crist,Jeff Legos,Stephen D. Rubin,Shonda M Little,Dirk Schadendorf +27 more
TL;DR: Dabrafenib plus trametinib, as compared with vemurafenib monotherapy, significantly improved overall survival in previously untreated patients with metastatic melanoma with BRAF V600E or V600K mutations, without increased overall toxicity.
Journal ArticleDOI
Improved Survival with MEK Inhibition in BRAF-Mutated Melanoma
Keith T. Flaherty,Caroline Robert,Peter Hersey,Paul C. Nathan,Claus Garbe,Mohammed M. Milhem,Lev V. Demidov,Jessica C. Hassel,Piotr Rutkowski,Peter Mohr,Reinhard Dummer,Uwe Trefzer,James Larkin,Jochen Utikal,Brigitte Dréno,Marta Nyakas,Mark R. Middleton,Juergen C. Becker,Michelle Casey,Laurie Sherman,Frank S. Wu,Daniele Ouellet,Anne-Marie Martin,Kiran Patel,Dirk Schadendorf +24 more
TL;DR: Tametinib, as compared with chemotherapy, improved rates of progression-free and overall survival among patients who had metastatic melanoma with a BRAF V600E or V600K mutation.
Journal ArticleDOI
Combined BRAF and MEK Inhibition versus BRAF Inhibition Alone in Melanoma
Georgina V. Long,Daniil Stroyakovskiy,Helen Gogas,Evgeny Levchenko,F. de Braud,James Larkin,Claus Garbe,T. Jouary,Axel Hauschild,Jean-Jacques Grob,V. Chiarion Sileni,Céleste Lebbé,Mario Mandalà,Michael Millward,Ana Arance,Igor Bondarenko,John B. A. G. Haanen,Johan Hansson,Jochen Utikal,Virginia Ferraresi,Nadezhda Kovalenko,Peter Mohr,V. Probachai,Dirk Schadendorf,Paul Nathan,Caroline Robert,Antoni Ribas,Douglas J. DeMarini,Jhangir G. Irani,Michelle Casey,Daniele Ouellet,Anne-Marie Martin,Ngocdiep T. Le,Kiran Patel,Keith T. Flaherty +34 more
TL;DR: A combination of dabraenib and trametinib, as compared with dabrafenib alone, improved the rate of progression-free survival in previously untreated patients who had metastatic melanoma with BRAF V600E or V600K mutations.
Journal ArticleDOI
Dabrafenib in patients with Val600Glu or Val600Lys BRAF-mutant melanoma metastatic to the brain (BREAK-MB): a multicentre, open-label, phase 2 trial
Georgina V. Long,Uwe Trefzer,Michael A. Davies,Richard F. Kefford,Paolo A. Ascierto,Paul B. Chapman,Igor Puzanov,Axel Hauschild,Caroline Robert,Alain Algazi,Laurent Mortier,Hussein Tawbi,Tabea Wilhelm,Lisa Zimmer,Julie Switzky,Suzanne Swann,Anne-Marie Martin,Mary E. Guckert,Vicki L. Goodman,Michael R. W. Streit,John M. Kirkwood,Dirk Schadendorf +21 more
TL;DR: Dabrafenib has activity and an acceptable safety profile in patients with Val600Glu BRAF-mutant melanoma and brain metastases irrespective of whether they are untreated or have been previously treated but have progressed.