K
Katja Schulze
Researcher at Genentech
Publications - 48
Citations - 1159
Katja Schulze is an academic researcher from Genentech. The author has contributed to research in topics: Atezolizumab & Medicine. The author has an hindex of 10, co-authored 31 publications receiving 470 citations.
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Journal ArticleDOI
Pertuzumab plus trastuzumab for HER2-amplified metastatic colorectal cancer (MyPathway): an updated report from a multicentre, open-label, phase 2a, multiple basket study.
Funda Meric-Bernstam,Herbert Hurwitz,Kanwal Pratap Singh Raghav,Robert R. McWilliams,Marwan Fakih,Ari M. Vanderwalde,Charles Swanton,Razelle Kurzrock,Howard A. Burris,Christopher Sweeney,Ron Bose,David R. Spigel,Mary Beattie,Steven Blotner,Alyssa Stone,Katja Schulze,Vaikunth Cuchelkar,John D. Hainsworth +17 more
TL;DR: Dual HER2-targeted therapy with pertuzumab plus trastuzumAB is well tolerated and could represent a therapeutic opportunity for patients with heavily pretreated, Her2-amplified metastatic colorectal cancer.
Journal ArticleDOI
Pertuzumab and trastuzumab for HER2-positive, metastatic biliary tract cancer (MyPathway): a multicentre, open-label, phase 2a, multiple basket study
Milind Javle,Mitesh J. Borad,Nilofer S. Azad,Razelle Kurzrock,Ghassan K. Abou-Alfa,Ghassan K. Abou-Alfa,Ben George,John D. Hainsworth,Funda Meric-Bernstam,Charles Swanton,Christopher Sweeney,Claire F. Friedman,Claire F. Friedman,Ron Bose,David R. Spigel,Yong Wang,Jonathan Levy,Katja Schulze,Vaikunth Cuchelkar,Arisha Patel,Howard A. Burris +20 more
TL;DR: The MyPathway trial as discussed by the authors evaluated the activity of US Food and Drug Administration-approved therapies in non-indicated tumours with potentially actionable molecular alterations, including HER2 amplification, overexpression, or both treated with a dual anti-HER2 regimen.
Journal ArticleDOI
Neoadjuvant atezolizumab in resectable non-small cell lung cancer (NSCLC): Interim analysis and biomarker data from a multicenter study (LCMC3).
David J. Kwiatkowski,Valerie W. Rusch,Jamie E. Chaft,Bruce E. Johnson,Alan Nicholas,Ignacio I. Wistuba,Robert E. Merritt,Jay M. Lee,Paul A. Bunn,Yan Tang,S. Phan,Saiama N. Waqar,Alexander Patterson,Eric B. Haura,Eric M. Toloza,Karen L. Reckamp,Dan J. Raz,Katja Schulze,A. Johnson,David P. Carbone +19 more
TL;DR: A large multicentre trial has shown that preoperative immune checkpoint inhibitor therapy may be of benefit in early-stage NSCLC and aims to extend the scope of this study to include further studies in patients with recurrent NSCLCs.
Journal ArticleDOI
Oncogene-specific differences in tumor mutational burden, PD-L1 expression, and outcomes from immunotherapy in non-small cell lung cancer.
Marcelo V. Negrao,Ferdinandos Skoulidis,Meagan Montesion,Katja Schulze,Ilze Bara,Vincent Shen,Hao Xu,Sylvia Hu,Dawen Sui,Yasir Elamin,Xiuning Le,Michael E. Goldberg,Karthikeyan Murugesan,Chang-Jiun Wu,Jianhua Zhang,David S. Barreto,Jacqulyne P. Robichaux,Alexandre Reuben,Tina Cascone,Kyle G. Mitchell,Lingzhi Hong,Waree Rinsurongkawong,Jack A. Roth,Stephen G. Swisher,Jack Lee,Anne Tsao,Vassiliki A. Papadimitrakopoulou,Don L. Gibbons,Bonnie S. Glisson,Gaurav Singal,Vincent A. Miller,Brian M. Alexander,Garrett M. Frampton,Lee A. Albacker,David S. Shames,Jianjun Zhang,John V. Heymach +36 more
TL;DR: In this article, the authors investigated oncogene-specific differences in these markers and clinical outcome and found that high TMB and PD-L1 expression are predictive for benefit from immune checkpoint blockade (ICB) treatment in non-small cell lung cancer.
Journal ArticleDOI
Targeted therapy for advanced salivary gland carcinoma based on molecular profiling: results from MyPathway, a phase IIa multiple basket study.
Razelle Kurzrock,Daniel W. Bowles,Hyunseok Kang,Funda Meric-Bernstam,John D. Hainsworth,David R. Spigel,Ron Bose,H. A. Burris,Christopher Sweeney,Michael S. Beattie,Steven Blotner,Katja Schulze,Vaikunth Cuchelkar,Charles Swanton +13 more
TL;DR: It is suggested that matched targeted therapy for SGC has promising efficacy, supporting molecular profiling in treatment determination and the clinical benefit rate was 67% and the median progression-free survival was 8.6 months.