Hans-Peter Goertz
Genentech
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Publication
Featured researches published by Hans-Peter Goertz.
Cancer | 2018
Maria Pisu; Andres Azuero; Karina I. Halilova; Courtney P. Williams; Kelly Kenzik; Elizabeth Kvale; Grant R. Williams; Karen Meneses; Margaret M. Sullivan; Supriya Kumar Yagnik; Hans-Peter Goertz; Gabrielle Betty Rocque
As the population of older adults with cancer continues to grow, the most important factors contributing to their health‐related quality of life (HRQOL) remain unclear.
Drugs - real world outcomes | 2017
Nicholas J. Robert; Hans-Peter Goertz; Pooja Chopra; Xiaolong Jiao; Bongin Yoo; Debra A. Patt; Vincent Antao
BackgroundPertuzumab (Perjeta®), a HER2/neu receptor antagonist, was approved by the US Food and Drug Administration in June 2012 for use in the first-line setting for patients with HER2-positive metastatic breast cancer (mBC).ObjectiveThis retrospective study investigated the clinical and demographic characteristics, treatment patterns, safety, and clinical outcomes for patients with HER2-positive mBC who received pertuzumab in the first-line setting in US community oncology practices.MethodsPatients with HER2-positive mBC, who initiated pertuzumab within 60 days of mBC diagnosis between June 2012 and June 2014, followed through December 2014, had ≥2 visits within the McKesson Specialty Health/US Oncology Network, and were not on clinical trials during the study period, were eligible. This study utilized iKnowMed electronic health records, Claims Data Warehouse, and Social Security Death Index. Progression-free survival (PFS) was assessed by Kaplan–Meier methods.ResultsA total of 266 patients met the selection criteria. A vast majority of the patients (249/266, 93.6%) received a trastuzumab + pertuzumab + taxane (H + P + T) regimen. The number of patients with prior adjuvant/neoadjuvant therapy was higher than the CLEOPATRA trial, but age (median 57 years) and percentage of visceral disease (74.8%) were similar. The most common adverse events were fatigue (50.8%), diarrhea (44.7%), nausea (35.3%), peripheral neuropathy (33.5%), neutropenia (24.9%), and rash (24.4%). The median PFS was 16.9 months (95% CI 14.2–19.7).ConclusionsIn this retrospective study of patients with HER2-positive mBC receiving pertuzumab in the first-line setting, most patients were treated with H + P + T. The safety and PFS of H + P + T were consistent with those observed in the pivotal trial.
Drugs - real world outcomes | 2016
Orsolya Lunacsek; Arliene Ravelo; Anna D. Coutinho; Sebastien J. Hazard; Mark R. Green; Joanne Willey; Michael Eaddy; Hans-Peter Goertz
BackgroundReal-world evidence is lacking on the impact of bevacizumab added to carboplatin/paclitaxel (Bev + CP) therapy versus CP alone for patients with non-squamous non-small cell lung cancer (NS-NSCLC), particularly in those excluded from clinical trials.MethodsThis is a retrospective electronic medical record analysis of patients who received first-line therapy with Bev + CP or CP between 1 October 2006 and 30 June 2013. We identified four subsets: elderly patients (≥65 years), patients with brain/central nervous system (CNS) metastases, patients with Eastern Cooperative Oncology Group performance status (ECOG PS) ≥2, and patients receiving anticoagulation. We used descriptive statistics to describe patient characteristics and treatment patterns and evaluated progression-free survival (PFS) and overall survival (OS) using survival analyses.ResultsThe study included 431 patients (Bev + CP: 231; CP: 200). The Bev + CP cohort was more likely to receive four or more cycles of induction therapy (72 vs. 50 %) and was more likely to receive maintenance therapy (45 vs. 21 %) than patients receiving CP. In the overall population, median PFS and OS were significantly longer in the Bev + CP cohort than in the CP cohort: 6.7 vs. 5.1 months (hazard ratio [HR] 0.74; 95 % confidence interval [CI] 0.59–0.92; p = 0.008) and 11.9 vs. 9.0 months (HR 0.57; 95 % CI 0.44–0.73; p < 0.001), respectively. Treatment with Bev + CP in patients aged ≥65 years and in those with brain/CNS metastases was also associated with a significant risk reduction in PFS (35 and 51 %, respectively; p < 0.05 for both) and OS (46 and 62 %, respectively; p < 0.05 for both) compared with CP alone.ConclusionBev + CP is associated with a significant improvement in PFS and OS in patients with NS-NSCLC and in subsets with brain/CNS metastases and those aged ≥65 years.
Journal of General Internal Medicine | 2015
Christina Brzezniak; Sacha Satram-Hoang; Hans-Peter Goertz; Carolina Reyes; Ashok Gunuganti; Christopher Gallagher; Corey A. Carter
Journal of Clinical Oncology | 2017
David L. Veenstra; Preeti S. Bajaj; Josh J. Carlson; Hans-Peter Goertz
Annals of Surgical Oncology | 2016
Eleftherios P. Mamounas; Christine Poulos; Hans-Peter Goertz; Juan Marcos Gonzalez; Amy Pugh; Vincent Antao
Journal of Clinical Oncology | 2018
Hans-Peter Goertz; Daniel Sheinson; Ning Wu
Journal of Clinical Oncology | 2017
Carolina Reyes; Minghan Dai; Hans-Peter Goertz; Keith L Dawson; John Hornberger
Journal of Clinical Oncology | 2017
Hannah Staunton; Supriya Kumar Yagnik; Nicola Williamson; Holly Spencer; Sharan Kaur; Bryan Bennett; Sarah Donelson; Dayo Jagun; Hans-Peter Goertz; Alisha Stein
BMC Health Services Research | 2017
Michael Stokes; Carolina Reyes; Yu Xia; Veronica Alas; Hans-Peter Goertz; Luke Boulanger