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Lenz, Heinz‐Josef

https://orcid.org/0000-0003-2178-9568

Mayo Clinic

University of Southern California

Citations 133

Multicenter Phase II Trial of Temsirolimus and Bevacizumab in Pancreatic Neuroendocrine Tumors
Hobday, Timothy J. , Qin, Rui , Reidy‐Lagunes, Diane , Moore, Malcolm J. , Kaubisch, Andreas , Shah, Manisha H. , Kindler, Hedy L. , Lenz, Heinz‐Josef , Erlichman, Charles , Shah, Manisha , Kindler, Hedy Lee, Chen, Helen, Strosberg, Jonathan , Chen, Helen

Journal of Clinical Oncology | December 9, 2014 | Volume: 33 | Issue: 14 | Pages: 1551-1556

10.1200/jco.2014.56.2082 Get It

Purpose There are few effective therapies for pancreatic neuroendocrine tumors (PNETs). Recent placebo-controlled phase III trials of the mammalian target of rapamycin (mTOR) inhibitor everolimus and the vascular endothelial growth factor (VEGF)/platelet-derived growth factor receptor inhibitor sunitinib have noted improved progression-free survival (PFS). Preclinical studies have suggested enhanced antitumor effects with combined mTOR and VEGF pathway–targeted therapy. We conducted a clinical trial to evaluate combination therapy against these targets in PNETs. Patients and Methods We conducted a two-stage single-arm phase II trial of the mTOR inhibitor temsirolimus 25 mg intravenously (IV) once per week and the VEGF-A monoclonal antibody bevacizumab 10 mg/kg IV once every 2 weeks in patients with well or moderately differentiated PNETs and progressive disease by RECIST within 7 months of study entry. Coprimary end points were tumor response rate and 6-month PFS. Results A total of 58 patients were enrolled, and 56 patients were eligible for response assessment. Confirmed response rate (RR) was 41% (23 of 56 patients). PFS at 6 months was 79% (44 of 56). Median PFS was 13.2 months (95% CI, 11.2 to 16.6). Median overall survival was 34 months (95% CI, 27.1 to not reached). For evaluable patients, the most common grade 3 to 4 adverse events attributed to therapy were hypertension (21%), fatigue (16%), lymphopenia (14%), and hyperglycemia (14%). Conclusion The combination of temsirolimus and bevacizumab had substantial activity and reasonable tolerability in a multicenter phase II trial, with RR of 41%, well in excess of single targeted agents in patients with progressive PNETs. Six-month PFS was a notable 79% in a population of patients with disease progression by RECIST criteria within 7 months of study entry. On the basis of this trial, continued evaluation of combination mTOR and VEGF pathway inhibitors is warranted.
Explaining the Unexplainable: EGFR Antibodies in Colorectal Cancer
Grothey, Axel, Lenz, Heinz‐Josef

Journal of Clinical Oncology | April 3, 2012 | Volume: 30 | Issue: 15 | Pages: 1735-1737

10.1200/jco.2011.40.4194 Get It

The Continuum of Care: A Paradigm for the Management of Metastatic Colorectal Cancer
Goldberg, Richard M. , Rothenberg, Mace L., Benson, Al B. , Blanke, Charles D. , Diasio, Robert B. , Grothey, Axel, Lenz, Heinz‐Josef , Meropol, Neal J. , Ramanathan, Ramesh K., Becerra, Carlos H.R., Wickham, Rita , Armstrong, Delma, Viele, Carol, Cutsem, Eric Van

The Oncologist | January 17, 2007 | Volume: 12 | Issue: 1 | Pages: 38-50

10.1634/theoncologist.12-1-38 Get It

Learning ObjectivesAfter completing this course, the reader should be able to: Discuss recent progress in the treatment of patients with advanced colorectal cancer.Define the continuum-of-care approach and how it may differ from our current approach to the treatment of patients with advanced colorectal cancer.Identify key factors in treatment selection for patients with advanced colorectal cancer.Explain the impact of each active drug in the treatment of advanced colorectal cancer and the impact of treatment with multiple agents over the course of the disease.CME Access and take the CME test online and receive 1 AMA PRA Category 1 Credit™ at CME.TheOncologist.com