John Leppert

Prof. John Leppert

Stanford University School of Medicine
+1
orcid

Research Focus & Metrics

Academic Career Length

28Years (1999-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 July 2006 in Clinical Cancer Research
Verified
Journal Article
Closed access
PDF file
APAllan Pantuck
Allan Pantuck
JLJohn Leppert
John Leppert
NZNazy Zomorodian
Nazy Zomorodian
WAWilliam Aronson
William Aronson
JHJenny Hong
Jenny Hong
ABArie Belldegrun
Arie Belldegrun
Purpose: Phytochemicals in plants may have cancer preventive benefits through antioxidation and via gene-nutrient interactions. We sought to determine the effects of pomegranate juice (a major source of antioxidants) consumption on prostate-specific antigen (PSA) progression in men with a rising PSA following primary therapy.

18 May 2007 in Cancer
Verified
Journal Article
Open access
PDF file
APAllan J. Pantuck
Allan J. Pantuck
DSDavid B. Seligson
David B. Seligson
TKTobias Klatte
Tobias Klatte
HYHong Yu
Hong Yu
JLJohn Leppert
John Leppert
RFRobert A. Figlin
Robert A. Figlin
BACKGROUND.: The mammalian target of rapamycin (mTOR) pathway is up‐regulated in many human cancers, and agents targeting the mTOR pathway are in various stages of clinical development. The goal of the study was to evaluate the potential and limitations of targeting the mTOR pathway in renal cell carcinoma (RCC).METHODS.: Immunohistochemical analysis using antibodies against pAkt, PTEN, p27, and pS6 was performed on a tissue microarray constructed from paraffin‐embedded specimens from 375 patients treated by nephrectomy for RCC. The expression was associated with pathological parameters and survival.RESULTS.: The mTOR pathway was more significantly altered in clear‐cell RCC, high‐grade tumors, and tumors with poor prognostic features. PS6 and PTEN showed the strongest associations with pathological parameters. Survival tree analysis regarding expression of cytoplasmic pAkt, nuclear pAkt, PTEN, cytoplasmic p27, and pS6 identified staining percentages of 40%, 10%, 75%, 7%, and 70%, respectively, as ideal cutoff values for stratification, with corresponding P‐values of .03, .001, .02, .005, and <.0001, respectively. Interestingly, high nuclear pAkt expression was associated with a favorable prognosis, whereas high cytoplasmic pAkt expression was associated with a poor prognosis. In multivariate Cox regression analysis, ECOG PS, T classification, N classification, M classification, cytoplasmic Akt, nuclear pAkt, PTEN, and pS6 were independent prognostic factors of DSS.CONCLUSIONS.: Components of the mTOR pathway are significantly associated with pathological features and survival. Not all RCC tumor types seem to be equally amenable to mTOR targeted therapy. PTEN, pAkt, p27, and pS6 may serve as surrogate parameters for patient selection and predicting prognosis. Patients with a highly activated mTOR pathway should benefit most from this therapy. External validation of our results is recommended. Cancer 2007. © 2007 American Cancer Society.

1 June 2005 in Journal of Urology
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Journal Article
Closed access
JLJohn S. Lam
John S. Lam
OSOleg Shvarts
Oleg Shvarts
JLJohn Leppert
John Leppert
RFRobert A. Figlin
Robert A. Figlin
ABArie S. Belldegrun
Arie S. Belldegrun
Renal cell carcinoma (RCC) has traditionally been staged using a purely anatomical staging system. Although current staging systems provide good prognostic information, data published in the last few years has led to significant controversies as to whether further revisions are needed and whether improvements can be made with the introduction of new, more accurate and predictive prognostic factors not currently included in traditional staging systems. This review highlights such controversies and provides an update on current staging modalities, prognostic factors and targeted molecular therapy for RCC. A comprehensive review of the peer reviewed literature was performed on the topic of current staging modalities, validated prognostic factors, predictive nomograms, molecular markers and targeted molecular therapy for RCC. A staging system for malignant disease such as RCC uses various characteristics of tumors to stratify patients into clinically meaningful categories, which can be used to provide patients with counseling regarding prognosis, select treatment modalities and determine eligibility for clinical trials. The TNM staging system is currently the most extensively used one. However, it has undergone recent systematic revision due to rapidly emerging data from longer patient followup. The identification of various histological and symptomatic factors has led groups at many centers to develop more comprehensive staging systems that integrate these factors and include patients with metastatic and local disease. While integrated staging systems have improved RCC staging, the recent discovery of molecular tumor markers is expected to revolutionize RCC staging in the future and lead to the development of new therapies based on molecular targeting. Staging systems for RCC serve as a valuable prognostic tool. Several new patient and tumor characteristics have been reported to be important prognostic factors and they have been integrated into current staging systems. In addition, the field of RCC is rapidly undergoing a revolution led by molecular markers and targeted therapies. With this information urologists will be updated with the most current and comprehensive staging strategies, and be provided with a glimpse of the molecular and patient specific staging and treatment paradigms that will in our opinion transform the future management of this malignancy.

1 August 2005 in Journal of Urology
Verified
Journal Article
Closed access
JLJohn S. Lam
John S. Lam
OSOleg Shvarts
Oleg Shvarts
JLJohn Leppert
John Leppert
APAllan J. Pantuck
Allan J. Pantuck
RFRobert A. Figlin
Robert A. Figlin
ABArie S. Belldegrun
Arie S. Belldegrun
Purpose: We created an evidence based postoperative surveillance protocol for patients with localized and locally advanced renal cell carcinoma (RCC) based on a risk group stratification sy...

1 March 2008 in Journal of Urology
Verified
Journal Article
Closed access
ABAlberto Breda
Alberto Breda
OOOreoluwa Ogunyemi
Oreoluwa Ogunyemi
JLJohn Leppert
John Leppert
JLJohn S. Lam
John S. Lam
PSPeter G. Schulam
Peter G. Schulam
Percutaneous nephrolithotomy has been the standard of care for intrarenal calculi greater than 2 cm. Flexible ureteroscopy with holmium laser lithotripsy is a minimally invasive treatment modality that is able to treat large intrarenal calculi with the potential to decrease morbidity, while maintaining a high level of efficacy. A total of 15 patients with a single intrarenal calculus 2 cm or greater were treated with retrograde ureteroscopic nephrolithotripsy. Lithotripsy was performed with a 7.2Fr flexible ureteroscope and 200 micron laser fiber. The stone-free rate was defined as the absence of any stones in the kidney or residual stone fragments less than 1 mm, which is too small to be extracted with a basket or a grasper. All patients underwent followup ureteroscopy within 15 days after the last procedure and renal ultrasound 30 days after the last treatment. There were a total of 15 intrarenal calculi 20 to 25 mm (mean 22) in diameter. The mean number of procedures was 2.3 (range 2 to 4). The overall stone-free rate was 93.3%. One patient (6.6%) had a residual 5 mm stone fragment in the lower pole of the kidney, which was followed expectantly for 2 years with no change in size. There were no major complications. There were 3 minor complications (20%), including 1 emergency room visit for fever and pain, and 2 cases of gross hematuria. All cases were performed on an outpatient basis. In select patients with a single intrarenal calculus 2 cm or greater small diameter flexible ureteroscopy with holmium laser lithotripsy may represent an alternative therapy to standard percutaneous nephrolithotomy with acceptable efficacy and low morbidity.

1 May 2009 in European Urology
Verified
Journal Article
Closed access
ABAlberto Breda
Alberto Breda
OOOreoluwa Ogunyemi
Oreoluwa Ogunyemi
JLJohn Leppert
John Leppert
PSPeter G. Schulam
Peter G. Schulam