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Y. J. Hei

Researcher at Novartis

Publications -  14
Citations -  1133

Y. J. Hei is an academic researcher from Novartis. The author has contributed to research in topics: Zoledronic acid & Prostate cancer. The author has an hindex of 8, co-authored 14 publications receiving 1067 citations.

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Bone Turnover Markers as Predictors of Skeletal Complications in Prostate Cancer, Lung Cancer, and Other Solid Tumors

TL;DR: Baseline and recent bone marker levels were predictive of negative clinical outcomes in patients with bone metastases secondary to prostate cancer and to NSCLC and other solid tumors, reflecting the key role of osteolysis in the development of skeletal complications.
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Natural history of rising serum prostate-specific antigen in men with castrate nonmetastatic prostate cancer.

TL;DR: Men with nonmetastatic prostate cancer and rising PSA despite androgen deprivation therapy have a relatively indolent natural history and baseline PSA and PSA velocity independently predict time to first bone metastasis and survival.
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Clinical Benefit of Zoledronic Acid in Patients with Lung Cancer and OtherSolid Tumors: Analysis Based on History of Skeletal Complications

TL;DR: This exploratory analysis demonstrates that patients with a history of SREs are at high risk for subsequent S REs, but zoledronic acid reduces skeletal morbidity regardless of S RE history.
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Clinical benefit of zoledronic acid in patients with lung cancer and other solid tumors: Analysis based on prior history of skeletal complications

TL;DR: This exploratory analysis demonstrates that patients with a history of SREs are at high risk of subsequent S REs, and zoledronic acid reduces skeletal morbidity regardless of a prior history ofSREs.
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Zoledronic acid versus pamidronate in patients with breast cancer and multiple myeloma who are at high risk for skeletal complications

TL;DR: This exploratory analysis suggests that patients with a history of SREs are at significantly higher risk of subsequent skeletal complications, and Zol was significantly more effective than Pam at reducing S REs in this subgroup.