James N. Ingle
Mayo Clinic
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Publication
Featured researches published by James N. Ingle.
Cancer | 1994
Lynn C. Hartmann; James N. Ingle; Lester E. Wold; Gist H. Farr; Joseph P. Grill; John Q. Su; Nita J. Maihle; James E. Krook; Thomas E. Witzig; Patrick C. Roche
Background. This study was designed to evaluate the prognostic importance of c‐erbB2 overexpression in a standardized cohort of patients with axillary lymph node positive breast cancer.
Cancer | 1993
Thomas M. Pisansky; James N. Ingle; Daniel J. Schaid; A. Curtis Hass; James E. Krook; John H. Donohue; Thomas E. Witzig; Lester E. Wold
Background. This analysis was conducted to evaluate the impact of selected clinical, histopathologic, and flow cytometric factors on sites of initial tumor relapse after postmastectomy adjuvant systemic therapy.
Cancer | 2000
Edith A. Perez; David W. Hillman; Philip J. Stella; James E. Krook; Lynn C. Hartmann; Tom R. Fitch; Alan K. Hatfield; James A. Mailliard; Suresh Nair; Carl G. Kardinal; James N. Ingle
This Phase II multicenter study evaluated the efficacy and toxicity of paclitaxel (200 mg/m2 by 3‐hour infusion) with carboplatin (area under the curve 6 mg/mL per minute) administered every 3 weeks as first‐line therapy for women with metastatic breast carcinoma.
Cancer | 1999
James N. Ingle; Vera J. Suman; Carl G. Kardinal; James E. Krook; James A. Mailliard; Michael H. Veeder; Charles L. Loprinzi; Robert J. Dalton; Lynn C. Hartmann; Cheryl A. Conover; Michael N. Pollak
Tamoxifen (TAM) is generally considered the hormonal agent of choice for postmenopausal women with hormone receptor positive breast carcinoma. The somatostatin analogues, including octreotide, have demonstrated inhibition of breast carcinoma cell lines and multiple endocrinologic actions, including reduction of insulin‐like growth factor I (IGF‐I), a potent mitogen for breast carcinoma cells. In an attempt to improve the efficacy of TAM, this randomized trial was performed.
Cancer | 1997
James N. Ingle; Patricia A. Johnson; Vera J. Suman; James B. Gerstner; James A. Mailliard; John K. Camoriano; Dean H. Gesme; Charles L. Loprinzi; Alan K. Hatfield; Lynn C. Hartmann
It is common practice to utilize a series of different hormonal agents in the treatment of postmenopausal women who, despite disease progression, continue to be candidates for hormonal therapy on a clinical basis. Letrozole is a new highly selective and potent aromatase inhibitor. There are limited data on third‐line hormonal therapy in general, and this study was undertaken to evaluate letrozole in this context.
Cancer | 1996
M.P.H. Steven R. Alberts M.D.; James N. Ingle; Patrick R. Roche; Stephen S. Cha; Lester E. Wold; Gist H. Farr; James E. Krook; H. Sam Wieand
The measurement of estrogen receptors (ER) in breast cancer specimens has traditionally been assessed with a dextran‐coated charcoal assay (DCCA). More recently the immunohistochemical staining (IHC) method has gained increasing popularity because of its ability to use fixed tissue, assess needle biopsies, and reduce cost. Controversy exists over the accuracy of IHC compared with that of DCCA in determining ER. We compared these two techniques using tumor tissue obtained from a large group of females with lymph node positive breast carcinoma with long term follow‐up.
Cancer | 1996
Madhav V. Dhodapkar; James N. Ingle; Stephen S. Cha; James A. Mailliard; H. Sam Wieand
Information regarding prognostic factors and survival in elderly women with metastatic breast cancer treated with tamoxifen is limited.
Cancer | 1994
James N. Ingle; John F. Foley; James A. Mailliard; James E. Krook; Lynn C. Hartmann; Sin-Ho Jung; Michael H. Veeder; Dean H. Gesme; Alan K. Hatfield; Richard M. Goldberg
Background. The fraction of breast cancer cells undergoing DNA synthesis at any one time is relatively low, which is problematic because most chemotherapeutic agents are most effective against dividing cells. Estrogens administered in vitro and in vivo can increase breast cancer cell proliferation. A randomized clinical trial was performed to determine if estrogenic recruitment could increase the effectiveness of combination chemotherapy.
Cancer | 1996
Thomas M. Pisansky; Charles L. Loprinzi; Stephen S. Cha; Robert J. Fitzgibbons; Clive S. Grant; A. Curtis Hass; Nicholas F. Reuter; Lester E. Wold; James N. Ingle; Carl G. Kardinal
This prospective trialiu was conducted to evaluate the outcome of patients treated with preoperative and postoperative chemotherapy, mastectomy, and irradiation for locoregionally advanced breast carcinoma.
Cancer | 1995
Madhav V. Dhodapkar; James N. Ingle; David L Ahmann