Gilchrist KW - Search Results

1

Prognostic potential of DNA flow cytometry measurements in node-negative breast cancer patients: preliminary analysis of an intergroup study (INT 0076).

Dressler LG, Eudey L, Gray R, Tormey DC, McGuire WL, Gilchrist KW, Clark GM, Osborne CK, Mansour EG, Abeloff MD. Dressler LG, et al. Among authors: gilchrist kw. J Natl Cancer Inst Monogr. 1992;(11):167-72. J Natl Cancer Inst Monogr. 1992. PMID: 1627424 Clinical Trial.

2

Tumor necrosis is a prognostic predictor for early recurrence and death in lymph node-positive breast cancer: a 10-year follow-up study of 728 Eastern Cooperative Oncology Group patients.

Gilchrist KW, Gray R, Fowble B, Tormey DC, Taylor SG 4th. Gilchrist KW, et al. J Clin Oncol. 1993 Oct;11(10):1929-35. doi: 10.1200/JCO.1993.11.10.1929. J Clin Oncol. 1993. PMID: 8410120

3

Chemotherapy versus observation in high-risk node-negative breast cancer patients.

Mansour EG, Eudey L, Tormey DC, Shatila AH, Osborne CK, Gilchrist KW, Cooper MR, Falkson G. Mansour EG, et al. Among authors: gilchrist kw. J Natl Cancer Inst Monogr. 1992;(11):97-104. J Natl Cancer Inst Monogr. 1992. PMID: 1627437 Clinical Trial.

4

Prognostic significance of S-phase fraction in good-risk, node-negative breast cancer patients.

Clark GM, Mathieu MC, Owens MA, Dressler LG, Eudey L, Tormey DC, Osborne CK, Gilchrist KW, Mansour EG, Abeloff MD, et al. Clark GM, et al. Among authors: gilchrist kw. J Clin Oncol. 1992 Mar;10(3):428-32. doi: 10.1200/JCO.1992.10.3.428. J Clin Oncol. 1992. PMID: 1740681

5

Adjuvant chemohormonal therapy with cyclophosphamide, methotrexate, 5-fluorouracil, and prednisone (CMFP) or CMFP plus tamoxifen compared with CMF for premenopausal breast cancer patients. An Eastern Cooperative Oncology Group trial.

Tormey DC, Gray R, Gilchrist K, Grage T, Carbone PP, Wolter J, Woll JE, Cummings FJ. Tormey DC, et al. Cancer. 1990 Jan 15;65(2):200-6. doi: 10.1002/1097-0142(19900115)65:2<200::aid-cncr2820650203>3.0.co;2-q. Cancer. 1990. PMID: 2403834 Clinical Trial.

6

Accumulation of p53 protein as a possible predictor of response to adjuvant combination chemotherapy with cyclophosphamide, methotrexate, fluorouracil, and prednisone for breast cancer.

Elledge RM, Gray R, Mansour E, Yu Y, Clark GM, Ravdin P, Osborne CK, Gilchrist K, Davidson NE, Robert N, et al. Elledge RM, et al. J Natl Cancer Inst. 1995 Aug 16;87(16):1254-6. doi: 10.1093/jnci/87.16.1254. J Natl Cancer Inst. 1995. PMID: 7563172 Clinical Trial. No abstract available.

7

Maintenance tamoxifen after induction postoperative chemotherapy in node-positive breast cancer patients: the Eastern Cooperative Oncology Group Trials.

Tormey DC, Gray R, Falkson HC, Gilchrist K, Abeloff MD, Falkson G. Tormey DC, et al. Recent Results Cancer Res. 1993;127:185-96. doi: 10.1007/978-3-642-84745-5_26. Recent Results Cancer Res. 1993. PMID: 8502815 Clinical Trial. No abstract available.

8

High DNA content and prognosis in lymph node positive breast cancer. A case control study by the University of Leiden and ECOG. (Eastern Cooperative Oncology Group).

Gilchrist KW, Gray R, van Driel-Kulker AM, Mesker WE, Ploem-Zaaijer JJ, Ploem JS, Taylor SG, Tormey DC. Gilchrist KW, et al. Breast Cancer Res Treat. 1993 Oct;28(1):1-8. doi: 10.1007/BF00666350. Breast Cancer Res Treat. 1993. PMID: 8123866

9

HER-2/neu in node-negative breast cancer: prognostic significance of overexpression influenced by the presence of in situ carcinoma.

Allred DC, Clark GM, Tandon AK, Molina R, Tormey DC, Osborne CK, Gilchrist KW, Mansour EG, Abeloff M, Eudey L, et al. Allred DC, et al. Among authors: gilchrist kw. J Clin Oncol. 1992 Apr;10(4):599-605. doi: 10.1200/JCO.1992.10.4.599. J Clin Oncol. 1992. PMID: 1548522 Clinical Trial.

10

Efficacy of adjuvant chemotherapy in high-risk node-negative breast cancer. An intergroup study.

Mansour EG, Gray R, Shatila AH, Osborne CK, Tormey DC, Gilchrist KW, Cooper MR, Falkson G. Mansour EG, et al. Among authors: gilchrist kw. N Engl J Med. 1989 Feb 23;320(8):485-90. doi: 10.1056/NEJM198902233200803. N Engl J Med. 1989. PMID: 2915651 Clinical Trial.

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