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| A rationale for expanding the endpoints for clinical trials in advanced pancreatic carcinoma |
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| Author(s): Rothenberg ML, Abbruzzese JL, Moore M, Portenoy RK, Robertson JM, Wanebo HJ |
| Source: CANCER Volume: 78 Issue: 3 Pages: 627-632 Supplement: Suppl. S Published: AUG 1 1996 |
| Times Cited: 68 References: 48 |
| Abstract: BACKGROUND. Using classical endpoints, such as response rate and survival, as the sole measures of benefit, little progress has been made in the treatment of advanced pancreatic carcinoma in the past 30 years. We challenge the assumption that response rate and survival are the only appropriate endpoints for clinical trials in this disease setting. METHOD. A review of the literature and roundtable discussion were undertaken.
RESULTS. Using current imaging techniques, it is inherently difficult to distinguish pancreatic tumor from normal pancreas, inflammatory tissue, local fibrosis, and unopacified bowel. As a result, objective tumor measurements are often imprecise, unreliable, and irreproducible. This difficulty may explain the wide variation in response rates reported in clinical trials even when the same therapies are used. Tumor-related symptoms, such as anorexia, weight loss, severe pain (requiring opioid analgesia), and impaired functional status, are prevalent and debilitating characteristics of this disease. Tools that can assess these symptoms in a consistent fashion over time have been developed and have been integrated into clinical trials to evaluate new drugs in this setting.
CONCLUSIONS. Systematic assessment of the impact of a new therapy on tumor-related symptoms may provide a sensitive and accurate way to identify useful new treatments for patients with advanced pancreatic carcinoma. Such analyses can be a useful complement to the classical endpoints of response rate and survival. (C) 1996 American Cancer Society.
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| Document Type: Proceedings Paper |
| Language: English |
Addresses:
1. UNIV TEXAS, HLTH SCI CTR, DIV MED ONCOL, SAN ANTONIO, TX 78284 USA 2. UNIV TEXAS, MD ANDERSON CANC CTR, DEPT GASTROINTESTINAL ONCOL, HOUSTON, TX USA 3. PRINCESS MARGARET HOSP, DEPT MED, TORONTO, ON M4X 1K9 CANADA 4. UNIV MICHIGAN, MED CTR, DEPT RADIAT ONCOL, ANN ARBOR, MI 48109 USA 5. MEM SLOAN KETTERING CANC CTR, DEPT NEUROL, NEW YORK, NY 10021 USA 6. BROWN UNIV, ROGER WILLIAMS GEN HOSP, SCH MED, DEPT SURG, PROVIDENCE, RI 02908 USA |
| Publisher: WILEY-LISS, DIV JOHN WILEY & SONS INC 605 THIRD AVE, NEW YORK, NY 10158-0012 |
| Subject Category: Oncology |
| IDS Number: UY778 |
| ISSN: 0008-543X |
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