Phase I clinical trial of allogeneic mixed lymphocyte culture (cytoimplant) delivered by endoscopic ultrasound−guided fine‐needle injection in patients with advanced pancreatic carcinoma

BACKGROUND To the authors' knowledge, there are no other published clinical studies that have employed either systemic or local biologic response modifiers in the treatment of patients with pancreatic carcinoma. The purpose of this study was to determine the feasibility and safety of allogeneic...

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Published in:Cancer Vol. 88; no. 6; pp. 1325 - 1335
Main Authors: Chang, Kenneth J., Nguyen, Phuong T., Thompson, James A., Kurosaki, Thomas T., Casey, Linda R., Leung, Edwin C., Granger, Gale A.
Format: Journal Article Conference Proceeding
Language:English
Published: New York John Wiley & Sons, Inc 15-03-2000
Wiley-Liss
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Summary:BACKGROUND To the authors' knowledge, there are no other published clinical studies that have employed either systemic or local biologic response modifiers in the treatment of patients with pancreatic carcinoma. The purpose of this study was to determine the feasibility and safety of allogeneic mixed lymphocyte culture (cytoimplant) delivered by endoscopic ultrasound (EUS)−guided fine‐needle injection (FNI) in patients with advanced pancreatic carcinoma. METHODS Eight patients with unresectable adenocarcinoma of the pancreas were enrolled: 4 patients in Stage II, 3 in Stage III, and 1 in Stage IV. Cytoimplants were delivered locally into the tumor using a novel EUS‐guided FNI technique. Escalating doses of 3, 6, or 9 billion cells were implanted into the pancreatic tumor by a single EUS‐guided FNI. Toxicity (modified National Cancer Institute criteria) was assessed at Day 1, Week 1, and Months 1 and 3. Clinical endpoints included Karnofsky performance status (KPS), CA 19‐9, tumor response (computed tomography and/or EUS), and survival with follow‐up examinations and imaging tests on months 3, 6, 9, 12, and 24. RESULTS There were no bone marrow, hemorrhagic, infectious, renal, cardiac, or pulmonary toxicities. There were 3 transient Grade 3 gastrointestinal toxicities, and 3 patients had transient episodes of hyperbilirubinemia that were reversed by replacement of biliary stents. Seven of 8 patients (86%) experienced low grade fever that responded to acetaminophen, and all fever was resolved within the first 4 weeks. There were no procedure‐related complications. There were 2 partial responses and 1 minor response, with a median survival of 13.2 months. CONCLUSIONS A single injection of cytoimplant immunotherapy by EUS‐guided FNI appears to be feasible and is not associated with substantial toxicity. Cancer 2000;88:1325–35. © 2000 American Cancer Society. To the authors' knowledge, this is the first published clinical trial to use allogeneic mixed lymphocyte culture (cytoimplant), a new form of immune therapy, combined with a novel nonsurgical delivery system (endoscopic ultrasound−guided fine‐needle injection) in the treatment of patients with advanced pancreas carcinoma. These preliminary results showed no substantial toxicities, 20%% partial responders, and a median survival of 13.2 months.
Bibliography:Dr. Chang served as a consultant to Applied Immunotherapeutics in 1997–1998.
ISSN:0008-543X
1097-0142
DOI:10.1002/(SICI)1097-0142(20000315)88:6<1325::AID-CNCR8>3.0.CO;2-T