Different response to the long-acting somatostatin analogues lanreotide and octreotide in a patient with a malignant carcinoid

Citation
M. Raderer et al., Different response to the long-acting somatostatin analogues lanreotide and octreotide in a patient with a malignant carcinoid, ONCOL-BASEL, 60(2), 2001, pp. 141-145
Citations number
23
Categorie Soggetti
Oncology,"Onconogenesis & Cancer Research
Journal title
ONCOLOGY
ISSN journal
00302414 → ACNP
Volume
60
Issue
2
Year of publication
2001
Pages
141 - 145
Database
ISI
SICI code
0030-2414(2001)60:2<141:DRTTLS>2.0.ZU;2-O
Abstract
Introduction: Somatostatin (SST) analogues are cornerstones in the symptoma tic management of patients suffering from carcinoid tumors, and antiprolife rative activity has also been reported for these agents. The most commonly applied SST analogues are octreotide (OCT) and lanreotide (LAN), which are both available in a slow release formulation. To the current knowledge, bot h OCT and LAN are thought to be equally effective for the management of var ious disorders. We report the case of a patient with a disseminated carcino id, who progressed during dose-intensified treatment with slow-release LAN in combination with interferon-alpha, but developed a pronounced response a fter treatment was switched to the application of a depot formulation of OC T. Case Report: A 46-year-old woman was admitted to our department for the evaluation of persistent flushing, diarrhea and dyspnea. After a diagnosis of metastatic carcinoid had been established, treatment with LAN (30 mg i.m . every 10 days) along with interferon-alpha 3 x 5 MU/week was initiated. I n spite of successful blocking of tumoral SST receptors as judged by SST re ceptor scintigraphy and subjective improvement of symptoms, the patient had progressive disease. As she refused chemotherapy, treatment was switched t o a depot formulation of OCT (20 mg i.m. every 4 weeks), resulting both in a disappearance of symptoms as well as tumor regression as seen on CT scann ing. Conclusion: To our knowledge, this is the first case demonstrating bot h a symptomatic as well as objective response to OCT following progression during therapy with LAN in a patient with a carcinoid tumor. Our results su ggest that refractoriness to treatment including a long-acting SST analogue does not automatically imply resistance to a related agent and should aler t clinicians to the potential of non-cross-resistance between SST analogues in neuroendocrine malignancies. Copyright (C) 2001 S. Karger AG, Basel.