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
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.