Octreotide scintigraphy and Chromogranin A do not predict clinical response in patients with octreotide acetate-treated hormone-refractory prostate cancer
(2006) In Prostate Cancer and Prostatic Diseases 9(1). p.92-98- Abstract
- In this pilot study, the predictive value of Octreotide scintigraphy (Octreoscan) and/or Chromogranin-A (CgA) was investigated in patients with hormone-refractory prostate cancer treated with Octreotide acetate. In total, 20 patients with progressive disease and bone metastases entered the trial. At baseline Octreoscan, CgA, PSA, alkaline phosphates (ALP) and two self-administered questionnaires (EORTC QLQ C-30 (v3) and brief pain index) were performed and a diary of the pharmaceutical was started. The treatment consisted of Octreotide (Sandostatin LAR) acetate 30 mg intramuscular injection every month. The blood samples and questionnaires were repeated every month until 3 months. Clinical responder was defined as a patient with increased... (More)
- In this pilot study, the predictive value of Octreotide scintigraphy (Octreoscan) and/or Chromogranin-A (CgA) was investigated in patients with hormone-refractory prostate cancer treated with Octreotide acetate. In total, 20 patients with progressive disease and bone metastases entered the trial. At baseline Octreoscan, CgA, PSA, alkaline phosphates (ALP) and two self-administered questionnaires (EORTC QLQ C-30 (v3) and brief pain index) were performed and a diary of the pharmaceutical was started. The treatment consisted of Octreotide (Sandostatin LAR) acetate 30 mg intramuscular injection every month. The blood samples and questionnaires were repeated every month until 3 months. Clinical responder was defined as a patient with increased global health score more than 10 units and stable or decreased pain score without an increase in analgesic. In all, 17 patients were treated per protocol, and four were assessed as clinical responders. Six patients developed a reduction in ALP (median -26%, range -5 to -78%). All patients increased in PSA. At baseline, three patients had a negative Octreoscan and the patients with positive lesions, demonstrated uptake of low intensity. At baseline the CgA was elevated above the normal range in 15 of the patients, and during treatment five patients decreased their CgA to the normal range. Neither baseline Octreoscan nor CgA could identify the clinical reponders. A minority of patients improves their health-related quality of life. The decrease and normalization of CgA levels in five patients during therapy indicates therapeutic activity but Octreoscan and CgA could not identify clinical responders. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/411353
- author
- Kalkner, Karl Mikael ; Acosta, Stefan LU ; Thorsson, Ola LU ; Frederiksen, Hans LU ; Nilsson, A ; Gustavsson, Bengt ; Elingsbo, Marie ; Stridsberg, M and Abrahamsson, Per-Anders LU
- organization
- publishing date
- 2006
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- somatostatin analog, prostate cancer, neuroendocrine differentiation
- in
- Prostate Cancer and Prostatic Diseases
- volume
- 9
- issue
- 1
- pages
- 92 - 98
- publisher
- Nature Publishing Group
- external identifiers
-
- pmid:16231013
- wos:000236690300027
- scopus:33644894779
- ISSN
- 1476-5608
- DOI
- 10.1038/sj.pcan.4500843
- language
- English
- LU publication?
- yes
- id
- f1a3da48-8d2a-41f7-8c4c-19f67abba743 (old id 411353)
- date added to LUP
- 2016-04-01 11:45:46
- date last changed
- 2023-09-15 06:50:56
@article{f1a3da48-8d2a-41f7-8c4c-19f67abba743, abstract = {{In this pilot study, the predictive value of Octreotide scintigraphy (Octreoscan) and/or Chromogranin-A (CgA) was investigated in patients with hormone-refractory prostate cancer treated with Octreotide acetate. In total, 20 patients with progressive disease and bone metastases entered the trial. At baseline Octreoscan, CgA, PSA, alkaline phosphates (ALP) and two self-administered questionnaires (EORTC QLQ C-30 (v3) and brief pain index) were performed and a diary of the pharmaceutical was started. The treatment consisted of Octreotide (Sandostatin LAR) acetate 30 mg intramuscular injection every month. The blood samples and questionnaires were repeated every month until 3 months. Clinical responder was defined as a patient with increased global health score more than 10 units and stable or decreased pain score without an increase in analgesic. In all, 17 patients were treated per protocol, and four were assessed as clinical responders. Six patients developed a reduction in ALP (median -26%, range -5 to -78%). All patients increased in PSA. At baseline, three patients had a negative Octreoscan and the patients with positive lesions, demonstrated uptake of low intensity. At baseline the CgA was elevated above the normal range in 15 of the patients, and during treatment five patients decreased their CgA to the normal range. Neither baseline Octreoscan nor CgA could identify the clinical reponders. A minority of patients improves their health-related quality of life. The decrease and normalization of CgA levels in five patients during therapy indicates therapeutic activity but Octreoscan and CgA could not identify clinical responders.}}, author = {{Kalkner, Karl Mikael and Acosta, Stefan and Thorsson, Ola and Frederiksen, Hans and Nilsson, A and Gustavsson, Bengt and Elingsbo, Marie and Stridsberg, M and Abrahamsson, Per-Anders}}, issn = {{1476-5608}}, keywords = {{somatostatin analog; prostate cancer; neuroendocrine differentiation}}, language = {{eng}}, number = {{1}}, pages = {{92--98}}, publisher = {{Nature Publishing Group}}, series = {{Prostate Cancer and Prostatic Diseases}}, title = {{Octreotide scintigraphy and Chromogranin A do not predict clinical response in patients with octreotide acetate-treated hormone-refractory prostate cancer}}, url = {{http://dx.doi.org/10.1038/sj.pcan.4500843}}, doi = {{10.1038/sj.pcan.4500843}}, volume = {{9}}, year = {{2006}}, }