
Brighton, UK
22 March 2004 - 24 March 2004
British Endocrine Societies
The efficacy of an octreotide test dose to predict the outcome of treatment for acromegaly with somatostatin LAR
Endocrinology, Christie Hospital, Manchester, UK.
In many centres a test dose (TD) of octreotide is administered prior to commencing LAR. The value of the TD as a predictor of subsequent response to therapy remains uncertain. We have studied the relationship of the GH response to a TD to the subsequent response to LAR in 26 patients (median age 59 years, range 20- 84). After baseline GH sampling, 50mcg subcutaneous octreotide was administered and sampling continued for six hours. Results of the TD were compared to the lowest mean GH achieved on LAR (77% achieved target GH of <5mU/l).
Median baseline GH was 17.7mU/l (range 2.2 to 180) and during the TD fell by a median of 76.7% (43.1 to 97.1) to a median of GH 3.4mU/l (1.0 to 26.6), with a positive correlation between baseline GH and nadir GH (r=0.733, p<0.001). Furthermore, a correlation was found between the nadir GH during the TD and the subsequent GH response to LAR (r=0.52, p=0.003), no such relationship existed for % fall in GH during the TD. Optimal predictive value of the TD was achieved with a TD GH nadir of <5mU/l. At this level the positive predictive value of the TD for a subsequent mean GH on LAR of <5mU/l was 87%, and 85% for >50% fall, but the former had a better negative predictive value of 50% compared to 0% for % fall.
Dividing patients by baseline GH <25, 25-50 and >50 mU/l reveals 87%, 33% and 0% respectively achieve a nadir GH <5mU/l during the TD, and during LAR 87%, 67% and 50% respectively achieve GH <5mU/l.
A relatively low baseline GH and a nadir during the TD of <5mU/l are both predictive of a good response to LAR therapy but a poor response during a TD does not exclude a good response to LAR therapy.
Endocrine Abstracts (2004) 7 P124