DOTA-D-Phe(1)-Tyr(3)-octreotide (DOTATOC), a newly developed somatostatin a
nalogue which can be stably labelled with the beta -emitter yttrium-90, can
be used for receptor-mediated internal radiotherapy. A 78-year-old woman s
uffering from a carcinoid of the small intestine with multiple metastases i
n the liver as well as mesenteric and supraclavicular lymph node metastases
was treated with this therapy after the disease had progressed under other
chemotherapy options employed years previously. The patient received four
single doses of Y-90-DOTATOC at 6-week intervals. yielding a cumulative dos
e of 9,620 MBq (5,659 MBq/m(2)). Restaging revealed stable metastatic disea
se. Serum creatinine and urea nitrogen levels were within the normal range
prior to starting and during DOTATOC therapy. However, 15 months after cess
ation of DOTATOC therapy, a progressive deterioration of renal function occ
urred, leading to end-stage renal disease. Urinalysis revealed a slight pro
teinuria of 700 mg/day without haematuria, leucocyturia or casts. There was
no obvious risk factor for chronic renal insufficiency except DOTATOC ther
apy. However. it was not feasible to use kidney biopsy to prove the presenc
e of radiation-induced nephritis. Intermittent haemodialysis was started as
the creatinine clearance declined to below 10 ml/min. Diuresis was not aff
ected. The presented case shows delayed renal insufficiency after a relativ
ely low cumulative dose of Y-90-DOTATOC (5,659 MBq/m(2)). This serious adve
rse event indicates that further studies are needed to evaluate which dose
of Y-90-DOTATOC, under which renal protection regimen, will provide optimal
management, balancing risks and benefits.