Radiolabelled somatostatin analogue(s) for peptide receptor scintigraphy and radionuclide therapy

Annals of Oncology, Jan 1999

E. P. Krenning, M. de Jong, P. P. M. Kooij, W. A. P. Breeman, W. H. Bakker, W. W. de Herder, C. H. J. van Eijck, D. J. Kwekkeboom, F. Jamar, S. Pauwels, et al.

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Radiolabelled somatostatin analogue(s) for peptide receptor scintigraphy and radionuclide therapy

E. P. Krenning 2 3 M. de Jong 2 3 P. P. M. Kooij 2 3 W. A. P. Breeman 2 3 W. H. Bakker 2 3 W. W. de Herder 1 2 C. H. J. van Eijck 0 2 D. J. Kwekkeboom 2 3 F. Jamar 2 S. Pauwels 2 R.Valkema 2 3 0 Surgery, University Hospital and Erasmus University Rotterdam (EUR) , The Netherlands 1 Department of Internal Medicine III 2 H.C-COOH I / N-<CH,),-N-<CH , ),.N 3 Department ofNuclear Medicine 4 Department of Nuclear Medicine, Catholic University ofLouvain , Brussels , Belgium Summary two years treatment, except that in a few patients a transient decline in platelets counts and lymphocyte subsets occurred. Background: Peptide receptor scintigraphy with the radioactive Promising beneficial effects on clinical symptoms, hormone somatostatin analogue, [mIn-DTPA0]octreotide, is a sensitive production and tumour proliferation were found. Of the 21 and specific technique to show in vivo the presence and abun- patients who received a cumulative dose of more than 20 GBq, dance of somatostatin receptors on various tumours. eight patients showed stabilisation of disease and six other Aim: With this technique primary tumours and metastases patients a reduction in size of tumours. There is a tendency of neuroendocrine cancers as well as of many other cancer-types towards better results in patients whose tumours have a higher can be localised. This technique is currently used to assess accumulation of the radioligand. the possibility of peptide receptor radionuclide therapy Conclusions: PRRT is feasible, also with m I n as radio(PRRT) with repeated administrations of high doses of [luIn- nuclide. Depending on the homogeneity of distribution of DTPA]octreotide. '"in emits Auger and conversion electrons tumour cells expressing peptide receptors and the size of the having a tissue penetration of 0.02-10 urn and 200 to 500 urn, tumour, P-emitting radionuclides, e.g., 90Y, labelled to DOTArespectively. chelated peptides, are also attractive candidates for PRRT. The Patients and methods: Thirty end-stage patients with mostly first PRRT trials with [90Y-DOTA,Tyr3]octreotide started neuroendocrine progressing tumours were treated with [ulIn- recently. DTPA]octreotide, up to a maximal cumulative patient dose of about 74 GBq, in a phase I trial. Key words: octreotide, peptide, radionuclide, scintigraphy, Results: There were no major clinical side effects after up to somatostatin, therapy Introduction The inhibitory effect of somatostatin on hormone secretion of various glands led to the concept of beneficial effects of somatostatin in the treatment of diseases, based on gland hyperfunction or overproduction of hormones by endocrine-active tumours. However, the tetradecapeptide SSj4 itself is unsuitable for routine treatment, because of its very short half-life of 3 minutes in man after intravenous injection due to rapid enzymatic degradation and because of its diversity of action, such as lowering insulin levels. Successful efforts have been undertaken to synthesise somatostatin analogues that are more resistant to enzymatic degradation. Introduction of D-amino acids and shortening of the molecule to the bioactive core sequence resulted in the eight amino acids-containing somatostatin-analogue octreotide (Figure 1). Somatostatin receptors are structurally related integral membrane glycoproteins. Recently, five different human somatostatin receptor types have been cloned. All subtypes bind SS!4 and SS2s (a polypeptide of 28 amino acids with SSi4 making up the C-terminus) with high affinity, while the affinity of numerous somatostatin analogues for the five different subtypes differs considerably [1-3]. Octreotide binds with high affinity to the sst2 (human somatostatin receptor subtype 2), while this analogue has a relatively low affinity for sst3 and sst5 Ala-Gly-Cys-Lys-Asn-Phe-Phe-Trp-Lys -Thr-Phe-Thr-Ser-Cys D-Phe-Cys-Phe-D-Trp-Lys-Thr-Cys-Thr(ol) [Tyr3]OCtreOtide D-Phe-Cys-Tyr-D-Trp-Lys-Thr-Cys-Thr (ol) and shows no binding to sstl and sst4 [1-4]. Octreotide scintigraphy is, therefore, based on the visualisation of (an) octreotide-binding somatostatin receptor(s), most probably the sst2 and sst5. Peptide receptor scintigraphy with the radioactive somatostatin analogue, [mIn-DTPA]octreotide (Figure 1), is a sensitive and specific technique to show in vivo the presence and abundance of somatostatin receptors on various tumours. In general, mapping of the presence of various peptide receptors on the cell membrane by peptide receptor scintigraphy (PRS) may become an attractive, non-invasive, harmless, easy-to-perform tool for an individual therapeutic approach of the cancer patient [5-8]. Also the detection of heterogeneous metastases (with regard to the expression of different peptide receptors or the accumulation of other radiolabeled ligands) becomes possible if a combination of radiolabeled peptides or of radiolabeled peptides with other radioligands (all labelled with different radionuclides) can be used. At the moment, examples of this approach are the use of 1) octreotide and MIBG scintigraphy in patients with metastasised pheochromocytoma and 2) octreotide and radioiodine scintigraphy in patients with metastasised differentiated thyroid cancer. One of the therapeutic options for patients with endocrine cancers is the use of non-radioactive peptides (or antagonists) but application of radiolabeled peptides for therapeutic use, possibly in combination with other radiolabeled ligands (e.g., MIBG or radioiodine) may become a new alternative or adjunct as well. A new and fascinating application is the use of radiolabeled peptides for PRRT. The success of the therapeutic strategy relies upon the amount of radioligand, which can be concentrated within tumour cells and the rates of internalization, degradation and recycling of both ligand and receptor will among other things determine this. Binding of several peptide hormones to specific surface receptors is generally followed by internalization of the ligand receptor complex via invagination of the plasma membrane [9, 10]. The resulting intracellular vesicles, termed endosomes, rapidly acidify, which causes the ligand to dissociate from the receptor. The ligand may be delivered to the lysosome [11] and the receptor recycles back to plasma membrane. The whole process takes approximately 15 min [9], and a single receptor can deliver numerous ligand molecules to the lysosomes. We have studied internalization and degradation of radiolabeled [DTPA]octreotide in the somatostatin receptor positive rat pancreatic tumour cell lines CA20948 and AR42J and in the somatostatin receptor negative human anaplastic thyroid tumour cell line ARO. We detected internalization of the radiopharmaceutical in vitro, in accordance with the findings of Andersson et al. [12], and found that this process was receptor specific and temperature dependent [13]. Receptor-mediated internalization of [inIn-DTPA0]octreotide will most probably result in degradation to "'in-DTPA-D-Phe, this metabolite is not capable passing the lysosomal membrane(s) [11]. For radiotherapeutic applications several radionuclides have been proposed and investigated for coupling to [DTPA]octreotide. 90Y, a suitable (3-emitting radionuclide, shows dissociation from this chelated peptide in serum, '"in labelled [DTPA]octreotide has an appropriate distribution profile in humans for PRS and PRRT [14, 15]. nlIn emits Auger- and conversion-electrons and can therefore be used to investigate its antiproliferative effect in cancer. Scintigraphy with [l"ln-DTPA]octreotide The efficacy of PRS with [ulIn-DTPA]octreotide was evaluated in a European multicenter trial (EMT) in 350 patients with a histologically or biochemically proven GEP tumour [7]. Tumour sites were detected by conventional imaging methods (CIM) in 88%, whereas somatostatin receptor scintigraphy was positive in 80%. The highest success rates of somatostatin receptor scintigraphy were observed with glucagonomas (100%), vipomas (88%), carcinoids (87%) and non-functioning islet cell tumours (ICT; 82%). The low detection rate (46%) noted for insulinomas is related to the lower incidence of sst2 somatostatin receptors on insulinoma cells. However, the overall 80% sensitivity found is somewhat lower than the 88% obtained at the Erasmus University Rotterdam (EUR) in 130 patients with GEP tumours. This may be related to important differences in scanning procedures such as the amount of radioligand administered (minimal dose of '"in of 200 MBq and at least 10 ug of peptide at EUR), the duration of the acquisition and the use of single photon emission computed tomography (SPECT, with a triple head camera at EUR). The fact that abdominal SPECT was not systematically performed in all patients of the EMT may explain that only 73% of gastrinoma patients had a positive scan compared to the 90%-100% sensitivity reported in other studies. In the EMT, a total of 388 sites were visualized with CIM in 308 out of the 350 patients. In addition to 297 known localisations, somatostatin receptor scintigraphy revealed another 166 unsuspected lesions. Forty percent of these unsuspected lesions were subsequently confirmed as true positive findings based on the results of additional imaging procedures or histology obtained during the one-year follow-up period. The clinical relevance of detecting additional tumour localizations is very dependent on the clinical status of the patient. The demonstration of an unsuspected lesion in a patient with known metastatic spread usually has little impact on the management. In contrast, the detection of unsuspected tumour sites in patients with a single known lesion or without any known lesion is important in that it may affect the selection for curative surgery, which remains the treatment of choice of patients with this type of tumours. In the cohort of 350 patients studied, 42 had no lesion detected by CIM and 178 were known to have a single tumour localisation prior to the study. Somatostatin receptor scintigraphy was positive in 11 of the 42 patients (25%) and 12 of 16 lesions revealed by somatostatin receptor scintigraphy were further confirmed as true positive. Somatostatin receptor scintigraphy demonstrated multiple tumour sites in 62 of the 178 patients (35%), 60% of these lesions were confirmed by follow-up (one year) procedures. A reply to an impact questionnaire was obtained for 235 patients. Overall, the scintigraphic findings led to management changes in 40% of the 235 patients. Gibril et al. compared in a prospective study the sensitivity of somatostatin receptor scintigraphy with that of CT, MRI, ultrasonography and selective angiography in the detection of primary and metastatic gastrinomas [16]. Their conclusion is that somatostatin receptor scintigraphy is the single most sensitive method for imaging either primary or metastatic liver lesions in patients with Zollinger-Ellison syndrome. The same group studied the effect of somatostatin receptor scintigraphy on clinical management based on the data of this comparative study [16, 17]. Since this technique altered management of 47% of the patients, they concluded that somatostatin receptor scintigraphy should be the initial imaging modality for patients with gastrinomas, also because of its superior sensitivity, high specificity, simplicity and cost-effectiveness. Furthermore, "it is likely that the conclusion drawn from this study can also be extended to other pancreatic endocrine tumour syndromes except insulinomas" [17]. PRRTwith['"ln-DTPA]octreotide After internalization of the radiopharmaceutical in tumour cells, the radioactive ligand is close to the nucleus. Since '"in emits not only gamma-rays, which are visualized during PRS, but also short-ranged Auger-electrons, an effect on tumour cell proliferation could be expected, as the radiotoxicity of Auger electrons is very high if their target, the DNA of the cell, is within the particle range [18-20]. Preclinical We performed PRRT studies in rats using ['"in-DTPA0]octreotide. To investigate receptor dependence of the therapeutic effects, we compared the effect of PRRT in animals inoculated with the somatostatin receptor positive CA20948 tumour cells in the portal vein of the liver and the somatostatin receptor negative CC531 tumour cells. Other groups of rats were co-injected with 1 mg octreotide, to investigate the effect of excess unlabeled peptide. All rats were sacrificed 21 days after inoculation of tumour cells and tumour growth was determined by counting the number of metastases on the surface of the liver lobes. Clinical The side-effects and antiproliferative effect of high, multiple radiotherapeutic doses of [IMIn-DTPA0]octreotide, using the Auger- and conversion-electrons emitted by '"in, are being investigated in patients and reported here preliminarily [14, 15, 21]. In this phase I study of therapy with [lllIn-DTPA]octreotide we included endstage patients with mainly a high tumour load of progressing neuroendocrine tumours. Patients and methods PTPA]octreotide and mlnCl3 (DRN 4901, 370 MBq/ml in HC1, pH = 1.5-1.9) were obtained from Mallinckrodt Medical BV (Petten, The Netherlands). [DTPA]octreotide was labelled with '"in as has been described previously [22]. Preclinical Rats in the experimental groups were injected with 370 MBq (0.5 ug) [mIn-DTPA]octreotide i.v. on day 1 and/or 8 after injection of tumour cells into the portal vein. Tumour inoculated rats in the control groups were injected with 0.5 ug unlabeled [DTPA]octreotide i.v. according to the same schedule. Clinical Since 1995, the typical doses per administration are 6000-7000 MBq '"in incorporated in 40-50 ug [DTPA]octreotide within 24 hours after production of '"in. It is given with at least two weeks intervals between administrations and a total of eight administrations is aimed at with extensions to 12-14 administrations. PRRT with ['"in-DTPA0]octreotide was applied after witnessed informed consent by the patient and approval by the medical ethics committee of our hospital. The following measurements, carried out prior to and between all administrations, served as parameters of possible side-effects: the usual hematological and chemical analyses of bone-marrow, liver, kidney and endocrine pancreatic (glucose or Hb Alc) function. Pituitary function (FreeT4, post-menopausal women: LH and FSH, men: testosterone) was assessed prior to and four weeks after the 4th and 8th administration of ["'ln-DTPA]octreotide: at these time points also possible effects on 1) the endocrine activity of the tumours and/or their production of specific serum markers, and 2) tumour-size (CTor MR!) were investigated. Pituitary-adrenal-axis function testing (metyrapone test) prior to and after eight administrations as well as long-term followup with three to four months' intervals was also investigated, if feasible. Dosimetry of (l"ln-DTPA|octreotide accumulation Scoring of tumour radioactivity uptake in patients prior to the start of treatment with ['"ln-DTPA]octreotide was done visually by using scintigrams obtained 24 hours after injection of a diagnostic dose (220 MBq) of ["'ln-DTPA]octreotide. The scoring grades used were 4 = intense, 3 = clear (higher than liver uptake), 2 = clear but faint (lower than or equal to liver uptake), 1 = equivocal and 0 = no accumulation. Patients were also scanned three and seven days after each administration of the radiotherapeutical dose. Percentage uptake of the administered dose in total body and in the most prominent tumour was calculated (data not shown). Uptakes decreased slowly or remained the same if the interval between the successive administrations was less than one month. In patients who had 6 or more administrations of 6000 to 7000 MBq of ['"ln-DTPA]octreotide with intervals of maximally one month between administrations, uptake in the tumour was still clearly visible after the last administration. Typical radiation doses to tissues with administered doses of 6000-7000 MBq ['"in-DTPA0]octreotide are: kidneys 300 - 1400 (depending on the relative biological effectiveness (RBE 1-20) for Auger electrons) cGy, spleen 200 cGy, liver 50 cGy, bone marrow 13 cGy (target organ for gamma photons), thyroid gland 25 cGy and pituitary 70 cGy [23]. Thus the critical organs are kidneys and spleen. With these administered doses the estimated tumour radiation doses are for a 10 gram tumour (assumptions: 1% uptake; effective half-life is equal to the physical half-life) 1700 and 6700 cGy (RBE for Auger electrons 1 and 20, respectively) and for a 100 gram tumour (1% uptake) 250 and 750 cGy, respectively. Pos effect (S + R) Results and discussion Abbreviations P - progression; S - stable; R - reduction in tumour size. * < 20 GBq and/or no FU 10.0- N = 21 Pre >20 >50 CUMULATIVE DOSE (GBq) of 1111n-DTPA-OCTREOTIDE Preclinical Pre >20 >50 CUMULATIVE DOSE (GBq) of 111ln-DTPA-OCTREOTIDE 7.5- N= 21 2 5- - Leuco's N= 21 21 12 Pre >20 >5O CUMULATIVE DOSE (GBq) of1'11n-DTPA-OCTREOTIDE N = 20 20 11 Pre >20 >50 >70 CUMULATIVE DOSE (GBq) of1111n-DTPA-OCTREOTIDE sfQP- strepto -in-pentetreotide J i l 1 11 H J i l 1 in Figure 4. The endocrine effect of [1"ln-DTPA]octreotide (or '"inpentetreotide) treatment (180 mCi or 6.7 GBq doses) in a patient with a very progressive, metastasised neuroendocrine tumour of the pancreas producing among other hormones insulin leading to profound hypoglycemia, which forced permanent hospitalization for iv. glucose administration. Between the 4th and 5th administration of ["'in-DTPA0]octreotide the patient could be discharged for a short period in which no special precautions had to be taken to maintain an euglycemia. Some tumours showed regression and others an increase in size. The effect of PRRT in this patient has been scored in the Table as 'progression'. The patient died in february 1996. start of ['"ln-DTPA0]octreotide therapy. In eight patients this treatment resulted in stable disease and in another six patients in actual tumour shrinkage. Thus, six out of 21 patients with progressive disease, who received an adequate dose of at least 20 GBq [H1InDTPA]octreotide, showed an antiproliferative effect. So far, it can be concluded that a response to treatment with ['"Tn-DTPA^octreotide, based on antiproliferative VOLUME GLUCAGON mln-Octreotlde -tgammaQT 8 10 12 2 4 6 S 10 12 2 4 6 8 9 11 1 3 5 7 9 12 90 | 91 | 92 | 93 94, MONTH-YEAR effects and a lowering of tumour markers in serum and/or urine, has been obtained if 1) the cumulative therapeutic dose of [luIn-DTPA]octreotide was at least about 20 GBq and 2) tumour uptake was at least grade 2 in order to get a stabilisation of disease and grade 3 or 4 for reduction in size of tumours (Table 1). The observed responses to this PRRT are in agreement with internalization of [luIn-DTPA]octreotide into tumour cells [because of the abundance of Auger and conversion electrons with a (very) short particle range or tissue penetration] and, with an antiproliferative effect induced by these electrons. Since it is at present not exactly known to what extent the radionuclide is localised intracellularly after administration of high amounts of [luIn-DTPA]octreotide, measurements of the actual radiation doses are not possible. It is to be expected that the radiotherapeutic use of radionuclides, such as 90Y, emitting the higher energies of (3-particles, coupled to (small) DOTA-chelated peptides, leads to higher radiation doses in a larger part of the tumour, also because of their more appropriate particle ranges or tissue penetration [24, 25]. In contrast to [90Y-DTPA]octreotide, 90Y labelled to [DOTA0,Tyr3]octreotide shows no dissociation from this DOTA chelated peptide in serum. The first two PRRT trials with [90Y-DOTA,Tyr3]octreotide started recently [26; Krenning, Kvols, Pauwels in Novartis B151 trial]. Based on the same assumptions as in section 3.1. and a similar biodistribution ('"in and 90Y labelled peptide) the estimated tumour radiation dose after an administered dose of 3.7 GBq 90Y-labelled peptide will be 16.500 cGy (10 g, 1% uptake) and 1800 cGy (100 g, 1% uptake). Estimated tissue doses are 2400 cGy for the kidneys, 150 NEUROENDOCRINE TUMOR 70% Prior Start After 11 X PRRT After hemihepa8/96 tectomy 11/96 DEPT. NUCLEAR MEDICINE UNIV. HOSP. ROTTERDAM cGy for the liver, and 1400 cGy for the spleen. Thus, tumours with an inhomogeneous distribution of cells expressing peptide receptors may then respond in a favourable way to this kind of treatment because of the better cross-fire. A problem during PRRT may be caused by the high uptake of 90Y-labelled peptide in the kidneys; small peptides in the blood plasma are filtered through the glomerular capillaries in the kidneys and subsequently reabsorbed almost completely (^90%) by the proximal tubular cells by carrier-mediated endocytosis. After the subsequent degradation process that takes place in the lysosomes of the tubular cells, their labeled degradation products are 'trapped' in the lysosomes [11]. This will cause a high dose of radioactivity in the kidneys, thereby reducing the possibilities for PRRT. We showed that the renal uptake of [niIn-DTPA]octreotide in rats could be reduced about 50% by single intravenous administration of 400 mg/kg L- or D-lysine [27, 28]. The membranes of renal tubular cells contain negatively charged sites, to which positively charged residues of peptides or proteins are thought to bind [29]. An inhibition of this binding process may explain the effects by administration of the positively charged amino acid lysine (both D- and L-lysine) on lnIn-DTPA-octreotide re-uptake [28]. The high tissue penetration of 90Y localised in tubular cells may affect the glomeruli and eventually induce a glomerular fibrosis. Measures have to be taken in order to decrease the renal accumulation of beta-emitting peptides when used for PRRT, e.g., with lysine infusions [27, 28]. In this study, in which [mIn-DTPA]octreotide was used, no special precautions were taken to lower renal uptake. In this phase I study of therapy with [1HIn-DTPA0]octreotide we only included end-stage patients with (neuroendocrine) tumours expressing a (rather) homogeneous distribution of somatostatin receptors and preferably high or modest accumulation of the radioligand. Based on our results with [mIn-DTPA]octreotide scintigraphy and given a relatively high accumulation of the radioligand in the tumour it is anticipated that patients with the following tumours might be candidates for this kind of treatment: most of (metastasised) GEP-tumours and paragangliomas, and 30% and 40% of malignant lymphomas and small-cell lung cancers, respectively. References


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E. P. Krenning, M. de Jong, P. P. M. Kooij, W. A. P. Breeman, W. H. Bakker, W. W. de Herder, C. H. J. van Eijck, D. J. Kwekkeboom, F. Jamar, S. Pauwels, R. Valkema. Radiolabelled somatostatin analogue(s) for peptide receptor scintigraphy and radionuclide therapy, Annals of Oncology, 1999, S23-S29, DOI: 10.1093/annonc/10.suppl_2.S23