Key result
[177Lu]Lu-DOTA-TATE appears safe in GEP-NENs with only minor hematological toxicity and no renal decline.
Why the study?
Hematological and renal toxicity of [177Lu]Lu-DOTA-TATE therapy in patients with well-differentiated unresectable or metastatic GEP-NENs needed evaluation.
Does [177Lu]Lu-DOTA-TATE therapy cause hematological and renal toxicity in patients with GEP-NENs?
Observational (n=29)
Does [177Lu]Lu-DOTA-TATE therapy cause hematological and renal toxicity in patients with GEP-NENs?
[177Lu]Lu-DOTA-TATE therapy is safe and well-tolerated in patients with GEP-NENs, causing only minor, clinically insignificant hematological toxicity and no renal toxicity.
Supports short-term tolerability in GEP-NENs; leaves open need for larger prospective safety confirmation.
Background/Objectives: Lutathera® ([177Lu]Lu-DOTA-TATE) is the first radiolabelled somatostatin (SST) analog approved for the treatment of patients with well-differentiated (G1 and G2) unresectable or metastatic gastro-entero-pancreatic neuro-endocrine-neoplasms (GEP-NENs). The bone marrow and kidneys are critical organs for RLT with [177Lu]Lu-DOTA-TATE. Our purpose was to evaluate hematological and renal toxicity in 29 patients (18 males, 11 females) treated with Lutathera®. Methods: According to standard protocols, four cycles of (177Lu)Lu-DOTA-TATE were administered every eight/nine weeks. Patients received pre-medication with anti-emetic and anti-acid drugs and a slow amino acid infusion for renal protection. Blood count and serum creatinine data were collected at three time points: before the first cycle, after the second cycle, and at the end of treatment. Results: We found that almost all hematological parameters significantly decreased between the baseline and/or interim and post-therapy evaluation, although without a clinical impact. The presence of total tumor load or bone metastases had no influence on these findings, while male patients showed less hematological toxicity than females. Conversely, creatinine levels did not vary during treatment. Conclusions: Our study confirms that [177Lu]Lu-DOTATATE RLT is safe and well tolerated despite some minor (grade 1) hematological toxicity.
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Carideo et al. (2024) conducted an observational in Well-differentiated (G1 and G2) unresectable or metastatic gastro-entero-pancreatic neuro-endocrine-neoplasms (GEP-NENs) (n=29). Lutathera® ([177Lu]Lu-DOTA-TATE) was evaluated on Hematological and renal toxicity. [177Lu]Lu-DOTA-TATE therapy in 29 patients with GEP-NENs was safe and well tolerated, causing only minor (grade 1) hematological toxicity and no changes in creatinine levels.
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