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Toxicity manifestations encountered in peptide receptor radionuclide therapy setting
被引:0
|作者:
Parghane, Rahul V.
[1
,2
]
Basu, Sandip
[1
,2
]
机构:
[1] Tata Mem Hosp, Radiat Med Ctr BARC, Mumbai, India
[2] Homi Bhabha Natl Inst, Mumbai, India
关键词:
Lu-177-DOTATATE;
nephrotoxicity and bone marrow toxicity;
neuroendocrine tumors (NET);
peptide receptor radionuclide therapy (PRRT);
toxicity of PRRT;
RADIOLABELED SOMATOSTATIN ANALOG;
ENETS CONSENSUS GUIDELINES;
NEUROENDOCRINE TUMORS;
BOWEL OBSTRUCTION;
TYR(3) OCTREOTATE;
PHASE-I;
EFFICACY;
PRRT;
LU-177-DOTATATE;
EXTRAVASATION;
D O I:
10.1111/jne.13464
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Peptide receptor radionuclide therapy (PRRT) has demonstrated immense promise as a treatment for patients with neuroendocrine tumors (NET) who have somatostatin receptor (SSTR) expression. PRRT significantly reduces tumor growth, stabilizes the disease, and prolongs survival in a significant percentage of patients with metastatic/advanced NET. It produces an important beneficial effect on the quality of life (QOL) and effectively alleviates symptoms in patients with NET. Overall, PRRT is typically well-tolerated and most of the side effects are usually transient and subside on their own. It is, however, crucial to be cognizant of the potential toxicities associated with this treatment. This awareness will enable physicians to promptly detect, effectively manage, and prevent these toxicities by identifying high-risk factors in NET patients. This review provides an in-depth overview for clinicians managing NET about the toxicity of PRRT. The toxicities are stratified into acute, subacute, and long-term based on their onset following PRRT. Potential high-risk factors in order to treat effectively and prevent these toxicities in NET patients are presented including the management strategy. This review also discusses novel insights, perspectives, and recent advancements in predicting, preventing, and managing toxicity associated with PRRT, while offering prospective future research directions to minimize clinical toxicity and maximize the therapeutic benefits of PRRT as a treatment strategy for NET patients.
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