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Comparison of the impact of 68Ga-DOTATATE and 18F-FDG PET/CT on clinical management in patients with neuroendocrine tumors

Comparison of the impact of 68Ga-DOTATATE and 18F-FDG PET/CT on clinical management in patients with neuroendocrine tumors
Comparison of the impact of 68Ga-DOTATATE and 18F-FDG PET/CT on clinical management in patients with neuroendocrine tumors
This study aimed to assess the clinical impact of 68Ga-DOTATATE and 18F-FDG with respect to the management plan and to evaluate the prognostic value of both tracers.

Methods: a total of 104 patients (55 male and 49 female; median age, 58 y; range, 20-90 y) with histologically proven neuroendocrine tumors (NETs) underwent both 68Ga-DOTATATE and 18F-FDG PET/CT. Twenty-eight patients (26.9%) had poorly differentiated tumors, and 76 (73.1%) had well differentiated tumors. PET/CT results and SUVs were compared with prognostic factors such as histologic grade (G1, G2, or G3, for low-grade [well differentiated], intermediate-grade [moderately differentiated], and high-grade [poorly differentiated], respectively), chromogranin A, and proliferation index (Ki-67).

Results: the 68Ga-DOTATATE and 18F-FDG PET/CT findings were discordant in 65 patients (62.5%) and concordant in 39 patients (37.5%). The results changed the therapeutic plan in 84 patients (80.8%). In 22 patients (21.1%), decision making was based on the 18F-FDG findings; in 32 (30.8%), on the findings with both radiotracers; and in 50 (48.1%), on the 68Ga-DOTATATE findings. The most frequent management decision based on 18F-FDG was initiation of chemotherapy (10 patients, 47.6%). The most common treatment decision due to 68Ga-DOTATATE was initiation of peptide receptor radionuclide therapy (14 patients, 27.4%). In 11 (39.2%) of 28 patients with poorly differentiated NETs, the management decision was based on only the 18F-FDG results. For 68Ga-DOTATATE, SUVmax was higher for G1 tumors and lower for G3 tumors (P 5 0.012). However, no significant differences in 18F-FDGderived SUVs were observed between different grades (P 5 0.38). The Mann-Whitney test showed significant differences in 68Ga-DOTATATE SUVmax between tumors with a Ki-67 of less than 5% and tumors with a Ki-67 of more than 5% (P 5 0.004), without significance differences in 18F-FDG SUVmax. Log-rank analysis showed statistically significant differences in survival for patients with bone metastasis versus soft-Tissue or no metastasis for both 18F-FDG (P 5 0.037) and 68Ga-DOTATATE (P 5 0.047). Overall survival declined rapidly with increasing grade (P 5 0.001), at an estimated 91 mo for G1, 59 mo for G2, and 48 mo for G3.

Conclusion: 18F-FDG PET/CT had no clinical impact on G1 NETs and a moderate impact on G2 NETs. However, in poorly differentiated NETs, 18F-FDG PET/CT plays a significant clinical role in combination with 68Ga-DOTATATE. 68Ga DOTATATE SUVmax relates to grade and Ki-67 and can be used prognostically. Key Words: 68Ga-DOTATATE; 18F-FDG PET/CT; neuroendocrine tumors; clinical impact; prognosis.
2159-662X
91-96
Panagiotidis, Emmanouil
9d13d090-665b-4660-b8f1-b611cc1f4857
Alshammari, Alshaima
cd7dc945-9ade-4aa0-8305-64ea1d2ee21d
Michopoulou, Sofia
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Skoura, Evangelia
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Naik, Keval
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Maragkoudakis, Emmanouil
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Mohmaduvesh, Mullan
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Al-Harbi, Mohammed
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Belda, Maria
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Caplin, Martyn E.
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Toumpanakis, Christos
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Bomanji, Jamshed
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Panagiotidis, Emmanouil
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Alshammari, Alshaima
cd7dc945-9ade-4aa0-8305-64ea1d2ee21d
Michopoulou, Sofia
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Skoura, Evangelia
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Naik, Keval
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Maragkoudakis, Emmanouil
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Mohmaduvesh, Mullan
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Al-Harbi, Mohammed
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Belda, Maria
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Caplin, Martyn E.
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Toumpanakis, Christos
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Bomanji, Jamshed
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Panagiotidis, Emmanouil, Alshammari, Alshaima, Michopoulou, Sofia, Skoura, Evangelia, Naik, Keval, Maragkoudakis, Emmanouil, Mohmaduvesh, Mullan, Al-Harbi, Mohammed, Belda, Maria, Caplin, Martyn E., Toumpanakis, Christos and Bomanji, Jamshed (2017) Comparison of the impact of 68Ga-DOTATATE and 18F-FDG PET/CT on clinical management in patients with neuroendocrine tumors. Journal of Nuclear Medicine, 58 (1), 91-96. (doi:10.2967/jnumed.116.178095).

Record type: Article

Abstract

This study aimed to assess the clinical impact of 68Ga-DOTATATE and 18F-FDG with respect to the management plan and to evaluate the prognostic value of both tracers.

Methods: a total of 104 patients (55 male and 49 female; median age, 58 y; range, 20-90 y) with histologically proven neuroendocrine tumors (NETs) underwent both 68Ga-DOTATATE and 18F-FDG PET/CT. Twenty-eight patients (26.9%) had poorly differentiated tumors, and 76 (73.1%) had well differentiated tumors. PET/CT results and SUVs were compared with prognostic factors such as histologic grade (G1, G2, or G3, for low-grade [well differentiated], intermediate-grade [moderately differentiated], and high-grade [poorly differentiated], respectively), chromogranin A, and proliferation index (Ki-67).

Results: the 68Ga-DOTATATE and 18F-FDG PET/CT findings were discordant in 65 patients (62.5%) and concordant in 39 patients (37.5%). The results changed the therapeutic plan in 84 patients (80.8%). In 22 patients (21.1%), decision making was based on the 18F-FDG findings; in 32 (30.8%), on the findings with both radiotracers; and in 50 (48.1%), on the 68Ga-DOTATATE findings. The most frequent management decision based on 18F-FDG was initiation of chemotherapy (10 patients, 47.6%). The most common treatment decision due to 68Ga-DOTATATE was initiation of peptide receptor radionuclide therapy (14 patients, 27.4%). In 11 (39.2%) of 28 patients with poorly differentiated NETs, the management decision was based on only the 18F-FDG results. For 68Ga-DOTATATE, SUVmax was higher for G1 tumors and lower for G3 tumors (P 5 0.012). However, no significant differences in 18F-FDGderived SUVs were observed between different grades (P 5 0.38). The Mann-Whitney test showed significant differences in 68Ga-DOTATATE SUVmax between tumors with a Ki-67 of less than 5% and tumors with a Ki-67 of more than 5% (P 5 0.004), without significance differences in 18F-FDG SUVmax. Log-rank analysis showed statistically significant differences in survival for patients with bone metastasis versus soft-Tissue or no metastasis for both 18F-FDG (P 5 0.037) and 68Ga-DOTATATE (P 5 0.047). Overall survival declined rapidly with increasing grade (P 5 0.001), at an estimated 91 mo for G1, 59 mo for G2, and 48 mo for G3.

Conclusion: 18F-FDG PET/CT had no clinical impact on G1 NETs and a moderate impact on G2 NETs. However, in poorly differentiated NETs, 18F-FDG PET/CT plays a significant clinical role in combination with 68Ga-DOTATATE. 68Ga DOTATATE SUVmax relates to grade and Ki-67 and can be used prognostically. Key Words: 68Ga-DOTATATE; 18F-FDG PET/CT; neuroendocrine tumors; clinical impact; prognosis.

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Accepted/In Press date: 30 June 2016
e-pub ahead of print date: 3 January 2017

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Local EPrints ID: 487902
URI: http://eprints.soton.ac.uk/id/eprint/487902
ISSN: 2159-662X
PURE UUID: 9f866166-b6d1-4295-b46f-b8d0db5d1d7e

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Date deposited: 08 Mar 2024 18:00
Last modified: 17 Mar 2024 07:57

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Contributors

Author: Emmanouil Panagiotidis
Author: Alshaima Alshammari
Author: Sofia Michopoulou
Author: Evangelia Skoura
Author: Keval Naik
Author: Emmanouil Maragkoudakis
Author: Mullan Mohmaduvesh
Author: Mohammed Al-Harbi
Author: Maria Belda
Author: Martyn E. Caplin
Author: Christos Toumpanakis
Author: Jamshed Bomanji

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