74 research outputs found
Active Lumbar Spondylodiscitis on [68Ga]Ga-PSMA-11 PET/CT Mimicking Bone Metastasis
We report a [68Ga]Ga-PSMA-11 positron emission tomography/computed tomography
(PET/CT) scan of a 71-year-old man with metastatic castration-resistant prostate cancer (mCRPC)
and concomitant active lumbar spondylodiscitis, both PSMA-positive on a PET/CT scan. This
interesting image should advise colleagues to consider spondylodiscitis as a differential diagnosis of
PSMA-positive findings in the spine, particularly if intervertebral space and soft tissue are involved
Systemic Mastocytosis Treatment with Midostaurin: [18F]FDG PET/CT as a Potential Monitoring Tool for Therapy Outcome
We report the case of a 68-year-old patient with diagnosed systemic mastocytosis and
histopathologically confirmed manifestations in the stomach and intestinal tract who underwent 18FFluorodeoxyglucose ([18F]FDG) positron-emission tomography/computed tomography (PET/CT)
pre- and post-6-month therapy with midostaurin, an established tyrosine kinase inhibitor. Posttherapeutic [18F]FDG PET/CT showed decreased multifocal tracer uptake in the known lesions in
the gastrointestinal tract, which was consistent with relief of the patientâs symptoms and decrease in
serum tryptase level. [18F]FDG PET/CT may thus be considered a potential method for monitoring
the outcome of midostaurin therapy in systemic mastocytosis
Histologically Confirmed Testicular Metastasis Revealed by [89Zr]Zr-PSMA-617 PET/CT in a Patient with Biochemical Recurrence of Prostate Cancer and Negative Conventional PSMA PET/CT Imaging
We present an interesting image of a testicular metastasis from prostate cancer revealed by
[
89Zr]Zr-PSMA-617 PET/CT imaging in a 70-year-old man with biochemical recurrence and negative
conventional [68Ga]Ga-PSMA-11 PET/CT imaging. This case should encourage the consideration of
[
89Zr]Zr-PSMA-617 PET/CT if conventional PSMA PET/CT imaging had failed to localize biochemical
recurrence, and may remind colleagues of this rare but potential metastatic localization in this setting
Striatal dopamine transporters and cognitive function in Parkinson's disease
Background
Idiopathic Parkinsonâs disease (PD) is characterized by clinical motor symptoms including hypokinesia, rigidity and tremor. In addition to the movement disorder, cognitive deficits are commonly described. In the present study, we applied FPâCIT SPECT to investigate the impact of nigrostriatal dopaminergic degeneration on cognitive function in PD patients.
Methods
Fiftyâfour PD patients underwent [123I]FPâCIT SPECT and CERAD (Consortium to Establish a Registry for Alzheimerâs Disease) testing. FPâCIT SPECT visualized the density of presynaptic dopamine transporters in both striata, each subdivided into a limbic, executive and sensorimotor subregion according to the atlas of Tziortzi et al (Cereb Cortex 24, 2014, 1165). CERAD testing quantified cognitive function.
Results
In the CERAD testing, PD patients exhibited deficits in the domains of semantic memory, attention, visuospatial function, nonâverbal memory and executive function. After correction for multiple testing, the performance of the subtests Figure Recall and TrailâMaking Test A correlated significantly with FPâCIT uptake into the ipsilateral executive subregion. The performance of the subtest Figure Saving correlated significantly with FPâCIT uptake into the contralateral executive subregion.
Conclusions
The significant correlation between cognitive function and density of nigrostriatal dopamine transporters, as assessed by FPâCIT SPECT, indicate that striatal dopaminergic pathwaysâprimarily the executive striatal subregionâare relevant to cognitive processing in PD
Strongly Radioiodine-Positive Pancreatic Adenocarcinoma Mimicking Metastasis of Differentiated Thyroid Cancer
We present an interesting image of a strikingly intense radioiodine accumulation of a
histologically proven pancreatic adenocarcinoma mimicking metastasis of differentiated thyroid
cancer in a 63-year-old woman with recurrence of papillary thyroid carcinoma undergoing radioiodine
therapy. This interesting image should draw attention to considering pancreatic adenocarcinoma in
radioiodine-positive pancreatic lesions
PSMA-Positive Follicular Thyroid Carcinoma Incidentally Detected by [68Ga]Ga-PSMA-11 PET/CT: Correlation with Immunohistology Confirms Neovascular PSMA-Expression
We present an interesting image of an intense PSMA-positive follicular thyroid carci noma incidentally detected by [68Ga]Ga-PSMA-11 PET/CT in a 76-year-old man with biochemical
recurrence of prostate cancer. Immunohistochemical staining demonstrated PSMA expression in
the endothelial cells of tumor tissue. This interesting image should remind colleagues to consider
malignant thyroid neoplasia in PSMA-positive thyroid lesions
Does PRRT with standard activities of 177Lu-octreotate really achieve relevant somatostatin receptor saturation in target tumor lesions?: insights from intra-therapeutic receptor imaging in patients with metastatic gastroenteropancreatic neuroendocrine tumors
Twenty plantain crop fields were sampled to identify Meloidogyne spp. in Tierralta and Valencia municipalities. Ten soil and root samples per field were taken to obtain the nematodes. Meloidogyne species classification was based on the perineal pattern of the female, shape of the stylet in females, males and juveniles (J2), and shape and number of rings on the cephalic region in J2 and males. Stylet length and dorsal oesophageal gland (DOG) on males, females and J2, body length, tail and hyaline tail region in J2 were measured to identify the specie of root-knot nematode. Meloidogyne spp. were found in 80% of the fields in Valencia, and 60% of the field in Tierralta. M. incognita and M. arenaria were detected. M. incognita was the most frequent species throughout the sampled area. Mixtures of both species were found in both municipalities. This is the first report of mixed M. incognita and M. arenaria associated to plantain crop in Colombia.Veinte cultivos de plĂĄtano fueron muestreados en los municipios de Tierralta y Valencia para identificar las especies de Meloidogyne asociadas a este cultivo. Diez muestras de suelos y raĂces fueron colectadas en cada de los lotes, las cuales fueron usadas para la obtenciĂłn de los nemĂĄtodos. La clasificaciĂłn de las especies se basĂł en las caracterĂsticas morfolĂłgicas (patrĂłn perineal de las hembras, forma del estilete de hembras, machos y juveniles (J2); forma y nĂșmero de anillos de la regiĂłn cefĂĄlica de J2 y machos) y morfomĂ©tricas (longitud del estilete y la distancia de la base del estilete a la desembocadura de la glĂĄndula dorsal (D.G.O) de hembras, machos y J2; longitud del cuerpo, la cola y la regiĂłn hialina de los J2. En el 80% de las fincas en Valencia se detectĂł la presencia de estos nematodos, mientras que el 60% de los predios en Tierralta fueron positivos para los mismos. Las especies encontradas fueron Meloidogyne incognita y M. arenaria. De estas, M. incognita fue la mĂĄs frecuente detectada en la zona productora de plĂĄtano en los dos municipios. Mezcla de especies fueron detectadas en ambos municipios. Se reporta por primera vez en Colombia las especies M. incognita y M. arenaria, asĂ como la mezcla de las mismas asociadas al cultivo de plĂĄtano
Molecular imaging and biochemical response assessment after a single cycle of [225Ac]Ac-PSMA-617/[177Lu]Lu-PSMA-617 tandem therapy in mCRPC patients who have progressed on [177Lu]Lu-PSMA-617 monotherapy
Rationale: Despite the promising results of prostate-specific membrane antigen (PSMA)-targeted 177Lu
radioligand therapy in metastatic castration-resistant prostate carcinoma (mCRPC), some patients do not
respond and other patients with initially good response develop resistance to this treatment. In this study,
we investigated molecular imaging and biochemical responses after a single cycle of
[225Ac]Ac-PSMA-617/[177Lu]Lu-PSMA-617 tandem therapy in patients who had progressed on
[177Lu]Lu-PSMA-617 monotherapy.
Methods: Seventeen patients with mCRPC were included in a retrospective, monocenter study.
Molecular imaging-based response was assessed by modified PERCIST criteria using the whole-body total
lesion PSMA (TLP) and molecular tumour volume (MTV) derived from [68Ga]Ga-PSMA-11 PET/CT.
Biochemical response was evaluated according to PCWG3 criteria using the prostate-specific antigen
(PSA) serum value. Concordance and correlation statistics as well as survival analyses were performed.
Results: Based on the molecular imaging-based response assessment, 5 (29.4%) patients showed partial
remission and 7 (41.2%) had stable disease. The remaining 5 (29.4%) patients had further progression,
four with an increase in TLP/MTV of >30% and one with stable TLP/MTV but appearance of new
metastases. Based on the biochemical response assessment, 5 (29.4%), 8 (47.1%), and 4 (23.5%) patients
showed partial remission, stable disease, and progressive disease, respectively. A comparison of the
response assessment methods showed a concordance of 100% (17/17) between TLP and MTV and 70.6%
(12/17) between TLP/MTV and PSA. Patients with partial remission, independently assessed by each
method, had better overall survival (OS) than patients with either stable or progressive disease. The
difference in OS was statistically significant for the molecular imaging response assessment (median OS
not reached vs. 8.3 m, p = 0.044), but not for the biochemical response assessment (median OS 18.1 m vs.
9.4 m, p = 0.468).
Conclusion: Based on both assessment methods, [225Ac]Ac-PSMA-617/[177Lu]Lu-PSMA-617 tandem
therapy is an effective treatment for the highly challenging cohort of patients with mCRPC who have
progressed on [177Lu]Lu-PSMA-617 monotherapy. Molecular imaging response and biochemical PSA
response were mostly concordant, though a considerable number of cases (29.4%) were discordant.
Molecular imaging response reflecting the change in total viable tumour burden appears to be superior to
PSA change in estimating survival outcome after tandem therapy
Addition of Standard Enzalutamide Medication Shows Synergistic Effects on Response to [177Lu]Lu-PSMA-617 Radioligand Therapy in mCRPC Patients with Imminent Treatment FailureâPreliminary Evidence of Pilot Experience
Well-received strong efficacy of prostate-specific membrane antigen (PSMA)-targeted
radioligand therapy (RLT) does not prevent patients from either early or eventual disease progression
under this treatment. In this study, we investigated co-medication with enzalutamide as a potential
re-sensitizer for PSMA-RLT in patients with imminent treatment failure on standard 177Lu-based
PSMA-RLT. Ten mCRPC patients who exhibited an insufficient response to conventional [177Lu]Lu PSMA-617 RLT received oral medication of enzalutamide 160 mg/d as an adjunct to continued PSMA RLT. Prostate-specific antigen (PSA) and standard toxicity screening lab work-up were performed
to assess the treatment efficacy and safety in these individuals. The mean PSA increase under
PSMA-RLT before starting the re-sensitizing procedure was 22.4 ± 26.5%. After the introduction of
enzalutamide medication, all patients experienced a PSA decrease, â43.4 ± 20.0% and â48.2 ± 39.0%,
after one and two cycles of enzalutamide-augmented PSMA-RLT, respectively. A total of 70% of
patients (7/10) experienced partial remission, with a median best PSA response of â62%. Moreover,
5/6 enzalutamide-naĂŻve patients and 2/4 patients who had previously failed enzalutamide exhibited
a partial remission. There was no relevant enzalutamide-induced toxicity observed in this small
cohort. This pilot experience suggests the synergistic potential of adding enzalutamide to PSMA-RLT
derived from the intra-individual comparison of 177Lu-based PSMA-RLT ± enzalutamide
Renal Safety of [177Lu]Lu-PSMA-617 Radioligand Therapy in Patients with Compromised Baseline Kidney Function
Background: Radioligand therapy (RLT) targeting prostate-specific membrane antigen
(PSMA) is an effective antitumor-treatment in metastatic castration-resistant prostate carcinoma
(mCRPC). Concerns of potential nephrotoxicity are based on renal tubular PSMA expression and the
resulting radiopharmaceutical retention during RLT, but data confirming clinically significant renal
toxicity are still lacking. In this study, patients with significantly impaired baseline kidney function
before initiation of therapy were investigated for treatment-associated nephrotoxicity and the potential relationship with administered activities of [177Lu]Lu-PSMA-617. Methods: Twenty-two mCRPC
patients with impaired renal function (glomerular filtration rate (GFR) †60 mL/min) who received
more than two cycles of [177Lu]Lu-PSMA-617 RLT (median 5 cycles and median 6-week time interval
between consecutive cycles) were analyzed in this study. Patients were treated within a prospective
patient registry (REALITY Study, NCT04833517). Cumulative administered activities ranged from
17.1 to 85.6 GBq with a median activity of 6.5 GBq per cycle. Renal function was closely monitored
during and after PSMA-RLT. Results: Mean pre-treatment GFR was 45.0 ± 10.7 mL/min. After two
(22/22 patients), four (20/22 patients), and six cycles (10/22 patients) of RLT, a significant increase
of GFR was noted (each p < 0.05). End-of-treatment GFR (54.1 ± 16.7 mL/min) was significantly
higher than baseline GFR (p = 0.016). Only one patient experienced deterioration of renal function
(change of CTCAE grade 2 to 3). The remaining patients showed no significant reduction of GFR,
including follow-up assessments (6, 9, and 12 months), and even showed improved (10/22 patients)
or unchanged (11/22 patients) CTCAE-based renal impairment grades during and after the end
of PSMA-RLT. No significant correlation between the change in GFR and per-cycle (p = 0.605) or
cumulative (p = 0.132) administered activities were found. Conclusions: As pre-treatment chronic
kidney failure did not lead to detectable RLT-induced deterioration of renal function in our study, the
nephrotoxic potential of [177Lu]Lu-PSMA-617 RLT may be overestimated and not of clinical priority
in the setting of palliative treatment in mCRPC. We suggest not to categorically exclude patients from
enrolment to PSMA-RLT due to renal impairment
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