Skeletal tumor burden on baseline 18F-fluoride PET/CT to predict bone marrow failure after radium-223.

2015 ◽  
Vol 33 (15_suppl) ◽  
pp. 11012-11012 ◽  
Author(s):  
Elba Etchebehere ◽  
John C. Araujo ◽  
Denai Milton ◽  
Patricia S Fox ◽  
Nancy Swanston ◽  
...  
2016 ◽  
Vol 41 (4) ◽  
pp. 268-273 ◽  
Author(s):  
Elba C. Etchebehere ◽  
John C. Araujo ◽  
Denái R. Milton ◽  
William D. Erwin ◽  
Richard E. Wendt ◽  
...  

2019 ◽  
Vol 52 (1) ◽  
pp. 33-40 ◽  
Author(s):  
Elba Etchebehere ◽  
Ana Emília Brito ◽  
Kalevi Kairemo ◽  
Eric Rohren ◽  
John Araujo ◽  
...  

Abstract Objective: To determine whether an interim 18F-fluoride positron-emission tomography/computed tomography (PET/CT) study performed after the third cycle of radium-223 dichloride (223RaCl2) therapy is able to identify patients that will not respond to treatment. Materials and Methods: We retrospectively reviewed 34 histologically confirmed cases of hormone-refractory prostate cancer with bone metastasis in patients submitted to 223RaCl2 therapy. All of the patients underwent baseline and interim 18F-fluoride PET/CT studies. The interim study was performed immediately prior to the fourth cycle of 223RaCl2. The skeletal tumor burden-expressed as the total lesion fluoride uptake above a maximum standardized uptake value of 10 (TLF10)-was calculated for the baseline and the interim studies. The percent change in TLF10 between the baseline and interim studies (%TFL10) was calculated as follows: %TFL10 = interim TLF10 - baseline TLF10 / baseline TLF10. End points were overall survival, progression-free survival, and skeletal-related events. Results: The mean age of the patients was 72.4 ± 10.2 years (range, 43.3-88.8 years). The %TLF10 was not able to predict overall survival (p = 0.6320; hazard ratio [HR] = 0.753; 95% confidence interval [CI]: 0.236-2.401), progression-free survival (p = 0.5908; HR = 1.248; 95% CI: 0.557-2.797) nor time to a bone event (p = 0.5114; HR = 1.588; 95% CI: 0.399-6.312). Conclusion: The skeletal tumor burden on an interim 18F-fluoride PET/CT, performed after three cycles of 223RaCl2, is not able to predict overall survival, progression-free survival, or time to bone event, and should not be performed to monitor response at this time.


2017 ◽  
Vol 2017 ◽  
pp. 1-10 ◽  
Author(s):  
Francesco Fiz ◽  
Samine Sahbai ◽  
Cristina Campi ◽  
Matthias Weissinger ◽  
Helmut Dittmann ◽  
...  

Rationale. Radium-223-Dichloride (Ra-223) is an alpha-emitter, used to treat bone metastases. Patients with high metastatic burden and/or with increased trabecular bone uptake could present a higher incidence of hematologic toxicity. We hypothesized that these two factors are predictors of bone marrow failure. Material and Methods. A computer algorithm discriminated between trabecular bone (BVol) and tumor metastases (MVol) within pretherapeutic whole-body skeletal SPECT/CT (N=47). The program calculated the metastatic invasion percent (INV%) as the MVol/(MVol+BVol) ratio and extracted the BVol mean counts. BVol counts were correlated to % drop of hemoglobin (Hb), leukocytes (WBC), and platelets (PLT) after 3/6 Ra-223 cycles. Patient-specific and computational-derived parameters were tested as predictors of hematologic toxicity with MANOVA. Results. BVol counts correlated with drop of Hb (R = 0,65, p<0.01) and PLT (R = 0,45, p<0.01). Appendicular BVol counts showed a better correlation (p<0.05, p<0.01, and p<0.001 for Hb, WBC, and PLT, resp.). INV% directly correlated with BVol counts (R = 0.68, p<0.001). At MANOVA, grade III/IV toxicity was predicted by INV% (p<0.01), by long-bone invasion (p<0.005), and by BVol counts (p<0.05). Conclusions. In patients with significant bone tumor burden, degree of bone invasion and trabecular bone uptake are predictors of subsequent bone marrow failure.


2020 ◽  
Author(s):  
SEVASTIAN MEDINA-ORNELAS ◽  
FRANCISCO OSVALDO GARCIA-PEREZ ◽  
MIGUEL Alvarez-Avitia ◽  
NORA SOBREVILLA-MORENO ◽  
ZAEL SANTANA-RIOS ◽  
...  

Abstract Objective: Evaluate impact after 223 Ra therapy and 18 F-NaF (sodium fluoride) PET/CT in the selection and evaluation of response in patients treated with 223 Ra in six different solid tumors. Material and Methods: Twenty patients with metastatic castration-resistant prostate cancer (mCRPC), seven metastatic castration-sensitive prostate cancer (mCSPC), three osteosarcoma, two breast cancer, two non-small cell lung cancer (NSCLC), one chondrosarcoma, one chordoma and one patient lung neuroendocrine carcinoma. Three groups of study were defined according total skeletal tumor-burden obtained by 18 F-NaF PET/CT, group 1 <1000cm 3 , group 2 1001–2999cm 3 and group 3 >3000cm 3 VOI´s. A semi-quantitative comparison was performed measuring the SUVmax values of VOIs values in all bone metastases in each patient previous to receive the first cycle of 223 Ra, after 3 and 6 cycles. Results: 30 patients non-progress disease was documented after 24±4 weeks. 8 patients progress disease was presented after three cycles of 223 Ra, two patients with osteosarcoma, four patients with mCRPC, one patient with chondrosarcoma and one patient with NSCLC. Group 1 patients showed better response rates compared to group 3 (p<0.05). Group 2 patients who showed improvement clinical and radiological, had prostate malignancies compared to those in the same group, but non-prostatic malignancies (p<0.05). No significant difference in group 2 patients compared to group 3 (p<0.67). Symptomatic skeletal-related event was observed in 7 patients. Conclusion: 18 F-NaF PET/CT allows to identify patients who show osteoblastic bone activity and discard or confirm progression in the interval PET/CT image, allowing change of treatment, reducing costs. High tumor-burden strongly suggests a poor response to treatment


Blood ◽  
2013 ◽  
Vol 122 (21) ◽  
pp. 1857-1857
Author(s):  
Yuki Nishida ◽  
Hiroki Sugihara ◽  
Masayuki Yamakura ◽  
Masami Takeuchi ◽  
Dai Chihara ◽  
...  

Abstract Background Modern imaging techniques such as whole body multidetector CT (MDCT) and 18F-fluorodeoxyglucose-positron emission tomography CT (PET-CT) are increasingly playing an important role in the diagnosis, staging, and treatment response monitoring of patients with MM because of limitations in hematological parameters. To date, however, few studies have evaluated the roles of MDCT and PET-CT in determining clinical outcome. This study was conducted to compare these two modalities for assessment of tumor burden and prognostic relevance in patients with symptomatic MM. Patients and methods Between December 2008 and November 2012, MDCT scans were performed in 64 newly diagnosed symptomatic MM patients as an initial evaluation of lytic bones and abnormal medullary and/or extramedullary lesions. Among them, PET-CT scan was performed in 56 patients. MDCT and PET-CT image acquisitions were as follows. MDCT was performed in a non-enhanced manner (acquisition time ∼45 s) and CT values (CTV) were measured using circular regions of interest for abnormal medullary lesions of the appendicular skeleton (AS; humerus and femur). The results were expressed in Hounsfield Units (HU). Since the normal CTV of yellow bone marrow ranges between -30 HU and -100 HU, we defined abnormal MDCT findings as marrow infiltration with CTV ≥ –30 HU, and the highest CTV among abnormal AS lesions was recorded in each patient. PET-CT was carried out according to the standard procedure. Data acquisition was performed in 3D mode. Field of view included the skull, upper limbs, and knees. The standardized uptake value (SUV) was calculated by the standard formula and the highest SUV (SUVmax) and SUV in the AS were collected. Visible areas of either focal or diffuse FDG uptake in bone were considered positive for myelomatous lesions. The numbers of abnormal lesions detected by these two modalities were investigated. CTV in MDCT and SUVmax in PET-CT were compared in relation to clinical variables and survival outcome. Statistical analyses were performed using STATA software ver. 12.0. Results Among 64 consecutive patients (36 male and 28 female, median age 71 yr, range 44 – 90), IgG, IgA, light chain only, and non-secretory subtypes were 34, 19, 10, and 1, respectively. Fifty-one patients and 34 patients were disease stage III according to the Durie-Salmon staging system (D-S) and International Staging System (ISS), respectively. Abnormal findings of AS were detected in 53 of 64 patients (82.8%) by MDCT. However, such findings were detected only in 15 patients (26.8%) by PET-CT. Patients with D-S stage III had significantly higher CTV on MDCT than those with D-S stage I or II (mean CTV: 16.94 HU vs -9.59 HU, p = 0.032). In correlation analysis between CTV, SUVmax, serum beta-2-microglobulin, the amount of M protein, and abnormal serum lactate dehydrogenase, a positive correlation was found between CTV and M protein (r = 0.36, p = 0.003), however, SUVmax by PET-CT was not significantly correlated with any variables. All patients were treated with bortezomib and/or lenalidomide-containing regimens. Based on IMWG response criteria, the numbers of patients achieving complete remission, very good partial response, partial response, and stable disease or less were 27, 14, 20, and 3, respectively. With median follow-up duration of 18.9 months (range: 2.9 – 52.7), one-year progression-free survival (PFS) and overall survival (OS) was 46.3% and 90.2%, respectively. With the cut-off value of CTV ≥ -10 HU, high CTV had significantly shorter PFS and OS (median PFS, 9.3 months vs. 19.5 months, p = 0.041, Figure 1; median OS, not reached, p = 0.018, Figure 2). However, with the cut-off value of SUVmax ≥ 6, high SUVmax was not associated with shorter PFS or OS. Conclusions MDCT had higher sensitivity for detection of abnormal medullary lesions in AS than PET-CT. As CTVs in MDCT were significantly associated with the amount of M protein and D-S stage, CTVs may reflect tumor burden of MM. Although the follow-up duration was relatively short, our results suggest that the presence of medullary lesions in AS with high CTV may be associated with poorer outcome in patients with symptomatic MM. Disclosures: No relevant conflicts of interest to declare.


2018 ◽  
Vol 46 (4) ◽  
pp. 378-383 ◽  
Author(s):  
Ana E. Brito ◽  
Felipe Mourato ◽  
Allan Santos ◽  
Camila Mosci ◽  
Celso Ramos ◽  
...  
Keyword(s):  
Pet Ct ◽  

2015 ◽  
Vol 56 (10) ◽  
pp. 1507-1512 ◽  
Author(s):  
E. M. Rohren ◽  
E. C. Etchebehere ◽  
J. C. Araujo ◽  
B. P. Hobbs ◽  
N. M. Swanston ◽  
...  
Keyword(s):  
Pet Ct ◽  

2015 ◽  
Vol 56 (8) ◽  
pp. 1177-1184 ◽  
Author(s):  
E. C. Etchebehere ◽  
J. C. Araujo ◽  
P. S. Fox ◽  
N. M. Swanston ◽  
H. A. Macapinlac ◽  
...  

Oncotarget ◽  
2017 ◽  
Vol 8 (22) ◽  
pp. 36001-36011 ◽  
Author(s):  
Ana E. Brito ◽  
Allan Santos ◽  
André Deeke Sasse ◽  
Cesar Cabello ◽  
Paulo Oliveira ◽  
...  

2021 ◽  
Author(s):  
hua jun wang ◽  
chenjie ZHOU ◽  
jianhua Wang

Abstract Background: Bone marrow metastasis is common in liver cancer and lung cancer, but there are few reports on bone marrow metastasis of colon cancer. So far, there are no research reports from mainland China; especially reports of bone marrow metastasis combined with septic shock as the main manifestation are even rarer. Case presentation: A 71-year-old elderly woman with sepsis as the first symptom, mainly manifested as high fever, low blood pressure, high inflammation indicators, etc. CT examination revealed mild inflammation of the lungs and no obvious abnormalities in the abdomen. Blood culture culture suggested Escherichia coli and Aeromonas hydrophila/caviae. After anti-infective treatment, the patient's sepsis symptoms improved significantly, but after repeated platelet transfusion, he still could not correct hypothrombosis. Finally, a large number of malignant cells were found through a bone marrow puncture smear, and further PET-CT examination confirmed that the ascending colon malignant tumor was accompanied by multiple metastases such as the liver and bones. The patient was eventually unable to tolerate surgery due to bone marrow failure and liver failure and died 3 weeks after admission.Conclusions: We hope that this case report can raise people’s awareness of the insidiousness of colon cancer and the possibility of metastasis to the bone marrow, especially for patients with progressive thrombocytopenia that is difficult to correct. Thrombocytopenia needs to be treated differently from sepsis.


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