Impact of baseline F-flotufolastat PET bone tumor volume for prognosticating severe hematologic toxicity in patients with metastatic castration-resistant prostate Cancer receiving Lu-PSMA-targeted radioligand therapy.
1/5 보강
PICO 자동 추출 (휴리스틱, conf 2/4)
유사 논문P · Population 대상 환자/모집단
환자: baseline F-flotufolastat-PET scans and complete hematologic profiles were analyzed
I · Intervention 중재 / 시술
추출되지 않음
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
Prior [Ra]Radiumdichloride treatment prognosticated severe thrombocytopenia (HR 6.43, p = 0.021). [CONCLUSION] Baseline F-flotufolastat-PET metrics and pretherapeutic clinical parameters are key prognostic factors for severe hematologic toxicity in mCRPC patients treated with [Lu]Lu-PSMA-I&T.
[PURPOSE] This retrospective analysis evaluated the prognostic value of baseline F-flotufolastat-PET bone tumor metrics for severe hematologic toxicity in metastatic castration-resistant prostate canc
- p-value p = 0.036
- p-value p < 0.001
APA
Karimzadeh A, Hansen K, et al. (2025). Impact of baseline F-flotufolastat PET bone tumor volume for prognosticating severe hematologic toxicity in patients with metastatic castration-resistant prostate Cancer receiving Lu-PSMA-targeted radioligand therapy.. European journal of nuclear medicine and molecular imaging, 52(12), 4434-4445. https://doi.org/10.1007/s00259-025-07200-7
MLA
Karimzadeh A, et al.. "Impact of baseline F-flotufolastat PET bone tumor volume for prognosticating severe hematologic toxicity in patients with metastatic castration-resistant prostate Cancer receiving Lu-PSMA-targeted radioligand therapy.." European journal of nuclear medicine and molecular imaging, vol. 52, no. 12, 2025, pp. 4434-4445.
PMID
40383857 ↗
Abstract 한글 요약
[PURPOSE] This retrospective analysis evaluated the prognostic value of baseline F-flotufolastat-PET bone tumor metrics for severe hematologic toxicity in metastatic castration-resistant prostate cancer (mCRPC) patients treated with [Lu]Lu-PSMA-I&T.
[METHODS] Data from 182 mCRPC patients with baseline F-flotufolastat-PET scans and complete hematologic profiles were analyzed. Bone lesions were semiautomatically delineated, and clinical parameters (e.g., pretreatments, lab results) were assessed. Hematologic adverse events (AEs) were defined per Common Terminology Criteria for Adverse Events version 5.0, with grades 3-4 considered severe. Cox regression was used to identify prognostic factors for AEs.
[RESULTS] Baseline bone tumor volume prognosticated leukocytopenia (HR 1.03 per 100 ml, p = 0.036), while the number of bone lesions was prognostic for anemia (HR 1.04 per 10 lesions, p < 0.001) and severe anemia (HR per 10 lesions 1.05, p = 0.009). Higher baseline hemoglobin correlated with reduced leukocytopenia (HR 0.74, p = 0.002), thrombocytopenia (HR 0.80, p = 0.033), and severe anemia (HR 0.52, p < 0.001). Baseline kidney dysfunction was linked to anemia (HR 2.46, p = 0.002) and severe anemia (HR 3.81, p = 0.023). Prior [Ra]Radiumdichloride treatment prognosticated severe thrombocytopenia (HR 6.43, p = 0.021).
[CONCLUSION] Baseline F-flotufolastat-PET metrics and pretherapeutic clinical parameters are key prognostic factors for severe hematologic toxicity in mCRPC patients treated with [Lu]Lu-PSMA-I&T.
[METHODS] Data from 182 mCRPC patients with baseline F-flotufolastat-PET scans and complete hematologic profiles were analyzed. Bone lesions were semiautomatically delineated, and clinical parameters (e.g., pretreatments, lab results) were assessed. Hematologic adverse events (AEs) were defined per Common Terminology Criteria for Adverse Events version 5.0, with grades 3-4 considered severe. Cox regression was used to identify prognostic factors for AEs.
[RESULTS] Baseline bone tumor volume prognosticated leukocytopenia (HR 1.03 per 100 ml, p = 0.036), while the number of bone lesions was prognostic for anemia (HR 1.04 per 10 lesions, p < 0.001) and severe anemia (HR per 10 lesions 1.05, p = 0.009). Higher baseline hemoglobin correlated with reduced leukocytopenia (HR 0.74, p = 0.002), thrombocytopenia (HR 0.80, p = 0.033), and severe anemia (HR 0.52, p < 0.001). Baseline kidney dysfunction was linked to anemia (HR 2.46, p = 0.002) and severe anemia (HR 3.81, p = 0.023). Prior [Ra]Radiumdichloride treatment prognosticated severe thrombocytopenia (HR 6.43, p = 0.021).
[CONCLUSION] Baseline F-flotufolastat-PET metrics and pretherapeutic clinical parameters are key prognostic factors for severe hematologic toxicity in mCRPC patients treated with [Lu]Lu-PSMA-I&T.
🏷️ 키워드 / MeSH 📖 같은 키워드 OA만
- Humans
- Male
- Prostatic Neoplasms
- Castration-Resistant
- Aged
- Bone Neoplasms
- Lutetium
- Middle Aged
- Prognosis
- Retrospective Studies
- Tumor Burden
- 80 and over
- Radiopharmaceuticals
- Hematologic Diseases
- Radioisotopes
- Glutamate Carboxypeptidase II
- Prostate-Specific Antigen
- Bone tumor metrics
- Hematologic toxicity
- PSMA radioligand therapy
- [177Lu]Lu-PSMA-I&T
- mCRPC
같은 제1저자의 인용 많은 논문 (2)
- Overview of selected completed prospective studies on PSMA-targeted radioligand therapy with [177Lu]Lu-PSMA-617 in metastatic castration-resistant prostate cancer.
- Overview of selected completed prospective studies on PSMA-targeted radioligand therapy with [177Lu]Lu-PSMA-617 in metastatic castration-resistant prostate cancer.
🏷️ 같은 키워드 · 무료전문 — 이 논문 MeSH/keyword 기반
- A Phase I Study of Hydroxychloroquine and Suba-Itraconazole in Men with Biochemical Relapse of Prostate Cancer (HITMAN-PC): Dose Escalation Results.
- Self-management of male urinary symptoms: qualitative findings from a primary care trial.
- Clinical and Liquid Biomarkers of 20-Year Prostate Cancer Risk in Men Aged 45 to 70 Years.
- Diagnostic accuracy of Ga-PSMA PET/CT versus multiparametric MRI for preoperative pelvic invasion in the patients with prostate cancer.
- Comprehensive analysis of androgen receptor splice variant target gene expression in prostate cancer.
- Clinical Presentation and Outcomes of Patients Undergoing Surgery for Thyroid Cancer.