The Value of Bone Marrow Assessment by FDG PET/CT, Biopsy and Aspirate in the Upfront Evaluation of Mantle Cell Lymphoma: A Nationwide Cohort Study.
Обработка статьи · этапы, ошибки и управление
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Ródenas Quiñonero Isabel, Marco-Ayala Javier, Chen-Liang Tzu-Hua, de la Cruz-Vicente Fátima, Baumann Tycho, Navarro José-Tomás, Martín García-Sancho Alejandro, Martin-Santos Taida, López-Jiménez Javier, Andreu Rafael, Parra-Virto Esther, Usas Andrea, Alonso David, Fernández-González Marta, Palomo Rumschisky Pablo, Frutos Laura, Navarro José Luis, Alvarez-Perez Rosa María, Sarandeses Pilar, Cortes Montserrat, Tamayo Pilar, Uña Jon, Martínez-Lorca Alberto, Ruiz Cristina, Lozano María Luisa, Ortuño Francisco José
Аннотация
OBJECTIVES: To evaluate the accuracy and prognostic impact of BMI assessed by PET/CT and BMB in a large series of MCL patients.
METHODS: We deconstructed the IPI-NCCN, MIPI, and MIPI-c indices and considered BMI as positive if indicated by a BMB, PET/CT scan, or a combination of both.
RESULTS: In the total cohort (n = 148), 110 patients had BMI detected by BMB and 33 by PET/CT. The sensitivity of BMB was higher than that of PET/CT (94.8% vs. 28.4%), as were its negative predictive value (84.2% vs. 27.8%) and accuracy (95.9% vs. 43.9%). In the total cohort, BMI detected by PET/CT showed a significant predictive value for PFS (p = 0.027), while BMB demonstrated independent prognostic value only in combination with PET/CT (p = 0.025). Among intensively treated patients (n = 128), PET/CT had significant clinical impact on PFS (p = 0.030), and when combined with BMB, it provided independent prognostic value for both PFS and OS (p = 0.026 and p = 0.033, respectively). Based on these findings, we propose a prognostic model (MCL-PET-I) that incorporates BMI by PET/CT, allowing for the identification of three groups with distinct clinical outcomes (p < 0.0001 for PFS and p = 0.00025 for OS).
CONCLUSIONS: In the upfront work of MCL, PET/CT-based BMI has greater prognostic impact, while BMB remains essential for staging. We propose the MCL-PET-I prognostic index, which effectively differentiates between clinical risk groups.