Cureus · 2025
Real-World Outcomes of PET-Adapted Treatment for Classic Hodgkin's Lymphoma: A Study From a Single Tertiary Care Center.
СтатьяНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
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.
Iftikhar Imran, Abbas Mansoor, Afzal Maryam, Bilal Hasan, Uzair Muhammad, Qasim Muhammad, Ahsan Bushra, Ahmad Usman, Imam Bokhari Syed Waqas
Аннотация
Background Classic Hodgkin's lymphoma (CHL) is frequently treated using a positron emission tomography (PET)-directed approach, as demonstrated in the Response-Adapted Therapy for Hodgkin Lymphoma (RATHL) trial. This study aimed to compare real-world patient outcomes with those reported in the RATHL trial for individuals with advanced-stage disease. Methods This retrospective study included 169 adult patients aged 18 years and older (range 20-66 years). Only patients who received treatment and subsequent follow-up at our institution were included in this study. Results The study population had a male-to-female ratio of 1.86:1, with a median age of 30 years. B symptoms were present in 119 patients (70.4%), while bulky disease (>33% of the transthoracic diameter or >10 cm elsewhere) was observed in 55 patients (32.5%). More than half (57.4%) had stage IV disease at diagnosis, and the median follow-up time was 4.79 years. The three-year overall survival rate was 92.3%, and the progression-free survival rate was 76.9%. Among the 49 patients in the interim PET-positive group, the three-year overall survival and progression-free survival rates were 83.7% and 57.1%, respectively. Of these, 17 (34.7%) received escalated therapy with bleomycin, etoposide, doxorubicin, cyclophosphamide, vincristine, procarbazine, and prednisone (BEACOPP), while 32 (65.7%) continued with doxorubicin, bleomycin, vinblastine, and dacarbazine (ABVD) or standard BEACOPP. No significant survival difference was observed between these treatment groups. In the interim PET-negative group of 104 patients, 84 (80.8%) received ABVD, while 20 (19.2%) received doxorubicin, vinblastine, and dacarbazine (AVD). Again, no significant difference in survival was noted between these two groups. When comparing the interim PET-positive cohort to the RATHL trial, the three-year overall survival rates were 83.7% versus 87.8% (p = 0.45), and the progression-free survival rates were 57.1% versus 67.5% (p = 0.17), with no statistically significant difference. Conclusion This study highlights excellent real-world outcomes for treating CHL using a PET-directed approach similar to the RATHL trial. However, despite PET-guided therapy, interim PET positivity remained associated with significantly lower overall survival and progression-free survival rates. De-escalation to AVD in the interim PET-negative group did not negatively affect survival outcomes. ABVD remains a viable treatment option for PET-positive patients with good tolerance, strong response, or near-complete remission with single-site residual disease, without compromising survival.