Cancer research and treatment · 2026
Incidence and Risk Factors for Development of Portal Hypertension and Sinusoidal Liver Injury Associated with T-DM1 in HER2-Positive Breast Cancer.
СтатьяНазвание и аннотация: Перевод пока не подготовлен
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.
Park Hee Woo, Jang Seo Yoon, Choi Ji Young, Chang Won, Na Hee Young, Lee Kyoung Ho, Kim Su Yeon, Seo Jeongmin, Chae Heejung, Suh Koung Jin, Kim Se Hyun, Kim Yu Jung, Jee Jongmin, Kim Jee Hyun, Jeong Sook-Hyang
Аннотация
PURPOSE: While an association between trastuzumab emtansine (T-DM1) and development of portal hypertension has been suggested, clinical studies on the incidence and risk factors remain limited.
MATERIALS AND METHODS: HER2-positive breast cancer patients treated with T-DM1 as adjuvant or palliative therapy were retrospectively enrolled. The composite endpoint of portal hypertension and sinusoidal liver injury was defined as development of splenomegaly and at least one among gastroesophageal varices, spontaneous portosystemic shunt, or portal hypertensive ascites; or biopsy-confirmed sinusoidal obstruction syndrome. Splenomegaly was defined as ≥50% increase in spleen volume, measured from CT images using a deep learning algorithm and reviewed by an independent radiologist. Univariable and multivariable analyses identified potential risk factors.
RESULTS: A total of 173 patients (median age: 53 (28-80)) were analyzed. Patients received a median of 14 (2-18) T-DM1 cycles in the adjuvant (n=62) and 11 (2-84) in the palliative setting (n=111). Portal hypertension and sinusoidal liver injury occurred in 31 (17.9%) (adjuvant; 11.3%, palliative; 21.6%), splenomegaly in 86 (49.7%) patients (adjuvant; 32.3%, palliative; 59.5%). Eight cases (4.6%) of liver-related T-DM1 discontinuation and 5 cases (2.9%) of significant liver-related complications were identified (4 variceal bleeding, one portosystemic encephalopathy). Age at T-DM1 treatment ≥60 years (OR 2.7, p=0.027), cumulative dose ≥55 mg/kg (OR 2.7, p=0.029), and baseline platelet count ≤150 × 109/L (OR 12.7, p=0.008) were identified as potential risk factors; however, the latter two associations should be interpreted with caution because the cumulative-dose association likely reflects prolonged T-DM1 exposure and the association observed for low baseline platelet count was derived from a very small subgroup of six patients.
CONCLUSION: Portal hypertension and sinusoidal liver injury are clinically significant in patients receiving T-DM1, warranting careful monitoring, especially in those with older age, low baseline platelet count, and prolonged T-DM1 exposure.
MATERIALS AND METHODS: HER2-positive breast cancer patients treated with T-DM1 as adjuvant or palliative therapy were retrospectively enrolled. The composite endpoint of portal hypertension and sinusoidal liver injury was defined as development of splenomegaly and at least one among gastroesophageal varices, spontaneous portosystemic shunt, or portal hypertensive ascites; or biopsy-confirmed sinusoidal obstruction syndrome. Splenomegaly was defined as ≥50% increase in spleen volume, measured from CT images using a deep learning algorithm and reviewed by an independent radiologist. Univariable and multivariable analyses identified potential risk factors.
RESULTS: A total of 173 patients (median age: 53 (28-80)) were analyzed. Patients received a median of 14 (2-18) T-DM1 cycles in the adjuvant (n=62) and 11 (2-84) in the palliative setting (n=111). Portal hypertension and sinusoidal liver injury occurred in 31 (17.9%) (adjuvant; 11.3%, palliative; 21.6%), splenomegaly in 86 (49.7%) patients (adjuvant; 32.3%, palliative; 59.5%). Eight cases (4.6%) of liver-related T-DM1 discontinuation and 5 cases (2.9%) of significant liver-related complications were identified (4 variceal bleeding, one portosystemic encephalopathy). Age at T-DM1 treatment ≥60 years (OR 2.7, p=0.027), cumulative dose ≥55 mg/kg (OR 2.7, p=0.029), and baseline platelet count ≤150 × 109/L (OR 12.7, p=0.008) were identified as potential risk factors; however, the latter two associations should be interpreted with caution because the cumulative-dose association likely reflects prolonged T-DM1 exposure and the association observed for low baseline platelet count was derived from a very small subgroup of six patients.
CONCLUSION: Portal hypertension and sinusoidal liver injury are clinically significant in patients receiving T-DM1, warranting careful monitoring, especially in those with older age, low baseline platelet count, and prolonged T-DM1 exposure.