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Thomas A. Abrams

harvard university medical affiliates
H指数:37
被引数:6,116

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A Summary of the HCC-CARE Symposium: Collaborative Approaches to Reaching Equity in Hepatocellular Carcinoma in Boston by 2030

HCC-CARE Symposium总结:到2030年在波士顿实现肝细胞癌公平性的协作方法

2025-07-160
OA
An open label, phase II trial of ERK inhibition alone and in combination with autophagy inhibition in patients with metastatic cancreatic cancer
2024-09-150
PRE
Clinical outcomes and ctDNA correlates for CAPOX BETR: a phase II trial of capecitabine, oxaliplatin, bevacizumab, trastuzumab in previously untreated advanced HER2+gastroesophageal adenocarcinoma
2024-08-091
OAAI
Plain language summary of the FOENIX-CCA2 study: futibatinib for people with advanced bile duct cancer

FOENIX-CCA2研究的简明语言摘要: futibatinib用于晚期胆管癌患者

2024-06-170
OAAI
A phase 1 expansion cohort study evaluating the safety and efficacy of the CHK1 inhibitor LY2880070 with low-dose gemcitabine in metastatic pancreatic adenocarcinoma
2024-01-160
PRE
A Phase I Expansion Cohort Study Evaluating the Safety and Efficacy of the CHK1 Inhibitor LY2880070 with Low-dose Gemcitabine in Patients with Metastatic Pancreatic Adenocarcinoma
2023-10-114
OA
PD-1 Blockade Induces Reactivation of Nonproductive T-Cell Responses Characterized by NF-κB Signaling in Patients with Pancreatic Cancer

PD-1阻断诱导胰腺癌患者以nf-κb信号为特征的非生产性T细胞反应的重新激活

2023-09-210
OAAI
Biliary Tract Cancers, Version 2.2023 Featured Updates to the NCCN Guidelines

胆道癌,2.2023版更新了NCCN指南

2023-07-0171
OA
Long term results and ctDNA correlatives for CAPOX BETR: A multi-center phase II trial of capecitabine, oxaliplatin, bevacizumab and trastuzumab for previously untreated HER2 positive metastatic gastroesophageal adenocarcinoma
2023-04-140
PRE
Combined PD-1, BRAF and MEK inhibition in BRAFV600E colorectal cancer: a phase 2 trial

在BRAFV600E结直肠癌中联合PD-1,BRAF和MEK抑制: 一项2期试验

2023-01-2678
OAAI
Futibatinib for FGFR2-Rearranged Intrahepatic Cholangiocarcinoma

Futibatinib治疗FGFR2-Rearranged肝内胆管癌

2023-01-19243
OA
FGFR2 Extracellular Domain In-Frame Deletions Are Therapeutically Targetable Genomic Alterations That Function as Oncogenic Drivers in Cholangiocarcinoma
2021-04-2961
OA