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Andreas Block

Researcher at University of Hamburg

Publications -  29
Citations -  1924

Andreas Block is an academic researcher from University of Hamburg. The author has contributed to research in topics: Genetic enhancement & Cancer. The author has an hindex of 10, co-authored 25 publications receiving 1107 citations. Previous affiliations of Andreas Block include Massachusetts Institute of Technology.

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Perioperative chemotherapy with fluorouracil plus leucovorin, oxaliplatin, and docetaxel versus fluorouracil or capecitabine plus cisplatin and epirubicin for locally advanced, resectable gastric or gastro-oesophageal junction adenocarcinoma (FLOT4): a randomised, phase 2/3 trial.

TL;DR: In this article, the safety and efficacy of the docetaxel-based triplet FLOT (fluorouracil plus leucovorin, oxaliplatin, and doceteaxel) as a perioperative therapy for patients with locally advanced, resectable tumours was reported.
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Histopathological regression after neoadjuvant docetaxel, oxaliplatin, fluorouracil, and leucovorin versus epirubicin, cisplatin, and fluorouracil or capecitabine in patients with resectable gastric or gastro-oesophageal junction adenocarcinoma (FLOT4-AIO): results from the phase 2 part of a multicentre, open-label, randomised phase 2/3 trial.

TL;DR: Findings from the phase 2 part of the FLOT4 trial, which compared histopathological regression in patients treated with a docetaxel-based triplet chemotherapy versus an anthracycline-based doublet chemotherapy before surgical resection, suggest FLOT was associated with significantly higher proportions of patients achieving pathological complete regression than was ECF/ECX.
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Implications of SARS-CoV-2 Infection and COVID-19 Crisis on Clinical Cancer Care: Report of the University Cancer Center Hamburg.

TL;DR: Support and potential perspectives are provided to generate a discussion basis on how to maintain high-end cancer care during such a crisis and how to conduct patients safely into the future.
Journal Article

Amplified Muc1-specific gene expression in colon cancer cells utilizing a binary system in adenoviral vectors.

TL;DR: These new adenoviral vectors combing highly efficient and specific transgene expression will contribute to the safety and efficacy of experimental approaches in cancer gene therapy and will contribute To overcome weak expression, which is much lower than the widely used cytomegalovirus-promoter.