Systemic treatment of advanced pancreatic cancer

被引:106
作者
Heinemann, Volker [1 ]
Haas, Michael [1 ]
Boeck, Stefan [1 ]
机构
[1] Univ Munich, Dept Oncol & Comprehens Canc Ctr, Klinikum Grosshadern, D-80539 Munich, Germany
关键词
Pancreatic cancer; Chemotherapy; Supportive therapy; Targeted therapy; PHASE-III TRIAL; MOLECULAR-WEIGHT HEPARIN; ARBEITSGEMEINSCHAFT-INTERNISTISCHE-ONKOLOGIE; ONCOLOGICO-ITALIA-MERIDIONALE; IRINOTECAN PLUS GEMCITABINE; RANDOMIZED CONTROLLED-TRIAL; NUCLEOSIDE TRANSPORTER 1; EARLY PALLIATIVE CARE; CELL LUNG-CANCER; VENOUS THROMBOEMBOLISM;
D O I
10.1016/j.ctrv.2011.12.004
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Pancreatic cancer belongs to the most malignant gastrointestinal cancers and, in its advanced stage, remains a deadly disease for nearly all affected patients. Treatment of metastatic adenocarcinoma of the pancreas not only involves chemotherapy and targeted therapy, but also requires attention to accompanying comorbidities as well as frequently intensive supportive treatment and psychosocial support. Gemcitabine-based combinations with fluoropyrimidines and platin analogs have essentially failed to provide a substantial prolongation of survival and may constitute a treatment option only in patients with a good performance status. Among targeted therapies, only the EGFR tyrosine kinase inhibitor erlotinib has shown activity which is marginal in the overall population, but clinically relevant in patients developing skin rash. New avenues of polychemotherapy are presently explored since the gemcitabine-free FOLFIRINOX-regimen (infusional 5-fluorouracil/folinic acid plus irinotecan and oxaliplatin) was shown to be markedly superior to gemcitabine in selected good-performance patients. Pancreatic cancer is notably characterized as a hypovascular tumor rich in desmoplastic stromal tissue. An innovative approach to treatment therefore focuses on peritumoral fibroblasts and aims to induce a depletion of the stroma either by inhibition of the hedgehog pathway or by targeting SPARC (secreted protein acidic and rich in cysteine) via application of albumin-bound paclitaxel. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:843 / 853
页数:11
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