Hepatocellular carcinoma (HCC) is the second cause of cancer–related deaths worldwide
constitutes a major global health problem. Although our understanding of the molecular
pathogenesis of hepatocellular HCC has improved, detected driver mutations are not yet
sufficiently reliable therapeutic targets.
The modern management of HCC is conceived only
within multidisciplinary schemes. Current systemic therapies are not curative and surgical
treatments remain the only potential curative treatments for selected patients with early stage HCC.
The role of parenchyma sparing liver resection for appropriately selected patients may
vary in different environments according to organ availability,and liver resection remains a
reliable curative method for HCC.
Meta-analyses have shown that clinical outcomes of
surgical resection are superior to ablative treatments in early stage HCC. Liver transplantation is
still the standard treatment for patients with early stage HCC. Lately the Milan Criteria are
considered too restrictive, still recognizing that the extension of transplantation criteria
beyond Milano criteria increases the risk of HCC recurrence.
Resection, ablation, transarterial
embolization and trans-arterial radiation are commonly applied to bridge patients to
transplant. Despite enormous advances in the therapy of HCC treatments at present, there
are currently no genuine breakthroughs for patients with HCC.
The Clinical Trials Planning
Meeting (CTPM) in HCC convened by the American Society of Clinical Oncology identified
the key knowledge gaps in HCC and define clinical research priorities. Major improvements
in survival provided by multimodal treatments witnessed in other cancers are not yet
available for HCC because effective systemic treatment modalities for HCC are still lacking.
Integration of bio-genetic tumor information into current tested treatment schemes and truly
multimodal surgery-based treatment schemes will enable the recruitment of less selected
patients in larger numbers to curative treatments.
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