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Journal Of Comparative Effectiveness Research

Publication date: 2019-03-01
Pages: 205 - 216
Publisher: Future Medicine

Author:

Geldof, Tine
Rawal, Smita ; Van Dyck, Walter ; Huys, Isabelle

Keywords:

Science & Technology, Life Sciences & Biomedicine, Health Care Sciences & Services, clinical studies, combination studies, comparative studies, immune-oncology, literature review, precision-oncology, real-world evidence, METASTATIC COLORECTAL-CANCER, CELL LUNG-CANCER, PHASE-III TRIAL, REAL-WORLD DATA, BREAST-CANCER, DOUBLE-BLIND, OPEN-LABEL, TRASTUZUMAB EMTANSINE, 1ST-LINE TREATMENT, CLINICAL-PRACTICE, Antineoplastic Agents, Immunological, Breast Neoplasms, Colorectal Neoplasms, Combined Modality Therapy, Female, Humans, Lung Neoplasms, Male, Medical Oncology, Melanoma, Treatment Outcome, 32 Biomedical and clinical sciences, 42 Health sciences

Abstract:

To achieve therapeutic innovation in oncology, already expensive novel medicines are often concomitantly combined to potentially enhance effectiveness. While this aggravates the pricing problem, comparing effectiveness of novel yet expensive (concomitant) treatments is much needed for healthcare decision-making to deliver effective but affordable treatments. This study reviewed published clinical trials and real-world studies of targeted and immune therapies. In total, 48 studies compared and/or combined multiple novel products on breast, colorectal, lung and melanoma cancers. To a great extent, products evaluated in each study were owned by one manufacturer. However, cross-manufacturer assessments are also needed. Next to costs and intensive market competition, the absence of a regulatory framework enforcing real-world multiproduct studies prevents these from being conducted. Trusted third parties could facilitate such real-world studies, for which appropriate and efficient data access is needed.