Maurie Markman, MD
The relevance of conducting and reporting well-designed, randomized trials to define optimal treatment for patients diagnosed with cancer is not open for debate. For example, modern oncologists could not fathom treating women with advanced epithelial ovarian cancer with cytotoxic chemotherapy without knowledge of preceding, decades-old controlled trial research that defined the central role of platinum-based combination cytotoxic chemotherapy in disease management, or, more recently, the potential of several maintenance strategies. The oncology community eagerly awaits the results of ongoing randomized trials that may further modify our therapeutic paradigms for the benefit of current and future patients.
Although this paradigm has demonstrated success, the traditional phase III randomized oncology trial model has come under increasing criticism, including over the validity of this approach in defining the clinical utility of new antineoplastic pharmaceutical agents and for what should be considered the standard of care in routine cancer management. For instance, the value of such studies is widely recognized as questionable when it comes to relating the findings to the real world of patients with cancer. The drawbacks include the lack of inclusion of more elderly populations that account for the majority of individuals with cancer, the general exclusion of patients with common comorbidities, and the difficulty of conducting randomized trials in molecularly defined subsets that may comprise less than 5% of patients with all but the most common cancer types.
Are Endpoints Meaningful?
One of the more difficult issues with randomized trials is defining endpoints that are clinically meaningful and objectively measurable while simultaneously permitting a statistically valid definitive analysis. As a result, the projected required sample size and the time necessary to confirm or refute a predefined study hypothesis may be either unrealistic or simply not acceptable to patients, clinicians, and society members who are waiting for the answer.
This is a critically important and reassuring report highlighting the long-term effects of a widely employed, health-related intervention. But one must inquire how relevant these results of a specific intervention (eg, drugs employed, dosages delivered, treatment schedules, duration of therapy, and age of initiation of treatment) are to what is considered routine or standard practice today. Further, will these results become the standard response to questions about the safety of menopausal hormonal therapy, despite current and future changes in routine management, until the results of the next phase III randomized trial are reported in the peer-reviewed literature?
Do Control Arms Reflect Guidelines?
Another recent question challenging the relevance of phase III randomized trials of antineoplastic agents is the selection of the control arms with which a novel experimental regimen is compared. In a concerning analysis examining phase III breast cancer clinical trials registered on the ClinicalTrials.gov website that included 229,000 women treated in 210 studies, the therapy tested in the control arms in 29% of the trials was not consistent with National Comprehensive Cancer Center Network guidelines.2
Further, the investigators examined clinical trials recruiting outside of the United States and compared them with German Gynecology Oncology Group guidelines and reached similar conclusions.
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