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Testing Targeted Therapies in Cancer using Structural DNA Alteration Analysis and Patient-Derived Xenografts
Published on: July 25, 2020
Molecular testing to deliver personalized chemotherapy recommendations: risking over and undertreatment
Timothée Olivier1,2, Vinay Prasad3
1Department of Oncology, Geneva University Hospital, 4 Gabrielle-Perret-Gentil Street, 1205, Geneva, Switzerland. timothee.olivier@hcuge.ch.
Background:
In the adjuvant setting of cancer treatment, de-escalation strategies have the goal of omitting or minimizing treatment in patients, without compromising outcomes. Historically, eligibility for adjuvant treatment solely relied on the patient's clinical and tumor's pathological characteristics. At the turn of the century, based on new biological understanding, molecular-based strategies were tested and sometimes implemented.
Main Body:
However, we illustrate how molecularly based de-escalation strategies may paradoxically lead to overtreatment. This may happen when the novel approach is tested in lieu of standard management and may not yield the same results when being implemented in addition to usual practice. In the DYNAMIC trial, adjuvant chemotherapy decision in stage II colon cancer was compared between a circulating tumor DNA (ctDNA)-based approach and the standard care. We show this may result in more patients receiving oxaliplatin-based chemotherapy and may expose a similar proportion of patients to chemotherapy if the novel strategy is implemented in addition to usual practice. The other potential risk is undertreatment. We provide an illustration of early breast cancer, where the decision of adjuvant chemotherapy based on the gene expression signature MammaPrint may lead to inferior outcomes as compared with the clinico-pathologic strategy. This may also happen when non-inferiority designs have large margins. Among solutions, it should be acknowledged that clinico-pathological features, like T4 in colon cancer, may not be abandoned and replaced by novel strategies in real-life practice. Therefore, novel strategies should be tested in addition to standard of care, and not in lieu of. Second, de-escalation trials should focus on the settings where the standard of care has a widespread agreement. This would avoid the risk of testing non-inferiority against an ineffective therapy, which guarantees successes without providing informative data.
Conclusion:
Simply because a molecular test is rational does not mean it can improve patient outcomes. Here, we highlight how molecular test-based strategies may result in either overtreatment or undertreatment. In the rapidly evolving field of medicine, where technological advances may be transformative, our piece highlights scientific pitfalls to be aware of when considering running such trials or before implementing novel strategies in daily practice.
Insights
Molecular de-escalation in cancer treatment may lead to overtreatment or undertreatment. Novel strategies should complement, not replace, standard care to ensure patient benefit and avoid trial pitfalls.
Area of Science:
- Oncology
- Translational Medicine
- Clinical Trial Design
Background:
- Adjuvant cancer treatment de-escalation aims to reduce therapy without compromising outcomes.
- Historically, treatment decisions relied on clinical and pathological factors.
- Molecular insights have driven the development of new de-escalation strategies.
Purpose of the Study:
- To illustrate potential pitfalls of molecularly based de-escalation strategies in cancer treatment.
- To highlight risks of overtreatment and undertreatment associated with novel approaches.
- To propose solutions for designing and implementing molecular de-escalation trials.
Main Methods:
- Analysis of molecularly based de-escalation strategies in clinical trials.
- Comparison of circulating tumor DNA (ctDNA)-based approach versus standard care in colon cancer (DYNAMIC trial).
- Evaluation of gene expression signature (MammaPrint) in early breast cancer treatment decisions.
Main Results:
- Molecular de-escalation may lead to overtreatment if tested in lieu of standard care.
- The DYNAMIC trial suggests potential for increased chemotherapy use.
- MammaPrint strategy may result in inferior outcomes compared to clinico-pathologic factors in breast cancer.
Conclusions:
- Molecular tests must demonstrate improved patient outcomes, not just rationality.
- Novel strategies should be tested alongside standard care, not as replacements.
- De-escalation trials require careful design, focusing on areas with established standard care.
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