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Relationship Between Tumor Response and Tumor-Related Symptoms in RAS Wild-Type Metastatic Colorectal Cancer: Retrospective Analyses From 3 Panitumumab Trials

Published on Dec 1, 2019in Clinical Colorectal Cancer3.176
· DOI :10.1016/j.clcc.2019.07.009
Julien Taieb46
Estimated H-index: 46
(Paris V: Paris Descartes University),
M. Geissler11
Estimated H-index: 11
+ 7 AuthorsMarie-Rose Peeters43
Estimated H-index: 43
Abstract
Abstract Background There is no standardised assessment of symptomatic events in metastatic colorectal cancer (mCRC), despite disease symptoms impacting treatment decisions. Data from 3 first-line panitumumab in mCRC trials were retrospectively analysed to assess whether early tumour shrinkage (ETS) and depth of response (DpR) are associated with time to occurrence of tumour-related symptoms. Patients and Methods Patients with RAS wild-type mCRC from PRIME, PEAK and study ‘314 were included. ETS was defined as a reduction of ≥ 30% in the sum-of-the-longest-diameters of lesions at 8 weeks. DpR was calculated as maximum percentage change in tumour size from baseline to nadir. The proportion of patients who developed symptoms (including a composite symptomatic endpoint) during study treatment was calculated. Results Overall, 659 patients were analysed. Onset of symptoms was delayed in patients with ETS ≥ 30% versus ETS Conclusion Both ETS and DpR were associated with delayed onset of symptoms in RAS wild-type mCRC patients. Treatments with high cytoreductive potential may delay symptom development. ClinicalTrials.gov Identifiers PRIME NCT00364013; PEAK NCT00819780; study ‘314 NCT00508404.
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