Hans-Joachim Schmoll, MD
Chemotherapy combinations are being examined in an effort to take the treatment paradigm of metastatic colorectal cancer (CRC) a few steps forward, says Hans-Joachim Schmoll, MD. While the FDA approvals of the PD-1 inhibitors nivolumab (Opdivo) and pembrolizumab (Keytruda) were significant, the treatments are specifically indicated for those with microsatellite instability-high disease, which comprises 15% of patients.
In an interview with OncLive, Schmoll, head of the Department of Oncology and Hematology, associate professor of internal medicine, at University Hospital Halle, discussed these updated CHARTA findings, the current role of chemotherapy in patients with metastatic CRC, and his predictions for the future CRC treatment landscape.
OncLive: Could you provide a recap of the final results of the CHARTA trial?
: CHARTA investigated the potential activity of a 4-drug regimen consisting of some standards in CRC management: FOLFOX plus bevacizumab with the addition of irinotecan. The question was, “Is it better in terms of response rate, PFS, and overall survival?” For that reason, we have treated 450 patients, and the primary endpoint of the study was improvement of the PFS at 9 months. The primary endpoint was met, meaning the PFS was increased at 9 months with the 4-drug regimen.
Has the role of chemotherapy evolved in any way in this landscape?
Chemotherapy is still there. We are now wondering how the chemotherapy triplet plus the VEGF inhibitor bevacizumab combination fare in relation to the cetuximab (Erbitux)- or EGFR inhibitor–based results. Based on our current knowledge of the 4-drug combination with bevacizumab, I would suggest that a patient with a RAS-wildtype and left-sided tumor, with liver or lung metastases, should probably undergo surgery to make long-term survival possible. Some patients should still [be treated with] the EGFR inhibitor, but you need to compare the data and see if you should just go for the FOLFIRI plus cetuximab, for example.
What is the biggest challenge in the treatment of patients with advanced CRC?
We need to have more active chemotherapies or targeted treatments—whatever it is, as long as it is active. We need more active combinations that can incite major responses in the majority of patients. Right now, we have a 60% to 70% response rate, but this is not enough. We need maximum responses to enable surgical resection of tumors, at least in those patients who have a specific biology—which is 50% of patients with liver or lung metastases.
It is difficult in CRC, as there are not many good targets. HER2 is one of the targets. Currently, there is a screening study checking the value of the drugs in first-line setting. This is a way forward.
What else is taking place in the CRC field that is important to highlight?
At the moment, there are many interesting things in biology going on, which are demonstrating new ways to go forward. It is all very early and experimental, and there is nothing that can go into routine [practice] any time soon. If you compare the amount of information and new preclinical investigation with molecular data in CRC, it shows that we are really accelerating our understanding for the future.
Schmoll HJ, Meinert FM, Cygon F, et al. CHARTA: FOLFOX/bevacizumab vs. FOLFOXIRI/bevacizumab in advanced colorectal cancer—Final results, prognostic and potentially predictive factors from the randomized phase II trial of the AIO. J Clin Oncol. 2017;35(15):3533. doi: 10.1200/JCO.2017.35.15_suppl.3533.
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