In our study, drug-drug interactions (DDIs) were assessed on a case-by-case basis by a team of oncologists, HCV-treating physicians and clinical pharmacy specialists. A meticulous search of online drug-interaction databases was performed for every regimen administered to our patients. Univariate and multivariate analyses of risk factors for serious AEs, including DDIs, were not possible because no clinically significant DDIs occurred.Jiang et al., 1 mention that another limitation of our study is the lack of a comparable control group. We agree that the use of controls could add additional information regarding the safety of these combinations. However, only a few patients needed dose modifications to the chemotherapeutic regimens, likely a result of the respective agents themselves and not clinically significant DDIs. One patient had a dose reduction of ribavirin for grade 3 anaemia, an AE that could lead to delayed count recovery and postponement of potentially curative chemotherapy. Also important is that all of the serious AEs for which the dose of chemotherapy was modified resolved after dose adjustments. Confronting data that affect special patient populations like HCV-infected patients with cancer is crucial. We emphasise that we do not advocate for routine use of DAAs and chemotherapy concomitantly, but when used under certain circumstances close monitoring is of the utmost importance. Larger studies, evaluating more chemotherapeutic regimens and DAAs in a controlled setting are warranted before this practice is implemented.