“…58,59 However, for the reasons mentioned above, FDA-approved epothilones (i.e., ixabepilone, which is licensed for the treatment of breast carcinoma) 60 and EGFR-targeting mAbs (i.e., cetuximab and panitumumab, which are currently employed for the treatment of head and neck cancer and colorectal carcinoma) [61][62][63] may not share this ability with patupilone and 7A7, respectively. Finally, it should be noted that some FDA-approved agents such as digoxin and digitoxin (which are licensed for the treatment of various cardiac disorders), 64 as well as zoledronic acid (which is commonly employed for the treatment of MM or hypercalcemia and bone lesions of oncological origin), 65 are very efficient at boosting the immunogenicity of otherwise non-immunogenic instances of cell death, although they are unable to elicit ICD per se. [66][67][68][69] These agents may be particularly relevant for the development of combinatorial chemotherapeutic regimens that actively engage the host immune system against malignant cells.…”