The patient achieved a partial response (C and D) after initial disease progression was noted at the first (data not shown) and second assessments (B). The identification of robust Pirarubicin Hydrochloride biomarkers that might predict the response of cancer patients to CTLA4-blocking agents is still a major, unsettled topic. cell death 1 (PDCD1, best known as PD-1) and its main ligand CD274 (best known as PD-L1), on the Pirarubicin Hydrochloride other hand.3 Based on accumulating clinical data, a further step into the future will undoubtedly involve the combinatorial and/or sequential administration of multiple checkpoints-blocking mAbs, as well as their association with conventional chemotherapeutic and/or active immunotherapy (e.g., anticancer vaccines). In spite of the steadily increasing incidence of this disease, the current therapeutic options against malignant mesothelioma (MM) are largely unsatisfactory. The combination of platinum-based chemotherapy and pemetrexed constitutes indeed the standard of care, being associated with a median survival of only 12 mo.4 Furthermore, second-line treatments remain an unsolved issue, since different cytotoxic chemotherapeutic and targeted anticancer agents have failed to exert clinical activity in MM patients.5 Seeking to assess the therapeutic potential of blocking CTLA4 in malignancies Pirarubicin Hydrochloride previously unexplored in this sense and generally associated with dismal prognosis, we designed the MESOT-TREM-2008 study. In this context, we investigated the clinical and immunological activity of the anti-CTLA4 mAb tremelimumab in unresectable MM patients who failed a first-line platinum-containing chemotherapeutic regimen. The preliminary results of this clinical trial have recently been published in em The Lancet Oncology /em .6 Though the primary endpoint Pirarubicin Hydrochloride of the study (i.e., objective response rate) was not met, 2 out of 29 patients treated with tremelimumab achieved a durable partial response, and 7 had a prolonged stabilization of disease, with a comprehensive disease control rate of 31%. Initial disease progression followed by a long-lasting Pirarubicin Hydrochloride partial response was observed in one patient (Fig.?1). Such an unusual pattern of response has been previously documented in metastatic melanoma patients receiving ipilimumab.7 Thus, our findings corroborate the notion that blocking CTLA4 can lead to peculiar clinical responses in patients affected by various tumor types. This implies that a careful assessment of disease progression is mandatory before the discontinuation of anti-CTLA4 therapy, as clinical benefits may be delayed.7 Such an aspect is highly relevant for patients with MM, a setting in which radiological assessments are central in the evaluation of disease progression and response to treatment.8 An additional typical feature of CTLA4 blockade is the induction of persistent disease stabilization. Indeed, a long-lasting stable Mouse monoclonal to S1 Tag. S1 Tag is an epitope Tag composed of a nineresidue peptide, NANNPDWDF, derived from the hepatitis B virus preS1 region. Epitope Tags consisting of short sequences recognized by wellcharacterizated antibodies have been widely used in the study of protein expression in various systems. disease was achieved by 24% of the MM patients enrolled in our study. The 1- and 2-y survival rates that we observed, 48.3% and 36.7%, respectively, compare quite favorably with available data for MM patients.5 Though limited by the small cohort size, our study identified a proportion of MM patients who may obtain long-term clinical benefits from tremelimumab, which is consistent with extensive clinical data collected in metastatic melanoma patients receiving ipilimumab.9 Open in a separate window Figure?1. CT scan of a malignant pleural mesothelioma patient receiving tremelimumab. (ACD) Computer tomography (CT) scans were performed at baseline (A) and after the second (day 180, B), fourth (day 470, C), and seventh (day 630, D) dose of tremelimumab. The patient achieved a partial response (C and D) after initial disease progression was noted at the first (data not shown) and second assessments (B). The identification of robust biomarkers that might predict the response of cancer patients to CTLA4-blocking agents is still a major, unsettled topic. In our study, we prospectively demonstrated that the increase in the absolute number of circulating CD4+ICOS+ T lymphocytes in the very early phases of treatment is predictive of an improved survival. However, the levels of CD4+ICOS+ T lymphocytes before therapy did not allow for the identification of patients who would experience a favorable disease outcome upon the administration of tremelimumab.6 This finding, which is in line with retrospective data obtained in metastatic melanoma patients treated with ipilimumab,9 suggests that the analysis of.