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      The role of ipilimumab after anti-PD-1 treatment: two case reports and a literature review.

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          Abstract

          Metastatic melanoma has been historically associated with a poor prognosis; however, the therapeutic landscape has experimented and impressive change in the last years due to rapid advances in the immunotherapy field. The first immunotherapy treatment for metastatic melanoma was ipilimumab (anti-CTLA-4), which showed a significant improvement of overall survival compared to chemotherapy. However, in 2015 anti-PD-1 pembrolizumab shown an improved overall survival, progression-free survival and response rate compared to ipilimumab with either a better toxicity profile. Moreover, other immunotherapy combinations and target therapies, such as BRAF and MEK inhibitors combinations, have shown better outcomes than ipilimumab. Thus, ipilimumab seems to have no role in frontline metastatic melanoma treatment and even their role in second line is being less frequent due to clinical efficacy of those other treatments. Actually, the role of ipilimumab in second line after anti-PD-1 progression is not clear although there is clinical evidence for its use. Here, we report two cases of treatment response with ipilimumab in second line setting after receiving anti-PD-1 combination. So that, ipilimumab may have a role after progression to an anti-PD-1 treatment.

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          Author and article information

          Journal
          Melanoma Res
          Melanoma research
          Ovid Technologies (Wolters Kluwer Health)
          1473-5636
          0960-8931
          Apr 2020
          : 30
          : 2
          Affiliations
          [1 ] Medical Oncology, Vall d´Hebron University Hospital.
          [2 ] Medical Oncology, Breast Cancer Unit and Melanoma and Other Skin Tumors Unit, Vall d´Hebron University Hospital.
          [3 ] Medical Oncology Melanoma and Other Skin Tumors Unit, Vall d´Hebron University Hospital, Barcelona, Spain.
          Article
          00008390-202004000-00013
          10.1097/CMR.0000000000000632
          31348136
          835ac2f3-f267-4adf-b64f-98ca9ec61dc5
          History

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