| Literature DB >> 30158286 |
Yoshihide Inayama1,2, Junzo Hamanishi3, Noriomi Matsumura4, Ryusuke Murakami1, Kaoru Abiko1, Ken Yamaguchi5, Tsukasa Baba1, Katsuyuki Horie6, Ikuo Konishi5, Masaki Mandai1.
Abstract
Platinum-resistant recurrent ovarian cancer is generally refractory to chemotherapy. Programmed cell death-1 (PD-1) signaling is a new target for antitumor therapy. The anti-PD-1 antibody nivolumab had a 10% durable complete response rate in our phase II clinical trial. However, how nivolumab affects sensitivity to subsequent chemotherapy remains unclear. We encountered several cases of unexpected antitumor response among patients who underwent palliative chemotherapy in the follow-up study of our phase II nivolumab trial (UMIN000005714). Several agents had an unexpected antitumor response in patients who were resistant or refractory to standard chemotherapeutic agents. In one patient, both pegylated liposomal doxorubicin (PLD) and nedaplatin (CDGP) resulted in partial response. In another patient, PLD and CDGP resulted in partial response and stable disease, respectively. These two patients remained alive on the cutoff date. These two cases raise the possibility that nivolumab might improve sensitivity to adequate chemotherapy for ovarian cancer. © AlphaMed Press 2018.Entities:
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Year: 2018 PMID: 30158286 PMCID: PMC6291322 DOI: 10.1634/theoncologist.2018-0167
Source DB: PubMed Journal: Oncologist ISSN: 1083-7159