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International journal of hematology · 2020

Safety and efficacy of anti-programmed cell death-1 monoclonal antibodies before and after allogeneic hematopoietic cell transplantation for relapsed or refractory Hodgkin lymphoma: a multicenter retrospective study.

СтатьяМногоцентровое исследованиеНазвание и аннотация: Перевод пока не подготовлен
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Ito Ayumu, Kim Sung-Won, Matsuoka Ken-Ichi, Kawakita Toshiro, Tanaka Takashi, Inamoto Yoshihiro, Toubai Tomomi, Fujiwara Shin-Ichiro, Fukaya Masafumi, Kondo Tadakazu, Sugita Junichi, Nara Miho, Katsuoka Yuna, Imai Yosuke, Nakazawa Hideyuki, Kawashima Ichiro, Sakai Rika, Ishii Arata, Onizuka Makoto, Takemura Tomonari, Terakura Seitaro, Iida Hiroatsu, Nakamae Mika, Higuchi Kohei, Tamura Shinobu, Yoshioka Satoshi, Togitani Kazuto, Kawano Noriaki, Suzuki Ritsuro, Suzumiya Junji, Izutsu Koji, Teshima Takanori, Fukuda Takahiro

Аннотация

We conducted a multicenter study on anti-programmed cell death-1 monoclonal antibodies (anti-PD-1 mAbs) before/after allogeneic hematopoietic cell transplantation (allo-HCT) for Hodgkin lymphoma. Anti-PD-1 mAbs were administered to 25 patients before allo-HCT and to 20 after allo-HCT. In pre-allo-HCT setting, the median interval from the last administration to allo-HCT was 59 days. After allo-HCT, 12 patients developed non-infectious febrile syndrome requiring high-dose corticosteroid. The cumulative incidences of grade II-IV acute graft-versus-host disease (aGvHD) were 47.1%. Eight patients who had GvHD prophylaxis with post-transplant cyclophosphamide (PTCy) had less frequent aGvHD (grade II-IV, 14.6% versus 58.8%; P = 0.086). The 1 year overall survival (OS), relapse/progression, and non-relapse mortality rates were 81.3%, 27.9%, and 8.4%. In post-allo-HCT setting, the median interval from allo-HCT to the first administration was 589 days. The overall and complete response rates were 75% and 40%. At 100 days after anti-PD-1 therapy, the cumulative incidences of grade II-IV aGvHD, moderate-to-severe chronic GvHD, and grade 3-4 immune-related toxicity were 15.0%, 30.0%, and 30.0%. While the 1 year relapse/progression rate was 47.4%, the 1 year OS probability was 89.7%. In conclusion, immune-related complications were frequent despite modifications of GvHD prophylaxis or anti-PD-1 mAb dosing. In anti-PD-1-mAb-pretreated patients, PTCy-based GvHD prophylaxis may be effective.

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты