TY - JOUR
T1 - Safety and efficacy of anti-programmed cell death-1 monoclonal antibodies before and after allogeneic hematopoietic cell transplantation for relapsed or refractory Hodgkin lymphoma
T2 - a multicenter retrospective study
AU - Ito, Ayumu
AU - Kim, Sung Won
AU - Matsuoka, Ken ichi
AU - Kawakita, Toshiro
AU - Tanaka, Takashi
AU - Inamoto, Yoshihiro
AU - Toubai, Tomomi
AU - Fujiwara, Shin ichiro
AU - Fukaya, Masafumi
AU - Kondo, Tadakazu
AU - Sugita, Junichi
AU - Nara, Miho
AU - Katsuoka, Yuna
AU - Imai, Yosuke
AU - Nakazawa, Hideyuki
AU - Kawashima, Ichiro
AU - Sakai, Rika
AU - Ishii, Arata
AU - Onizuka, Makoto
AU - Takemura, Tomonari
AU - Terakura, Seitaro
AU - Iida, Hiroatsu
AU - Nakamae, Mika
AU - Higuchi, Kohei
AU - Tamura, Shinobu
AU - Yoshioka, Satoshi
AU - Togitani, Kazuto
AU - Kawano, Noriaki
AU - Suzuki, Ritsuro
AU - Suzumiya, Junji
AU - Izutsu, Koji
AU - Teshima, Takanori
AU - Fukuda, Takahiro
N1 - Publisher Copyright:
© 2020, Japanese Society of Hematology.
PY - 2020/11/1
Y1 - 2020/11/1
N2 - 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.
AB - 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.
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U2 - 10.1007/s12185-020-02960-4
DO - 10.1007/s12185-020-02960-4
M3 - Article
C2 - 32748216
AN - SCOPUS:85088949811
SN - 0925-5710
VL - 112
SP - 674
EP - 689
JO - International Journal of Hematology
JF - International Journal of Hematology
IS - 5
ER -