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 - Funding Information:
We thank all the patients whose data were reported in this study. We are also indebted to the medical, nursing, and clinical staff at all participating institutions for their care for each patient. This work was supported by a grant from the National Cancer Center Research and Development Fund (29-A-14).
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.
KW - Allogeneic hematopoietic cell transplantation
KW - Anti-PD-1 monoclonal antibody
KW - Hodgkin lymphoma
KW - Immune checkpoint inhibitor
UR - http://www.scopus.com/inward/record.url?scp=85088949811&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85088949811&partnerID=8YFLogxK
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 -