TY - JOUR
T1 - Cancer Immunotherapy Trials Network 12
T2 - Pembrolizumab in HIV-Associated Kaposi Sarcoma
AU - Lurain, Kathryn
AU - Ramaswami, Ramya
AU - Ekwede, Irene
AU - Eulo, Vanessa
AU - Goyal, Gaurav
AU - Menon, Manoj
AU - Odeny, Thomas A.
AU - Sharon, Elad
AU - Wagner, Michael J.
AU - Wang, Chia Ching Jackie
AU - Bhardwaj, Nina
AU - Friedlander, Philip A.
AU - Abdul-Hay, Maher
AU - Cornejo Castro, Elena M.
AU - Labo, Nazzarena
AU - Marshall, Vickie Ann
AU - Miley, Wendell
AU - Moore, Kyle
AU - Roshan, Romin
AU - Whitby, Denise
AU - Kask, Angela Shaulov
AU - Kaiser, Judith
AU - Han, Emma
AU - Wright, Anna
AU - Yarchoan, Robert
AU - Fling, Steven P.
AU - Uldrick, Thomas S.
N1 - Publisher Copyright:
© 2024 by American Society of Clinical Oncology.
PY - 2024
Y1 - 2024
N2 - PURPOSE Cancer Immunotherapy Trials Network 12 demonstrated safety of pembrolizumab in treating advanced cancer in people with HIV. Here, we report results of the Kaposi sarcoma (KS) cohort. METHODS In this multicenter phase I trial, we enrolled participants with HIV-associated KS on antiretroviral therapy with CD41 ≥50 cells/mL and HIV plasma RNA <200 copies/mL. Pembrolizumab 200 mg intravenously was administered once every 3 weeks for up to 35 cycles. The primary end point was safety, and the secondary end point was KS response by modified AIDS Clinical Trials Group Criteria. RESULTS Thirty-two cisgender men enrolled with baseline median CD41 T-cell count of 274 cells/mL. All but nine participants had received previous systemic KS therapy. Participants received a median of 11 cycles of pembrolizumab (range, 1-35). Sixty-six percent had grade ≥1 treatment-emergent adverse events, including one death from polyclonal KS herpesvirus–related B-cell lymphoproliferation. Thirty-one percent had ≥one immune-mediated AEs (imAEs) with 25% requiring systemic steroids. In 29 participants with evaluable KS, the overall response rate (ORR) was 62.1% (95% CI, 42.3 to 79.3) and did not differ by CD41 T-cell count. ORR in the eight participants with evaluable disease without previous KS therapy was 87.5% (95% CI, 47.3 to 99.7). Median duration of response (DOR) was not reached, and the Kaplan-Meier estimate of DOR of ≥12 months was 92.3% (95% CI, 56.6 to 98.8). Median progression-free survival was 28.2 months (95% CI, 4.2 to noncalculable). CONCLUSION Pembrolizumab yielded a high rate of durable responses in HIV-associated KS. imAEs were successfully managed with standard guidelines.
AB - PURPOSE Cancer Immunotherapy Trials Network 12 demonstrated safety of pembrolizumab in treating advanced cancer in people with HIV. Here, we report results of the Kaposi sarcoma (KS) cohort. METHODS In this multicenter phase I trial, we enrolled participants with HIV-associated KS on antiretroviral therapy with CD41 ≥50 cells/mL and HIV plasma RNA <200 copies/mL. Pembrolizumab 200 mg intravenously was administered once every 3 weeks for up to 35 cycles. The primary end point was safety, and the secondary end point was KS response by modified AIDS Clinical Trials Group Criteria. RESULTS Thirty-two cisgender men enrolled with baseline median CD41 T-cell count of 274 cells/mL. All but nine participants had received previous systemic KS therapy. Participants received a median of 11 cycles of pembrolizumab (range, 1-35). Sixty-six percent had grade ≥1 treatment-emergent adverse events, including one death from polyclonal KS herpesvirus–related B-cell lymphoproliferation. Thirty-one percent had ≥one immune-mediated AEs (imAEs) with 25% requiring systemic steroids. In 29 participants with evaluable KS, the overall response rate (ORR) was 62.1% (95% CI, 42.3 to 79.3) and did not differ by CD41 T-cell count. ORR in the eight participants with evaluable disease without previous KS therapy was 87.5% (95% CI, 47.3 to 99.7). Median duration of response (DOR) was not reached, and the Kaplan-Meier estimate of DOR of ≥12 months was 92.3% (95% CI, 56.6 to 98.8). Median progression-free survival was 28.2 months (95% CI, 4.2 to noncalculable). CONCLUSION Pembrolizumab yielded a high rate of durable responses in HIV-associated KS. imAEs were successfully managed with standard guidelines.
UR - http://www.scopus.com/inward/record.url?scp=85207959342&partnerID=8YFLogxK
U2 - 10.1200/JCO.24.00640
DO - 10.1200/JCO.24.00640
M3 - Article
C2 - 39356983
AN - SCOPUS:85207959342
SN - 0732-183X
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
M1 - JCO.24.00640
ER -