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A Randomized Phase 2 Study of Pembrolizumab With or Without Radiation in Patients With Recurrent or Metastatic Adenoid Cystic Carcinoma.
Mahmood, Umair; Bang, Andrew; Chen, Yu-Hui; Mak, Raymond H; Lorch, Jochen H; Hanna, Glenn J; Nishino, Mizuki; Manuszak, Claire; Thrash, Emily M; Severgnini, Mariano; Sanborn, Matthew; Sridharan, Vishwajith; Margalit, Danielle N; Tishler, Roy B; Busse, Paul M; Willers, Henning; Mamon, Harvey J; Yoo, Hyung-Jin; Pai, Sara I; Wirth, Lori J; Haddad, Robert I; Chau, Nicole G; Schoenfeld, Jonathan D.
Afiliación
  • Mahmood U; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Bang A; Department of Radiation Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Chen YH; Department of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Mak RH; Department of Radiation Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Lorch JH; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Hanna GJ; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Nishino M; Department of Imaging, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Manuszak C; Center for Immuno-Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Thrash EM; Center for Immuno-Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Severgnini M; Center for Immuno-Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Sanborn M; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Sridharan V; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Margalit DN; Department of Radiation Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Tishler RB; Department of Radiation Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Busse PM; Department of Radiation Oncology, Massachusetts General Hospital, Boston, Massachusetts.
  • Willers H; Department of Radiation Oncology, Massachusetts General Hospital, Boston, Massachusetts.
  • Mamon HJ; Department of Radiation Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Yoo HJ; Division of Vascular and Endovascular Surgery, Massachusetts General Hospital, Boston, Massachusetts.
  • Pai SI; Division of Surgical Oncology, Department of Surgery, Massachusetts General Hospital, Boston, Massachusetts.
  • Wirth LJ; Department of Medical Oncology, Massachusetts General Hospital, Boston, Massachusetts.
  • Haddad RI; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Chau NG; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Schoenfeld JD; Department of Radiation Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts. Electronic address: jonathan_schoenfeld@dfci.harvard.edu.
Int J Radiat Oncol Biol Phys ; 109(1): 134-144, 2021 01 01.
Article en En | MEDLINE | ID: mdl-32781104
ABSTRACT

PURPOSE:

We evaluated the safety and efficacy of pembrolizumab (pembro) ± radiation therapy (RT) in a phase 2 study among patients with progressive, metastatic adenoid cystic carcinoma (ACC). METHODS AND MATERIALS Eligible patients had metastatic ACC with progression within the last year and ≥1 measurable lesion. Patients were randomized to pembro alone or with RT to 30 Gy in 5 fractions (pembroRT). The primary endpoint was objective response rate outside the RT field. Secondary endpoints included progression-free survival (PFS), overall survival (OS), and local RT responses.

RESULTS:

We randomized 20 patients (10 per arm) from 2017 to 2018. We did not observe objective response outside of the radiation treatment field; stable disease (SD) was the best response in 12 (60%) patients and was not different per arm (7 pembro, 5 pembroRT, P = .65). A tumor growth rate decrease (TGR) of >25% was noted among 7 of 12 patients and >75% in 4 patients. There were local responses in the irradiated field among all evaluable pembroRT patients. Median PFS and OS were 4.5/not reached for pembroRT and 6.6 / 27.2 months for pembro patients. One patient developed grade 3 liver enzyme elevation after 27 cycles of therapy. Correlative analyses confirm low levels of programmed death-ligand 1 expression (PD-L1), and CD8 infiltrating T-cells. We identified associations between local response and both MYB/NFIB translocation and PD-L1 expression and between changes in systemic immune populations and RT.

CONCLUSIONS:

Pembrolizumab and pembroRT were well tolerated. We observed no objective responses, but 60% of patients with PD before the study achieved SD, the majority with decreased TGR and half (n = 10) with clinical benefit (SD >6 months). We observed favorable local responses within the RT field. Additional strategies are needed to further delay progression and effect response.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Carcinoma Adenoide Quístico / Anticuerpos Monoclonales Humanizados Tipo de estudio: Clinical_trials Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Int J Radiat Oncol Biol Phys Año: 2021 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Carcinoma Adenoide Quístico / Anticuerpos Monoclonales Humanizados Tipo de estudio: Clinical_trials Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Int J Radiat Oncol Biol Phys Año: 2021 Tipo del documento: Article