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Retrospective Review of Outcomes After Radiation Therapy for Oligoprogressive Disease on Immune Checkpoint Blockade.
Mahmood, Umair; Huynh, Mai Anh; Killoran, Joseph H; Qian, Jack M; Bent, Eric H; Aizer, Ayal A; Mak, Raymond H; Mamon, Harvey J; Balboni, Tracy A; Gunasti, Lauren; Ott, Patrick A; Awad, Mark M; Schoenfeld, Jonathan D.
Afiliação
  • Mahmood U; Department of Radiation Oncology.
  • Huynh MA; Department of Radiation Oncology.
  • Killoran JH; Department of Radiation Oncology.
  • Qian JM; Department of Radiation Oncology.
  • Bent EH; Department of Radiation Oncology.
  • Aizer AA; Department of Radiation Oncology.
  • Mak RH; Department of Radiation Oncology.
  • Mamon HJ; Department of Radiation Oncology.
  • Balboni TA; Department of Radiation Oncology.
  • Gunasti L; Department of Radiation Oncology.
  • Ott PA; Melanoma Disease Center.
  • Awad MM; Lowe Center for Thoracic Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Schoenfeld JD; Department of Radiation Oncology. Electronic address: jonathan_schoenfeld@dfci.harvard.edu.
Int J Radiat Oncol Biol Phys ; 114(4): 666-675, 2022 11 15.
Article em En | MEDLINE | ID: mdl-35643252
PURPOSE: We retrospectively evaluated outcomes after radiation therapy for patients with oligoprogression on immune checkpoint inhibitors (ICI). METHODS AND MATERIALS: We identified patients irradiated to ≤5 progressive lesions while receiving ICI between 2010 and 2020. We excluded patients whose systemic therapy was switched after radiation but before progression. We evaluated predictors of local control (LC), progression-free survival (PFS) and overall survival (OS). RESULTS: We screened 1423 patients and identified 120 who were eligible; the most common histologies were lung cancer (n = 59) and melanoma (n = 36). The median number of oligoprogressive lesions was 1. For the median LC of irradiated oligoprogressive lesions, PFS and OS were not reached at 6.41 (4.67-7.66) and 29.80 (22.54-43.33) months, respectively. Tumor histology, radiated site, or radiation modality were not associated with LC, PFS, or OS. Local response to radiation (P < .0001) and radiation of newly developed lesions (P = .02) were associated with LC. Predictors of PFS on univariate and multivariate analyses were best response to radiation (P = .006) and high programmed death ligand 1 tumor proportion score (P = .02). On multivariate analyses, OS was associated with cumulative oligoprogressive lesion volumes (P = .02) and duration of ICI before oligoprogression (P = .03). CONCLUSIONS: Promising outcomes were observed among patients irradiated for oligoprogression on ICI, especially those with a favorable local response, high tumor programmed death ligand 1 expression, and those receiving ICI for longer periods before oligoprogression. These data can help identify patients well suited for radiation therapy versus those who should switch systemic treatment.
Assuntos

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Carcinoma Pulmonar de Células não Pequenas / Neoplasias Pulmonares Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Int J Radiat Oncol Biol Phys Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Carcinoma Pulmonar de Células não Pequenas / Neoplasias Pulmonares Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Int J Radiat Oncol Biol Phys Ano de publicação: 2022 Tipo de documento: Article