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Outcomes on anti-VEGFR-2/paclitaxel treatment after progression on immune checkpoint inhibition in patients with metastatic gastroesophageal adenocarcinoma.
Kankeu Fonkoua, Lionel A; Chakrabarti, Sakti; Sonbol, Mohamad B; Kasi, Pashtoon M; Starr, Jason S; Liu, Alex J; Nevala, Wendy K; Maus, Rachel L; Bois, Melanie C; Pitot, Henry C; Chandrasekharan, Chandrikha; Ross, Helen J; Wu, Tsung-Teh; Graham, Rondell P; Villasboas, Jose C; Weiss, Matthias; Foster, Nathan R; Markovic, Svetomir N; Dong, Haidong; Yoon, Harry H.
Afiliação
  • Kankeu Fonkoua LA; Department of Oncology, Mayo Clinic, Rochester, Minnesota, USA.
  • Chakrabarti S; Department of Hematology, Mayo Clinic, Rochester, Minnesota, USA.
  • Sonbol MB; Department of Oncology, Mayo Clinic, Rochester, Minnesota, USA.
  • Kasi PM; Department of Oncology, Medical College of Wisconsin, Wauwatosa, Wisconsin, USA.
  • Starr JS; Department of Oncology, Mayo Clinic, Phoenix, Arizona, USA.
  • Liu AJ; Department of Oncology, Mayo Clinic, Jacksonville, Florida, USA.
  • Nevala WK; Department of Oncology, University of Iowa, Iowa City, Iowa, USA.
  • Maus RL; Department of Oncology, Mayo Clinic, Jacksonville, Florida, USA.
  • Bois MC; Department of Oncology, Mayo Clinic, Phoenix, Arizona, USA.
  • Pitot HC; Department of Hematology, Mayo Clinic, Rochester, Minnesota, USA.
  • Chandrasekharan C; Department of Immunology, Mayo Clinic, Rochester, Minnesota, USA.
  • Ross HJ; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.
  • Wu TT; Department of Oncology, Mayo Clinic, Rochester, Minnesota, USA.
  • Graham RP; Department of Oncology, University of Iowa, Iowa City, Iowa, USA.
  • Villasboas JC; Department of Oncology, Mayo Clinic, Phoenix, Arizona, USA.
  • Weiss M; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.
  • Foster NR; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.
  • Markovic SN; Department of Hematology, Mayo Clinic, Rochester, Minnesota, USA.
  • Dong H; Department of Immune Monitoring Core, Mayo Clinic, Rochester, Minnesota, USA.
  • Yoon HH; ThedaCare Cancer Care, Appleton, Wisconsin, USA.
Int J Cancer ; 149(2): 378-386, 2021 07 15.
Article em En | MEDLINE | ID: mdl-33739449
Through our involvement in KEYNOTE-059, we unexpectedly observed durable responses in two patients with metastatic gastroesophageal adenocarcinoma (mGEA) who received ramucirumab (anti-VEGFR-2)/paclitaxel after immune checkpoint inhibition (ICI). To assess the reproducibility of this observation, we piloted an approach to administer ramucirumab/paclitaxel after ICI in more patients, and explored changes in the immune microenvironment. Nineteen consecutive patients with mGEA received ICI followed by ramucirumab/paclitaxel. Most (95%) did not respond to ICI, yet after irRECIST-defined progression on ICI, all patients experienced tumor size reduction on ramucirumab/paclitaxel. The objective response rate (ORR) and progression-free survival (PFS) on ramucirumab/paclitaxel after ICI were higher than on the last chemotherapy before ICI in the same group of patients (ORR, 58.8% vs 11.8%; PFS 12.2 vs 3.0 months; respectively). Paired tumor biopsies examined by imaging mass cytometry showed a median 5.5-fold (range 4-121) lower frequency of immunosuppressive forkhead box P3+ regulatory T cells with relatively preserved CD8+ T cells, post-treatment versus pre-treatment (n = 5 pairs). We then compared the outcomes of these 19 patients with a separate group who received ramucirumab/paclitaxel without preceding ICI (n = 68). Median overall survival on ramucirumab/paclitaxel was longer with (vs without) immediately preceding ICI (14.8 vs 7.4 months) including after multivariate analysis, as was PFS. In our small clinical series, outcomes appeared improved on anti-VEGFR-2/paclitaxel treatment when preceded by ICI, in association with alterations in the immune microenvironment. However, further investigation is needed to determine the generalizability of these data. Prospective clinical trials to evaluate sequential treatment with ICI followed by anti-VEGF(R)/taxane are underway.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Aged / Humans / Male / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Aged / Humans / Male / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article