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Assessment of Clinical Response Following Atezolizumab and Bevacizumab Treatment in Patients With Neuroendocrine Tumors: A Nonrandomized Clinical Trial.
Halperin, Daniel M; Liu, Suyu; Dasari, Arvind; Fogelman, David; Bhosale, Priya; Mahvash, Armeen; Estrella, Jeannelyn S; Rubin, Laura; Morani, Ajaykumar C; Knafl, Mark; Overeem, Tim A; Fu, Szu-Chin; Solis, Luisa M; Parra Cuentas, Edwin; Verma, Anuj; Chen, Hong-Lei; Gite, Swati; Subashchandrabose, Priya; Dervin, Shannon; Schulze, Katja; Darbonne, Walter C; Yun, Cindy; Wistuba, Ignacio I; Futreal, P Andrew; Woodman, Scott E; Yao, James C.
Afiliação
  • Halperin DM; Department of Gastrointestinal Medical Oncology, University of Texas MD Anderson Cancer Center, Houston.
  • Liu S; Department of Biostatistics, University of Texas MD Anderson Cancer Center, Houston.
  • Dasari A; Department of Gastrointestinal Medical Oncology, University of Texas MD Anderson Cancer Center, Houston.
  • Fogelman D; Department of Gastrointestinal Medical Oncology, University of Texas MD Anderson Cancer Center, Houston.
  • Bhosale P; Department of Radiology, University of Texas MD Anderson Cancer Center, Houston.
  • Mahvash A; Department of Interventional Radiology, University of Texas MD Anderson Cancer Center, Houston.
  • Estrella JS; Department of Pathology, University of Texas MD Anderson Cancer Center, Houston.
  • Rubin L; Department of Biostatistics, University of Texas MD Anderson Cancer Center, Houston.
  • Morani AC; Department of Radiology, University of Texas MD Anderson Cancer Center, Houston.
  • Knafl M; Department of Genomic Medicine, University of Texas MD Anderson Cancer Center, Houston.
  • Overeem TA; Department of Genomic Medicine, University of Texas MD Anderson Cancer Center, Houston.
  • Fu SC; Department of Genomic Medicine, University of Texas MD Anderson Cancer Center, Houston.
  • Solis LM; Department of Translational Molecular Pathology, University of Texas MD Anderson Cancer Center, Houston.
  • Parra Cuentas E; Department of Translational Molecular Pathology, University of Texas MD Anderson Cancer Center, Houston.
  • Verma A; Department of Translational Molecular Pathology, University of Texas MD Anderson Cancer Center, Houston.
  • Chen HL; Department of Translational Molecular Pathology, University of Texas MD Anderson Cancer Center, Houston.
  • Gite S; Department of Translational Molecular Pathology, University of Texas MD Anderson Cancer Center, Houston.
  • Subashchandrabose P; Department of Translational Molecular Pathology, University of Texas MD Anderson Cancer Center, Houston.
  • Dervin S; Genentech, Inc, South San Francisco, California.
  • Schulze K; Genentech, Inc, South San Francisco, California.
  • Darbonne WC; Genentech, Inc, South San Francisco, California.
  • Yun C; Genentech, Inc, South San Francisco, California.
  • Wistuba II; Department of Translational Molecular Pathology, University of Texas MD Anderson Cancer Center, Houston.
  • Futreal PA; Department of Genomic Medicine, University of Texas MD Anderson Cancer Center, Houston.
  • Woodman SE; Department of Genomic Medicine, University of Texas MD Anderson Cancer Center, Houston.
  • Yao JC; Department of Gastrointestinal Medical Oncology, University of Texas MD Anderson Cancer Center, Houston.
JAMA Oncol ; 8(6): 904-909, 2022 06 01.
Article em En | MEDLINE | ID: mdl-35389428
ABSTRACT
Importance Therapies for patients with advanced well-differentiated neuroendocrine tumors (NETs) have expanded but remain inadequate, with patients dying of disease despite recent advances in NET therapy. While patients with other cancers have seen long-term disease control and tumor regression with the application of immunotherapies, initial prospective studies of single-agent programmed cell death 1 inhibitors in NET have been disappointing.

Objective:

To evaluate the response rate following treatment with the combination of the vascular endothelial growth factor inhibitor bevacizumab with the programmed cell death 1 ligand 1 inhibitor atezolizumab in patients with advanced NETs. Design, Setting, and

Participants:

This single-arm, open-label nonrandomized clinical study in patients with rare cancers included 40 patients with advanced, progressive grade 1 to 2 NETs (20 with pancreatic NETs [pNETs] and 20 with extrapancreatic NETs [epNETs]) treated at a tertiary care referral cancer center between March 31, 2017, and February 19, 2019. Data were analyzed from June to September 2021.

Interventions:

Patients received intravenous bevacizumab and atezolizumab at standard doses every 3 weeks until progression, death, or withdrawal. Main Outcomes and

Measures:

The primary end point was objective radiographic response using Response Evaluation Criteria in Solid Tumors, version 1.1, with progression-free survival (PFS) as a key secondary end point.

Results:

Following treatment of the 40 study patients with bevacizumab and atezolizumab, objective response was observed in 4 patients with pNETs (20%; 95% CI, 5.7%-43.7%) and 3 patients with epNETs (15%; 95% CI, 3.2%-37.9%). The PFS was 14.9 (95% CI, 4.4-32.0) months and 14.2 (95% CI, 10.2-19.6) months in these cohorts, respectively. Conclusions and Relevance In this nonrandomized clinical trial, findings suggest that clinical responses in patients with NET may follow treatment with the combination of bevacizumab and atezolizumab, with a PFS consistent with effective therapies. Trial Registration ClinicalTrials.gov Identifier NCT03074513.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Tumores Neuroendócrinos Tipo de estudo: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Tumores Neuroendócrinos Tipo de estudo: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article