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Phase II study of neoadjuvant checkpoint blockade in patients with surgically resectable undifferentiated pleomorphic sarcoma and dedifferentiated liposarcoma.
Keung, Emily Z; Lazar, Alexander J; Torres, Keila E; Wang, Wei-Lien; Cormier, Janice N; Ashleigh Guadagnolo, B; Bishop, Andrew J; Lin, Heather; Hunt, Kelly K; Bird, Justin; Lewis, Valerae O; Patel, Shreyaskumar R; Wargo, Jennifer A; Somaiah, Neeta; Roland, Christina L.
Afiliação
  • Keung EZ; Departments of Surgical Oncology, The University of Texas MD Anderson Cancer Center, 1400 Pressler St., FCT17.6054, Unit 1484, Houston, TX, 77030, USA.
  • Lazar AJ; Departments of Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
  • Torres KE; Departments of Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
  • Wang WL; Departments of Surgical Oncology, The University of Texas MD Anderson Cancer Center, 1400 Pressler St., FCT17.6054, Unit 1484, Houston, TX, 77030, USA.
  • Cormier JN; Departments of Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
  • Ashleigh Guadagnolo B; Departments of Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
  • Bishop AJ; Departments of Surgical Oncology, The University of Texas MD Anderson Cancer Center, 1400 Pressler St., FCT17.6054, Unit 1484, Houston, TX, 77030, USA.
  • Lin H; Departments of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
  • Hunt KK; Departments of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
  • Bird J; Departments of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
  • Lewis VO; Departments of Surgical Oncology, The University of Texas MD Anderson Cancer Center, 1400 Pressler St., FCT17.6054, Unit 1484, Houston, TX, 77030, USA.
  • Patel SR; Departments of Orthopaedic Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
  • Wargo JA; Departments of Orthopaedic Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
  • Somaiah N; Departments of Sarcoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
  • Roland CL; Departments of Surgical Oncology, The University of Texas MD Anderson Cancer Center, 1400 Pressler St., FCT17.6054, Unit 1484, Houston, TX, 77030, USA.
BMC Cancer ; 18(1): 913, 2018 Sep 24.
Article em En | MEDLINE | ID: mdl-30249211
ABSTRACT

BACKGROUND:

Soft tissue sarcomas are a heterogeneous and rare group of solid tumors of mesenchymal origin that can arise anywhere in the body. Although surgical resection is the mainstay of treatment for patients with localized disease, disease recurrence is common and 5-year overall survival is poor (~ 65%). Both radiation therapy and conventional chemotherapy are used to reduce local and distant recurrence. However, the utility of radiation therapy is often limited by disease location (in the case of retroperitoneal sarcomas, for instance) while systemic therapy with conventional lines of chemotherapy offer limited efficacy and are often poorly tolerated and associated with significant toxicity. Within the past decade, major advances have been made in the treatment of other malignancies including melanoma, renal cell carcinoma, and non-small cell lung carcinoma with the advent of immune-checkpoint inhibitors such as ipilimumab (anti-CTLA4), pembrolizumab (anti-PD1), and nivolumab (anti-PD1). The recently published SARC028 (NCT02301039), an open label, phase II, multicenter trial of pembrolizumab in patients with advanced bone and soft tissue sarcomas reported promising activity in select histologic subtypes of advanced STS, including undifferentiated pleomorphic sarcoma and dedifferentiated liposarcoma.

METHODS:

There is a clear need for novel and effective adjuncts in the treatment of STS. We hypothesize that immune checkpoint blockade will be effective in patients with surgically resectable primary or locally recurrent dedifferentiated liposarcoma and undifferentiated pleomorphic sarcoma when administered in the neoadjuvant setting. The primary aim of this phase II, single-center, open label, randomized non-comparative trial is to determine the pathologic response to neoadjuvant nivolumab monotherapy and combination nivolumab/ipilimumab in patients with resectable dedifferentiated liposarcoma of the retroperitoneum or undifferentiated pleomorphic sarcoma of the trunk or extremity treated with concurrent standard of care neoadjuvant radiation therapy.

DISCUSSION:

This study will help define the role of single agent anti-PD1 and combination anti-CTLA4 and anti-PD1 therapy in patients with surgically resectable dedifferentiated liposarcoma and undifferentiated pleomorphic sarcoma. TRIAL REGISTRATION ClinicalTrials.gov NCT03307616 , registered October 12, 2017.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sarcoma / Protocolos Clínicos / Terapia de Alvo Molecular / Antineoplásicos Imunológicos / Lipossarcoma Tipo de estudo: Clinical_trials / Etiology_studies / Guideline / Incidence_studies / Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sarcoma / Protocolos Clínicos / Terapia de Alvo Molecular / Antineoplásicos Imunológicos / Lipossarcoma Tipo de estudo: Clinical_trials / Etiology_studies / Guideline / Incidence_studies / Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article