Abstract

Simple SummarySince the first introduction of the oligometastatic state with a low burden of metastases in non-small cell lung cancer, accumulating evidence from retrospective and prospective studies has shown that a local aggressive, multimodality treatment may significantly improve the prognosis in these patients. Local aggressive treatment includes a systemic therapy of micrometastatic disease, as well as a radical resection of the primary tumor and surgical resection and/or radiation therapy of distant metastases. However, patient selection and treatment allocation remain a central challenge in oligometastatic disease. In this review, we aimed to address the current evidence on criteria for patient selection for local aggressive treatment in non-small cell lung cancer.One-fourth of all patients with metastatic non-small cell lung cancer presents with a limited number of metastases and relatively low systemic tumor burden. This oligometastatic state with limited systemic tumor burden may be associated with remarkably improved overall and progression-free survival if both primary tumor and metastases are treated radically combined with systemic therapy. This local aggressive therapy (LAT) requires a multidisciplinary approach including medical oncologists, radiation therapists, and thoracic surgeons. A surgical resection of the often advanced primary tumor should be part of the radical treatment whenever feasible. However, patient selection, timing, and a correct treatment allocation for LAT appear to be essential. In this review, we aimed to summarize and discuss the current evidence on patient selection criteria such as characteristics of the primary tumor and metastases, response to neoadjuvant or first-line treatment, molecular characteristics, mediastinal lymph node involvement, and other factors for LAT in oligometastatic NSCLC.

Highlights

  • Lung cancer is the most common cause of cancer-related death worldwide and results in more than 36 million disability-adjusted life years globally [1,2]

  • In 1995, Hellman and Weichselbaum first described an oligometastatic state of cancer with low systemic tumor burden, few distant metastases, and presumably a less aggressive cancer biology that was associated with an improved survival [9]

  • A metastatic disease might be amenable to local aggressive therapy (LAT), which may include surgical resection of the primary tumor and metastatic lesions and/or a stereotactic body radiation therapy (SBRT)

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Summary

Introduction

Lung cancer is the most common cause of cancer-related death worldwide and results in more than 36 million disability-adjusted life years globally [1,2]. In 1995, Hellman and Weichselbaum first described an oligometastatic state of cancer with low systemic tumor burden, few distant metastases, and presumably a less aggressive cancer biology that was associated with an improved survival [9] In this stage, a metastatic disease might be amenable to local aggressive therapy (LAT), which may include surgical resection of the primary tumor and metastatic lesions and/or a stereotactic body radiation therapy (SBRT). A metastatic disease might be amenable to local aggressive therapy (LAT), which may include surgical resection of the primary tumor and metastatic lesions and/or a stereotactic body radiation therapy (SBRT) This new concept resulted in a paradigm shift where metastatic NSCLC would not per definition be incurable but require a multi-disciplinary treatment approach to address both the localized primary and metastatic tumor lesions, as well as disseminated, circulating tumor cells [10].

Definition and Staging of Oligometastatic Non-Small Cell Lung Cancer
Surgical Treatment for Oligometastatic Non-Small Cell Lung Cancer
Radiation Therapy for Oligometastatic Non-Small Cell Lung Cancer
Patient Selection Criteria for Local Aggressive Therapy
Site of the Primary Tumor
Site of Metastases
Mediastinal Lymph Node Involvement
Synchronous and Metachronous Metastases
Performance Status
Response to Systemic Therapy and Oligoprogressive Disease
Histopathological and Molecular Markers
Quality of Life
Findings
Conclusions and Outlook
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