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Measuring the Integration of Stereotactic Ablative Radiotherapy Plus Surgery for Early-Stage Non-Small Cell Lung Cancer: A Phase 2 Clinical Trial.
Palma, David A; Nguyen, Timothy K; Louie, Alexander V; Malthaner, Richard; Fortin, Dalilah; Rodrigues, George B; Yaremko, Brian; Laba, Joanna; Kwan, Keith; Gaede, Stewart; Lee, Ting; Ward, Aaron; Warner, Andrew; Inculet, Richard.
Affiliation
  • Palma DA; Department of Radiation Oncology, London Health Sciences Centre, London, Ontario, Canada.
  • Nguyen TK; Department of Oncology, Western University, London, Ontario, Canada.
  • Louie AV; Department of Radiation Oncology, London Health Sciences Centre, London, Ontario, Canada.
  • Malthaner R; Currently with Department of Radiation Oncology, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada.
  • Fortin D; Department of Radiation Oncology, London Health Sciences Centre, London, Ontario, Canada.
  • Rodrigues GB; Department of Oncology, Western University, London, Ontario, Canada.
  • Yaremko B; Currently with Department of Radiation Oncology, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada.
  • Laba J; Department of Surgery, Division of Thoracic Surgery, London Health Sciences Centre, London, Ontario, Canada.
  • Kwan K; Department of Surgery, Division of Thoracic Surgery, London Health Sciences Centre, London, Ontario, Canada.
  • Gaede S; Department of Radiation Oncology, London Health Sciences Centre, London, Ontario, Canada.
  • Lee T; Department of Oncology, Western University, London, Ontario, Canada.
  • Ward A; Department of Radiation Oncology, London Health Sciences Centre, London, Ontario, Canada.
  • Warner A; Department of Oncology, Western University, London, Ontario, Canada.
  • Inculet R; Department of Radiation Oncology, London Health Sciences Centre, London, Ontario, Canada.
JAMA Oncol ; 5(5): 681-688, 2019 May 01.
Article in En | MEDLINE | ID: mdl-30789648
ABSTRACT
IMPORTANCE Stereotactic ablative radiotherapy (SABR) is a standard treatment option in patients with medically inoperable early-stage non-small cell lung cancer (NSCLC), yet the pathologic complete response (pCR) rate after SABR is unknown. Neoadjuvant SABR in patients with cancer who are fit for resection has been hypothesized to improve local control and induce antitumor immune activity, potentially leading to better outcomes.

OBJECTIVES:

To determine the pCR rate after SABR and to assess oncologic and toxicity outcomes after a combined approach of neoadjuvant SABR followed by surgery. DESIGN, SETTING, AND

PARTICIPANTS:

A phase 2, single-arm trial, with patient accrual from September 30, 2014, to August 15, 2017 (median follow-up, 19 months), was performed at a tertiary academic cancer center. Patients 18 years or older with T1T2N0M0 NSCLC and good performance status, with adequate pulmonary reserve to undergo surgical resection, were studied.

INTERVENTIONS:

Patients underwent neoadjuvant SABR using a risk-adapted fractionation scheme followed by surgery 10 weeks later. MAIN OUTCOMES AND

MEASURES:

The pCR rate as determined by hematoxylin-eosin staining.

RESULTS:

Forty patients (mean [SD] age, 68 [8] years; 23 [58%] female) were enrolled. Thirty-five patients underwent surgery and were evaluable for the primary end point. The pCR rate was 60% (95% CI, 44%-76%). The 30- and 90-day postoperative mortality rates were both 0%. Grade 3 or 4 toxic effects occurred in 7 patients (18%). In patients receiving surgery, 2-year overall survival was 77% (95% CI, 48%-91%), local control was 100% (95% CI, not defined), regional control was 53% (95% CI, 22%-76%), and distant control was 76% (95% CI, 45%-91%). Quality of life did not decline after treatment, with no significant changes in mean Functional Assessment of Cancer Therapy for Lung-Trial Outcome Index score during the first year of follow-up. CONCLUSIONS AND RELEVANCE The pCR rate after SABR for early-stage NSCLC was 60%, lower than hypothesized. The combined approach had toxic effects comparable to series of surgery alone, and there was no perioperative mortality. Further studies are needed to evaluate this combined approach compared with surgical resection alone. TRIAL REGISTRATION ClinicalTrials.gov identifier NCT02136355.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Radiosurgery / Carcinoma, Non-Small-Cell Lung / Lung Neoplasms Type of study: Clinical_trials / Prognostic_studies Aspects: Patient_preference Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: JAMA Oncol Year: 2019 Document type: Article Affiliation country: Canada

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Radiosurgery / Carcinoma, Non-Small-Cell Lung / Lung Neoplasms Type of study: Clinical_trials / Prognostic_studies Aspects: Patient_preference Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: JAMA Oncol Year: 2019 Document type: Article Affiliation country: Canada