Abstract

BackgroundSCLC has limited treatment options and inadequate preclinical models. Promising activity of arsenic trioxide (ASO) recorded in conventional preclinical models of SCLC supported the clinical evaluation of ASO in patients. We assessed the efficacy of ASO in relapsed SCLC patients and in corresponding patient-derived xenografts (PDX).MethodsSingle arm, Simon 2-stage, phase II trial to enroll patients with relapsed SCLC who have failed at least one line of therapy. ASO was administered as an intravenous infusion over 1–2 h daily for 4 days in week 1 and for 2 days in weeks 2–6 of an 8-week cycle. Treatment continued until disease progression. Pretreatment tumor biopsy was employed for PDX generation through direct implantation into subcutaneous pockets of SCID mice without in vitro manipulation and serially propagated for five generations. Ex vivo efficacy of cisplatin (3 mg/kg i.p. weekly) and ASO (3.75 mg/kg i.p. every other day) was tested in PDX representative of platinum sensitive and platinum refractory SCLC.ResultsThe best response in 17 evaluable patients was stable disease in 2 (12 %), progressive disease in 15 (88 %) patients and median time-to-progression of seven (range 1–7) weeks. PDX was successfully grown in 5 of 9 (56 %) transplanted biopsy samples. Serially-propagated PDXs preserved characteristic small cell histology and genomic stability confirmed by immunohistochemistry, short tandem repeat (STR) profiling and targeted sequencing. ASO showed in vitro cytotoxicity but lacked in vivo efficacy against SCLC PDX tumor growth.ConclusionsCisplatin inhibited growth of PDX derived from platinum-sensitive SCLC but was ineffective against PDX from platinum-refractory SCLC. Strong concordance between clinical and ex vivo effects of ASO and cisplatin in SCLC supports the use of PDX models to prescreen promising anticancer agents prior to clinical testing in SCLC patients.Trial Registration The study was registered at http://www.clinicaltrials.gov (NCT01470248)Electronic supplementary materialThe online version of this article (doi:10.1186/s12967-016-0861-5) contains supplementary material, which is available to authorized users.

Highlights

  • Small cell lung cancer (SCLC) has limited treatment options and inadequate preclinical models

  • Other objectives were to determine the progression free survival and overall survival associated with single agent arsenic tri‐ oxide (ASO) in refractory SCLC and to correlate the clinical efficacy observed in patients with the activity in corresponding patient-derived xenografts (PDX) generated using pretreatment tumor biopsies obtained from patients enrolled on study

  • In order to test whether the PDX model could predict efficacy of other agents beyond cisplatin, we evaluated the in vivo efficacy of ON.01910.Na, a novel agent, targeting polo-like kinase 1 (PLK1), which was previously identified as a promising target in SCLC [17]

Read more

Summary

Introduction

SCLC has limited treatment options and inadequate preclinical models. Promising activity of arsenic tri‐ oxide (ASO) recorded in conventional preclinical models of SCLC supported the clinical evaluation of ASO in patients. Preclinical data in SCLC cell lines revealed the presence of a rare sub-clone with a stem-cell phenotype characterized by surface receptor expression of CD44, CD133, multi-drug resistance gene (MDR1) and urokinase plasminogen activator receptor (uPAR) [6,7,8]. This cell population frequently exhibits primary resistance to frontline chemotherapy agents including cisplatin and etoposide [7, 8]. These cells possess a high capacity for self-renewal, differentiation into adult cancer cells and increased tumorigenesis in clonogenic assays

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.