Circulating tumor cells as a prognostic factor in patients with small cell lung cancer

Igawa,Satoshi; Gohda,Keigo; Fukui,Tomoya; Ryuge,Shinichiro; Otani,Sakiko; Masago,Akinori; Sato,Jun; Murakami,Katsuhiro; Maki,Sachiyo; Katono,Ken; Takakura,Akira; Sasaki,Jiichiro; Satoh,Yukitoshi; Masuda,Noriyuki

doi:10.3892/ol.2014.1940

May-2014 Volume 7 Issue 5

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May-2014 Volume 7 Issue 5

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Article

Circulating tumor cells as a prognostic factor in patients with small cell lung cancer

Authors:
- Satoshi Igawa
- Keigo Gohda
- Tomoya Fukui
- Shinichiro Ryuge
- Sakiko Otani
- Akinori Masago
- Jun Sato
- Katsuhiro Murakami
- Sachiyo Maki
- Ken Katono
- Akira Takakura
- Jiichiro Sasaki
- Yukitoshi Satoh
- Noriyuki Masuda
View Affiliations / Copyright

Affiliations: Department of Respiratory Medicine, Kitasato University School of Medicine, Sagamihara, Kanagawa 252‑0374, Japan, Central Research Laboratories, Sysmex Corporation, Kobe, Hyōgo 651‑2271, Japan, Department of Thoracic Surgery, Kitasato University School of Medicine, Sagamihara, Kanagawa 252‑0374, Japan
Pages: 1469-1473
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Published online on: March 5, 2014

https://doi.org/10.3892/ol.2014.1940
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Abstract

The detection of circulating tumor cells (CTCs) in peripheral blood is currently an important field of study. Detection of CTCs by the OBP‑401 assay (TelomeScan®) has previously been reported to be useful in the diagnosis, prognosis and evaluation of therapeutic efficacy in breast and gastric cancer. The aim of the present study was to evaluate the OBP‑401 assay as a novel method of detecting CTCs of small cell lung cancer (SCLC) patients and to evaluate whether CTC count is associated with prognosis. Prospectively, 30 consecutively diagnosed SCLC patients who had commenced chemotherapy or chemoradiotherapy were enrolled as subjects of the current study. Peripheral blood specimens were collected from the SCLC patients prior to and following the initiation of treatment and the viable CTCs were detected in the specimens following incubation with a telomerase‑specific, replication‑selective, oncolytic adenoviral agent, which was carrying the green fluorescent protein gene. CTCs were detected in 29 patients (96%). The group of 21 patients with a CTC count of <2 cells/7.5 ml prior to treatment (baseline) had a significantly longer median survival time than the group of eight patients with a CTC count of ≥2 cells/7.5 ml prior to treatment (14.8 and 3.9 months, respectively; P=0.007). The results of a multivariate analysis showed that the baseline CTC count was an independent prognostic factor for survival time (hazard ratio, 3.91; P=0.026). Among the patients that achieved a partial response to treatment, patients who had a CTC count of <2 cells/7.5 ml following two cycles of chemotherapy tended to have a longer median progression‑free survival compared with patients who had a CTC count of ≥2 cell/7.5 ml (8.3 and 3.8 months, respectively; P=0.07). Therefore, CTCs may be detected via OBP‑401 assay in SCLC patients and the CTC count prior to treatment appears to be a strong prognostic factor.

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Journals

International Journal of Molecular Medicine

International Journal of Oncology

Molecular Medicine Reports

Oncology Reports

Experimental and Therapeutic Medicine

Oncology Letters

Biomedical Reports

Molecular and Clinical Oncology

World Academy of Sciences Journal

International Journal of Functional Nutrition

International Journal of Epigenetics

Medicine International

Circulating tumor cells as a prognostic factor in patients with small cell lung cancer

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Abstract

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