Stevenson H C, Gazdar A F, Linnoila R I, Russell E K, Oie H K, Steinberg S M, Ihde D C
National Cancer Institute-Navy Medical Oncology Branch, Bethesda, MD 20814.
J Clin Oncol. 1989 Jul;7(7):923-31. doi: 10.1200/JCO.1989.7.7.923.
The ability to establish a continuously growing tumor cell line from fresh tumor specimens has been associated with shortened survival in some human malignancies. Therefore, we assessed the relationship between survival and in vitro tumor cell growth from specimens obtained during routine staging procedures in 68 consecutive patients with untreated, extensive-stage small-cell lung cancer (SCLC) who received etoposide/cisplatin chemotherapy. Three groups of SCLC patients could be distinguished: (1) 23 patients in whom a tumor cell line was established in vitro; (2) 28 patients in whom tumor-containing specimens were cultured but in vitro growth did not occur; and (3) 17 patients in whom no tumor-containing specimen could be procured. No significant difference in response rates to chemotherapy of the three groups was noted. Poor performance status (P2 = .001), male gender (P2 = .0008), liver metastases (P2 = .0033), brain metastases (P2 = .0152), and the ability to obtain a tumor-containing specimen from the patient for laboratory culture (P2 = .0005) were all significant independent predictors of decreased survival in this patient population. While the ability to obtain a tumor cell specimen for cell culture using routine staging and diagnostic procedures identified patients with shortened survival, we found no significant survival differences between patients whose tumor cell specimens grew in cell culture v those that did not (median survival of 7 months v 11 months, P2 = .72). Our study indicates that the clinical outcome of extensive-stage SCLC patients from whom tumor cell lines can be established is not significantly different than in those cases from whom tumor-containing specimens could not be grown in vitro.
从新鲜肿瘤标本中建立持续生长的肿瘤细胞系的能力,在一些人类恶性肿瘤中与生存期缩短有关。因此,我们评估了68例未经治疗的广泛期小细胞肺癌(SCLC)患者在常规分期程序中获取的标本的体外肿瘤细胞生长与生存期之间的关系,这些患者接受了依托泊苷/顺铂化疗。可将三组SCLC患者区分开来:(1)23例在体外建立了肿瘤细胞系的患者;(2)28例培养了含肿瘤标本但未发生体外生长的患者;(3)17例未获取到含肿瘤标本的患者。三组患者对化疗的反应率未观察到显著差异。较差的体能状态(P2 = 0.001)、男性(P2 = 0.0008)、肝转移(P2 = 0.0033)、脑转移(P2 = 0.0152)以及从患者获取含肿瘤标本用于实验室培养的能力(P2 = 0.0005),均是该患者群体生存期缩短的显著独立预测因素。虽然使用常规分期和诊断程序获取肿瘤细胞标本用于细胞培养的能力可识别出生存期缩短的患者,但我们发现肿瘤细胞标本在细胞培养中生长的患者与未生长的患者之间生存期无显著差异(中位生存期分别为7个月和11个月,P2 = 0.72)。我们的研究表明,能够建立肿瘤细胞系的广泛期SCLC患者的临床结局,与无法在体外培养出含肿瘤标本的患者相比,无显著差异。