Smerage Jeffrey B, Barlow William E, Hortobagyi Gabriel N, Winer Eric P, Leyland-Jones Brian, Srkalovic Gordan, Tejwani Sheela, Schott Anne F, O'Rourke Mark A, Lew Danika L, Doyle Gerald V, Gralow Julie R, Livingston Robert B, Hayes Daniel F
Jeffrey B. Smerage, Anne F. Schott, and Daniel F. Hayes, University of Michigan Comprehensive Cancer Center, Ann Arbor; Gordan Srkalovic, Sparrow Regional Cancer Center, Lansing; Sheela Tejwani, Henry Ford Hospital, Detroit, MI; William E. Barlow and Danika L. Lew, SWOG Statistical Center; Julie R. Gralow, Seattle Cancer Care Alliance, Seattle, WA; Gabriel N. Hortobagyi, University of Texas MD Anderson Cancer Center, Houston, TX; Eric P. Winer, Dana-Farber Cancer Institute, Boston, MA; Brian Leyland-Jones, Avera Cancer Institute, Sioux Falls, SD; Mark A. O'Rourke, Greenville Health System Cancer Institute/Greenville Community Clinical Oncology Program, Greenville, SC; Gerald V. Doyle, Immunicon, Huntingdon Valley, PA; and Robert B. Livingston, University of Arizona Cancer Center, Tucson, AZ.
J Clin Oncol. 2014 Nov 1;32(31):3483-9. doi: 10.1200/JCO.2014.56.2561. Epub 2014 Jun 2.
Increased circulating tumor cells (CTCs; five or more CTCs per 7.5 mL of whole blood) are associated with poor prognosis in metastatic breast cancer (MBC). A randomized trial of patients with persistent increase in CTCs tested whether changing chemotherapy after one cycle of first-line chemotherapy would improve the primary outcome of overall survival (OS).
Patients with MBC who did not have increased CTCs at baseline remained on initial therapy until progression (arm A). Patients with initially increased CTCs that decreased after 21 days of therapy remained on initial therapy (arm B). Patients with persistently increased CTCs after 21 days of therapy were randomly assigned to continue initial therapy (arm C1) or change to an alternative chemotherapy (arm C2).
Of 595 eligible and evaluable patients, 276 (46%) did not have increased CTCs (arm A). Of those with initially increased CTCs, 31 (10%) were not retested, 165 were assigned to arm B, and 123 were randomly assigned to arm C1 or C2. No difference in median OS was observed between arm C1 and C2 (10.7 and 12.5 months, respectively; P = .98). CTCs were strongly prognostic. Median OS for arms A, B, and C (C1 and C2 combined) were 35 months, 23 months, and 13 months, respectively (P < .001).
This study confirms the prognostic significance of CTCs in patients with MBC receiving first-line chemotherapy. For patients with persistently increased CTCs after 21 days of first-line chemotherapy, early switching to an alternate cytotoxic therapy was not effective in prolonging OS. For this population, there is a need for more effective treatment than standard chemotherapy.
循环肿瘤细胞(CTCs;每7.5毫升全血中CTCs数量达到或超过5个)增多与转移性乳腺癌(MBC)患者的不良预后相关。一项针对CTCs持续增加的患者的随机试验,检验了在一线化疗一个周期后更换化疗方案是否能改善总生存期(OS)这一主要结局。
基线时CTCs未增多的MBC患者继续初始治疗直至疾病进展(A组)。初始CTCs增多但治疗21天后减少的患者继续初始治疗(B组)。治疗21天后CTCs持续增多的患者被随机分配继续初始治疗(C1组)或更换为另一种化疗方案(C2组)。
在595例符合条件且可评估的患者中,276例(46%)CTCs未增多(A组)。在初始CTCs增多的患者中,31例(10%)未再次检测,165例被分配至B组,123例被随机分配至C1组或C2组。C1组和C2组的中位OS无差异(分别为10.7个月和12.5个月;P = 0.98)。CTCs具有很强的预后价值。A组、B组和C组(C1组和C2组合并)的中位OS分别为35个月、23个月和13个月(P < 0.001)。
本研究证实了CTCs在接受一线化疗的MBC患者中的预后意义。对于一线化疗21天后CTCs持续增多的患者,早期更换为另一种细胞毒性治疗方案并不能有效延长OS。对于这一人群,需要比标准化疗更有效的治疗方法。