Gamma knife radiosurgery for brain metastasis of nonsmall cell lung cancer: Is there a difference in outcome between morning and afternoon treatment?

Cancer - Tập 117 Số 2 - Trang 414-420 - 2011
Douglas A. Rahn1, Dibyendu K. Ray2, David Schlesinger3, Ladislau Steiner3,4, Jason P. Sheehan3,1, John O’Quigley5, Tyvin A. Rich1
1Department of Radiation Oncology, The University of Virginia Health Sciences Center, Charlottesville, Virginia
2Department of Neurological Surgery, Oregon Health and Science University, Portland, Oregon
3Department of Neurological Surgery, The University of Virginia Health Sciences Center, Charlottesville, Virginia
4Department of Radiology and Neuroradiology, The University of Virginia Health Sciences Center, Charlottesville, Virginia
5Department of Biostatistics, The University of Virginia Health Sciences Center, Charlottesville, Virginia

Tóm tắt

AbstractBACKGROUND:

Circadian cell‐cycle progression causes fluctuating radiosensitivity in many tissues, which could affect clinical outcomes. The purpose of this study was to determine whether outcomes of single‐session gamma knife radiosurgery (GKRS) for metastatic nonsmall cell lung cancer (NSCLC) differ based on treatment time.

METHODS:

Fifty‐eight patients received GKRS between 10:00 am and 12:30 pm and 39 patients received GKRS between 12:30 pm and 3:00 pm. The mean peripheral dose was 18.6 Gy. The mean tumor size was 7.3 cm3. Magnetic resonance imaging was used to score local control at 3 months. Cause of death (COD) was categorized as central nervous system (CNS)‐related or systemic.

RESULTS:

Demographic and disease characteristics of the 2 groups were similar. Local control at 3 months was achieved in 97% (35/36) of patients who underwent GKRS early in the day versus 67% (8/12) of patients who underwent GKRS later in the day (chi‐square, P = .014). Early GKRS was associated with better survival (median 9.5 months) than late GKRS (median 5 months) (Kaplan‐Meier log‐rank test, P = .025). Factors contributing to better survival in a Cox regression model included early treatment time (P = .004) and recursive partition analysis class (P < .001). Cause of death in the early treatment group was CNS‐related in 6% (3/47) of patients versus 24% (8/34) of patients in the late treatment group (chi‐square test, P = .026).

CONCLUSIONS:

GKRS for metastatic NSCLC had better local control, better survival, and a lower rate of CNS‐related cause of death when given earlier in the day versus later in the day. These retrospective data should encourage future study in brain radiosurgery and non‐CNS stereotactic body radiotherapy series. Cancer 2011. © 2010 American Cancer Society.

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Tài liệu tham khảo

Kubota S, 1989, Prediction of radiosensitivity by DNA analysis, Gan No Rinsho., 35, 1572

10.1016/j.ijrobp.2004.03.005

10.1080/09553008814551091

10.1016/0300-9629(84)90633-9

Haus E, 1974, Circadian susceptibility‐resistance cycle of bone marrow cells to whole body x‐irradiation in Balb/c mice, Chronobiologia., 1974, 115

10.1080/09553008214551791

10.1080/09553009114550171

10.1152/ajpregu.2001.280.5.R1476

10.1007/s004410050997

10.1007/s10517-005-0234-1

Frentz G, 1991, On circadian rhythms in human epidermal cell proliferation, Acta Derm Venereol., 71, 85, 10.2340/00015555718587

Moller U, 1984, Circadian‐stage dependence of methotrexate in a keratinized epithelium. An in‐vivo study using flow cytometry on the hamster cheek pouch epithelium, Cell Tissue Kinet., 17, 483

10.1007/BF00417387

Smaaland R, 1993, DNA synthesis and ploidy in non‐Hodgkin's lymphomas demonstrate intrapatient variation depending on circadian stage of cell sampling, Cancer Res., 53, 3129

10.1016/0016-5085(91)90019-H

10.1002/ijc.21591

10.1016/S0002-9440(10)65306-0

10.1016/S0002-9440(10)64135-1

10.1016/j.ijrobp.2008.07.009

10.3322/canjclin.57.1.43

10.1148/radiol.2423051707

10.1016/S0360-3016(96)00619-0

10.1016/S0360-3016(99)00549-0

10.1259/0007-1285-48-568-312

Hall EJ, 2005, Time, dose, and fractionation in radiotherapy, 378

Thames HD, 1987, Fractionation in Radiotherapy

10.1016/j.mehy.2006.08.020

10.1007/s10552-005-9003-8

10.1016/j.neuroscience.2006.03.037

10.1016/S0303-7207(01)00548-2

10.1126/science.1086271

Hrushesky W, 1992, The application of chronobiology to cancer medicine, 2666

10.1200/JCO.1993.11.7.1403

10.1002/j.2326-1951.1994.tb03773.x

Bjarnason G, 1994, Cancer chronotherapy, 240

10.1081/CBI-120002595

10.1016/j.molcel.2006.03.038

10.1074/jbc.M705576200

10.1016/j.tcb.2007.07.001

10.1073/pnas.0812638106