Inhaled Granulocyte-Macrophage Colony Stimulating Factor for First Pulmonary Recurrence of Osteosarcoma: Effects on Disease-Free Survival and Immunomodulation. A Report From the Children's Oncology Group

被引:66
作者
Arndt, Carola A. S. [1 ]
Koshkina, Nadya V. [2 ]
Inwards, Carrie Y. [1 ]
Hawkins, Douglas S. [3 ]
Krailo, Mark D. [4 ]
Villaluna, Doojduen [5 ]
Anderson, Peter M. [2 ]
Goorin, Allen M. [6 ]
Blakely, Martin L. [7 ]
Bernstein, Mark [8 ]
Bell, Sharon A. [1 ]
Ray, Kaylee [9 ]
Grendahl, Darryl C. [1 ]
Marina, Neyssa [10 ]
Kleinerman, Eugenie S. [2 ]
机构
[1] Mayo Clin, Rochester, MN 55905 USA
[2] Univ Texas MD Anderson Canc Ctr, Houston, TX 77030 USA
[3] Seattle Childrens Hosp, Seattle, WA USA
[4] Univ So Calif, Los Angeles, CA USA
[5] Childrens Oncol Grp, Arcadia, CA USA
[6] Dana Farber Canc Inst, Boston, MA 02115 USA
[7] Univ Tennessee, Ctr Hlth Sci, Memphis, TN 38163 USA
[8] IWK Hlth Ctr, Halifax, NS, Canada
[9] Doernbecher Hosp Children, Portland, OR USA
[10] Stanford Univ, Med Ctr, Stanford, CA 94305 USA
关键词
EARLY LYMPHOCYTE RECOVERY; GM-CSF; AEROSOL GEMCITABINE; ANTITUMOR IMMUNITY; PROGNOSTIC-FACTORS; LUNG METASTASES; FAS EXPRESSION; CELLS; CHEMOTHERAPY; THERAPY;
D O I
10.1158/1078-0432.CCR-10-0662
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Purpose: Osteosarcoma most commonly recurs in the lung. Based on preliminary data on the antitumor effects of granulocyte-macrophage colony stimulating factor (GM-CSF) in animal models, and promising phase I trials, we embarked on a feasibility study of inhaled GM-CSF in patients with first isolated pulmonary recurrence of osteosarcoma. Experimental Design: Forty-three eligible patients received inhaled GM-CSF at doses from 250 to 1,750 mu g twice daily on alternate weeks. Following two cycles, patients underwent thoracotomy to resect tumor and analyze pulmonary nodules for expression of Fas/Fas ligand (Fas/FasL), and the presence of dendritic cells by immunostaining for CD1a, clusterin, and S100. Following surgery, patients received 12 additional cycles of therapy on alternating weeks or until progression. Event-free survival and survival, and feasibility of therapy delivery were evaluated. Results: Dose escalation to 1,750 mu g twice daily was feasible with no dose-limiting toxicity. Mean scores for Fas/FasL in nodules from patients with bilateral recurrence who underwent unilateral thoracotomy pretreatment (using a scoring system of 0-3) were 1.3 and 0.88, respectively, compared with 0.78 and 0.62 in nodules resected following two cycles of therapy. Only 11 of 30 nodules postinhalation were positive for CD1a, 4 of 30 for S100, and 6 of 30 for clusterin. Event-free and overall survival at 3 years were 7.8% and 35.4%, respectively. Conclusions: Inhalation of GM-CSF at doses from 250 to 1,750 mu g twice daily on alternate weeks was feasible with low toxicity. However, no detectable immunostimulatory effect in pulmonary metastases or improved outcome postrelapse was seen. Clin Cancer Res; 16(15); 4024-30. (C) 2010 AACR.
引用
收藏
页码:4024 / 4030
页数:7
相关论文
共 31 条
[1]
Anderson PM, 1999, CLIN CANCER RES, V5, P2316
[2]
[Anonymous], J AEROSOL MED PULM D
[3]
Emerging applications of recombinant human granulocyte-macrophage colony-stimulating factor [J].
Armitage, JO .
BLOOD, 1998, 92 (12) :4491-4508
[4]
Granulocyte-macrophage colony-stimulating factor improves immunological parameters in patients with refractory solid tumours receiving second-line chemotherapy: Correlation with clinical responses [J].
Baxevanis, CN ;
Tsavaris, NB ;
Papadhimitriou, SI ;
Zarkadis, IK ;
Papadopoulos, NG ;
Bastounis, EA ;
Papamichail, M .
EUROPEAN JOURNAL OF CANCER, 1997, 33 (08) :1202-1208
[5]
Bernstein Z. P., 1997, Blood, V90, p133A
[6]
Treatment of osteosarcoma at first recurrence after contemporary therapy - The Memorial Sloan-Kettering Cancer Center Experience [J].
Chou, AJ ;
Merola, PR ;
Wexler, LH ;
Gorlick, RG ;
Vyas, YM ;
Healey, JH ;
LaQuaglia, MP ;
Huvos, AG ;
Meyers, PA .
CANCER, 2005, 104 (10) :2214-2221
[7]
Early lymphocyte recovery as a prognostic indicator for high-risk Ewing sarcoma [J].
De Angulo, Guillermo ;
Hernandez, Mike ;
Morales-Arias, Jaime ;
Herzog, Cynthia E. ;
Anderson, Peter ;
Wolff, Johannes ;
Kleinerman, Eugenie S. .
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 2007, 29 (01) :48-52
[8]
The intriguing role of polymorphonuclear neutrophils in antitumor reactions [J].
Di Carlo, E ;
Forni, G ;
Lollini, P ;
Colombo, MP ;
Modesti, A ;
Musiani, P .
BLOOD, 2001, 97 (02) :339-345
[9]
VACCINATION WITH IRRADIATED TUMOR-CELLS ENGINEERED TO SECRETE MURINE GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR STIMULATES POTENT, SPECIFIC, AND LONG-LASTING ANTITUMOR IMMUNITY [J].
DRANOFF, G ;
JAFFEE, E ;
LAZENBY, A ;
GOLUMBEK, P ;
LEVITSKY, H ;
BROSE, K ;
JACKSON, V ;
HAMADA, H ;
PARDOLL, D ;
MULLIGAN, RC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (08) :3539-3543
[10]
Recurrences following primary osteosarcoma in adolescents and adults previously treated with chemotherapy [J].
Duffaud, F ;
Digue, L ;
Mercier, C ;
Dales, JP ;
Baciuchka-Palmaro, M ;
Volot, F ;
Thomas, P ;
Favre, R .
EUROPEAN JOURNAL OF CANCER, 2003, 39 (14) :2050-2057