Granulocyte growth factors in the treatment of non-small cell lung cancer (NSCLC)

被引:18
作者
Grossi, Francesco [1 ]
Tiseo, Marcello [1 ]
机构
[1] Ist Nazl Ric Canc, Div Med Oncol A, Dis Management Team Lung Canc, I-16132 Genoa, Italy
关键词
non-small cell lung cancer; neutropenia; febrile neutropenia; granulocyte growth factors;
D O I
10.1016/j.critrevonc.2005.09.002
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Neutropenia and subsequent infections are common events that limit treatment of non-small cell lung cancer (NSCLC). Granulocyte growth factors (G- and GM-CSF) have been introduced in clinical practice and their use has yielded a reduction of the infection risk related to chemotherapy and a dose increase of drug delivery. Randomized clinical trials have shown that granulocyte colony-stimulating factors and, more recently, the longer-acting pegylated granulocyte colony-stimulating factor (pegfilgrastim) effectively reduce the incidence and severity of neutropenia and of its complications. Recommendations for the use of haematopoietic colony-stimulating factors from the American Society of Clinical Oncology (ASCO) have been published in 1994 and updated in 1996,1997 and 2000. Recently, moreover, National Comprehensive Cancer Network (NCCN) guidelines for the myeloid growth factors in cancer treatment make available. Chemotherapy-associated myelosuppression is a major limitation of anticancer therapy also in early stage, local advanced and metastatic NSCLC. Recently, dose-dense chemotherapy has been shown to improve the outcome in early stage breast cancer and non-Hodgkin's lymphoma. However, few randomized trials have been reported on chemotherapy with or without granulocyte growth factors as primary prophylaxis in NSCLC. Presently, there is no evidence for a benefit in response rate and survival from the use of granulocyte growth factors as support of chemotherapy, in particular, for locally advanced and metastatic NSCLC. In clinical practice, the role of granulocyte growth factors for NSCLC treatment should be limited following the guidelines. An appropriate use of granulocyte growth factors may reduce the overall cost of treatment and improve the quality of life, important aims in the treatment of patients with local advanced or metastatic NSCLC. In the future, we need to identify patients who can benefit from granulocyte growth factors for optimize the schedule and doses, in advanced disease and also, after the recent positive results of adjuvant chemotherapy, in early stages. This review summarizes the present knowledge on the use of granulocyte growth factors in NSCLC. (c) 2005 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:221 / 230
页数:10
相关论文
共 77 条
[41]   PACLITAXEL AND CARBOPLATIN IN COMBINATION IN THE TREATMENT OF ADVANCED NON-SMALL-CELL LUNG-CANCER - A PHASE-II TOXICITY, RESPONSE, AND SURVIVAL ANALYSIS [J].
LANGER, CJ ;
LEIGHTON, JC ;
COMIS, RL ;
ODWYER, PJ ;
MCALEER, CA ;
BONJO, CA ;
ENGSTROM, PF ;
LITWIN, S ;
OZOLS, RF .
JOURNAL OF CLINICAL ONCOLOGY, 1995, 13 (08) :1860-1870
[42]   PHASE-I TRIAL OF HIGH-DOSE ETOPOSIDE, HIGH-DOSE CISPLATIN, AND REINFUSION OF AUTOLOGOUS BONE-MARROW FOR LUNG-CANCER [J].
LAZARUS, HM ;
SPITZER, TR ;
CREGER, RJ .
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 1990, 13 (02) :107-112
[43]   Cisplatin-based adjuvant chemotherapy in patients with completely resected non-small-cell lung cancer [J].
Le Chevalier, T ;
Arriagada, R ;
Le Péchoux, C ;
Grunenwald, D ;
Dunant, A ;
Pignon, JP ;
Tarayre, M ;
Abratt, R ;
Arriagada, R ;
Bergman, B ;
Gralla, R ;
Grunenwald, D ;
Le Chevalier, T ;
Orlowski, T ;
Papadakis, E ;
Pinel, MIS ;
Araujo, C ;
Della Torre, H ;
de Solchaga, MM ;
Abdi, E ;
Blum, R ;
Ball, D ;
Basser, R ;
De Boer, R ;
Bishop, J ;
Brigham, B ;
Davis, S ;
Fox, D ;
Richardson, G ;
Wyld, D ;
Pirker, R ;
Humblet, Y ;
Delaunois, L ;
Van Meerbeeck, JP ;
Germonpre, P ;
Vansteenkiste, J ;
Nackaerts, K ;
Pinel, MIS ;
Vauthier, G ;
Younes, RN ;
Arriagada, R ;
Baeza, R ;
Carvajal, P ;
Kleinman, S ;
Orlandi, L ;
Castro, C ;
Godoy, J ;
Kosatova, K ;
Gaafar, R ;
Azarian, R .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 350 (04) :351-360
[44]   A brief intensive cisplatin-based outpatient chemotherapy regimen with filgrastim and megestrol acetate support for advanced non-small cell lung cancer: results of a phase II trial [J].
Levitan, N ;
Dowlati, A ;
Craffey, M ;
Tahsildar, H ;
MacKay, W ;
McKenney, J ;
Remick, SC .
LUNG CANCER, 1998, 22 (03) :227-234
[45]  
Lyman Gary H, 2003, Cancer Control, V10, P487
[46]  
Masutani M, 1999, ONCOL REP, V6, P1045
[47]   Phase II trial of docetaxel and vinorelbine in patients with advanced non-small-cell lung cancer [J].
Miller, VA ;
Krug, LM ;
Ng, KK ;
Pizzo, B ;
Perez, W ;
Heelan, RT ;
Kris, MG .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (06) :1346-1350
[48]   A phase II study of irinotecan and infusional cisplatin with recombinant human granulocyte colony-stimulating factor support for advanced non-small-cell lung cancer [J].
Mori, K ;
Machida, S ;
Yoshida, T ;
Yoshida, M ;
Kano, Y ;
Tominaga, K .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 1999, 43 (06) :467-470
[49]   Phase II trial of dose intensification with cisplatin and carboplatin plus vindesine in patients with inoperable non-small cell lung cancer [J].
Nakanishi, Y ;
Takayama, K ;
Kawasaki, M ;
Yatsunami, J ;
Inutsuka, S ;
Wakamatsu, K ;
Tsuruta, N ;
Hara, N .
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 1997, 20 (04) :393-397
[50]  
*NAT COMPR CANC NE, 2005, MY GROWTH FACT CANC