Toxicity and health-related quality of life in breast cancer patients receiving adjuvant docetaxel, doxorubicin, cyclophosphamide (TAC) or 5-fluorouracil, doxorubicin and cyclophosphamide (FAC):: impact of adding primary prophylactic granulocyte-colony stimulating factor to the TAC regimen

被引:153
作者
Martin, M. [1 ]
Lluch, A.
Segui, M. A.
Ruiz, A.
Ramos, M.
Adrover, E.
Roriguez-Lescure, A.
Grosse, R.
Calvo, L.
Fernandez-Chacon, C.
Roset, M.
Anton, A.
Isla, D.
Martinez del Prado, P.
Iglesias, L.
Zaluski, J.
Arcusa, A.
Loez-Vega, J. M.
Munoz, M.
Mel, J. R.
机构
[1] Hosp Univ San Carlos, Med Oncol Serv, Madrid, Spain
[2] H Clin Univ Valencia, Valencia, Spain
[3] Corp Sanitaria Parc Tauli, Sabadell, Spain
[4] Inst Valenciano Oncol, Valencia, Spain
[5] Ctr Oncol Galicia, La Coruna, Spain
[6] H Gen Univ Alicante, Alicante, Spain
[7] H Gen Univ Elche, Elche, Spain
[8] Klin & Poliklin Gynakol, Halle, Germany
[9] CH Univ Juan Canalejo, La Coruna, Spain
[10] PIVOTAL, Madrid, Spain
[11] HORE, Barcelona, Spain
[12] H Univ Miguel Servet, Zaragoza, Spain
[13] H Clin Univ Lozano Blesa, Zaragoza, Spain
[14] H De Basurto, Bilbao, Spain
[15] H Univ Virgen Rocio, Seville, Spain
[16] Wielkopolskie Ctr Onkol, Poznan, Poland
[17] H de Terrassa, Terrassa, Spain
[18] H Univ Marques Valdecilla, Santander, Spain
[19] Hosp Clin Barcelona, Barcelona, Spain
[20] CH Xeral Calde, Lugo, Spain
关键词
adjuvant chemotherapy; docetaxel; TAC; G-CSF; filgrastim; lenograstim; operable breast cancer;
D O I
10.1093/annonc/mdl135
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The aim of the study was to analyse the toxicity and health related quality of life (HRQoL) of breast cancer patients treated with FAC (5-fluorouracil, doxorubicin, cyclophosphamide) and TAC (docetaxel, doxorubicin, cyclophosphamide) with and without primary prophylactic G-CSF (PPG). Patients and methods: This was a phase III study to compare FAC and TAC as adjuvant treatment of high-risk node-negative breast cancer patients. After the entry of the first 237 patients, the protocol was amended to include PPG in the TAC arm due to the high incidence of febrile neutropenia. A total of 1047 evaluable patients from 49 centres in Spain, two in Poland and four in Germany were included in the trial. Side-effects and the scores of the EORTC QLQ-C30 and QLQ BR-23 questionnaires were compared in the three groups (FAC, TAC pre-amendment and TAC post-amendment). Results: The addition of PPG to TAC significantly reduced the incidence of neutropenic fever, grade 2-4 anaemia, asthenia, anorexia, nail disorders, stomatitis, myalgia and dysgeusia. Patient QoL decreased during chemotherapy, more with TAC than FAC, but returned to baseline values afterwards. The addition of PPG to TAC significantly reduced the percentage of patients with clinically relevant Global Health Status deterioration (10 or more points over baseline value) at the end of chemotherapy (64% versus 46%, P < 0.03). Conclusions: The addition of PPG significantly reduces the incidence of neutropenic fever associated with TAC chemotherapy as well as that of some TAC-induced haematological and extrahaematological side-effects. The HRQoL of patients treated with TAC is worse than that of those treated with FAC but improves with the addition of PPG, particularly in the final part of chemotherapy treatment.
引用
收藏
页码:1205 / 1212
页数:8
相关论文
共 20 条
[1]   THE EUROPEAN-ORGANIZATION-FOR-RESEARCH-AND-TREATMENT-OF-CANCER QLQ-C30 - A QUALITY-OF-LIFE INSTRUMENT FOR USE IN INTERNATIONAL CLINICAL-TRIALS IN ONCOLOGY [J].
AARONSON, NK ;
AHMEDZAI, S ;
BERGMAN, B ;
BULLINGER, M ;
CULL, A ;
DUEZ, NJ ;
FILIBERTI, A ;
FLECHTNER, H ;
FLEISHMAN, SB ;
DEHAES, JCJM ;
KAASA, S ;
KLEE, M ;
OSOBA, D ;
RAZAVI, D ;
ROFE, PB ;
SCHRAUB, S ;
SNEEUW, K ;
SULLIVAN, M ;
TAKEDA, F .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1993, 85 (05) :365-376
[2]  
Abe O, 2005, LANCET, V366, P2087, DOI 10.1016/s0140-6736(05)66544-0
[3]  
Aggarwal B.B., 1995, HUMAN CYTOKINES THEI
[4]  
[Anonymous], 2000, HEMATOLOGY BASIC PRI
[5]   Life-threatening sepsis associated with adjuvant doxorubicin plus docetaxel for intermediate-risk breast cancer [J].
Brain, EGC ;
Bachelot, T ;
Serin, D ;
Kirscher, S ;
Graic, Y ;
Eymard, JC ;
Extra, JM ;
Combe, M ;
Fourme, E ;
Noguès, C ;
Rouëssé, J .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2005, 293 (19) :2367-2371
[6]  
Gabrilove J, 2000, SEMIN HEMATOL, V37, P1
[7]   EFFECT OF GRANULOCYTE COLONY-STIMULATING FACTOR ON NEUTROPENIA AND ASSOCIATED MORBIDITY DUE TO CHEMOTHERAPY FOR TRANSITIONAL-CELL CARCINOMA OF THE UROTHELIUM [J].
GABRILOVE, JL ;
JAKUBOWSKI, A ;
SCHER, H ;
STERNBERG, C ;
WONG, G ;
GROUS, J ;
YAGODA, A ;
FAIN, K ;
MOORE, MAS ;
CLARKSON, B ;
OETTGEN, HF ;
ALTON, K ;
WELTE, K ;
SOUZA, L .
NEW ENGLAND JOURNAL OF MEDICINE, 1988, 318 (22) :1414-1422
[8]   Meeting highlights: International Consensus Panel on the Treatment of Primary Breast Cancer [J].
Goldhirsch, A ;
Glick, JH ;
Gelber, RD ;
Senn, HJ .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1998, 90 (21) :1601-1608
[9]   A conversation with Lee Alvin DuBridge - Part II [J].
Goodstein, JR .
PHYSICS IN PERSPECTIVE, 2003, 5 (03) :281-309
[10]   The impact of hemoglobin levels on fatigue and quality of life in cancer patients [J].
Holzner, B ;
Kemmler, G ;
Greil, R ;
Kopp, M ;
Zeimet, A ;
Raderer, M ;
Hejna, M ;
Zöchbauer, S ;
Krajnik, G ;
Huber, H ;
Fleischhacker, WW ;
Sperner-Unterweger, B .
ANNALS OF ONCOLOGY, 2002, 13 (06) :965-973