Addition of rituximab to cyclophosphamide, doxorubicin, vincristine, and prednisolone therapy has a high risk of developing interstitial pneumonia in patients with non-Hodgkin lymphoma

被引:49
作者
Katsuya, Hiroo
Suzumiya, Junji [2 ]
Sasaki, Hidenori
Ishitsuka, Kenji
Shibata, Takao [3 ]
Takamatsu, Yasushi
Tamura, Kazuo [1 ]
机构
[1] Fukuoka Univ Hosp, Dept Med Oncol & Hematol, Jonan Ku, Fukuoka 8140180, Japan
[2] Fukuoka Univ, Chikushi Hosp, Dept Internal Med, Chikushino, Japan
[3] Murakami Karindou Hosp, Dept Internal Med, Fukuoka, Japan
关键词
Rituximab; interstitial pneumonitis; Pneumocystis jirovecii pneumonia; COLONY-STIMULATING FACTOR; ACUTE LUNG INJURY; CHEMOTHERAPY PLUS RITUXIMAB; B-CELL LYMPHOMA; ELDERLY-PATIENTS; G-CSF; CHOP; DIAGNOSIS; BLEOMYCIN; ASSAY;
D O I
10.3109/10428190903258780
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
There are a few reports suggesting that rituximab (RTX) might be a risk for interstitial pneumonitis (IP). We also experienced such patients in the era of RTX. Here, we reviewed all the patients with non-Hodgkin lymphoma who were treated with RTX-CHOP-like regimen (R-CHOP) to determine the risk of developing IP. One of 59 (1.7%) patients who received CHOP alone and 8 of 129 (6.2%) patients who were treated with R-CHOP experienced IP (p = 0.28). Furthermore, three of eight patients who have had IP during R-CHOP were confirmed having Pneumocystis jirovecii pneumonia (PCP). PCP occurred during the fourth, sixth, and seventh cycle of chemotherapy, respectively. Among the patients treated by R-CHOP, 3 of 32 (9%) patients whose lymphocyte counts were <1000/mu L before chemotherapy developed PCP, while 70 patients whose lymphocyte counts were >1000/mu L did not (p = 0.03). In four of eight patients, IP occurred during the administration of granulocyte-colony stimulating factor. RTX seems to have a certain risk to induce IP including PCP. Patients with lymphoma who were treated by R-CHOP regimen, might be considered as PCP prophylactic, especially if the number of lymphocytes is low at the beginning of chemotherapy.
引用
收藏
页码:1818 / 1823
页数:6
相关论文
共 22 条
[1]   Granulocyte colony-stimulating factor exacerbates the acute lung injury and pulmonary fibrosis induced by intratracheal administration of bleomycin in rats [J].
Adachi, K ;
Suzuki, M ;
Sugimoto, T ;
Suzuki, S ;
Niki, R ;
Oyama, A ;
Uetsuka, K ;
Nakamaya, H ;
Doi, K .
EXPERIMENTAL AND TOXICOLOGIC PATHOLOGY, 2002, 53 (06) :501-510
[2]  
ADLER D, 2008, REV MED SUISSE, V4, P2528
[3]   G-CSF and IL-8 but not GM-CSF correlate with severity of pulmonary neutrophilia in acute respiratory distress syndrome [J].
Aggarwal, A ;
Baker, CS ;
Evans, TW ;
Haslam, PL .
EUROPEAN RESPIRATORY JOURNAL, 2000, 15 (05) :895-901
[4]   Effect of granulocyte colony-stimulating factor on bleomycin-induced acute lung injury and pulmonary fibrosis [J].
Azoulay, E ;
Herigault, S ;
Levame, M ;
Brochard, L ;
Schlemmer, B ;
Harf, A ;
Delclaux, C .
CRITICAL CARE MEDICINE, 2003, 31 (05) :1442-1448
[5]   Exacerbation with granulocyte colony-stimulating factor of prior acute lung injury during neutropenia recovery in rats [J].
Azoulay, É ;
Attalah, H ;
Yang, K ;
Herigault, S ;
Jouault, H ;
Brun-Buisson, C ;
Brochard, L ;
Harf, A ;
Schlemmer, B ;
Delclaux, C .
CRITICAL CARE MEDICINE, 2003, 31 (01) :157-165
[6]   Granulocyte colony-stimulating factor or neutrophil-induced pulmonary toxicity: Myth or reality? Systematic review of clinical case reports and experimental data [J].
Azoulay, E ;
Attalah, H ;
Harf, A ;
Schlemmer, B ;
Delclaux, C .
CHEST, 2001, 120 (05) :1695-1701
[7]  
Bienvenu J, 2001, Hematol J, V2, P378, DOI 10.1038/sj.thj.6200133
[8]  
Brusamolino E, 2006, HAEMATOLOGICA, V91, P496
[9]  
Burton C, 2003, NEW ENGL J MED, V348, P2690
[10]   CHOP chemotherapy plus rituximab compared with CHOP alone in elderly patients with diffuse large-B-cell lymphoma. [J].
Coiffier, B ;
Lepage, E ;
Brière, J ;
Herbrecht, R ;
Tilly, H ;
Bouabdallah, R ;
Morel, P ;
Van den Neste, E ;
Salles, G ;
Gaulard, P ;
Reyes, F ;
Gisselbrecht, C .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 346 (04) :235-242