Cohen Jonathon B, Bucur Silvana, Winton Elliott F, Sinha Rajni, Heffner Leonard T, King Nassoma, Lonial Sagar, Langston Amelia A, Waller Edmund K, Hutchison-Rzepka Amanda, Colbert Amanda, Lechowicz Mary Jo, Flowers Christopher R
Department of Hematology and Medical Oncology, Emory University, Winship Cancer Institute, Atlanta, GA.
Department of Hematology and Medical Oncology, Emory University, Winship Cancer Institute, Atlanta, GA.
Clin Lymphoma Myeloma Leuk. 2015 Sep;15(9):514-8. doi: 10.1016/j.clml.2015.06.009. Epub 2015 Jul 3.
Granulocyte-monocyte colony stimulating factor (GM-CSF) is a hematopoietic cytokine with immunomodulatory activity that has preclinical evidence for enhancement of antitumor immunity when administered in combination with chemotherapy. We evaluated the utility of GM-CSF with chemoimmunotherapy in patients with indolent non-Hodgkin lymphoma (NHL) and chronic lymphocytic leukemia (CLL) in a pilot study.
Patients with previously untreated, relapsed, or refractory indolent NHL or CLL were treated with GM-CSF, rituximab, fludarabine, and cyclophosphamide or mitoxantrone for a maximum of 6 cycles.
Sixteen patients were enrolled, including 1 patient who did not receive study therapy. Of the 15 remaining patients, 6 received cyclophosphamide and 9 received mitoxantrone in combination with fludarabine, rituximab, and GM-CSF. The overall response rate for all patients was 87%. Nine patients have subsequently had relapse of their disease, and 6 remained in remission at last study contact. There were no toxic deaths during the study.
GM-CSF-based chemoimmunotherapy was well-tolerated and resulted in a high response rate and warrants evaluation in larger studies.
粒细胞-单核细胞集落刺激因子(GM-CSF)是一种具有免疫调节活性的造血细胞因子,临床前证据表明,与化疗联合使用时可增强抗肿瘤免疫力。在一项初步研究中,我们评估了GM-CSF联合化疗免疫疗法在惰性非霍奇金淋巴瘤(NHL)和慢性淋巴细胞白血病(CLL)患者中的效用。
既往未治疗、复发或难治性惰性NHL或CLL患者接受GM-CSF、利妥昔单抗、氟达拉滨和环磷酰胺或米托蒽醌治疗,最多6个周期。
共纳入16例患者,其中1例未接受研究治疗。其余15例患者中,6例接受环磷酰胺治疗,9例接受米托蒽醌联合氟达拉滨、利妥昔单抗和GM-CSF治疗。所有患者的总缓解率为87%。9例患者随后疾病复发,6例在最后一次研究随访时仍处于缓解状态。研究期间无毒性死亡病例。
基于GM-CSF的化疗免疫疗法耐受性良好,缓解率高,值得在更大规模的研究中进行评估。