Predictors of local recurrence after rituximab-based chemotherapy alone in stage III and IV diffuse large B-cell lymphoma: guiding decisions for consolidative radiation.
Predictors of local recurrence after rituximab-based chemotherapy alone in stage III and IV diffuse large B-cell lymphoma: guiding decisions for consolidative radiation.
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在第三阶段和IV弥漫大型B细胞淋巴瘤中,仅基于利妥昔单抗化疗后局部复发的预测因素:巩固辐射的指导决定。
DOI:
10.1016/j.ijrobp.2015.01.025
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发表时间:
2015-05-01
影响因子:
7
通讯作者:
Khan, Mohammad K.
中科院分区:
文献类型:
--
作者:
Jegadeesh, Naresh;Rajpara, Raj;Esiashvili, Natia;Shi, Zheng;Liu, Yuan;Okwan-Duodu, Derrick;Flowers, Christopher R.;Khan, Mohammad K.
The role of consolidative radiotherapy (RT) for stage III and IV DLBCL in the era of rituximab is not well defined. There is evidence that some patients with bulky disease may benefit, but patient selection criteria are not well established. We sought to identify a subset of patients who experienced a high local failure rate after receiving rituximab-based chemotherapy alone and hence may benefit from the addition of consolidative RT. 211 stage III and IV DLBCL patients treated between August 1999 and January 2012 were reviewed. Of these, 89 had a complete response to systemic therapy including rituximab and received no initial RT. Kaplan-Meier analysis and Cox proportional hazards regression were performed with local recurrence (LR) as the primary outcome. Median follow-up was 43.9 months. 50% experienced LR at 5 years. In multivariate analysis tumor ≥ 5 cm and stage III disease were associated with increased risk of LR. Five year LR free survival for patients with ≥ 5 cm lesions were 47.4% versus 74.7% for patients with < 5cm lesions (p = 0.01). In patients with < 5 cm tumors, SUVmax was ≥15 in all patients with LR. Five year LR free survival was 100% in SUV < 15 versus 68.8% in SUV≥15 (p=0.10). Advanced stage DLBCL patients who are stage III or with disease ≥ 5 cm appear to be at an increased risk for LR. Patients with < 5 cm disease and SUVmax≥15 may be at higher risk for LR. These patients may benefit from consolidative RT following chemoimmunotherapy.
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影响因子:
158.5
作者:
Miller, TP;Dahlberg, S;Fisher, RI
通讯作者:
Fisher, RI
DOI:
10.1016/j.ijrobp.2011.12.067
发表时间:
2012-11-01
影响因子:
7
作者:
Dorth, Jennifer A.;Prosnitz, Leonard R.;Kelsey, Chris R.
通讯作者:
Kelsey, Chris R.
DOI:
10.1016/0360-3016(94)90352-2
发表时间:
1994-11-15
影响因子:
7
作者:
AVILES, A;DELGADO, S;DIAZMAQUEO, JC
通讯作者:
DIAZMAQUEO, JC
影响因子:
3.5
作者:
Miyazaki, Yukihiro;Nawa, Yuichiro;Miyagawa, Masao;Kohashi, Sumiko;Nakase, Koichi;Yasukawa, Masaki;Hara, Masamichi
通讯作者:
Hara, Masamichi
DOI:
10.1200/jco.2009.27.3441
发表时间:
2010-09-20
期刊:
Journal of clinical oncology : official journal of the American Society of Clinical Oncology
影响因子:
--
作者:
Phan, Jack;Mazloom, Ali;Dabaja, Bouthaina Shbib
通讯作者:
Dabaja, Bouthaina Shbib