- Research article
- Open Access
- Open Peer Review
Is there a role for consolidative radiotherapy in the treatment of aggressive and localized Non-Hodgkin Lymphoma? A systematic review with meta-analysis
© dos Santos et al.; licensee BioMed Central Ltd. 2012
- Received: 26 October 2011
- Accepted: 27 June 2012
- Published: 13 July 2012
Chemotherapy is the mainstay of non-Hodgkin lymphoma (NHL) treatment. Based on expert opinion, the use of radiotherapy (RT) is currently preferred in some institutions as consolidative treatment for patients with localized disease. The lack of conclusive data coming from conflicting studies about the impact of treatment demands a systematic review, which could provide the most reliable assessment for clinical decision-making. We evaluate the addition of RT post-CT, for aggressive and localized NHL (ALNHL).
Randomized controlled trials (RCT) that evaluated chemotherapy alone versus chemotherapy plus RT were searched in databases. The outcomes were overall survival (OS), progression-free survival (PFS), overall response rate (ORR) and toxicity. Risk ratio (RR) and hazard ratio (HR) with their respective 95% confidence intervals (CI) were calculated using a fized-effect model.
Four trials (1,796 patients) met the inclusion criteria. All trials tested the use of RT after systemic therapy comprising anthracycline-based chemotherapy. This systematic review showed that RT enhances PFS after chemotherapy (hazard ratio [HR] 0.81; 95% CI 0.67-0.98; p = 0.03), with no impact on ORR and OS. Some heterogeneity between trials could limit the conclusions about OS. Toxicity data could not be pooled due to differences in reporting adverse events.
This systematic review with meta-analysis shows no improvement in survival when adding RT to systemic therapy for ALNHL. Our conclusions are limited by the available data. Further evaluations of new RT technologies and its association with biologic agents are needed.
- Non-Hodgkin lymphoma
- Consolidative radiotherapy
- Systematic review
Non-Hodgkin lymphoma (NHL) is the sixth most common cause of cancer death in the world . About 300,000 new cases of NHL occur every year, accounting for nearly 3% of all new cases of cancer. Among them, more than half will die due to NHL .
There are several classifications currently in use for NHL that are somewhat overlapping. The Revised European American Lymphoma (REAL) classification  was initially proposed. However, a REAL-based classification is now widely accepted, also known as the World Health Organization (WHO) classification for hematologic malignancies. This classification is based on cell of origin, maturity, morphology, immunophenotype, genetic and clinical features . Considered outdated by many, the International Working Formulation  (WF) had divided NHL in low, intermediate and high grade, based on morphology and natural history. It remains important because studies designed more than 10 years ago were based on this classification.
In some series, more than one third of patients with NHL have an aggressive phenotype. For patients with localized disease, radiotherapy (RT) was the first curative approach and continues to be a part of combined modality therapy [6–8]. Previous studies have shown that almost 70% of patients with localized NHL can be cured by RT alone [9, 10]. However, the high relapse rate outside the radiation field justifies the requirement of chemotherapy in this setting [11, 12].
Since the early 1980s, the synergistic effect of both modalities has been evaluated, and their combination widely advocated in the treatment of patients with NHL [13–17]. The benefit of this strategy was first shown in a randomized trial including 316 patients, comparing RT versus chemotherapy versus combined therapy . In this trial, the combination arm had better failure-free survival and OS when compared to chemotherapy alone, or RT alone arms. The use of RT after systemic therapy is frequently recommended, based on expert opinion, to improve local control of the disease, and possibly to diminish relapse and death .
The lack of conclusive data coming from conflicting studies about the impact of treatment demands a systematic review, which could provide the most reliable assessment for clinical decision-making. The aim of this systematic review is to assess whether adding RT to standard chemotherapy for aggressive and localized NHL (ALNHL) has an impact on local tumor control and survival.
This study was approved by the Ethics Committee at Universidade Estadual de Campinas.
Types of studies
Randomized controlled trials (RCT) were included comparing chemotherapy and consolidative RT versus chemotherapy alone for patients with ALNHL.
Types of participants
Participants included adults with ALNHL, without previous treatment. We defined localized disease as Ann Arbor stage I and stage II with contiguous disease encompassed by a radiation field . We defined aggressive NHL according to the WF , the REAL classification , or the WHO classification . In older trials, an intermediate or a high-grade classification was permitted.
Types of outcome measures
The primary outcome was OS. Secondary outcomes of interest were PFS, response to therapy and safety. PFS encompassed the term disease-free survival (DFS), used when there was no residual disease.
Search strategies for identification of studies
We performed an electronic database search  in MEDLINE, EMBASE, Cochrane Central Register of Controlled Trials – CENTRAL and LILACS (until January 2010); electronic or hand searching of the conference proceedings between 1980 and 2009 of the American Society of Clinical Oncology (ASCO), the American Society for Therapeutic Radiology and Oncology (ASTRO), the American Society of Hematology (ASH), the European Conference on Clinical Oncology (ECCO) and the European Society of Medical Oncology (ESMO). Reference list of all recovered trials and relevant reviews were also considered. For electronic databases, we used a sensitive search strategy with words linked to NHL and RT.
Titles and abstracts of studies identified from search strategy were screened independently by two reviewers (LVS and JPL), according to the eligibility criteria described above. Disagreements in the trial selection were resolved by discussion and a third reviewer was invited to give his opinion (ADS) if consensus was not reached. Full-text versions of all eligible studies were obtained for quality assessment and data extraction.
The quality of each individual study was assessed independently by two reviewers (LVS and ADS) using the published manuscript. A specific data extraction form was designed for assessment of quality features of studies, such as randomization, allocation concealment, intention-to-treat principle, similarity of treatment arms according to known prognostic factors, follow up and drop-outs [22, 23]. Disagreements were discussed among the group until consensus was reached.
A data extraction form was designed previously, and included the following items: general identification information (authors, title, journal, date of publication, protocol name, and duplication of publication), trial, type of patients, intervention characteristics, and reported outcomes. Data extraction was performed independently by two reviewers (LVS and JPL) and disagreements were resolved by consensus. When it was not possible to obtain data from the published trial, we tried to contact the authors to provide the information or additional data.
Data were directly extracted from the published data, or estimated from survival curves using the methods described by Parmar and colleagues . Calculations were carried out using the spreadsheet provided by Tierney and colleagues .
Statistical analysis and synthesis
Details regarding the main methodological dimensions empirically linked to bias as described by Deeks and colleagues  were extracted and the methodological quality of each selected trial was assessed by two reviewers (LVS and ADS). Special attention was given to the generation and concealment of the sequence of randomization, whether an intention-to-treat analysis was performed or not, and source of funding. These data were applied in sensitivity analyses to test the stability of the results.
Review Manager 5 software (RevMan 5; The Nordic Cochrane Centre, The Cochrane Collaboration, Copenhagen, Denmark) was used to perform the meta-analysis. For time-to-event variables, the effect of the treatment for each single study was expressed as a hazard ratio (HR) of chemotherapy plus RT arm over the chemotherapy alone arm. The 95% confidence interval (CI) was calculated for each point estimate. For dichotomous variables, the effect of treatment was calculated as a risk ratio (RR), and presented with the correspondent 95% CI. Data were analyzed using Mantel-Haenszel fixed-effect method.
Statistical heterogeneity of the results of the trials was assessed by the chi-square test , expressed with the I 2 index, as described by Higgins and colleagues . When heterogeneity was detected, a possible explanation for it was intensively pursued. If a reasonable cause was found, a separate analysis was then performed. When the cause was not apparent and heterogeneity was caused by divergent data in terms of direction of results, we chose not to pool the data. Publication bias was evaluated by the Egger test [29, 30].
Description of studies and quality assessment
Main characteristics of selected trials related to biasTrial
Year of Publication
GELA LNH 93-1
GELA LNH 93-4
Study population and therapy
Age and PS 0-1
CHOP x 8
WF groups D-J (DLBCL 75%); stage I to II non-bulky
> 60y = 49% 0-1 = 96%
0-1 = 71%
CHOP x 3 + RT
>60y = 50% 0-1 = 97%
0-1 = 74%
IFRT 40-55 Gy
CHOP x 8
WF H-J (DLBCL 83%); stage I bulky to II; complete responders to CHOP only
Median 60y 0-1 = 93%
II 70% E 52%, B20%
CHOP x 8 + RT
Median 58y 0-1 = 96%
II 68% E 45% B22%
IFRT 30 Gy
GELA LNH 93-1
ACVBP + CT
WF H-J or anaplastic according to uKC (DLBCL 81%); 15-60y; aaIPI = 0†; stages I to II
Median 46y 0-1 = 100%
II 32% E 46%
0 = 96%†
CHOP x 3 + RT
Median 47y 0-1 = 100%
II 32% E 52%
0 = 95%†
IFRT 40 Gy
GELA LNH 93-4
CHOP x 4
WF H-J or anaplastic according to uKC (DLBCL 80%); >60y; aaIPI = 0†; stages I to II
Median 69y 0-1 = 99%
II 32% Bu 8%
0 = 95%†
CHOP x 4 + RT
Median 68y 0-1 = 99%
II 34% Bu 9%
0 = 95%†
IFRT 40 Gy
The Southwest Oncology Group (SWOG) 8736 trial  included 401 patients with intermediate- or high-grade NHL. Stages I and II were allowed, except those with stage II and bulky disease. Participants were randomized to receive 8 cycles of CHOP or 3 cycles of CHOP plus involved-field radiation therapy (IFRT) with doses of 40 to 55 Gy. The trial was designed to address if the addition of RT may allow the use of less cycles of chemotherapy. Approximately 20% of the patients had two or more risk factors (international prognostic index [IPI] ≥ 2) . Complete response occurred in 73% of chemotherapy patients, and in 75% of chemotherapy plus RT patients. With a median follow-up of 4.4 years, five-year PFS was 64% for CHOP x 8, and 77% for CHOP x 3 plus RT (p = 0.03). Five-year OS was 72% and 82% (p = 0.02), respectively. In an updated analysis, the results showed an excess of late relapses and deaths due to lymphoma in the combined-modality treatment. PFS and OS curves of the two arms overlapped at 7 and 9 years, respectively . Unfortunately, it was impossible to use these updated results in meta-analysis, due to lack of extractable data.
The ECOG 1484 trial  included patients with a less favorable prognosis. All patients had at least bulky or extranodal disease, most of them were in stage II, and only high-grade NHL was allowed. This study included 352 patients receiving 8 cycles of CHOP. Those who achieved complete response (61%) were randomized to receive involved field radiation treatment (IFRT) with doses of 30 Gy (n = 103) or observation (n = 112). There were imbalances between groups, with patients allocated to receive RT presenting more mediastinal involvement and bulky disease. Six-year DFS was 53% for observation and 69% for RT (p = .05), and six-year OS rates were 67% and 79% (p = .23), respectively. The trial was designed to detect a 20% improvement in two-year DFS using a one-sided significance test. Thus, the sample size was not adequate to detect a survival advantage of consolidative RT.
In the Groupe d'Etudes des Lymphomes de l'Adulte (GELA) LNH 93–1 trial , 647 patients with ALNHL under 60 years and without age-adjusted IPI risk factors  (ECOG-PS < 2 and normal lactate dehydrogenase [LDH]) were randomized to receive an intensified induction chemotherapy (ACVBP) and a consolidative chemotherapy regimen or 3 cycles of CHOP plus 40 Gy IFRT. Bulky disease was present in 11% of patients and extranodal involvement in 50%. Complete response rate was 93% for chemotherapy alone and 92% for combined modality treatment. Five-year PFS was 82% for ACVBP versus 74% for CHOP plus RT (p < 0.001). Five-year OS was 90% and 81%, respectively (p = 0.001).
The GELA LNH 93–4 trial  randomized 576 patients older than 60 with ALNHL and without age-adjusted IPI risk factors  to receive 4 cycles of CHOP alone or 4 cycles of CHOP plus 40 Gy IFRT. Bulky disease was present in 9% of patients and extranodal involvement in 48%. Accrual was interrupted earlier due to increasing evidence that rituximab could improve efficacy in patients with aggressive NHL [37, 38]. With a median follow-up of 7 years, 5-year PFS was 61% for CHOP alone and 64% for CHOP plus RT (p = 0.56), and 5-year OS was 72% and 68%, respectively (p = 0.54).
Effects of interventions
Pooling data from trials whose arms had the same chemotherapy regimen (791 patients) [34, 35] showed that the addition of RT to systemic therapy resulted in no improvement in PFS (HR 0.86; 95% CI 0.69-1.06; p = 0.16). In this analysis, it was not possible to exclude heterogeneity among trials (p = 0.17; I² = 46%).
Again, data from ECOG 1484 trial  could not be obtained for an intention-to-treat analysis due to lack of an adequate description of results. Thus, estimation was made from the published overall survival (OS) curve from “as treated” patients. Although all trials [31, 32, 34, 35] reported data of survival analysis comprising 1,796 patients, results from four trials could not be pooled due to heterogeneity among them (p = 0.0009; I² = 82%). Even excluding the ECOG 1484 trial, there was still heterogeneity detected among trials (p = 0.0009; I² = 86%). The GELA LNH 93–1 trial  seemed to be mainly responsible for the heterogeneity, again, possibly due to considerable differences in intensity and duration between systemic therapy in both arms. However, even excluding the GELA LNH 93–1 trial , we could still detect heterogeneity among trials (p = 0.04; I² = 68%).
Pooling data only from the studies whose arms had the same chemotherapy regimen [34, 35], the addition of RT showed no improvement in OS (HR 1.00; 95% CI 0.79-1.26; p = 0.99). Even in this analysis, there was considerable heterogeneity among trials (p = 0.15; I² = 51%).
In the SWOG 8736 trial  there were no differences in life-threatening toxicity or death between chemotherapy alone and chemotherapy plus RT arms (30% and 40%; p = 0.06; one death in each arm). Patients assigned to chemotherapy alone arm had more congestive heart failure than patients assigned to chemotherapy plus RT arm. More patients in the chemotherapy alone arm did not complete the assigned regimen (28 and 3 patients, respectively, p < 0.01).
In the ECOG 1484 trial , toxicity was described according to the phase of therapy (chemotherapy and then RT or observation). There was only one grade 4 adverse event (thrombocytopenia) in the RT arm and none in the observation arm. GELA LNH 93-1  and 93-4  did not describe toxicity individually for each arm, but life-threatening toxicity appeared to occur in a small number of patients.
Due to differences in reporting adverse events, it was not feasible to pool toxicity data. Radiation therapy appeared to be well tolerated, with side effects dependent mainly on the location of disease.
Risk of bias
There was no evidence of publication bias (Egger’s test: p = 0.52). The methodological characteristics of the selected trials included in this meta-analysis (described in Table 1) had no impact on the results obtained, as confirmed by the sensitivity analysis performed [this data is available upon request].
Early stage aggressive NHL is a heterogeneous group of diseases with a high potential of cure. Systemic therapy has been the mainstream of therapy for more than 20 years. Additionally, RT had shown to increase regional control, which may lead to improvement in survival. Other possible secondary benefits of radiotherapy could be the diminishing of chemotherapy late effects.
Considering that relapses usually occur at the site of disease, and RT alone can cure up to 70% of patients, it seems rational to test RT after chemotherapy in patients with ALNHL. The achievement of local control could be, in this setting, a surrogate of survival improvement.
Since the publication of the SWOG 8736 trial , radiation therapy has become the standard therapy in North America. Unfortunately, the benefit of the treatment in prolonging PFS and OS has not been sustained over the years . The ECOG 1484 trial  evaluated the addition of RT in patients with complete response with unfavorable results. In the trial, DFS (but not OS) was better in the combination arm. The GELA LNH 93–1 trial  compared short-course chemotherapy regimen plus RT to an intensified chemotherapy regimen. The group receiving the ACVBP regimen showed improved survival when compared to the group receiving CHOP for 8 cycles  for non-localized NHL or CHOP plus RT for localized disease . Despite that, the more intensive regimen has not been widely accepted due to long term adverse events, like acute myelogenous leukemia, myelodysplastic syndrome and lung cancer . This is especially important for patients with one IPI risk factor , in whom cure rates usually exceed 80% with CHOP-based chemotherapy [31, 32]. Thus, some advocate ACVBP should not be considered a valid alternative to CHOP in patients without high risk of recurrence. Recently, ACVBP plus rituximab (R-ACVBP) was compared to CHOP plus rituximab in young patients with advanced diffuse large B-cell lymphoma. With a median follow up of 44 months, R-ACVBP improved overall survival . Long term follow up is needed to address long term adverse events.
Both the GELA LNH 93-1  and SWOG 8736 [32, 33] trials suggested that radiotherapy cannot replace inadequate chemotherapy regimens. The GELA LNH 93–4 trial  evaluated the addition of RT to 4 cycles of CHOP in the treatment of elderly patients with ALNHL. No improvements in terms of PFS or OS were observed. Five-year PFS in the chemotherapy alone arm was 61%, comparable to 64% in the chemotherapy alone arm after 8 cycles of CHOP in the SWOG trial in younger patients with a more favorable prognosis .
This systematic review showed that RT could enhance PFS after chemotherapy, with no impact on ORR and OS. Heterogeneity among trials limits a definite conclusion. The interventions under study and trial design characteristics, such as definition of outcomes, inclusion criteria, risk factors and statistical considerations can cause substantial differences when pooling data, and may constitute the major causes of heterogeneity found in the current meta-analysis. Our results are consistent with those addressed in an overview published in 2003 . The high efficacy of chemotherapy in inducing remission of ALNHL would increase the number of subjects in clinical trials evaluating the role of consolidative RT. Thus, all included trials were individually underpowered to assess improvement of response rate, PFS and OS.
More recently, rituximab has been incorporated into the treatment of patients with NHL, with clear benefits in PFS and OS [37, 38]. Now the combination of rituximab with a CHOP-based chemotherapy regimen has been considered as the standard treatment for aggressive NHL patients. There is still no prospective trial evaluating the role of RT in the era of targeted therapy, so far the role of radiation after chemotherapy plus rituximab remains speculative. Recently, a retrospective study suggested improvement in both OS and PFS with consolidative RT after rituximab-CHOP chemotherapy. This improvement occurred in both early (I and II) and advanced stage (III and IV) . Despite these gains, these evidences are not sufficient to support or repel the use of consolidative RT in ALNHL. The possible interaction between rutuximab and radiation therapy makes the results of these combinations unpredictable. Thus, radiation therapy should be studied in this new context, and cannot be considered a standard of care until its benefit is proven. Some studies have recently addressed the role of radiation therapy in the management of localized disease in patients with positive Positron Emission Tomography (PET) after chemotherapy [43–45]. Radiation therapy yielded interesting survival results in this subset of patients, providing a rational selection tool for consolidative radiotherapy.
There are still many unanswered questions regarding the management of early stage aggressive NHL. The ideal chemotherapy regimen, its optimal duration, the duration of rituximab treatment, the benefits of adding RT and its dose are important issues that need further evaluation by high-quality RCT. Our systematic review suggests that RT prolongs PFS and can be considered an option for patients who cannot tolerate a high dose or prolonged schedule of chemotherapy. Further evaluation of RT after chemotherapy is still needed.
In conclusion, RT prolongs PFS, with no impact on OS. It must be considered an option for patients who cannot tolerate a high dose or prolonged schedule of chemotherapy. Further investigation of the role of RT in the era of targeted therapy is needed.
The authors received no specific funding for this study.
- Ries L, Melbert D, Krapcho M, Stinchcomb D, Howlader N, MJ H, et al: SEER Cancer Statistics Review, 1975–2005. Journal [serial on the Internet]. 2007, Date: Available from:http://seer.cancer.gov/csr/1975_2005 Google Scholar
- Parkin DM, Bray FI, Devesa SS: Cancer burden in the year 2000. The global picture. Eur J Cancer. 2001, 37 (Suppl 8): S4-66.View ArticlePubMedGoogle Scholar
- Harris NL, Jaffe ES, Stein H, Banks PM, Chan JK, Cleary ML, et al: A revised European-American classification of lymphoid neoplasms: a proposal from the International Lymphoma Study Group. Blood. 1994, 84 (5): 1361-1392.PubMedGoogle Scholar
- Harris NL, Jaffe ES, Diebold J, Flandrin G, Muller-Hermelink HK, Vardiman J, et al: World Health Organization classification of neoplastic diseases of the hematopoietic and lymphoid tissues: report of the Clinical Advisory Committee meeting-Airlie House, Virginia, November 1997. J Clin Oncol. 1999, 17 (12): 3835-3849.PubMedGoogle Scholar
- NCI: National Cancer Institute sponsored study of classifications of non-Hodgkin's lymphomas: summary and description of a working formulation for clinical usage. The Non-Hodgkin's Lymphoma Pathologic Classification Project. Cancer. 1982, 49 (10): 2112-2135.View ArticleGoogle Scholar
- Nieder C, Licht T, Andratschke N, Peschel C, Molls M: Influence of differing radiotherapy strategies on treatment results in diffuse large-cell lymphoma: a review. Cancer Treat Rev. 2003, 29 (1): 11-19. 10.1016/S0305-7372(02)00094-4.View ArticlePubMedGoogle Scholar
- Gustavsson A, Osterman B, Cavallin-Stahl E: A systematic overview of radiation therapy effects in non-Hodgkin's lymphoma. Acta Oncol. 2003, 42 (5–6): 605-619.View ArticlePubMedGoogle Scholar
- Lee CK: Evolving role of radiation therapy for hematologic malignancies. Hematol Oncol Clin North Am. 2006, 20 (2): 471-503. 10.1016/j.hoc.2006.01.020.View ArticlePubMedGoogle Scholar
- Hagberg H, Pettersson U, Glimelius B, Sundstrom C: Prognostic factors in non-Hodgkin lymphoma stage I treated with radiotherapy. Acta Oncol. 1989, 28 (1): 45-50. 10.3109/02841868909111180.View ArticlePubMedGoogle Scholar
- Vaughan Hudson B, Vaughan Hudson G, MacLennan KA, Anderson L, Linch DC: Clinical stage 1 non-Hodgkin's lymphoma: long-term follow-up of patients treated by the British National Lymphoma Investigation with radiotherapy alone as initial therapy. Br J Cancer. 1994, 69 (6): 1088-1093. 10.1038/bjc.1994.213.View ArticlePubMedPubMed CentralGoogle Scholar
- Jones SE, Miller TP, Connors JM: Long-term follow-up and analysis for prognostic factors for patients with limited-stage diffuse large-cell lymphoma treated with initial chemotherapy with or without adjuvant radiotherapy. J Clin Oncol. 1989, 7 (9): 1186-1191.PubMedGoogle Scholar
- Osterman B, Cavallin-Stahl E, Hagberg H, Linden O, Lenner P: High-grade non-Hodgkin's lymphoma stage I. A retrospective study of treatment, outcome and prognostic factors in 213 patients. Acta Oncol. 1996, 35 (2): 171-177. 10.3109/02841869609098498.View ArticlePubMedGoogle Scholar
- Connors JM, Klimo P, Fairey RN, Voss N: Brief chemotherapy and involved field radiation therapy for limited-stage, histologically aggressive lymphoma. Ann Intern Med. 1987, 107 (1): 25-30.View ArticlePubMedGoogle Scholar
- Longo DL: Combined modality therapy for localized aggressive lymphoma: enough or too much?. J Clin Oncol. 1989, 7 (9): 1179-1181.PubMedGoogle Scholar
- Longo DL, Glatstein E, Duffey PL, Ihde DC, Hubbard SM, Fisher RI, et al: Treatment of localized aggressive lymphomas with combination chemotherapy followed by involved-field radiation therapy. J Clin Oncol. 1989, 7 (9): 1295-1302.PubMedGoogle Scholar
- Tondini C, Zanini M, Lombardi F, Bengala C, Rocca A, Giardini R, et al: Combined modality treatment with primary CHOP chemotherapy followed by locoregional irradiation in stage I or II histologically aggressive non-Hodgkin's lymphomas. J Clin Oncol. 1993, 11 (4): 720-725.PubMedGoogle Scholar
- van der Maazen RW, Noordijk EM, Thomas J, Raemaekers JM, Meerwaldt JH: Combined modality treatment is the treatment of choice for stage I/IE intermediate and high grade non-Hodgkin's lymphomas. Radiother Oncol. 1998, 49 (1): 1-7. 10.1016/S0167-8140(98)00066-8.View ArticlePubMedGoogle Scholar
- Aviles A, Delgado S, Ruiz H, de la Torre A, Guzman R, Talavera A: Treatment of non-Hodgkin's lymphoma of Waldeyer's ring: radiotherapy versus chemotherapy versus combined therapy. Eur J Cancer B Oral Oncol. 1996, 32B (1): 19-23.View ArticlePubMedGoogle Scholar
- Wirth A: The rationale and role of radiation therapy in the treatment of patients with diffuse large B-cell lymphoma in the Rituximab era. Leuk Lymphoma. 2007, 48 (11): 2121-2136. 10.1080/10428190701636468.View ArticlePubMedGoogle Scholar
- Lymphoid neoplasms. American Joint Committee on Cancer: AJCC Cancer Staging Manual. 2002, Springer, New York, NY, 393-406. 6View ArticleGoogle Scholar
- Dickersin K, Scherer R, Lefebvre C: Identifying relevant studies for systematic reviews. BMJ. 1994, 309 (6964): 1286-1291. 10.1136/bmj.309.6964.1286.View ArticlePubMedPubMed CentralGoogle Scholar
- Verhagen AP, de Vet HC, de Bie RA, Kessels AG, Boers M, Bouter LM, et al: The Delphi list: a criteria list for quality assessment of randomized clinical trials for conducting systematic reviews developed by Delphi consensus. J Clin Epidemiol. 1998, 51 (12): 1235-1241. 10.1016/S0895-4356(98)00131-0.View ArticlePubMedGoogle Scholar
- Jadad AR, Moore RA, Carroll D, Jenkinson C, Reynolds DJ, Gavaghan DJ, et al: Assessing the quality of reports of randomized clinical trials: is blinding necessary?. Control Clin Trials. 1996, 17 (1): 1-12. 10.1016/0197-2456(95)00134-4.View ArticlePubMedGoogle Scholar
- Parmar MK, Torri V, Stewart L: Extracting summary statistics to perform meta-analyses of the published literature for survival endpoints. Stat Med. 1998, 17 (24): 2815-2834. 10.1002/(SICI)1097-0258(19981230)17:24<2815::AID-SIM110>3.0.CO;2-8.View ArticlePubMedGoogle Scholar
- Tierney JF, Stewart LA, Ghersi D, Burdett S, Sydes MR: Practical methods for incorporating summary time-to-event data into meta-analysis. Trials. 2007, 8: 16-10.1186/1745-6215-8-16.View ArticlePubMedPubMed CentralGoogle Scholar
- Deeks JJ AD, Bradburn MJ: Systematic reviews in health care: Metaanalisys in context. 2001, BMJ Publication Group, London, 2Google Scholar
- DerSimonian R, Laird N: Meta-analysis in clinical trials. Control Clin Trials. 1986, 7 (3): 177-188. 10.1016/0197-2456(86)90046-2.View ArticlePubMedGoogle Scholar
- Higgins JP, Thompson SG, Deeks JJ, Altman DG: Measuring inconsistency in meta-analyses. BMJ. 2003, 327 (7414): 557-560. 10.1136/bmj.327.7414.557.View ArticlePubMedPubMed CentralGoogle Scholar
- Egger M, Davey Smith G, Schneider M, Minder C: Bias in meta-analysis detected by a simple, graphical test. BMJ. 1997, 315 (7109): 629-634. 10.1136/bmj.315.7109.629.View ArticlePubMedPubMed CentralGoogle Scholar
- Sterne JA, Egger M, Smith GD: Systematic reviews in health care: Investigating and dealing with publication and other biases in meta-analysis. BMJ. 2001, 323 (7304): 101-105. 10.1136/bmj.323.7304.101.View ArticlePubMedPubMed CentralGoogle Scholar
- Reyes F, Lepage E, Ganem G, Molina TJ, Brice P, Coiffier B, et al: ACVBP versus CHOP plus radiotherapy for localized aggressive lymphoma. N Engl J Med. 2005, 352 (12): 1197-1205. 10.1056/NEJMoa042040.View ArticlePubMedGoogle Scholar
- Miller TP, Dahlberg S, Cassady JR, Adelstein DJ, Spier CM, Grogan TM, et al: Chemotherapy alone compared with chemotherapy plus radiotherapy for localized intermediate- and high-grade non-Hodgkin's lymphoma. N Engl J Med. 1998, 339 (1): 21-26. 10.1056/NEJM199807023390104.View ArticlePubMedGoogle Scholar
- Miller T, Leblanc M, Spier C, et al: CHOP alone compared with CHOP plus radiotherapy for early stage aggressive non-Hodgkin’s lymphomas: Update of the Southwest Oncology Group (SWOG) Randomized trial. Blood. 2001, 98: a724-View ArticleGoogle Scholar
- Horning SJ, Weller E, Kim K, Earle JD, O'Connell MJ, Habermann TM, et al: Chemotherapy with or without radiotherapy in limited-stage diffuse aggressive non-Hodgkin's lymphoma: Eastern Cooperative Oncology Group study 1484. J Clin Oncol. 2004, 22 (15): 3032-3038. 10.1200/JCO.2004.06.088.View ArticlePubMedGoogle Scholar
- Bonnet C, Fillet G, Mounier N, Ganem G, Molina TJ, Thieblemont C, et al: CHOP alone compared with CHOP plus radiotherapy for localized aggressive lymphoma in elderly patients: a study by the Groupe d'Etude des Lymphomes de l'Adulte. J Clin Oncol. 2007, 25 (7): 787-792. 10.1200/JCO.2006.07.0722.View ArticlePubMedGoogle Scholar
- A predictive model for aggressive non-Hodgkin's lymphoma: The International Non-Hodgkin's Lymphoma Prognostic Factors Project. N Engl J Med. 1993, 329 (14): 987-994.View ArticleGoogle Scholar
- Vose JM, Link BK, Grossbard ML, Czuczman M, Grillo-Lopez A, Gilman P, et al: Phase II study of rituximab in combination with chop chemotherapy in patients with previously untreated, aggressive non-Hodgkin's lymphoma. J Clin Oncol. 2001, 19 (2): 389-397.PubMedGoogle Scholar
- Coiffier B, Lepage E, Briere J, Herbrecht R, Tilly H, Bouabdallah R, et al: CHOP chemotherapy plus rituximab compared with CHOP alone in elderly patients with diffuse large-B-cell lymphoma. N Engl J Med. 2002, 346 (4): 235-242. 10.1056/NEJMoa011795.View ArticlePubMedGoogle Scholar
- Tilly H, Lepage E, Coiffier B, Blanc M, Herbrecht R, Bosly A, et al: Intensive conventional chemotherapy (ACVBP regimen) compared with standard CHOP for poor-prognosis aggressive non-Hodgkin lymphoma. Blood. 2003, 102 (13): 4284-4289. 10.1182/blood-2003-02-0542.View ArticlePubMedGoogle Scholar
- Andre M, Mounier N, Leleu X, Sonet A, Brice P, Henry-Amar M, et al: Second cancers and late toxicities after treatment of aggressive non-Hodgkin lymphoma with the ACVBP regimen: a GELA cohort study on 2837 patients. Blood. 2004, 103 (4): 1222-1228.View ArticlePubMedGoogle Scholar
- Recher C, Coiffier B, Haioun C, Molina TJ, Ferme C, Casasnovas O, et al: Intensified chemotherapy with ACVBP plus rituximab versus standard CHOP plus rituximab for the treatment of diffuse large B-cell lymphoma (LNH03-2B): an open-label randomised phase 3 trial. Lancet. 2011, 378 (9806): 1858-1867. 10.1016/S0140-6736(11)61040-4.View ArticlePubMedGoogle Scholar
- Phan J, Mazloom A, Jeffrey Medeiros L, Zreik TG, Wogan C, Shihadeh F, et al: Benefit of consolidative radiation therapy in patients with diffuse large B-cell lymphoma treated with R-CHOP chemotherapy. J Clin Oncol. 2010, 28 (27): 4170-4176. 10.1200/JCO.2009.27.3441.View ArticlePubMedGoogle Scholar
- Pommier P, Dussart S, Girinsky T, Chabaud S, Lagrange JL, Nguyen TD, et al: Impact of 18 F-fluoro-2-deoxyglucose positron emission tomography on treatment strategy and radiotherapy planning for stage I-II Hodgkin disease: a prospective multicenter study. Int J Radiat Oncol Biol Phys. 2011, 79 (3): 823-828. 10.1016/j.ijrobp.2009.11.048.View ArticlePubMedGoogle Scholar
- Dorth JA, Chino JP, Prosnitz LR, Diehl LF, Beaven AW, Coleman RE, et al: The impact of radiation therapy in patients with diffuse large B-cell lymphoma with positive post-chemotherapy FDG-PET or gallium-67 scans. Ann Oncol. 2011, 22 (2): 405-410. 10.1093/annonc/mdq389.View ArticlePubMedGoogle Scholar
- Halasz LM, Jacene HA, Catalano PJ, Van den Abbeele AD, Lacasce A, Mauch PM, et al: Combined Modality Treatment for PET-Positive Non-Hodgkin Lymphoma: Favorable Outcomes of Combined Modality Treatment for Patients With Non-Hodgkin Lymphoma and Positive Interim or Postchemotherapy FDG-PET. Int J Radiat Oncol Biol Phys. 2012, 83 (5): e647-e654. 10.1016/j.ijrobp.2012.01.060.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://0-www.biomedcentral.com.brum.beds.ac.uk/1471-2407/12/288/prepub
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