Increased Risk of Second Lung Cancer in Hodgkin’s Lymphoma Survivors: A Meta-analysis

Lung ◽  
2012 ◽  
Vol 191 (1) ◽  
pp. 117-134 ◽  
Author(s):  
Ezzeldin M. Ibrahim ◽  
Ghieth A. Kazkaz ◽  
Khaled M. Abouelkhair ◽  
Mubarak M. Al-Mansour ◽  
Turki M. Al-Fayea ◽  
...  
2006 ◽  
Vol 24 (10) ◽  
pp. 1568-1574 ◽  
Author(s):  
Nadejda Y. Mudie ◽  
Anthony J. Swerdlow ◽  
Craig D. Higgins ◽  
Paul Smith ◽  
Zongkai Qiao ◽  
...  

Purpose To assess long-term site-specific risks of second malignancy following non-Hodgkin's lymphoma (NHL) in relation to treatment and demographic factors. Patients and Methods A cohort of 2,456 patients with NHL who were first treated from 1973 to 2000 and were younger than 60 years from centers in the British National Lymphoma Investigation were observed, and occurrences of second malignancy was compared with expectations based on general population cancer rates in England and Wales. Results In total, 123 second malignancies occurred. Relative risks (RRs) were significantly elevated for all malignancies combined (RR = 1.3; 95% CI, 1.1 to 1.6) and for leukemia (RR = 8.8; 95% CI, 5.1 to 14.1) and lung cancer (RR = 1.6; 95% CI, 1.1 to 2.3). RRs of malignancy overall diminished significantly with increasing age at first treatment. Leukemia risk was significantly increased after chemotherapy (RR = 10.5; 95% CI, 5.0 to 19.3) and mixed-modality treatment (RR = 13.0; 95% CI, 5.2 to 26.7). Relative risks of lung (RR = 1.9; 95% CI, 1.1 to 3.1) and colorectal (RR = 2.1; 95% CI, 1.1 to 3.6) cancers were significantly raised following chemotherapy. Conclusion NHL patients are at elevated risk of developing second malignancy, particularly leukemia and lung cancer. The relative risk is greater with patients who are younger at first treatment. Chemotherapy predisposes patients toan increased risk of leukemia, and possibly lung and colorectal cancers. The role of specific drug treatments in the etiology of solid cancers after NHL deserves further investigation.


Blood ◽  
2010 ◽  
Vol 116 (21) ◽  
pp. 5089-5089
Author(s):  
Nishant Tageja ◽  
Ivo Ditah ◽  
Zartash Gul

Abstract Abstract 5089 Background – Obesity is linked with altered immune function and chronic inflammatory response; multiple studies have related autoimmune and chronic inflammatory processes with an increased risk of non-Hodgkin's lymphoma. However, epidemiological studies on the relation between excess body weight and risk of non-Hodgkin's lymphoma have yielded inconsistent results. The objective of this study is to examine the relationship between obesity, as measured by body mass index (BMI), and risk of non-Hodgkin's lymphoma in a meta-analysis of epidemiological studies. Methods – We performed a comprehensive search of MEDLINE, EMBASE and CINAHL databases for studies on BMI and non-Hodgkin's lymphoma that were published from 1966 to June 2010. Search terms included body mass index, BMI, or obesity combined with lymphoma. The reference lists of identified articles were manually reviewed to identify additional papers. Key Inclusion Criteria - cohort or case–control studies reporting NHL incidence or mortality as an outcome, BMI (body weight in kilograms divided by the square of height in meters) as the exposure of interest, and relative risks (RRs) or odds ratios with their 95% confidence intervals (CIs) as the outcome measures. Data Extraction and Statistical analysis - Two reviewers independently extracted study information and data. Where multiple outcome measures were reported, the most adjusted for was used. Before analysis, all studies were tested for publication bias using the Begg's and Egger's test. Pooled RRs with 95% confidence intervals (CI) were calculated using the random-effects meta-analysis model if heterogeneity was present; otherwise, the fixed-effects model was used. All statistical analyses were performed using Stata software, version 9.0 (Stata-Corp, College Station, TX). Results – Twenty-five studies (17 cohort and 8 case-control studies) with 40,279 participants met the inclusion criteria. Compared to individuals with BMI < 25.0 kg/m2, the summary RRs for non-Hodgkin's lymphoma were 1.05 (95% CI, 1.01–1.10) and 1.15 (95% CI, 1.06–1.25) for overweight (BMI between 25 and 30 kg/m2) and obese (BMI > 30.0 kg/m2) individuals respectively. By histological subtypes, obesity was associated with a statistically significant increase risk of diffuse large B-cell lymphoma (RR, 1.23; 95% CI, 1.11–1.37; n = 13 studies) but not with follicular lymphoma (RR, 1.11; 95% CI, 0.97–1.27; n = 13 studies) or small lymphocytic lymphoma/chronic lymphocytic leukemia (RR, 0.95; 95% CI, 0.84–1.07; n = 8 studies). There was no evidence of publication bias. Conclusions – The results of this meta-analysis suggest that compared to normal weight individuals, overweight and obese individuals have a 5% and 15% increased risk of non-Hodgkin's lymphoma respectively. Though statistically significant, these proportions are relatively small and perhaps may be accounted for by residual confounding. Larger, long term prospective studies will be needed to conclusively define the magnitude and strength of the association between body weight and non-Hodgkin lymphoma. Disclosures: Off Label Use: High dose Melphalan is not FDA approved as conditioning regimen for Autologous stem cell transplant.


2011 ◽  
Vol 29 (29) ◽  
pp. 3900-3906 ◽  
Author(s):  
Jorge J. Castillo ◽  
Samir Dalia ◽  
Helen Shum

Introduction Previous studies have suggested a relationship between smoking and Hodgkin's lymphoma (HL). The main objective of this study was to evaluate this potential association with a meta-analysis of observational studies. Patients and Methods A literature search was undertaken through December 2010 looking for observational studies evaluating the association between smoking and HL. From 714 articles, 17 were included in this study. Outcome was calculated and reported as odds ratio (OR). Heterogeneity was assessed by using the I2 index. Publication bias was evaluated by trim-and-fill analysis. Quality assessment was performed with the Newcastle-Ottawa scale. Results Our analysis showed an OR of developing HL of 1.35 (95% CI, 1.17 to 1.56; P < .001) in current smokers. Former smokers did not have an increased risk of HL. In subset analyses of current smokers, men and older individuals had ORs of HL of 1.78 (95% CI, 1.46 to 2.17; P < .001) and 1.77 (95% CI, 1.23 to 2.54; P = .002), respectively. In addition, the OR of HL was increased in individuals who smoke more than 20 cigarettes per day, have smoked more than 20 years, or have smoked more than 15 pack-years at 1.51 (95% CI, 1.16 to 1.98; P = .002), 1.84 (95% CI, 1.47 to 2.32; P < .001), and 1.97 (1.53 to 2.54; P < .001), respectively. Meta-regression analyses showed a relative OR of HL of 1.007 (95% CI, 1.001 to 1.013; P = .025) per cigarette per day and of 1.013 (95% CI, 1.006 to 1.019; P < .001) per year of smoking. Conclusion Smoking seems to increase the odds of developing HL in current smokers. The risk of HL is higher in men and older individuals and increases with higher intensity and longer duration of smoking.


2018 ◽  
Vol 28 (3) ◽  
pp. 222-230 ◽  
Author(s):  
Ling  Qin ◽  
Hui-Yang  Deng ◽  
Sheng-Jiang  Chen ◽  
Wei Wei

Background: Epidemiologic studies have suggested hair dye to be a risk factor for many cancers. However, previous studies on the association between the personal use of hair dye and risk of non-Hodgkin’s lymphoma (NHL) have been inconclusive. Methods: The PubMed, Embase, Cochrane Library, and Web of Science databases, as well as the references cited in included studies, were searched for relevant studies up to February 10, 2015. Odds ratios (OR) with 95% confidence intervals (CI) were applied to assess the strength of the association. Publication bias was evaluated using a funnel plot by Egger’s and Begg’s tests. Results: A total of 16 studies were included in the analysis, including 13 case-control studies and 3 cohort studies. The present meta-analysis results revealed that the risk of NHL in a high population of hair dye users was 14% (OR 1.14, 95% CI 1.01–1.29). Furthermore, individuals who used more than 20 pack-years of hair dye had increased risk of NHL. Conclusion: The outcomes indicate that hair dye use increases the risk of NHL, especially for females. Hence, people who frequently use hair dyes or have been using hair dyes for more than 20 years should minimize their exposure to hair dye products to prevent the risk of NHL.


2011 ◽  
Vol 22 (8) ◽  
pp. 1845-1858 ◽  
Author(s):  
M. Pirani ◽  
R. Marcheselli ◽  
L. Marcheselli ◽  
A. Bari ◽  
M. Federico ◽  
...  

Blood ◽  
2009 ◽  
Vol 114 (22) ◽  
pp. 1652-1652
Author(s):  
Meena Sunil ◽  
Tarisha Mixon ◽  
Erin Reid ◽  
Mary Jo Lechowicz

Abstract Abstract 1652 Poster Board I-678 Introduction Hodgkin lymphoma (HL) is one of the most common non-acquired immunodeficiency syndrome (AIDS)-defining tumors in human immunodeficiency virus (HIV)-infected patients. Studies have shown that HIV infected individuals have approximately a 7.5-fold (Goedert et al 1998) to nearly 13-fold increased risk for HL compared with the general population (Biggar et al. 2006, Engels 2006). The outcomes for patients with HL and HIV (HIV-HL) were described as inferior to HIV-negative patients. The existing literature regarding response and survival data is mainly comprised of small and/or retrospective studies. We reviewed the literature for the purpose of examining a larger HIV HL cohort for response rates and survival in the HAART era. Methods We searched PUBMED, OVID & Google Scholar (1980- July 2009) and ASH (2004-2008) & ASCO (2004-2009) Annual Meeting Abstracts. Key words used were ‘Hodgkin's Lymphoma’, ‘Hodgkin's Disease',’ HIV/AIDS', HAART, therapeutic outcomes, concomitant chemotherapy & HAART/antiretroviral therapy, non AIDS malignancies. Criteria for inclusion of studies were: 1) Upfront treatment of HL HIV infected patients with chemotherapy, with or without radiotherapy, with or without antiretroviral drugs/ HAART. 2) Reported in English 3) Studies with outcome measures of treatment for HIV-HL patients such as complete response (CR) rates, and/or at least one type of survival statistic. We also examined references from above articles as well as review articles, studies on pathogenesis & histologic features of HIV-HL, and epidemiologic studies for additional references. Studies that did not clearly report on a comprehensive cohort were excluded given increased probability of reporting bias. Primary outcome measures were CR rates, and 1- and 2-year overall survival rates. The data extracted included pre-treatment patient characteristics such as median age, sex, histological diagnosis, clinical staging, site of involvement, median CD4 cell counts, treatment regimen used, use or not of antiretrovirals/HAART & prophylactic agents with chemotherapy, response to treatment, toxicity, opportunistic infections, median follow up time, relapse, disease progression, death from treatment or infections. Summary CR and OS estimates were calculated based on the assumption of fixed effects and using the Mantel-Haenszel method. Results 12 articles met inclusion criteria for meta-analysis of CR and/or OS. The overall CR rate was 72% (95% CI 67-77%) with 1- and 2-year OS of 78% (95% CI 73-82%) and 69% (95% CI 67-77%), respectively (Figure 1). Advanced stage was present in 63%, and histology other than nodular sclerosing in 76%. Mean baseline CD4 count was 212 (3-887); 59% of subject received HAART with chemotherapy. Death during treatment occurred in 7% and relapse was reported in 14%. Conclusions Adverse baseline characteristics including advanced disease and histology other than NS persist in the HAART era. Response and survival rates are improved compared to pre-HAART era but remain lower than rates found in the HIV-negative population. Further prospective trials need to be done to examine improvements in treatment for this patient population. Disclosures No relevant conflicts of interest to declare.


BMC Cancer ◽  
2012 ◽  
Vol 12 (1) ◽  
Author(s):  
Ezzeldin M Ibrahim ◽  
Khaled M Abouelkhair ◽  
Ghieth A Kazkaz ◽  
Osama A Elmasri ◽  
Meteb Al-Foheidi

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