scholarly journals Quadruple Multiple Primary Malignancies: Early Detection of Second Primary Malignancy by Esophagogastroduodenoscopy/Colonoscopy Is Crucial for Patients with Classic Kaposi’s Sarcoma

Diagnostics ◽  
2020 ◽  
Vol 10 (4) ◽  
pp. 218
Author(s):  
Nobuyuki Maruyama ◽  
Yuko Okubo ◽  
Masato Umikawa ◽  
Akiko Matsuzaki ◽  
Akira Hokama ◽  
...  

Currently, Kaposi’s sarcoma (KS) is treated following the recommendations of international guidelines. These guidelines recommend esophagogastroduodenoscopy/colonoscopy for detecting multicentric KS of visceral lesions. Second primary malignancies (SPMs) are also a common KS complication; however, information on their detection and treatment is unfortunately not yet indicated in these guidelines. This paper reports on an 86-year-old man who suffered from quadruple primary malignancies: skin classic KS with colon adenocarcinoma, oral squamous cell carcinoma (maxilla), and well-differentiated stomach adenocarcinoma. Gastric cancer was incidentally detected during esophagogastroduodenoscopy, which was performed to detect visceral KS. We suggest that esophagogastroduodenoscopy/colonoscopy be routinely performed during the follow-up of patients with KS. As SPMs are crucial complications in patients with KS, these malignancies should be detected as early as possible.

2020 ◽  
pp. ijgc-2020-001946
Author(s):  
Julie My Van Nguyen ◽  
Danielle Vicus ◽  
Sharon Nofech-Mozes ◽  
Lilian T Gien ◽  
Marcus Q Bernardini ◽  
...  

ObjectiveOvarian clear cell carcinoma has unique clinical and molecular features compared with other epithelial ovarian cancer histologies. Our objective was to describe the incidence of second primary malignancy in patients with ovarian clear cell carcinoma.MethodsRetrospective cohort study of patients with ovarian clear cell carcinoma at two tertiary academic centers in Toronto, Canada between May 1995 and June 2017. Demographic, histopathologic, treatment, and survival details were obtained from chart review and a provincial cancer registry. We excluded patients with histologies other than pure ovarian clear cell carcinoma (such as mixed clear cell histology), and those who did not have their post-operative follow-up at these institutions.ResultsOf 209 patients with ovarian clear cell carcinoma, 54 patients developed a second primary malignancy (25.8%), of whom six developed two second primary malignancies. Second primary malignancies included: breast (13), skin (9), gastrointestinal tract (9), other gynecologic malignancies (8), thyroid (6), lymphoma (3), head and neck (4), urologic (4), and lung (4). Eighteen second primary malignancies occurred before the index ovarian clear cell carcinoma, 35 after ovarian clear cell carcinoma, and 7 were diagnosed concurrently. Two patients with second primary malignancies were diagnosed with Lynch syndrome. Smoking and radiation therapy were associated with an increased risk of second primary malignancy on multivariable analysis (OR 3.69, 95% CI 1.54 to 9.07, p=0.004; OR 4.39, 95% CI 1.88 to 10.6, p=0.0008, respectively). However, for patients developing second primary malignancies after ovarian clear cell carcinoma, radiation therapy was not found to be a significant risk factor (p=0.17). There was no significant difference in progression-free survival (p=0.85) or overall survival (p=0.38) between those with second primary malignancy and those without.ConclusionPatients with ovarian clear cell carcinoma are at increased risk of second primary malignancies, most frequently non-Lynch related. A subset of patients with ovarian clear cell carcinoma may harbor mutations rendering them susceptible to second primary malignancies. Our results may have implications for counseling and consideration for second primary malignancy screening.


Blood ◽  
2012 ◽  
Vol 119 (12) ◽  
pp. 2764-2767 ◽  
Author(s):  
Meletios A. Dimopoulos ◽  
Paul G. Richardson ◽  
Nancy Brandenburg ◽  
Zhinuan Yu ◽  
Donna M. Weber ◽  
...  

Abstract In a retrospective pooled analysis of 11 clinical trials of lenalidomide-based therapy for relapsed/refractory multiple myeloma (MM; N = 3846), the overall incidence rate (IR, events per 100 patient-years) of second primary malignancies (SPMs) was 3.62. IR of invasive (hematologic and solid tumor) SPMs was 2.08, consistent with the background incidence of developing cancer. In a separate analysis of pooled data from pivotal phase 3 trials of relapsed or refractory MM (N = 703), the overall IR of SPMs was 3.98 (95% confidence interval [CI], 2.51-6.31) with lenalidomide/dexamethasone and 1.38 (95% CI, 0.44-4.27) with placebo/dexamethasone; IRs of nonmelanoma skin cancers were 2.40 (95% CI, 1.33-4.33) and 0.91 (95% CI, 0.23-3.66), respectively; IRs of invasive SPMs were 1.71 (95% CI, 0.86-3.43) and 0.91 (95% CI, 0.23-3.66), respectively. The risk of SPMs must be taken into account before initiating lenalidomide treatment. In the context of the observed survival benefit in relapsed or refractory MM patients, the benefit/risk profile of lenalidomide/dexamethasone remains positive.


Cancer ◽  
1980 ◽  
Vol 45 (6) ◽  
pp. 1472-1479 ◽  
Author(s):  
Bijan Safai ◽  
Valerie Mike ◽  
Gaetano Giraldo ◽  
Elke Beth ◽  
Robert A. Good

2015 ◽  
Vol 2015 ◽  
pp. 1-8 ◽  
Author(s):  
Michele L. Santangelo ◽  
Carmen Criscitiello ◽  
Andrea Renda ◽  
Stefano Federico ◽  
Giuseppe Curigliano ◽  
...  

Immunodeficiency is associated with higher cancer incidence. However, it is unknown whether there is a link between immunodeficiency and development of multiple primary malignancies. In the present study we analyse this link focusing on kidney-transplanted patients, as they are at higher risk of developing cancer due to the chronic assumption of immunosuppressants. We followed up 1200 patients who underwent kidney transplantation between 1980 and 2012. A total of 77/1200 kidney-transplanted patients developed cancer and 24 of them developed multiple cancers. Most multiple cancers were synchronous with a nonsignificant association between cancer and rejection episodes. In the general cancer population, one-ninth of patients are at higher risk of developing a second tumor over a lifetime; hence it would be reasonable to conclude that, from a merely theoretical and statistical viewpoint, long-term transplanted patients potentially have a higher risk of developing MPMs. However, data did not confirm this assumption, probably because these patients die before a second primary malignancy appears. Despite many observations on the increased incidence of different tumor types in immunodeficient patients and despite immunosuppression certainly being a predisposing factor for the multicancer syndrome, data so far are not robust enough to justify a correlation between immunodeficiency and multiple primary malignancies in transplanted patients.


2014 ◽  
Vol 99 (1) ◽  
pp. 52-55 ◽  
Author(s):  
Vilvapathy Senguttuvan Karthikeyan ◽  
Sarath Chandra Sistla ◽  
Ramachandran Srinivasan ◽  
Debdatta Basu ◽  
Lakshmi C. Panicker ◽  
...  

Abstract Multiple primary malignant neoplasm is the occurrence of a second primary malignancy in the same patient within 6 months of the detection of first primary (synchronous), or 6 months or more after primary detection (metachronous). Multiple primary malignant neoplasms are not very frequently encountered in clinical practice. The relative risk for a second primary malignancy increases by 1.111-fold every month from the detection of the first primary malignancy in any individual. We present 2 patients treated for carcinoma of the breast who developed a metachronous primary malignancy in the stomach to highlight the rare occurrence of multiple primary malignant neoplasms. These tumors were histologically dissimilar, with distinct immunohistochemical parameters. The importance lies in carefully identifying the second primary malignancies, not dismissing them as metastases, and treating them accordingly.


2020 ◽  
Author(s):  
Xuqi Sun ◽  
Jinbin Chen ◽  
Juncheng Wang ◽  
Zhongguo Zhou ◽  
Li Xu ◽  
...  

Abstract Background:Hepatocellular carcinoma (HCC) survivors are increasing due to the improvement of survival. Follow-up scheme to prevent recurrence is routinely recommended, but are these patients exposed to increased risks of second malignancies remains unknown. We aimed to identify risk factors for second primary malignancies (SPM) among HCC survivors and develop a predicting model accordingly. Methods: We identified HCC patients in the Surveillance, Epidemiology, and End Results (SEER) database from 2004 to 2014. For the incidence of specific SPMs, standardized incidence ratios (SIRs) were calculated. The proportional hazard model was performed in order to discover hazards of SPM, and a competing-risk nomogram was developed to stratify patients with different incidences for SPM. Results:The crude incidence of SPM was 2.70% in HCC survivors, with the SIR of 1.09. HCC survivors had significantly higher incidences of SPM in the following sites: oral cavity and pharynx, stomach, intra and extrahepatic bile duct, lung and bronchus, kidney and renal pelvis, thyroid and lymphatic system (p< 0.05). Patients with diagnosed age at 61-75 years old, smaller tumor size, better histologic differentiation, earlier AJCC stage or surgical history had higher risks for SPM. The c-index of the competing-risk nomogram was 0.663. The cumulative incidences of SPM were significantly different among each quartile of patients stratified by the predicting model (p< 0.05). Conclusion:HCC survivors had an excess risk for SPMs, especially those with promising prognostic factors. This nomogram was the first competing-risk model for identifying high-risk cohort and assist clinical screening.


Blood ◽  
2011 ◽  
Vol 118 (21) ◽  
pp. 3958-3958
Author(s):  
Pedram Razavi ◽  
Kristin A Rand ◽  
Sikander Ailawadhi

Abstract Abstract 3958 Introduction: Recent advances in the treatment of multiple myeloma (MM) have lead to improved patient outcomes and significant improvement in MM survival. Reports from ongoing randomized clinical trials have suggested that there may be an association between the types of treatment received, particularly certain novel therapeutic agents, and a higher incidence of second primary malignancies (SPM) among MM patients. In this analysis, we explored current patterns and trends in incidence and survival of MM between 1973–2008 to better characterize MM patients with second primary malignancies. Methods: We used data from the National Cancer Institute Surveillance Epidemiology and End Results Program (SEER) to examine the incidence and survival trends in MM by SPM status between 1973–2008. We included all cases with MM as the first primary malignancy and calculated the age-adjusted annual incidence rates (AIR per 100,000) stratified by those with single primary (SP) MM and those with MM as the first of multiple primaries (FMP). All cases that were not microscopically confirmed or those with an MM diagnosis coded only from autopsy- or death certificates were excluded from the analysis. We used joinpoint regression models to calculate the annual percent change (APC) and to determine the best fitting line or set of lines that describes the MM temporal trends. A Monte Carlo permutation method was used to test for significance. We used multivariate Cox proportional hazard models to estimate the hazard ratios (HR) and 95% confidence intervals (95% CI) for MM by SPM status, and all analyses were further stratified by year of diagnosis, age, sex, and race/ethnicity. Results: A total of 61,411 cases of MM were recorded in all SEER registries between the years 1973 and 2008. The final analysis included 49,801 SP and 3090 FMP cases. Overall, the AIR of MM was 5.31 (95% CI 5.26–5.36). The AIR of SP MM was 4.33 (95% CI 4.28–4.38) and 0.28 (95% CI 0.27–0.29) for FMP MM. Compared to women, men were 1.41 times (95% CI 1.38–1.44) and 1.95 times as likely to develop SP MM and FMP MM, respectively. African-Americans had the highest rate of SP MM (AIR 9.09; 95% CI 8.85–9.34) and FMP MM (AIR 0.69; 95% CI 0.62–0.76). We observed no significant trend in AIR of SP MM between 1973–2008 (APC 0.03). The rate of FMP MM was relatively stable, however we observed a small but statistically significant increasing trend in incidence between 1973 and 1992 (APC 2.9), followed by a decreasing trend between 1992 and 2008 (APC −3.2). The rate ratio of FMP to SP MM has remained stable at approximately 6% from 1973–2008. The overall hazard ratio of mortality was 0.59 (95% CI 0.56–0.61) with a median survival of 3.6 years in the FMP MM versus 1.7 years in the SP MM patients. There was a statistically significant improvement in the survival of SP MM patients over the past three decades (P for trend < 0.001), with the most prominent increase in the 2002–2008 period with a HR of 0.67 (95% CI 0.64–0.69) when compared to those diagnosed in the 1973–1981 period. In contrast, the survival of FMP MM patients remained constant (P for trend=0.39). Although SP MM patients show a significant increase in survival over time, FMP MM survival remained stable and significantly higher. We further stratified the survival analysis by age, sex, and race/ethnicity. In all stratified analyses, FMP MM patients had a significantly better outcome compared to SP MM patients. Conclusions: Although there has been significant improvement in survival for patients with SP MM in recent years, our results provide an epidemiologic evidence suggestive of a subtype of MM with a better outcome, yet a higher risk of secondary primary malignancies. The incidence rate and outcome of this possible subtype has remained unchanged over the last three decades. These findings are replicated when stratified by gender, race, age, and year of diagnosis. Recent advancements of MM treatment have seemed to only increase the survival of SP MM patients, while the survival of FMP MM patients remained stable. Further studies are needed to explore the potential genetic heterogeneity between MM with and without second primary malignancies. Disclosures: No relevant conflicts of interest to declare.


Author(s):  
Manjunath I. Nandennavar ◽  
Veerendra Angadi ◽  
Shashidhar V. Karpurmath ◽  
Roshan Jacob

Background: The presence of second synchronous or metachronous primary malignancies in a cancer patient is not a rare phenomenon. Our study is an endeavour to present data on the frequency, types, and outcomes of double primary malignancies in Indian cancer patients.Methods: This was a retrospective study conducted in 28 cancer patients diagnosed with histologically confirmed double malignancy. Retrospective data of the cancer site, patient’s age at the presentation, gender, type of cancer (synchronous/metachronous), treatment, and outcome were recorded from patients presented with double malignancies from January 2012 to January 2019.Results: Among 28 patients (18 females; 10 males) with multiple primary malignancies, 10 (35.7%) and 18 patients (64.3%), respectively, had synchronous and metachronous primary malignancies. Overall, breast, gynecological, head, and neck cancer were the most common primary malignancies. Gastrointestinal tract, breast, and lung cancer emerged to be the most common second primary malignancy sites. Squamous cell carcinoma (SCC) and invasive ductal carcinoma (IDC) were the most common histopathological types of double malignancies. The majority of the patients received appropriate treatment for both the malignancies.Conclusions: Data from the present study clearly suggest that the occurrence of second primary malignancy is not rare in Indian cancer patients. The double malignancies can occur at any stage and for any type of cancer. Hence, we wish to highlight that the clinician should always be aware of the possibility of developing second malignancy either during evaluation or in follow up of a patient with malignancy.


Blood ◽  
2018 ◽  
Vol 132 (Supplement 1) ◽  
pp. 2991-2991
Author(s):  
Jin Seok Kim ◽  
Yanfang Liu ◽  
Kyoung Hwa Ha ◽  
Hong Qiu ◽  
Lee Anne Rothwell ◽  
...  

Abstract Background: Information about the epidemiology, treatment and clinical outcome of patients with B-cell Non-Hodgkin Lymphoma (BNHL) are limited and fragmented across Asia. Disparities in economy, health-care infrastructure, and access/reimbursement to novel drugs mean that treatment options and outcomes vary across the region. There is a need for improved understanding of real world treatment practices and outcomes in BNHL in Asian countries. Purpose: To describe incidence, clinical and treatment patterns and survival of patients with BNHL in South Korea. Methods: We conducted a retrospective cohort study using claims data from the National Health Insurance Service that covers 98% of all residents in South Korea. Newly diagnosed patients aged ≥18 years with a confirmed diagnosis of BNHL during the period 01 January 2006 to 31 December 2015 were enrolled. All eligible patients were followed up until death, dis-enrolment or the end of the observational period (December 31, 2015), whichever occurred first. Patients with pre-existing primary cancers were excluded. Standardized annual incidence, prevalence and morality rates were estimated. Overall survival and occurrence of second primary malignancies were estimated using Kaplan-Meier methods. Results: A total of 19,500 patients with newly diagnosed BNHL were included in the cohort analysis. At diagnosis, the mean age of patients was 59.5 years, 60.0% were 19-64 years of age and 54.0% were male. Diffuse large cell B-cell lymphoma (DLCBCL) was the most common diagnosis in each study year (53.1% to 58.7% of patients annually). The most commonly used first-line treatment regimens included rituximab-based combinations for the majority of patients with DLCBL, Follicular Lymphoma (FL), Mantle Cell Lymphoma (MCL), or Chronic lymphocytic leukemia/ Small Lymphocytic Lymphoma (CLL/SLL), radiation for patients with Marginal Zone Lymphoma (MZL), and chlorambucil or cyclophosphamide for patients with Waldenström's Macroglobulinemia (WM). The overall incidence of BNHL increased over time, from 5.96 per 100,000 in 2011 to 6.99 per 100,000 population in (Table). BNHL prevalence increased steadily each year, and was 2.5-fold higher in 2015 than in 2011. The mortality rate increased by 50% over the same period, from 1.38 per 100,000 to 2.09 per 100,000 population. There was a trend of increasing incidence of some BNHL sub-types, mainly DLBCL, Follicular Lymphoma (FL), and Marginal Zone Lymphoma (MZL), over time (Fig. 1). There were 4009 patients between 2006-2015 (20.6%) who were diagnosed with at least one second primary malignancy more than 180 days after their BNHL diagnosis. The majority (96%) had a solid tumor; incidence rate of 5.93 per 100 person-years versus 0.24 per 100 person-years for hematological malignancies. By year 5, the cumulative hazard for developing a second primary malignancy was highest for CLL/SLL (25%) and lowest (18%) for FL. By year 8-9, the cumulative risk of developing a second primary malignancy was similar among the BHNL sub-types (Fig. 2). Five-year survival was 88% (95% Confidence interval [CI] 86-90) for MZL, 79% (95% CI 76-81) for FL, 62% (95% CI 59-66) for CLL/SLL, 60% (95% CI 59-61) for DLBCL, 54% (95% CI 47-63) for WM and 53% (95% CI 46-60) for MCL. Overall survival by year 9 was highest in patients with CLL/SLL and FL, lowest for WM (Fig. 3). Conclusion: The incidence, prevalence and mortality of BNHL appears to be increasing in Korea, and the occurrence of second primary malignancies is high. BNHL remains an important unmet medical need in South Korea. Disclosures Liu: Janssen Research & Development, LLC: Employment, Equity Ownership. Qiu:Janssen Research & Development, LLC: Employment, Equity Ownership. Rothwell:Janssen Research & Development, LLC: Employment, Equity Ownership.


2021 ◽  
Author(s):  
Yandong Shen ◽  
Luke Coyle ◽  
Ian Kerridge ◽  
William Stevenson ◽  
Christopher Arthur ◽  
...  

Chronic lymphocytic leukaemia (CLL) is invariably accompanied by some degree of immune failure. CLL patients have a high rate of second primary malignancy (SPM) compared to the general population. We comprehensively documented the incidence of all forms of SPM including skin cancer (SC), solid organ malignancy (SOM), second haematological malignancy (SHM), and separately Richter's Syndrome (RS) across all therapy eras. Among the 517 CLL/SLL patients, the overall incidence of SPMs with competing risks were SC 31.07%, SOM 25.99%, SHM 5.19% and RS 7.55%. Melanoma accounted for 30.3% of SC. Squamous cell carcinoma (SCC), including 8 metastatic SCCs, was 1.8 times more than basal cell carcinoma (BCC), a reversal of the typical BCC:SCC ratio. The most common SOM were prostate (6.4%) and breast (4.5%). SHM included 7 acute myeloid leukaemia and 5 myelodysplasia of which 8 were therapy-related. SPMs are a major health burden with 44.9% of CLL patients with at least one, and apart from SC, associated with significantly reduced overall survival. Dramatic improvements in CLL treatment and survival have occurred with immunochemotherapy and targeted therapies but mitigating SPM burden will be important to sustain further progress.  


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