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1 with cancer types (first cancer, recurrence, second primary cancer).
2 cancer, of whom 1,088 were diagnosed with a second primary cancer.
3 -up (mean: 4.7 years), 279 women developed a second primary cancer.
4 risk factors to reduce risk of developing a second primary cancer.
5 d cancer recurrence, and 57 (2%) developed a second primary cancer.
6 a strong suggestion of an increased risk of second primary cancers.
7 id conditions such as obesity, diabetes, and second primary cancers.
8 intent radiation therapy is the induction of second primary cancers.
9 , of which 1243 (33.2%) were obesity-related second primary cancers.
10 virus-related, and hormone-related first and second primary cancers.
12 eath, and hazard ratios (HRs) and 95% CIs of second primary cancer adjusted for sex, age and year of
13 egarding the long-term incidence and risk of second primary cancer after radiotherapy vs nonradiother
14 respectively) and recipients who developed a second primary cancer after transplantation (aHRs, 1.01;
15 of patients with cancer recurrence and/or a second primary cancer after transplantation are unknown.
16 examines the risk factors and predictors of second primary cancers after being diagnosed with neuroe
18 r Registry were used to evaluate the risk of second primary cancers among a retrospective population-
20 odels were used to estimate the incidence of second primary cancer and death, and hazard ratios (HRs)
21 y in 75 trials yielded rate ratios (RRs) for second primary cancers and cause-specific mortality and
22 eriods of follow-up, the AER for deaths from second primary cancers and circulatory causes increased
23 f the excess number of deaths observed while second primary cancers and circulatory deaths together a
24 s of childhood cancer, excess mortality from second primary cancers and circulatory diseases continue
27 atients with multiple gene abnormalities had second primary cancers, and an additional patient had mu
28 ndary cancers, including metastatic cancers, second primary cancers, and cancers of unknown primaries
30 tients died of recurrent cancer, two died of second primary cancers, and four died of other causes.
32 revious history of malignancy, recurrent and second primary cancers are infrequent after renal transp
34 surveillance and screening for recurrence or second primary cancers, assessment and management of lon
35 for breast cancer recurrence, screening for second primary cancers, assessment and management of phy
37 the radiotherapy cohort had a higher risk of second primary cancer compared with those in the nonradi
38 lated from 2 months until the diagnosis of a second primary cancer, death, loss to follow-up, or Dece
39 is not associated with an increased risk of second primary cancers, either solid or hematologic, and
40 to <25), there was 15% increased risk of any second primary cancer for those who had overweight (25 t
41 set of patients alive, recurrence-free, and second primary cancer-free (disease-free survival [OS|DF
42 S-mutated tumors were more likely to develop second primary cancers (HR = 2.76, 95% CI, 1.34 to 5.70;
43 RCA1, BRCA2, and ERCC2 to the development of second primary cancer in breast cancer survivors, provid
45 ing should be offered to women who develop a second primary cancer in the ipsilateral or contralatera
48 gated the absolute and relative incidence of second primary cancers in a large cohort of Danish cance
49 kewise, retinoids prevent the development of second primary cancers in head/neck and lung cancer pati
51 a first primary melanoma, 23.7% developed a second primary cancer, including 12.7% who developed a s
52 1.48), with greater risk for obesity-related second primary cancers, including a 40% increased risk f
54 break-induced senescence as the mechanism of second primary cancer initiation, with clinically releva
55 erstanding the absolute risk of developing a second primary cancer is important to guide patient surv
57 and factors associated with development of a second primary cancer (melanoma versus other) after diag
60 iscontinuation in 6 patients (6%) because of second primary cancers (n = 4) and infection (n = 2).
63 sis showed a 10-year cumulative incidence of second primary cancers of 12.1% (95% CI, 9.6 to 14.9) af
64 3.9%) participants received a diagnosis of a second primary cancer, of which 1243 (33.2%) were obesit
66 an 1 year after diagnosis, (4) occurrence of second primary cancer or death within 1 year or less aft
67 By March 15, 2005, 394 events (recurrent, second primary cancer, or death before recurrence) had b
68 tic recurrence at other sites, occurrence of second primary cancer, or death resulting from noncancer
70 mary cancer should be carefully screened for second primary cancers, particularly for cancers that ar
74 y survivorship (~3 years postdiagnosis) with second primary cancer (SPC) risk among 533 endometrial c
76 e past are at increased risk of developing a second primary cancer (SPC), including second primary br
78 data for racial and ethnic disparities after second primary cancers (SPCs) are lacking despite the gr
79 in penile and vulvar/vaginal cancers and in second primary cancers (SPCs) following these cancers ar
80 t investigating the distribution and risk of second primary cancers (SPCs) in multiple myeloma (MM) s
81 d radiotherapy were more likely to develop a second primary cancer than patients who did not receive
83 ed in the rates of treatment-related deaths, second primary cancers, thromboembolic events, and perip
86 Cohort identification and information on second primary cancers was obtained from the Danish Canc
87 ent-free survival (with events that included second primary cancers) was significantly improved with
88 hough the incidence and risk of developing a second primary cancer were low, it is important to discu
89 en radiation exposure and risks of first and second primary cancers were quantified using Poisson reg
90 urvivors are at increased risk of developing second primary cancers, with lung cancer being the most