Literature DB >> 32239432

Incidence of second malignancies in individuals diagnosed with malignant peripheral nerve sheath tumors.

Lindsay A Williams1,2,3, Christopher L Moertel2,3,4, Michaela Richardson1, Erin L Marcotte5,6,7.   

Abstract

BACKGROUND: The incidence of malignant peripheral nerve sheath tumors (MPNSTs) is low in the general population, although individuals with Neurofibromatosis Type I (NF1) are particularly susceptible. These tumors generally have a high probability of metastasis. The rate and types of second malignancies (SMNs) after a primary diagnosis of MPNST are not well characterized. We aimed to quantify the rate of SMNs among individuals with a first primary MPNST using population-based data.
METHODS: We estimated age-standardized incidence rates (SIRs) for SMNs among 1,579 primary MPNST cases between ages 0-85+ using SEER 18 (2000-2015). We estimated incidence rate ratios (IRRs) and 95% confidence intervals (95% CI) for SMNs in MPNST cases compared with general population rates. We conducted sex-stratified and age-restricted analyses (< 30 years at diagnosis).
RESULTS: Seven percent (108/1579) of MPNST cases developed a SMN (SIR of 4635 cases/million). Compared to the general population, MPNST cases were more likely to develop SMNs (IRR: 29.3; 95% CI 23.8-34.8) and had a much higher rate of second MPNSTs (IRR: 15,992.9; 95% CI 9594.5-22,391.3). Aside from a second MPNST, second cancers were frequently diagnosed in the breast, lung, skin, and soft tissue in females and were myeloid and skin malignancies in males. When restricted to < 30 years of age, second MPNSTs were the most common cancers diagnosed.
CONCLUSIONS: The rate of SMNs among MPNST cases is tremendously higher than that observed among individuals with other cancers, particularly for second MPNSTs. These findings suggest rates of SMNs may also be higher in NF1 individuals.

Entities:  

Keywords:  Epidemiology; MPNST; SEER; Second malignancies

Mesh:

Year:  2020        PMID: 32239432      PMCID: PMC7285390          DOI: 10.1007/s11060-020-03478-9

Source DB:  PubMed          Journal:  J Neurooncol        ISSN: 0167-594X            Impact factor:   4.130


  33 in total

1.  Distinctive Cancer Associations in Patients With Neurofibromatosis Type 1.

Authors:  Elina Uusitalo; Matti Rantanen; Roope A Kallionpää; Minna Pöyhönen; Jussi Leppävirta; Heli Ylä-Outinen; Vincent M Riccardi; Eero Pukkala; Janne Pitkäniemi; Sirkku Peltonen; Juha Peltonen
Journal:  J Clin Oncol       Date:  2016-02-29       Impact factor: 44.544

2.  Long-term follow-up of von Recklinghausen neurofibromatosis. Survival and malignant neoplasms.

Authors:  S A Sørensen; J J Mulvihill; A Nielsen
Journal:  N Engl J Med       Date:  1986-04-17       Impact factor: 91.245

Review 3.  Treatment of neurofibromatosis 1-associated malignant peripheral nerve sheath tumors: a systematic review.

Authors:  Muhibullah S Tora; Dimitrios Xenos; Pavlos Texakalidis; Nicholas M Boulis
Journal:  Neurosurg Rev       Date:  2019-06-17       Impact factor: 3.042

4.  Peripheral nerve sheath tumors. Histogenesis, classification, and prognosis.

Authors:  S I Hajdu
Journal:  Cancer       Date:  1993-12-15       Impact factor: 6.860

5.  Malignant peripheral nerve sheath tumours in neurofibromatosis 1.

Authors:  D G R Evans; M E Baser; J McGaughran; S Sharif; E Howard; A Moran
Journal:  J Med Genet       Date:  2002-05       Impact factor: 6.318

6.  Monosomy 7 myelodysplastic syndrome and other second malignant neoplasms in children with neurofibromatosis type 1.

Authors:  J M Maris; S R Wiersma; N Mahgoub; P Thompson; R J Geyer; C G Hurwitz; B J Lange; K M Shannon
Journal:  Cancer       Date:  1997-04-01       Impact factor: 6.860

Review 7.  Neurofibromatosis type 1.

Authors:  Jacqueline L Anderson; David H Gutmann
Journal:  Handb Clin Neurol       Date:  2015

8.  Malignant peripheral nerve sheath tumors: Analysis of the national cancer database.

Authors:  Alia Mowery; Daniel Clayburgh
Journal:  Oral Oncol       Date:  2019-09-13       Impact factor: 5.337

9.  Management and prognosis of malignant peripheral nerve sheath tumors: The experience of the French Sarcoma Group (GSF-GETO).

Authors:  T Valentin; A Le Cesne; I Ray-Coquard; A Italiano; G Decanter; E Bompas; N Isambert; J Thariat; C Linassier; F Bertucci; J O Bay; A Bellesoeur; N Penel; S Le Guellec; T Filleron; C Chevreau
Journal:  Eur J Cancer       Date:  2016-01-26       Impact factor: 9.162

10.  A prospective study of neurofibromatosis type 1 cancer incidence in the UK.

Authors:  L Walker; D Thompson; D Easton; B Ponder; M Ponder; I Frayling; D Baralle
Journal:  Br J Cancer       Date:  2006-06-20       Impact factor: 7.640

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