echemi logo
Product
  • Product
  • Supplier
  • Inquiry
    Home > Active Ingredient News > Antitumor Therapy > Risk factors for recurrence of orbital meningioma and coping strategies

    Risk factors for recurrence of orbital meningioma and coping strategies

    • Last Update: 2022-10-20
    • Source: Internet
    • Author: User
    Search more information of high quality chemicals, good prices and reliable suppliers, visit www.echemi.com







    Mariniello G, Center for Neuroscience at the Federico II University of Naples, Italy, analyzed risk factors for SOM recurrence and discussed ways to deal with SOM recurrence, and the results were published online
    in the May 2022 issue of World Neurosurgery.


    —Excerpted from the article chapter


    Ref: Mariniello G, et al.
    World Neurosurg.
    2022 May; 161:e514-e522.
    doi: 10.
    1016/j.
    wneu.
    2022.
    02.
    048.
    Epub 2022 Feb 26


    Research background




    Spheno-orbital meningiomas (SOM) often spread along surrounding structures, invading the sphenoid, orbit and dura, and even growing into the orbital apex, optic tube, and supraorbital fissure
    .

    To cure, it is necessary to remove the entire tumor and the invaded durum and bone, and open the sinuses if necessary, which is difficult
    to operate.

    With a high recurrence rate
    of maximal safe resection while preserving function.

    Mariniello G, Center for Neuroscience at the Federico II University of Naples, Italy, analyzed risk factors for SOM recurrence and discussed ways to deal with SOM recurrence, and the results were published online
    in the May 2022 issue of World Neurosurgery.


    Research methods



    The study retrospectively analyzed the clinical data of 80 patients with orbital meningiomas admitted between 1990 and 2014, and the inclusion criteria for patients were meningiomas that simultaneously span from intracranial to intraorbital growth; Exceptions are sphenoid crest meningioma without intraorbital extension, meningioma that grows isolated in the orbit, WHO grade III meningioma, and patients
    with loss to follow-up.

    The researchers divided 80 patients into two groups; Among them, 30 cases of postoperative recurrence were in the relapse group, and 50 cases of non-recurrence after surgery were in the non-recurrence group, with an average follow-up of 136 months (5-336 months).


    87% of women in the relapse group, with an average age of 48 years; Women in the non-relapse group accounted for 80% of the population, with a mean age of 45 years
    .

    In the relapsed group, except for one patient who had no exophthalmos, the rest had different degrees of exophthalmos
    .

    63% of the relapsed group had visual field defects and 40% of eye movement disorders; 56% of the non-recurrence group had visual field defects and 32% of eye movement disorders; There was no statistically significant difference
    between the two groups.

    By tumor location and extension range, there were 4 types: type I (lateral and superior lateral) 20 cases, type II (medial and inferior medial) 13 cases, type III (orbital apex) 30 cases, type IV (diffusion extended to the orbit) 17 cases
    .

    There was a statistically different recurrence rate between type I + II and type III + IV (P=0.
    004).


    Both type III and IV tumors invade the optic neural tube, type II 69% invade, type I only 15% invade.


    Forty-eight cases extended to the anterior bed process, 52 cases extended to the supraorbital fissure, 47 cases extended to the orbital apex, 3 cases extended to the ethmoid sinus and sphenoid sinus, and 3 cases extended to the infratemporal fossa
    .

    There was a statistically significant difference in the proportion of epiorbital fissures, infratemporal fossa, ethmoid sinuses and sphenoid sinuses between the relapsed group and the non-relapsed group (P=0.
    0049), while there was no statistical difference
    in the rest.



    All patients with type I underwent lateral orbital approach, 11 patients with type II.
    , all type III.
    and 13 patients with type IV underwent superior orbital pterygoid approach, 2 patients with type II underwent superior orbital pterygoid approach + medial orbital open approach, 3 patients with type IV.
    underwent frontal temporal orbital zygomatic approach, and 1 patient with type IV.
    underwent medial orbitotomy
    .

    All patients with type I, 77% of type II, 63% of type III, and 18% of type IV patients had complete resection (Simpson grade 1 and 2).


    Patients with grades 1 and 2 of first surgical resection had significantly lower recurrence rates than patients with grades 3 and 4 of Simpson (P=0.
    0032 and P=0.
    0002).


    Patients with grades 1 and 2 of resection had significantly longer progression-free survival at 5 years than patients with grades 3 and 4 of Simpson (P=0.
    0004 and P=0.
    0001).



    Research results



    Of the patients, 52 were WHO Class I and 28 were WHO Class
    II.

    There were 19 cases of WHO class II in the relapsed group and 9 cases of WHO class II in the non-relapse group (P=0.
    0001).


    Of all patients, 40 had improved visual acuity after surgery, 7 had deterioration, and 5 had deterioration
    in oculomotor function.

    In the relapse group, 21 cases had exacerbation of exophthalmos, 4 cases of deterioration of visual acuity, and 5 cases of simultaneous exophthalmos and visual acuity deterioration
    .

    In the relapsing group, 18 patients received complete re-operation without radiotherapy, and the remaining 4 cases of postoperative total resection and 8 cases of postoperative subtotal resection were reoperated or radiotherapy
    .

    Of the 9 cases of third surgery, 2 cases did not recur after total resection, and the remaining 7 cases had re-progression of tumors, of which 3 cases had no indication for
    reoperation.

    Three cases died in the non-relapse group and 10 patients in the relapsed group had second postoperative progression, of which 4 died
    .



    Conclusion of the study



    The risk of recurrence of orbital meningiomas depends on the degree of tumor resection, whether the tumor extends to the supraorbital fissure, infratemporal fossa, sphenoid sinus and other sites before surgery, and WHO grade
    .

    The coping strategy for recurrent meningiomas is surgery to stop tumor progression, while radiotherapy
    is the option for patients with recurrent WHO class II.

    Because meningiomas progress slowly, patients whose tumors infiltrate the skull even after multiple surgeries have a longer survival and a higher quality of life
    .


    This article is an English version of an article which is originally in the Chinese language on echemi.com and is provided for information purposes only. This website makes no representation or warranty of any kind, either expressed or implied, as to the accuracy, completeness ownership or reliability of the article or any translations thereof. If you have any concerns or complaints relating to the article, please send an email, providing a detailed description of the concern or complaint, to service@echemi.com. A staff member will contact you within 5 working days. Once verified, infringing content will be removed immediately.

    Contact Us

    The source of this page with content of products and services is from Internet, which doesn't represent ECHEMI's opinion. If you have any queries, please write to service@echemi.com. It will be replied within 5 days.

    Moreover, if you find any instances of plagiarism from the page, please send email to service@echemi.com with relevant evidence.