[Adrenocortical carcinomas: therapeutic advances in 2011].

Author: CaronPh, GrunenwaldS

Paper Details 
Original Abstract of the Article :
Adrenocortical cancer (ACC) is a rare aggressive malignancy with a poor prognosis (5-year survival: 45 %). Their management requires multidisciplinary expertise. Complete resection by an expert surgeon is the only curative treatment. Very few adjuvant treatments are available and their efficacy is n...See full text at original site
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引用元:
https://doi.org/10.1016/S0003-4266(11)70004-X

データ提供:米国国立医学図書館(NLM)

Adrenocortical Carcinomas: Therapeutic Advances in 2011

This study reviews the current landscape of [adrenocortical cancer (ACC)] treatment. The researchers discuss the challenges of managing this rare and aggressive form of cancer, highlighting the importance of [multidisciplinary expertise] and [complete surgical resection]. They also explore the role of [mitotane], [radiotherapy], and [chemotherapy] in treating ACC and discuss the ongoing research into novel therapies, including [tyrosine kinase inhibitors] and [treatments targeting the IGF-1 receptor].

The Fight Against Adrenocortical Cancer: A Collaborative Approach

The study underscores the need for a [multidisciplinary approach] to treating [ACC]. The researchers emphasize the importance of [complete surgical resection] as the only curative treatment option for this aggressive cancer. They also highlight the challenges of managing [mitotane] therapy, balancing its efficacy with potential side effects. The study's findings reinforce the need for ongoing research into new and effective treatments for ACC.

Navigating the Treatment Landscape for Adrenocortical Cancer

This research provides a comprehensive overview of current treatment options for [ACC]. The study's findings underscore the need for continued research into [targeted therapies] for this rare and aggressive cancer. Exploring new treatment approaches, including [tyrosine kinase inhibitors] and [IGF-1 receptor inhibitors], holds promise for improving outcomes for patients with ACC.

Dr. Camel's Conclusion

Adrenocortical cancer is a formidable foe, like a mirage shimmering in the desert, offering false hope. This research provides a valuable roadmap for navigating the challenges of treating this rare and aggressive cancer. We must continue to explore innovative treatments and develop collaborative approaches to improve outcomes for those facing this difficult diagnosis.

Date :
  1. Date Completed 2012-02-17
  2. Date Revised 2016-10-31
Further Info :

Pubmed ID

22008276

DOI: Digital Object Identifier

10.1016/S0003-4266(11)70004-X

Related Literature

SNS
PICO Info
in preparation
Languages

French

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