Phase I study of the antiangiogenic antibody bevacizumab and the mTOR/hypoxia-inducible factor inhibitor temsirolimus combined with liposomal doxorubicin: tolerance and biological activity.

Author: FalchookGerald, FuSiqing, HelgasonThorunn, HongDavid, KurzrockRazelle, LevenbackCharles, MoroneyJohn, MoulderStacy, NaingAung, WhelerJennifer

Paper Details 
Original Abstract of the Article :
PURPOSE: Preclinical data suggest that combining the mTOR/hypoxia-inducible factor (HIF) inhibitor temsirolimus and the antiangiogenesis antibody bevacizumab may augment antitumor activity as well as resensitize cells to anthracyclines. EXPERIMENTAL DESIGN: We initiated a phase I study of bevacizum...See full text at original site
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引用元:
https://doi.org/10.1158/1078-0432.CCR-12-1158

データ提供:米国国立医学図書館(NLM)

The Antiangiogenic Antibody Bevacizumab and Temsirolimus Combined with Liposomal Doxorubicin: A Promising Combination Therapy

Cancer treatment is like a race against time, and we're always looking for ways to get ahead of the curve. This research delves into the fascinating world of [oncology] and explores a novel combination therapy involving bevacizumab, temsirolimus, and liposomal doxorubicin. This study aims to understand the safety and efficacy of this triple threat against various advanced malignancies. The researchers employed a modified 3 + 3 design and dose expansion in responsive tumor types to investigate the effects of this combination. Their findings show that this combination is generally well-tolerated and offers a promising [response rate]. This regimen achieved a 21% rate of stable disease ≥ 6 months and a 21% rate of partial or complete remission. Particularly promising results were observed in patients with parotid gland adenocarcinoma, metaplastic breast cancer, and endometrial endometrioid carcinoma, suggesting that this combination therapy could be particularly beneficial for these specific cancers. Interestingly, the study also highlights the potential role of PIK3CA and PTEN mutations in predicting response to this regimen. This research presents a valuable addition to the field of [oncology], offering hope for patients with advanced cancers.

The Study's Implication: Hope for Specific Cancers

The research suggests that this triple-drug regimen could be a valuable option for treating certain types of cancer. The researchers found that the treatment was particularly effective for patients with parotid gland adenocarcinoma, metaplastic breast cancer, and endometrial endometrioid carcinoma. This finding suggests that this combination therapy could be a promising new treatment approach for these types of cancer. Moreover, the study also provides insights into the potential role of PIK3CA and PTEN mutations in predicting response to this regimen.

The Research's Implications on Patient Care

This research opens up new avenues for treating specific cancer types. The combination of bevacizumab, temsirolimus, and liposomal doxorubicin may offer a more effective and tolerable treatment option for patients with parotid gland adenocarcinoma, metaplastic breast cancer, and endometrial endometrioid carcinoma. Furthermore, understanding the role of PIK3CA and PTEN mutations could guide personalized treatment strategies for patients with these cancers. While this study shows promise, further research is needed to confirm its long-term efficacy and safety. We're excited to see how this research translates into better treatment options for patients.

Dr.Camel's Conclusion

This research highlights the importance of personalized medicine and the power of combining different treatment modalities to combat cancer. Just like a skilled camel caravan leader carefully chooses the best route across the desert, researchers are diligently exploring the most effective treatment strategies for various cancers.

Date :
  1. Date Completed 2013-05-23
  2. Date Revised 2020-12-19
Further Info :

Pubmed ID

22927482

DOI: Digital Object Identifier

10.1158/1078-0432.CCR-12-1158

Related Literature

SNS
PICO Info
in preparation
Languages

English

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