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When would you consider sequential chemotherapy and radiation rather than concurrent for early stage cervical cancer with high risk pathologic features?

The recently released STARS phase 3 RCT found improved DFS, decreased distant recurrence, with reduced toxicities for chemotherapy (cisplatin + taxol) followed by RT versus concurrent chemo-radiation.
2 Answers
Mednet Member
Radiation Oncology · Vanderbilt-Ingram Cancer Center
Answered on

How much of the results of the STARS (Huang et al., PMID 33443541) (showing improved DFS with SCRT compared to CCRT) driven by only a 62% completion rate of CCRT (compared to 73.4% in SCRT, p< 0.001) as per the specified protocol is unknown.

While the authors state within their results section that the per-protocol analysis showed statistical superiority of SCRT, that is true only for the comparison to RT alone, as per Figure 2C within the paper.

I have not seen a combination Cis/Taxol delivered in the US - more common is CarboTaxol, which as per a previously referenced trial within the introduction of STARS, did not show any statistical benefit to sequential use of CarboTaxol + RT vs CRT w/ cisplatin (Sehouli et al., PMID 22357252).

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Mednet MemberInvited Expert
Radiation Oncology · University of Kentucky
Answered on

A critical review of this paper is not appropriate in this forum. Yes, I would consider it. No, I don't believe that this paper creates a new standard of care at this point. The differences in OS are very small, and the overall compliance with the SCRT arm is still less than 75% (drop out rate mostly due to chemotherapy toxicity). I would say that it is an option, especially in the very high risk population with positive LN's.

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