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. 2014 Mar 21;7(1):175–181. doi: 10.1159/000360983

Table 1.

Summary of assessments and clinical decisions

Time frame Clinical decision Assessments Commentary
November 2006 Therapy switch to fulvestrant plus zoledronic acid Imaging – PD – Decision to switch therapy based on imaging that showed PD in November 2006
[CTC] – low

July 2007 Continuation of fulvestrant plus zoledronic acid treatment Imaging – PR – Marginal [CTC] agreed with good performance status
Clinical – performance status: good
[CTC] – marginal – Continued fulvestrant plus zoledronic acid therapy
[CEA] – elevated, stable
[CA 27.29] – elevated, stable – Imaging showed equivocal response

December 2007 Continuation of fulvestrant plus zoledronic acid treatment Imaging – MR – Imaging response, performance status, and absence of CTCs indicate good prognosis
Clinical – performance status: good
[CTC] – absent
[CEA] – elevated, stable – Continued treatment
[CA 27.29] – elevated

February 2008 Continuation of fulvestrant plus zoledronic acid treatment Clinical – performance status: reporting increasing pain – Clinical symptoms and increased [CTC] suggest progression
[CTC] – low
[CEA] – elevated, stable – Treated with radiation
[CA 27.29] – increasing

May 2008 Therapy switch to Abraxane plus bevacizumab Imaging – PD – All assessments suggesting progression
[CTC] – elevated
[CEA] – elevated – Therapy switched to Abraxane plus bevacizumab
[CA 27.29] – elevated

August 2008 Discontinue bevacizumab Clinical – ulceration on foot – Stably absent CTCs agree with prior PR on imaging
[CTC] – absent
– Bevacizumab discontinued to address treatment-related AEs

September 2008 Discontinue Abraxane Clinical – neuropathy – Continued absence of CTCs
[CTC] – stably absent – Drug holiday to address treatment-related AEs

PD = Progressive disease; PR = partial response; MR = mixed response; [CTC] = CTC concentration; [CEA] = CEA concentration; [CA 27.29] = CA 27.29 concentration; AE = adverse effect.