| Literature DB >> 28032641 |
Dominik P Modest1,2, Sebastian Stintzing1,2, Ludwig Fischer von Weikersthal3, Thomas Decker4, Alexander Kiani5, Ursula Vehling-Kaiser6, Salah-Eddin Al-Batran7, Tobias Heintges8, Christian Lerchenmüller9, Christoph Kahl10, Gernot Seipelt11, Frank Kullmann12, Werner Scheithauer13, Thomas Kirchner2,14, Andreas Jung2,14, Martina Stauch15, Jobst Christian von Einem1, Markus Moehler16, Swantje Held17, Volker Heinemann1,2.
Abstract
We explored the association of early tumor shrinkage (ETS) and non-ETS with efficacy of first-line and consecutive second-line treatment in patients with KRAS wild-type metastatic colorectal cancer treated in FIRE-3. Assessment of tumor shrinkage was based on the sum of longest diameters of target lesions, evaluated after 6 weeks of treatment. Shrinkage was classified as ETS (shrinkage by ≥ 20%), mETS (shrinkage by 0 to <20%), mPD (minor progression >0 to <20%) and PD (progression ≥20%). Overall survival (OS) was 33.2 (95% CI 28.0-38.4) months in ETS patients, while non-ETS was associated with less favorable outcome (mETS 24.0 (95% CI 21.2-26.9) months, mPD 19.0 (95% CI 13.0-25.0) months, PD 12.8 (95% CI 11.1-14.5) months). Differences in PFS of first-line therapy were less pronounced. ETS subgroups defined in first-line therapy also correlated with efficacy of second-line therapy. Progression-free survival in second-line (PFS2nd) was 6.5 months (5.8-7.2) for ETS, and was 5.6 (95% CI 4.7-6.5) months for mETS, 4.9 (95% CI 3.7-6.1) months for mPD and 3.3 (95% CI 2.3-4.3) months for PD. PFS of first-line and PFS2nd showed a linear correlation (Bravais-Pearson coefficient: 0.16, p = 0.006). While ETS is associated with the most favorable outcome, non-ETS represents a heterogeneous subgroup with distinct characteristics of less favorable initial tumor response to treatment. This is the first analysis to demonstrate that early tumor response observed during first-line FOLFIRI-based therapy may also relate to efficacy of second-line treatment. Early response parameters may serve as stratification factors in trials recruiting pretreated patients.Entities:
Keywords: KRAS; RAS; bevacizumab; cetuximab; colorectal cancer; early tumor shrinkage; sequence
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Year: 2017 PMID: 28032641 DOI: 10.1002/ijc.30592
Source DB: PubMed Journal: Int J Cancer ISSN: 0020-7136 Impact factor: 7.396