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Oxaliplatin retreatment in metastatic colorectal cancer: Systematic review and future research opportunities

期刊

CANCER TREATMENT REVIEWS
卷 91, 期 -, 页码 -

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.ctrv.2020.102112

关键词

Colorectal cancer; FOLFOX; XELOX; CAPOX; Rechallenge; Reintroduction

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资金

  1. Fondazione Regionale Ricerca Biomedica Regione Lombardia [CP 12/2018 IANG CRC]
  2. FONDAZIONE AIRC [21091]
  3. H2020 grant [635342-2 MoTriColor]
  4. AIRC [20685, 21923]
  5. Terapia Molecolare Tumori by Fondazione Oncologia Niguarda Onlus
  6. AIRC-CRUK-FC AECC Accelerator Award [22795]
  7. Genomic-Based Triage for Target Therapy in Colorectal Cancer Ministero della Salute [NET 02352137]
  8. Ministero Salute
  9. Fondazione Piemontese per la Ricerca sul Cancro-ONLUS 5 per mille 2015 Ministero della Salute
  10. FPRC 5xmille 2017 Ministero Salute PTCRC-Intra 2020 (REGENERATION-YIG 2020 project)
  11. TRANSCAN-2 JTC 2014 INTRACOLOR [TRS-2015-00000060]
  12. Fondazione AIRC under MFAG 2017 [20236]

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Background: Oxaliplatin represents a main component of cytotoxic treatment regimens in colorectal cancer (CRC). Given its efficacy, oxaliplatin is frequently re-administered in the context of the continuum of care in metastatic CRC (mCRC). However, efficacy and tolerability of this therapeutic strategy has not been comprehensively assessed. Methods: We performed a systematic review of the literature on September 19th 2020, according to PRISMA criteria 2009. The research was performed on PubMed, ASCO Meeting Library, ESMO library and ClinicalTrials.gov for citations or ongoing trials. Results: 64 records were retrieved and 13 included in the systematic review: 8 full-text articles, 4 abstracts and 1 ongoing clinical trial. According to readministration timing, studies were classified as rechallenge/reintroduction (n = 8) or stop & go/intermittent therapeutic strategies (n = 4). The studies presented wide heterogeneity in terms of efficacy (Response Rate 6-31%; Disease Control Rate 39-79%; median Progression-Free Survival 3.1-7 months). Those patients who received retreatment after prior adjuvant oxaliplatin or exploiting a stop-&-go strategy appeared to achieve better outcomes. However, no formal comparisons on treatment outcomes were feasible. The most frequent grade 3 or higher adverse events were hematologic toxicities (5-27%), peripheral neuropathy (5-14%) and hypersensitivity reactions (5-20%). Conclusions: Retreatment with oxaliplatin for mCRC is practiced based on scarce and heterogeneous data indicating efficacy and manageable toxicity. The best strategy to exploit this approach remains to be defined, and the most promising research avenue to improve therapeutic index of oxaliplatin is represented by selection of responder patients whose tumors harbor molecular defects in the DNA damage repair pathway.

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