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Real-world treatment patterns and outcomes in refractory metastatic colorectal cancer.
Chiang, C L; Choi, H C; Lam, K O; Chan, B Y; Lee, S F; Yeung, S Y; Lau, K S; Chan, S Y; Choy, T S; Yuen, K K.
  • Chiang CL; Department of Clinical Oncology, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.
  • Choi HC; Clinical Oncology Center, The University of Hong Kong-Shenzhen Hospital, Shenzhen, China.
  • Lam KO; Department of Clinical Oncology, Queen Mary Hospital, Hong Kong, China.
  • Chan BY; Department of Clinical Oncology, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.
  • Lee SF; Department of Clinical Oncology, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.
  • Yeung SY; Clinical Oncology Center, The University of Hong Kong-Shenzhen Hospital, Shenzhen, China.
  • Lau KS; Department of Clinical Oncology, Queen Mary Hospital, Hong Kong, China.
  • Chan SY; Department of Clinical Oncology, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.
  • Choy TS; Department of Clinical Oncology, Tuen Mun Hospital, Hong Kong, China.
  • Yuen KK; Department of Clinical Oncology, Tuen Mun Hospital, Hong Kong, China.
Asia Pac J Clin Oncol ; 15 Suppl 2: 5-13, 2019 Mar.
Article en En | MEDLINE | ID: mdl-30887726
ABSTRACT

AIM:

To investigate treatment patterns and outcomes of metastatic colorectal cancer (mCRC) patients beyond second progression (PD2) since regorafenib and TAS-102 became available in Hong Kong.

METHODS:

The clinical records of consecutive mCRC patients who were treated beyond PD2 at Department of Clinical Oncology, Queen Mary Hospital between June 2013 and February 2018, were retrospectively reviewed.

RESULTS:

Of 176 PD2 patients (76.7% Eastern Cooperative Oncology Group performance status 0/1 and a median follow-up time of 6.6 [range, 0.4-37.2] months), 104 (59%) underwent palliative care only and 72 (41%) received active third-line (3L) treatment regorafenib (n = 22), TAS-102 (n = 6), chemotherapy + antiepidermal growth factor receptor (n = 12), chemotherapy + antivascular endothelial growth factor (n = 28) or clinical trials (n = 4). Patients on active 3L treatment had significantly longer OS than those on palliative care only 11.7 versus 5.5 months (adjusted hazard ratio = 0.41, 95% confidence interval 0.28-0.61, P < 0.001). For those on active treatment, OS was significantly associated with the time from diagnosis of metastasis to PD2 (P < 0.001) and post-3L treatments (P = 0.009). When analyzing treatment eligibility according to trial criteria, half of the eligible patients (54/109) did not receive active treatment, but both eligible and ineligible patients achieved better OS when receiving active 3L treatment versus palliative care only (P < 0.001 and P = 0.002). No unexpected toxicity was reported.

CONCLUSION:

Active 3L and beyond treatment significantly prolonged OS versus palliative care, even in selected "trial ineligible" patients. Given a high rate of palliation only care in eligible patients, improved patient access to medicine and counseling may be needed to maximize outcomes.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Cuidados Paliativos / Neoplasias Colorrectales / Protocolos de Quimioterapia Combinada Antineoplásica / Resistencia a Antineoplásicos Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Año: 2019 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Cuidados Paliativos / Neoplasias Colorrectales / Protocolos de Quimioterapia Combinada Antineoplásica / Resistencia a Antineoplásicos Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Año: 2019 Tipo del documento: Article