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- Publisher Website: 10.1111/ajco.13114
- Scopus: eid_2-s2.0-85063078728
- PMID: 30887726
- WOS: WOS:000462609500001
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Article: Real‐world treatment patterns and outcomes in refractory metastatic colorectal cancer
Title | Real‐world treatment patterns and outcomes in refractory metastatic colorectal cancer |
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Authors | |
Keywords | metastatic colorectal cancer palliative care refractory regorafenib trifluridine/tipiracil (TAS-102) |
Issue Date | 2019 |
Publisher | Wiley-Blackwell Publishing Ltd. The Journal's web site is located at http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1743-7563 |
Citation | Asia-Pacific Journal of Clinical Oncology, 2019, v. 15 n. S2, p. 5-13 How to Cite? |
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. |
Persistent Identifier | http://hdl.handle.net/10722/275710 |
ISSN | 2023 Impact Factor: 1.4 2023 SCImago Journal Rankings: 0.531 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Chiang, CL | - |
dc.contributor.author | Choi, HC | - |
dc.contributor.author | Lam, KO | - |
dc.contributor.author | Chan, BY | - |
dc.contributor.author | Lee, SF | - |
dc.contributor.author | Yeung, SY | - |
dc.contributor.author | Lau, KS | - |
dc.contributor.author | Chan, SY | - |
dc.contributor.author | Choy, TS | - |
dc.contributor.author | Yuen, KK | - |
dc.date.accessioned | 2019-09-10T02:48:05Z | - |
dc.date.available | 2019-09-10T02:48:05Z | - |
dc.date.issued | 2019 | - |
dc.identifier.citation | Asia-Pacific Journal of Clinical Oncology, 2019, v. 15 n. S2, p. 5-13 | - |
dc.identifier.issn | 1743-7555 | - |
dc.identifier.uri | http://hdl.handle.net/10722/275710 | - |
dc.description.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. | - |
dc.language | eng | - |
dc.publisher | Wiley-Blackwell Publishing Ltd. The Journal's web site is located at http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1743-7563 | - |
dc.relation.ispartof | Asia-Pacific Journal of Clinical Oncology | - |
dc.subject | metastatic colorectal cancer | - |
dc.subject | palliative care | - |
dc.subject | refractory | - |
dc.subject | regorafenib | - |
dc.subject | trifluridine/tipiracil (TAS-102) | - |
dc.title | Real‐world treatment patterns and outcomes in refractory metastatic colorectal cancer | - |
dc.type | Article | - |
dc.identifier.email | Chiang, CL: chiangcl@hku.hk | - |
dc.identifier.email | Lam, KO: lamkaon@hku.hk | - |
dc.identifier.authority | Chiang, CL=rp02241 | - |
dc.identifier.authority | Lam, KO=rp01501 | - |
dc.description.nature | link_to_OA_fulltext | - |
dc.identifier.doi | 10.1111/ajco.13114 | - |
dc.identifier.pmid | 30887726 | - |
dc.identifier.scopus | eid_2-s2.0-85063078728 | - |
dc.identifier.hkuros | 303028 | - |
dc.identifier.volume | 15 | - |
dc.identifier.issue | S2 | - |
dc.identifier.spage | 5 | - |
dc.identifier.epage | 13 | - |
dc.identifier.isi | WOS:000462609500001 | - |
dc.publisher.place | United Kingdom | - |
dc.identifier.issnl | 1743-7555 | - |