Efficacy of second-line chemotherapy after a first-line triplet in patients with metastatic colorectal cancer

被引:4
|
作者
Bazarbashi, S. [1 ]
Hakoun, A. M. [2 ]
Gad, A. M. [1 ,3 ]
Elshenawy, M. A. [1 ,4 ]
Aljubran, A. [1 ]
Alzahrani, A. M. [1 ]
Eldali, A. [5 ]
机构
[1] King Faisal Specialist Hosp & Res Ctr, Oncol Ctr, POB 3354, Riyadh 11211, Saudi Arabia
[2] Alfaisal Univ, Coll Med, Res Off, Riyadh, Saudi Arabia
[3] Ain Shams Univ, Fac Med, Clin Oncol & Nucl Med Dept, Cairo, Egypt
[4] Menoufia Univ, Clin Oncol & Nucl Med Dept, Fac Med, Shibin Al Kawm, Egypt
[5] King Faisal Specialist Hosp & Res Ctr, Res Ctr, Dept Biostat Epidemiol & Sci Comp, Riyadh, Saudi Arabia
关键词
Colorectal cancer; metastatic; second-line treatments; triplet chemotherapy; systemic therapy; PHASE-III TRIAL; COMBINATION CHEMOTHERAPY; INFUSIONAL FLUOROURACIL; IRINOTECAN FOLFOXIRI; RANDOMIZED PHASE-3; PLUS IRINOTECAN; OXALIPLATIN; LEUCOVORIN; BEVACIZUMAB; FOLFIRI;
D O I
10.3747/co.26.4217
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Exposing patients with metastatic colorectal cancer (MCRC) to all three active chemotherapeutic agents (oxaliplatin, irinotecan, fluorouracil) has improved survival. The benefit of second-line chemotherapy after a first-line triplet is not clearly defined. We evaluated the efficacy of second-line chemotherapy in patients who had received first-line triplet therapy. Methods The medical records of patients treated on a prospective trial of first-line triplet therapy were reviewed for second-line treatment. Univariate and multivariate analyses were performed to establish factors of prognostic significance. Results Of the 53 patients who received first-line triplet therapy, 28 (53%) received second-line chemotherapy [13 men; 8 with a colon primary; mutant KRAS in 10, wild-type in 15, and unknown status in 3; Eastern Cooperative Oncology Group performance status (PS) of 1 in 16 patients, PS 2 in 3, PS 3 in 2, and unknown in 7; involved organs: liver in 17 patients, lung in 16, and peritoneum in 8]. Second-line chemotherapy consisted of XELOX or FOLFOX in 13 patients, XELIRI or FOLFIRI in 12, and single-agent irinotecan in 3. Concurrent bevacizumab was given in 16 patients (57%), and cetuximab, in 2 (7%). Median survival was 28.0 months [95% confidence interval (CI): 22.8 months to 33.2 months] for patients receiving second-line therapy and 23.0 months (95% CI: 13.2 months to 32.8 months) for those not receiving it. Best response was partial in 6 patients (21%), stable disease in 11 (39%), and progressive disease in 11 (39%). Median progression-free survival was 4.8 months (95% CI: 2.4 months to 9.6 months), and overall survival was 15 months (95% CI: 9.6 months to 20.4 months). Conclusions Second-line chemotherapy after first-line triplet therapy in mete is feasible and suggests efficacy comparable to that reported for second-line therapy after a doublet, regardless of the agent used.
引用
收藏
页码:E24 / E29
页数:6
相关论文
共 50 条
  • [1] SECOND-LINE TREATMENTS IN PATIENTS WITH METASTATIC COLORECTAL CANCER PROGRESSED AFTER FIRST-LINE FOLFOXIRI
    Fornaro, Lorenzo
    Vasile, Enrico
    Masi, Gianluca
    Loupakis, Fotios
    Salvatore, Lisa
    Stasi, Irene
    Baldi, Giacomo Giulio
    Cupini, Samanta
    Barbara, Cecilia
    Pfanner, Elisabetta
    Brunetti, Isa Maura
    Di Donato, Samantha
    Caponi, Sara
    Allegrini, Giacomo
    Antonuzzo, Andrea
    Ricci, Sergio
    Chiara, Silvana
    Vitello, Stefano
    Andreuccetti, Michele
    Falcone, Alfredo
    [J]. ANNALS OF ONCOLOGY, 2009, 20
  • [2] Second-line treatments in patients with metastatic colorectal cancer progressed after first-line FOLFOXIRI
    Masi, G.
    Vasile, E.
    Loupakis, F.
    Fornaro, L.
    Salvatore, L.
    Cupini, S.
    Stasi, I.
    Brunetti, I. M.
    Andreuccetti, M.
    Falcone, A.
    [J]. EJC SUPPLEMENTS, 2009, 7 (02): : 346 - 347
  • [3] Second-line chemotherapy after early disease progression during first-line chemotherapy containing bevacizumab for patients with metastatic colorectal cancer
    Shun Yamamoto
    Kengo Nagashima
    Takeshi Kawakami
    Seiichiro Mitani
    Masato Komoda
    Yasushi Tsuji
    Naoki Izawa
    Kentaro Kawakami
    Yoshiyuki Yamamoto
    Akitaka Makiyama
    Kentaro Yamazaki
    Toshiki Masuishi
    Taito Esaki
    Takako Eguchi Nakajima
    Hiroyuki Okuda
    Toshikazu Moriwaki
    Narikazu Boku
    [J]. BMC Cancer, 21
  • [4] Second-line chemotherapy after early disease progression during first-line chemotherapy containing bevacizumab for patients with metastatic colorectal cancer
    Yamamoto, Shun
    Nagashima, Kengo
    Kawakami, Takeshi
    Mitani, Seiichiro
    Komoda, Masato
    Tsuji, Yasushi
    Izawa, Naoki
    Kawakami, Kentaro
    Yamamoto, Yoshiyuki
    Makiyama, Akitaka
    Yamazaki, Kentaro
    Masuishi, Toshiki
    Esaki, Taito
    Nakajima, Takako Eguchi
    Okuda, Hiroyuki
    Moriwaki, Toshikazu
    Boku, Narikazu
    [J]. BMC CANCER, 2021, 21 (01)
  • [6] Secondary treatment and predictive factors for second-line chemotherapy after first-line oxaliplatin-based therapy in metastatic colorectal cancer
    Sorbye, Halfdan
    Berglund, Ake
    Tveit, Kjell Magne
    Ogreid, Dagfinn
    Wanderas, Eva Hoff
    Wentzel-Larsen, Tore
    Dahl, Olav
    Glimelius, Bengt
    [J]. ACTA ONCOLOGICA, 2007, 46 (07) : 982 - 988
  • [7] SECOND-LINE CHEMOTHERAPY AFTER FIRST-LINE IRINOTECAN, OXALIPLATIN AND 5-FU/LV (FOLFOXIRI) IN METASTATIC COLORECTAL CANCER (MCRC) PATIENTS (PTS)
    Marcucci, L.
    Cupini, S.
    Masi, G.
    Allegrini, G.
    Cerri, E.
    Loupakis, F.
    Ricci, S.
    Brunetti, I.
    Fontana, E.
    Falcone, A.
    [J]. ANNALS OF ONCOLOGY, 2004, 15 : 60 - 60
  • [8] Efficacy of second line chemotherapy following first line triplet chemotherapy in advanced colorectal cancer (ACRC)
    Hakoun, A. M.
    Gad, A. M.
    Alzahrani, A.
    Aljubran, A.
    Bazarbashi, S.
    [J]. ANNALS OF ONCOLOGY, 2016, 27
  • [10] Clinical benefits of stabilization after second-line chemotherapy in patients with metastatic colorectal cancer
    Henry-Launois, B
    Becouarn, Y
    Aussage, P
    [J]. BULLETIN DU CANCER, 1999, 86 (02) : 195 - 201