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Treatment Patterns and Prognosis of Palliative Chemotherapy Combined With Targeting Agents in Patients With Unresectable Metastatic Colorectal Cancer: CHOICE, A Multicenter Longitudinal Observational Study.
Kim, Jwa Hoon; Cha, Yongjun; Shin, Sang Joon; Park, Young Suk; Kang, Jung Hun; Kim, Chan; Lim, Sung Hee; Kang, Myoung Joo; Kim, Jong Gwang; Hwang, In Gyu; Choi, Jong-Kwon; Shin, Seong Hoon; Kang, Seok Yun; Lee, Sang-Cheol; Lim, Seung Taek; Kim, Jung Sun; Jeung, Hei-Cheul; Kang, Myoung Hee; Choi, In Sil; Ryu, Hye Won; Lee, Kyung Hee; Lee, Moon Hee; Lee, Ji Young; Park, Ji Hyun; Jeon, So-Yeon; Lee, Namsu; Park, Chi-Young; Kim, Yeul Hong.
Affiliation
  • Kim JH; Division of Oncology, Department of Internal Medicine, Korea University Anam Hospital, Korea University College of Medicine, Seoul, Republic of Korea.
  • Cha Y; Center for Colon Cancer, National Cancer Center, Goyang, Republic of Korea.
  • Shin SJ; Division of Medical Oncology, Department of Internal Medicine, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, Republic of Korea.
  • Park YS; Division of Hematology-Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.
  • Kang JH; Department of Internal Medicine, Gyeongsang University Hospital, Jinju, Republic of Korea.
  • Kim C; Department of Medical Oncology, CHA Bundang Medical Center, CHA University, Seongnam, Republic of Korea.
  • Lim SH; Division of Hematology-Oncology, Department of Internal Medicine, Soon Chun Hyang University, Bucheon Hospital, Bucheon-si, Republic of Korea.
  • Kang MJ; Department of Hemato-oncology, Inje University, Haeundae Paik Hospital, Busan, Republic of Korea.
  • Kim JG; Department of Oncology/Hematology, Kyungpook National University Chilgok Hospital, School of Medicine, Kyungpook National University, Daegu, Republic of Korea.
  • Hwang IG; Department of Internal Medicine, Chung-Ang University Hospital, Chung-Ang University College of Medicine, Seoul, Republic of Korea.
  • Choi JK; Division of Hematology and Medical Oncology, Department of Internal Medicine, Konyang University Hospital, Daejeon, Republic of Korea.
  • Shin SH; Department of Internal Medicine, Kosin University Gospel Hospital, Kosin University College of Medicine, Busan, Republic of Korea.
  • Kang SY; Department of Hematology-Oncology, Ajou University School of Medicine, Suwon, Republic of Korea.
  • Lee SC; Department of Internal Medicine, Soonchunhyang University Cheonan Hospital, Cheonan, Republic of Korea.
  • Lim ST; Department of Oncology, Yonsei University Wonju College of Medicine, Wonju, Republic of Korea.
  • Kim JS; Division of Hematology/Oncology, Department of Internal Medicine, Korea University Ansan Hospital, Korea University College of Medicine, Gyeonggi-do, Republic of Korea.
  • Jeung HC; Division of Medical Oncology, Department of Internal Medicine, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea.
  • Kang MH; Division of Hematology-Oncology, Department of Internal Medicine, Gyeongsang National University Changwon Hospital, Gyeongsang National University College of Medicine, Changwon, Republic of Korea.
  • Choi IS; Department of Internal Medicine, Seoul Metropolitan Government-Seoul National University Boramae Medical Center, Seoul, Republic of Korea.
  • Ryu HW; Division of Hematology and Oncology, Department of Internal Medicine, Chungnam National University Hospital, Chungnam National University College of Medicine, Daejeon, Republic of Korea.
  • Lee KH; Department of Internal Medicine, Yeungnam University College of Medicine, Daegu, Republic of Korea.
  • Lee MH; Department of Hematology-Oncology, Inha University College of Medicine and Hospital, Incheon, Republic of Korea.
  • Lee JY; Department of Oncology, Inje University Busan Paik Hospital, Inje University College of Medicine, Busan, Republic of Korea.
  • Park JH; Department of Internal Medicine, Konkuk University Medical Center, Konkuk University School of Medicine, Seoul, Republic of Korea.
  • Jeon SY; Department of Internal Medicine, Jeonbuk National University Medical School, Jeonju, Republic of Korea.
  • Lee N; Division of Hematology and Oncology, Department of Internal Medicine, Soonchunhyang University Seoul Hospital, Seoul, Republic of Korea.
  • Park CY; Department of Internal Medicine, Hemato-oncology, Chosun University Hospital, Gwangju, Republic of Korea.
  • Kim YH; Division of Oncology, Department of Internal Medicine, Korea University Anam Hospital, Korea University College of Medicine, Seoul, Republic of Korea; jhmnkim@naver.com.
Anticancer Res ; 44(1): 347-359, 2024 Jan.
Article in En | MEDLINE | ID: mdl-38160001
ABSTRACT
BACKGROUND/

AIM:

This study investigated the treatment patterns and prognosis of patients with metastatic or unresectable colorectal cancer (mCRC) treated with chemotherapy with targeting agents. PATIENTS AND

METHODS:

This longitudinal multicenter study included 963 patients with mCRC who were treated in Korea between 2016 and 2020. Treatment patterns and efficacy were compared according to the mutation status and clinical factors.

RESULTS:

As first-line therapy, most of the patients (83.5%) received FOLFOX plus bevacizumab (35.4%), followed by FOLFIRI plus bevacizumab (18.8%), FOLFIRI plus cetuximab (17.0%), and FOLFOX plus cetuximab (12.3%). Bevacizumab was the most frequent agent (78.8%) combined with chemotherapy in RAS-mutated CRC, while cetuximab (57.2%) in RAS wild-type CRC. Cetuximab was frequently combined with a doublet regimen in patients with left-sided CRC than in those with right-sided CRC (34.4% vs. 16%). As second-line therapy, most patients (63.4%) also received doublet regimens with bevacizumab, and FOLFIRI plus aflibercept was administered in 15.1%. The objective response rate with FOLFIRI plus cetuximab was significantly higher in patients with left-sided CRC than in those with right-sided CRC (59.2% vs. 30.8%, p=0.008) and marginally higher in patients with RAS wild-type CRC than in those with RAS-mutated CRC (55.6% vs. 0.0%, p=0.092). Progression-free survival (PFS) with FOLFOX plus bevacizumab was significantly shorter than that with FOLFIRI plus bevacizumab (p=0.030) in RAS-mutated CRC, whereas there were no significant differences between regimens in RAS wild-type CRC.

CONCLUSION:

In patients with unresectable metastatic colorectal cancer, doublet chemotherapy with targeting agents is the most common therapy and efficacy depends on the mutation status as well as clinical factors.
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Full text: 1 Database: MEDLINE Main subject: Rectal Neoplasms / Colorectal Neoplasms / Colonic Neoplasms Limits: Humans Language: En Year: 2024 Type: Article

Full text: 1 Database: MEDLINE Main subject: Rectal Neoplasms / Colorectal Neoplasms / Colonic Neoplasms Limits: Humans Language: En Year: 2024 Type: Article