Phase II study of S-1-based sequential combination chemotherapy including oxaliplatin plus bevacizumab and irinotecan with or without cetuximab for metastatic colorectal cancer: the SOBIC trial.


Journal

International journal of clinical oncology
ISSN: 1437-7772
Titre abrégé: Int J Clin Oncol
Pays: Japan
ID NLM: 9616295

Informations de publication

Date de publication:
Jul 2020
Historique:
received: 04 01 2020
accepted: 06 03 2020
pubmed: 23 3 2020
medline: 2 9 2020
entrez: 23 3 2020
Statut: ppublish

Résumé

Fluorouracil and leucovorin combined with oxaliplatin or irinotecan plus bevacizumab (Bmab) or cetuximab (Cmab) are now widely accepted treatment options as first-line or second-line chemotherapy for metastatic colorectal cancer (mCRC). Sequential chemotherapy with oral 5-FU backbone for mCRC without using central venous ports is beneficial for both patients and physicians. We designed the SOBIC trial to validate the effectiveness of the first- and second-line oral combination chemotherapy for mCRC. From May 2010 through March 2013, 52 patients were enrolled from 47 institutions in the Hyogo Colorectal Cancer Surgery Group. First-line chemotherapy was S-1 + oxaliplatin (SOX) plus Bmab, and second-line chemotherapy after first-line failure was irinotecan + S-1 (IRIS) + Cmab, IRIS + Bmab, or IRIS based on the KRAS status. The 50 finally included patients received first-line chemotherapy. Second-line therapy was administered to 20 patients (40%): 12 patients received IRIS + Cmab and 8 patients received IRIS + Bmab. The median follow-up period was 48.6 months (range 35-67 months). The median second progression-free survival was 24.2 months (95% confidence interval [CI] 17.7-35.2). The response rate after first- and second-line chemotherapy was 46.7% and 15%, respectively. The median overall survival was 35.2 months (95% CI: 27.8 to not reached). The main grade 3-4 adverse events were sensory neuropathy (18%) and fatigue (10%). There were no treatment-related deaths. Sequential S-1-based combination regimens including oxaliplatin, irinotecan, Bmab, and Cmab were beneficial for patients with mCRC.

Sections du résumé

BACKGROUND BACKGROUND
Fluorouracil and leucovorin combined with oxaliplatin or irinotecan plus bevacizumab (Bmab) or cetuximab (Cmab) are now widely accepted treatment options as first-line or second-line chemotherapy for metastatic colorectal cancer (mCRC). Sequential chemotherapy with oral 5-FU backbone for mCRC without using central venous ports is beneficial for both patients and physicians. We designed the SOBIC trial to validate the effectiveness of the first- and second-line oral combination chemotherapy for mCRC.
PATIENTS AND METHODS METHODS
From May 2010 through March 2013, 52 patients were enrolled from 47 institutions in the Hyogo Colorectal Cancer Surgery Group. First-line chemotherapy was S-1 + oxaliplatin (SOX) plus Bmab, and second-line chemotherapy after first-line failure was irinotecan + S-1 (IRIS) + Cmab, IRIS + Bmab, or IRIS based on the KRAS status.
RESULTS RESULTS
The 50 finally included patients received first-line chemotherapy. Second-line therapy was administered to 20 patients (40%): 12 patients received IRIS + Cmab and 8 patients received IRIS + Bmab. The median follow-up period was 48.6 months (range 35-67 months). The median second progression-free survival was 24.2 months (95% confidence interval [CI] 17.7-35.2). The response rate after first- and second-line chemotherapy was 46.7% and 15%, respectively. The median overall survival was 35.2 months (95% CI: 27.8 to not reached). The main grade 3-4 adverse events were sensory neuropathy (18%) and fatigue (10%). There were no treatment-related deaths.
CONCLUSION CONCLUSIONS
Sequential S-1-based combination regimens including oxaliplatin, irinotecan, Bmab, and Cmab were beneficial for patients with mCRC.

Identifiants

pubmed: 32200481
doi: 10.1007/s10147-020-01657-2
pii: 10.1007/s10147-020-01657-2
doi:

Substances chimiques

Drug Combinations 0
Oxaliplatin 04ZR38536J
S 1 (combination) 150863-82-4
Tegafur 1548R74NSZ
Bevacizumab 2S9ZZM9Q9V
Oxonic Acid 5VT6420TIG
Irinotecan 7673326042
Cetuximab PQX0D8J21J
Leucovorin Q573I9DVLP
Fluorouracil U3P01618RT

Types de publication

Clinical Trial, Phase II Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1285-1290

Auteurs

Yoshihiko Nakamoto (Y)

Department of Surgery, Meiwa Hospital, Nishinomiya, Hyogo, 663-8186, Japan. myy2000815@gmail.com.

Masafumi Noda (M)

Division of Lower GI Surgery, Department of Surgery, Hyogo College of Medicine, Nishinomiya, Japan.

Ryuichi Mikami (R)

Department of Surgery, Kobe City Medical Center West Hospital, Kobe, Japan.

Yukihiko Tokunaga (Y)

Department of Surgery, Japan Post Kyoto Teishin Hospital, Kyoto, Japan.

Tatsuo Okumoto (T)

Department of Surgery, Himeji St. Mary's Hospital, Himeji, Japan.

Takashi Kawamura (T)

Department of Surgery, Kakogawa City Hospital, Kakogawa, Japan.

Hidetoshi Fujiwara (H)

Department of Surgery, Sanda City Hospital, Sanda, Japan.

Sadayuki Doi (S)

Department of Surgery, Kawanishi City Hospital, Kawanishi, Japan.

Naohiro Tomita (N)

Division of Lower GI Surgery, Department of Surgery, Hyogo College of Medicine, Nishinomiya, Japan.

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Classifications MeSH