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Early Tumor Shrinkage and Depth of Response as Predictors of Survival for Advanced Biliary Tract Cancer: An Exploratory Analysis of JCOG1113.
Okano, Naohiro; Morizane, Chigusa; Okusaka, Takuji; Sadachi, Ryo; Kataoka, Tomoko; Kobayashi, Satoshi; Ikeda, Masafumi; Ozaka, Masato; Mizutani, Tomonori; Sugimori, Kazuya; Todaka, Akiko; Shimizu, Satoshi; Mizuno, Nobumasa; Yamamoto, Tomohisa; Sano, Keiji; Tobimatsu, Kazutoshi; Katanuma, Akio; Gotoh, Kunihito; Yamaguchi, Hironori; Ishii, Hiroshi; Ohba, Akihiro; Furuse, Junji; Ueno, Makoto.
Affiliation
  • Okano N; Department of Medical Oncology, Kyorin University Faculty of Medicine, Tokyo, Japan.
  • Morizane C; Department of Hepatobiliary and Pancreatic Oncology, National Cancer Center Hospital, Tokyo, Japan.
  • Okusaka T; Department of Hepatobiliary and Pancreatic Oncology, National Cancer Center Hospital, Tokyo, Japan.
  • Sadachi R; JCOG Data Center/Operations Office, National Cancer Center Hospital, Tokyo, Japan.
  • Kataoka T; JCOG Data Center/Operations Office, National Cancer Center Hospital, Tokyo, Japan.
  • Kobayashi S; Department of Gastroenterology, Kanagawa Cancer Center, Yokohama, Japan.
  • Ikeda M; Department of Hepatobiliary and Pancreatic Oncology, National Cancer Center Hospital East, Kashiwa, Japan.
  • Ozaka M; Hepato-Biliary-Pancreatic Medicine Department, Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.
  • Mizutani T; Department of Medical Oncology, Kyorin University Faculty of Medicine, Tokyo, Japan.
  • Sugimori K; Gastroenterological Center, Yokohama City University Medical Center, Yokohama, Japan.
  • Todaka A; Division of Gastrointestinal Oncology, Shizuoka Cancer Center, Shizuoka, Japan.
  • Shimizu S; Department of Gastroenterology, Saitama Cancer Center, Saitama, Japan.
  • Mizuno N; Department of Gastroenterology, Aichi Cancer Center Hospital, Nagoya, Japan.
  • Yamamoto T; Department of Surgery, Kansai Medical University Hospital, Osaka, Japan.
  • Sano K; Department of Surgery, Teikyo University School of Medicine, Tokyo, Japan.
  • Tobimatsu K; Division of Gastroenterology, Department of Internal Medicine, Kobe University Graduate School of Medicine, Kobe, Japan.
  • Katanuma A; Center for Gastroenterology, Teine Keijinkai Hospital, Sapporo, Japan.
  • Gotoh K; Department of Surgery, National Hospital Organization Osaka National Hospital, Osaka, Japan.
  • Yamaguchi H; Department of Clinical Oncology, Jichi Medical University, Tochigi, Japan.
  • Ishii H; Clinical Research Center, Chiba Cancer Center, Chiba, Japan.
  • Ohba A; Department of Hepatobiliary and Pancreatic Oncology, National Cancer Center Hospital, Tokyo, Japan.
  • Furuse J; Department of Medical Oncology, Kyorin University Faculty of Medicine, Tokyo, Japan.
  • Ueno M; Department of Gastroenterology, Kanagawa Cancer Center, Yokohama, Japan.
Oncologist ; 29(1): e97-e107, 2024 Jan 05.
Article in En | MEDLINE | ID: mdl-37531645
ABSTRACT

BACKGROUND:

Recent studies suggest that early tumor shrinkage (ETS) and depth of response (DpR) reflect outcomes of chemotherapy in various cancers. This study evaluated the association of ETS and DpR with clinical outcomes using data from JCOG1113, which demonstrated the non-inferiority of gemcitabine plus S-1 (GS) to gemcitabine plus cisplatin (GC) for chemotherapy-naïve advanced biliary tract cancer. MATERIAL AND

METHODS:

In total, 354 (289 with measurable target lesions) patients enrolled in JCOG1113 were divided into ETS-unachieved and ETS-achieved groups (≥20% tumor reduction at week 6) and DpR-low and DpR-high groups (≥40% maximum shrinkage) until 12 weeks after enrollment. The impact of ETS and DpR on survival outcome was evaluated using the multivariable Cox proportional hazard model.

RESULTS:

The proportions of patients in the ETS-achieved and DpR-high groups were similar between the 2 treatment arms. The hazard ratios (HRs) of progression-free survival (PFS) and overall survival (OS) for the ETS-achieved group were 0.70 (95% confidence interval (CI), 0.52-0.93) and 0.60 (95%CI, 0.44-0.81), respectively. The HRs of PFS and OS for the DpR-high group were 0.67 (95%CI, 0.48-0.94) and 0.64 (95%CI, 0.46-0.90), respectively. In the subpopulation treatment effect pattern plot analysis, most patients in the ETS-achieved group in the GC arm did not experience disease progression after 12 weeks from the landmark.

CONCLUSION:

As on-treatment markers, ETS and DpR were effective tools. ETS was clinically useful, because it can be used to evaluate the outcomes of treatment early at a specific time.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bile Duct Neoplasms / Biliary Tract Neoplasms / Colorectal Neoplasms Type of study: Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Oncologist Journal subject: NEOPLASIAS Year: 2024 Document type: Article Affiliation country: Japan

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bile Duct Neoplasms / Biliary Tract Neoplasms / Colorectal Neoplasms Type of study: Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Oncologist Journal subject: NEOPLASIAS Year: 2024 Document type: Article Affiliation country: Japan