Literature DB >> 18497506

Short time to progression under first-line chemotherapy is a negative prognostic factor for time to progression and residual survival under second-line chemotherapy in advanced pancreatic cancer.

Christina Herrmann1, Ulrich Abel, Wolfgang Stremmel, Dirk Jaeger, Thomas Herrmann.   

Abstract

OBJECTIVES: Second-line chemotherapy is widely used in advanced pancreatic cancer. However, only few data exist concerning the question who might benefit from second-line therapy. We intended to identify prognostic factors for time to second progression (TTP2) and residual survival following second-line chemotherapy of patients with advanced pancreatic cancer.
METHODS: We performed a retrospective cohort study on 78 patients who started palliative chemotherapy at our department from January 2004 to June 2006 due to advanced adenocarcinoma of the pancreas. 46 patients who progressed following first-line therapy were analyzed.
RESULTS: In multivariate analyses, time to first progression (TTP1) <6 months and elevated LDH at the time of diagnosis were shown to be strong and highly significant independent prognostic factors for TTP2 and residual survival. For patients with TTP1 <6 months, prognosis was poor with a median residual survival of 4.4 versus 7.5 months for those with TTP1 > or =6 months.
CONCLUSION: In our cohort of patients with advanced pancreatic cancer treated with second-line chemotherapy, TTP1 <6 months is a strong negative prognostic factor for TTP2 and residual survival. 2008 S. Karger AG, Basel.

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Year:  2008        PMID: 18497506     DOI: 10.1159/000134477

Source DB:  PubMed          Journal:  Oncology        ISSN: 0030-2414            Impact factor:   2.935


  5 in total

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Authors:  L Gutierrez-Sainz; D Viñal; J Villamayor; D Martinez-Perez; J A Garcia-Cuesta; I Ghanem; A Custodio; J Feliu
Journal:  Clin Transl Oncol       Date:  2021-04-17       Impact factor: 3.405

2.  FOLFOX as second-line chemotherapy in patients with pretreated metastatic pancreatic cancer from the FIRGEM study.

Authors:  Aziz Zaanan; Isabelle Trouilloud; Theofano Markoutsaki; Mélanie Gauthier; Anne-Claire Dupont-Gossart; Thierry Lecomte; Thomas Aparicio; Pascal Artru; Anne Thirot-Bidault; Fanny Joubert; Daniella Fanica; Julien Taieb
Journal:  BMC Cancer       Date:  2014-06-14       Impact factor: 4.430

3.  Modified FOLFIRINOX as a second-line therapy following gemcitabine plus nab-paclitaxel therapy in metastatic pancreatic cancer.

Authors:  Masashi Sawada; Akiyoshi Kasuga; Takafumi Mie; Takaaki Furukawa; Takanobu Taniguchi; Koshiro Fukuda; Yuto Yamada; Tsuyoshi Takeda; Ryo Kanata; Masato Matsuyama; Takashi Sasaki; Masato Ozaka; Naoki Sasahira
Journal:  BMC Cancer       Date:  2020-05-20       Impact factor: 4.430

4.  A randomised phase II study of modified FOLFIRI.3 vs modified FOLFOX as second-line therapy in patients with gemcitabine-refractory advanced pancreatic cancer.

Authors:  C Yoo; J Y Hwang; J-E Kim; T W Kim; J S Lee; D H Park; S S Lee; D W Seo; S K Lee; M-H Kim; D J Han; S C Kim; J-L Lee
Journal:  Br J Cancer       Date:  2009-10-13       Impact factor: 7.640

5.  Efficacy of Capecitabine Plus Oxaliplatin Combination Chemotherapy for Advanced Pancreatic Cancer after Failure of First-Line Gemcitabine-Based Therapy.

Authors:  Kwang Hyun Chung; Ji Kon Ryu; Jun Hyuk Son; Jae Woo Lee; Dong Kee Jang; Sang Hyub Lee; Yong-Tae Kim
Journal:  Gut Liver       Date:  2017-03-15       Impact factor: 4.519

  5 in total

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