Evidence map›Paper›PMID 27211249›Full record

ArticleJournal of gastrointestinal cancer2016

Second-Line Palliative Chemotherapy in Advanced Gall Bladder Cancer, CAP-IRI: Safe and Effective Option.

Anant Ramaswamy, Vikas Ostwal, Nikhil Pande, Arvind Sahu, Sunny Jandyal, Mukta Ramadwar, Nitin Shetty, Shraddha Patkar, Mahesh Goel, Sudeep Gupta

Abstract read
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In one paragraph

Article in Journal of gastrointestinal cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.2field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 18 citations in OpenAlex.

  1. Trial
  2. Risk score for malignancy in patients with suspicious gallbladder lesions: Retrospective analysis of 175 cases.Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology · 2026
    Article
  3. Gallbladder cancer: Progress in the Indian subcontinent.World journal of clinical oncology · 2024
    Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Observational
  9. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Anant RamaswamyDepartment of Medical Oncology, TMH, E. Borges Road, Parel, Mumbai, 400012, India.
Vikas OstwalDepartment of Medical Oncology, TMH, E. Borges Road, Parel, Mumbai, 400012, India. dr.vikas.ostwal@gmail.com.
Nikhil PandeDepartment of Medical Oncology, TMH, E. Borges Road, Parel, Mumbai, 400012, India.
Arvind SahuDepartment of Medical Oncology, TMH, E. Borges Road, Parel, Mumbai, 400012, India.
Sunny JandyalDepartment of Medical Oncology, TMH, E. Borges Road, Parel, Mumbai, 400012, India.
Mukta RamadwarDepartment of Pathology, TMH, Mumbai, 400012, India.
Nitin ShettyDepartment of Interventional Radiology, TMH, Mumbai, 400012, India.
Shraddha PatkarDepartment of Surgical Oncology, TMH, Mumbai, 400012, India.
Mahesh GoelDepartment of Surgical Oncology, TMH, Mumbai, 400012, India.
Sudeep GuptaDepartment of Medical Oncology, TMH, E. Borges Road, Parel, Mumbai, 400012, India.
Borgess Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionGall bladder cancer (GBC) has high prevalence in the Indo-Gangetic belt in India. While the first-line chemotherapy (CT1) has been established as gemcitabine-platinum doublet in advanced GBC, there is no standard recommendation or guidelines regarding feasibility of second-line therapy.

methodsWe performed a retrospective analysis of all patients who received second-line of chemotherapy (CT2) at our institution from July 2012 to December 2014. Patient records were examined for efficacy and toxicity of administered CT2, along with response rates (RR) and survival. Potential prognostic factors were also evaluated.

resultsEighty-seven patients received CT2 in the predefined period. Ninety-nine percent of patients had received a gemcitabine-based regimen as CT1 with a median progression-free survival (PFS) of 5 months before CT2. 51.7 % patients had undergone surgery prior with 5.7 % patients having received radiotherapy previously. Prior to beginning CT2, PS was 0/1 in 67.8 % patients, albumin was >4 g% in 40.2 % and CA 19.9 was raised in a majority (66.7 %) patients, respectively. As per institution protocol, a majority of patients (89.6 %) were administered CAP-IRI regimen. Overall RR and disease control rates (DCR) were 21.8 % and 41.3 %, respectively. Median progression-free survival (PFS) and overall survival (OS) were 6 and 8 months, with no significant differences between CAP-IRI and other regimens. Adverse effects were tolerable, with dose reduced upfront in 23 % patients and 11.5 % patients during subsequent cycles of CT. ECOG Performance Status (PS) of 0/1 was a significant prognostic variable for OS on multivariate analysis (p = 0.003).

conclusionCAP-IRI is a well-tolerated second-line chemotherapeutic regimen in patients with advanced GBC. Careful selection of patients is required when administering second-line chemotherapy to advanced GBC patients, with particular emphasis on ECOG PS.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsCohort StudiesDeoxycytidineFemaleGallbladder NeoplasmsGemcitabineHumansHydrocarbons, ChlorinatedMaleMiddle AgedPalliative CarePrognosisProspective StudiesRetrospective StudiesDeoxycytidineGemcitabineHydrocarbons, ChlorinatedCAP-IRIGall bladder cancerSecond-line chemotherapy

Identifiers

PMID27211249
OpenAlexW2403585105

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.