Evidence map›Paper›PMID 40496305›Full record

ArticleEcancermedicalscience2025

Bevacizumab in recurrent epithelial ovarian cancer: real-world experience from a tertiary cancer hospital in India.

Ranti Ghosh, Debarshi Lahiri, Debjit Ghosh, Kushal Sen, Debanjan Chakraborty, Tapas Maji, Suparna Mazumder, Ranajit Mandal, Arit Bhattacharjee, Jayanta Chakrabarti

Abstract read
In one paragraph

Article in Ecancermedicalscience, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Ranti GhoshDepartment of Radiation Oncology, Chittaranjan National Cancer Institute, 37, SP Mukherjee Road, Kolkoata 700026, India.
Debarshi LahiriDepartment of Radiation Oncology, Chittaranjan National Cancer Institute, 37, SP Mukherjee Road, Kolkoata 700026, India.
Debjit GhoshDepartment of Radiation Oncology, Chittaranjan National Cancer Institute, 37, SP Mukherjee Road, Kolkoata 700026, India.
Kushal SenDepartment of Radiation Oncology, Chittaranjan National Cancer Institute, 37, SP Mukherjee Road, Kolkoata 700026, India.
Debanjan ChakrabortyDepartment of Radiation Oncology, Chittaranjan National Cancer Institute, 37, SP Mukherjee Road, Kolkoata 700026, India.
Tapas MajiDepartment of Radiation Oncology, Chittaranjan National Cancer Institute, 37, SP Mukherjee Road, Kolkoata 700026, India.
Suparna MazumderDepartment of Radio-Diagnosis, Chittaranjan National Cancer Institute, 37, SP Mukherjee Road, Kolkoata 700026, India.
Ranajit MandalDepartment of Gynae-Oncology, Chittaranjan National Cancer Institute, 37, SP Mukherjee Road, Kolkoata 700026, India.
Arit BhattacharjeeDepartment of Radiation Oncology, Chittaranjan National Cancer Institute, 37, SP Mukherjee Road, Kolkoata 700026, India.
Jayanta ChakrabartiDepartment of Surgical Oncology, Chittaranjan National Cancer Institute, 37, SP Mukherjee Road, Kolkoata 700026, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: In combination with chemotherapy, bevacizumab, a humanised monoclonal antibody against angiogenesis, significantly increases progression-free survival (PFS) in recurrent epithelial ovarian cancer (EOC). However, due to financial constraints, real-world experience with bevacizumab in EOC is lacking in Indian populations. This study assessed bevacizumab's efficacy with chemotherapy in platinum-sensitive and resistant EOC in resource-limited Indian populations. Method and materials: This retrospective study was conducted at a regional cancer hospital in eastern India. Platinum-sensitive and resistant recurrent EOC patients were enrolled between 2021 and 2024. Patients' demographic and treatment details were retrieved from hospital medical records. All patients received bevacizumab 7.5 mg/kg IV dose with chemotherapy followed by maintenance till disease progression or inadvertent toxicity occurred. Primary endpoints were PFS and objective response rate (ORR); secondary endpoints were overall survival (OS) and safety. Kaplan-Meier plot generated PFS and OS survival curves. Results: 48 patients were enrolled. With a median follow-up of 37 months, 46% of patients progressed on bevacizumab. The median duration of PFS was 17 months (95% CI, 14.31-19.68); it was slightly higher in platinum-sensitive patients at 18 months (95% CI, 14.25-21.74). Half of the patients achieved partial response, with an ORR of 66%. Median OS was not reached due to fewer events. The 3-year OS rate was 83%. About 15 patients who progressed on bevacizumab were able to receive further chemotherapy lines. No new safety concerns were noted. Only 4.2% of patients developed grade 3 proteinuria, one developed arterial thrombosis and two had grade 3 thrombocytopenia. Only one patient died due to a GI fistula. Conclusion: Bevacizumab plus chemotherapy followed by bevacizumab maintenance till disease progression significantly improved PFS in recurrent EOC. This real-world finding suggests a crucial insight into effective treatment options for financially compromised Indian populations with recurrent EOC.

Indexed as

bevacizumabepithelial ovarian canceroutcomerecurrent

Identifiers

PMID40496305
PMCPMC12149230

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