Retrospective analysis of the efficacy and safety of neoadjuvant gemcitabine and cisplatin in muscle-invasive bladder cancer.

dc.contributor.author

Meleis, Laura

dc.contributor.author

Moore, Russell

dc.contributor.author

Inman, Brant A

dc.contributor.author

Harrison, Michael R

dc.date.accessioned

2022-02-01T01:25:09Z

dc.date.available

2022-02-01T01:25:09Z

dc.date.issued

2020-03

dc.date.updated

2022-02-01T01:25:08Z

dc.description.abstract

Background

Neoadjuvant cisplatin-based combination chemotherapy for muscle-invasive bladder cancer (MIBC) improves overall and disease-free survival. However, there is much debate over the optimal neoadjuvant regimen. Gemcitabine plus cisplatin (GC) has been the neoadjuvant regimen of choice for many institutions for patients with MIBC based on data extrapolated from the metastatic setting. Based on recent data, many institutions are transitioning to variations of methotrexate, vinblastine, doxorubicin, and cisplatin (MVAC) as the neoadjuvant regimen of choice.

Objective

To assess the effectiveness and safety of neoadjuvant chemotherapy with gemcitabine plus cisplatin in patients with muscle-invasive bladder cancer prior to cystectomy.

Methods

This is a single-center, retrospective, cohort study at Duke University Hospital (DUH). Patients included had MIBC and received gemcitabine plus cisplatin chemotherapy prior to a cystectomy. The primary endpoint was to assess the pathologic complete response (pCR) rate in MIBC after treatment with gemcitabine and cisplatin. Patients were split into two groups, those who received their chemotherapy at DUH, and those who received their chemotherapy at an outside facility.

Results

Overall pCR rate for all patients (n = 36) was 14%. The pCR rates for patients in the Duke Chemotherapy Group (n = 17) and in the Community Chemotherapy Group (n = 19) were 24% and 5%, respectively. GC was overall well tolerated in most patients with few adverse events ≥ grade 3.

Conclusions

This retrospective study demonstrates a consistent pCR rate (24% in Duke Chemotherapy Group) for neoadjuvant GC in MIBC compared with other literature. The overall pCR rate for all patients was 14%.
dc.identifier.issn

1078-1552

dc.identifier.issn

1477-092X

dc.identifier.uri

https://hdl.handle.net/10161/24268

dc.language

eng

dc.publisher

SAGE Publications

dc.relation.ispartof

Journal of oncology pharmacy practice : official publication of the International Society of Oncology Pharmacy Practitioners

dc.relation.isversionof

10.1177/1078155219845434

dc.subject

Humans

dc.subject

Muscle Neoplasms

dc.subject

Neoplasm Invasiveness

dc.subject

Cisplatin

dc.subject

Deoxycytidine

dc.subject

Antineoplastic Agents

dc.subject

Antimetabolites, Antineoplastic

dc.subject

Antineoplastic Combined Chemotherapy Protocols

dc.subject

Disease-Free Survival

dc.subject

Treatment Outcome

dc.subject

Neoadjuvant Therapy

dc.subject

Retrospective Studies

dc.subject

Cohort Studies

dc.subject

Adult

dc.subject

Aged

dc.subject

Aged, 80 and over

dc.subject

Middle Aged

dc.subject

Female

dc.subject

Male

dc.subject

Urinary Bladder Neoplasms

dc.title

Retrospective analysis of the efficacy and safety of neoadjuvant gemcitabine and cisplatin in muscle-invasive bladder cancer.

dc.type

Journal article

duke.contributor.orcid

Inman, Brant A|0000-0002-6060-4485

duke.contributor.orcid

Harrison, Michael R|0000-0003-3776-8892

pubs.begin-page

330

pubs.end-page

337

pubs.issue

2

pubs.organisational-group

Duke

pubs.organisational-group

School of Medicine

pubs.organisational-group

Clinical Science Departments

pubs.organisational-group

Institutes and Centers

pubs.organisational-group

Medicine

pubs.organisational-group

Surgery

pubs.organisational-group

Medicine, Medical Oncology

pubs.organisational-group

Surgery, Urology

pubs.organisational-group

Duke Cancer Institute

pubs.publication-status

Published

pubs.volume

26

Files

Original bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
Meleis JOncPharmPrac 2020.pdf
Size:
277.91 KB
Format:
Adobe Portable Document Format