Evidence map›Paper›PMID 40145628›Full record

ArticleCancer medicine2025

The Impact of Carboplatin Dosing Design Using Adjusted Serum Creatinine on Carboplatin Plus Paclitaxel Therapy for Ovarian Cancer.

Shu Kato, Kaede Baba, Kanako Mamishin, Mao Uematsu, Mai Shimura, Akira Hirota, Misao Fukuda, Nobuyuki Takahashi, Takehiro Nakao, Hiromichi Nakajima and 8 more

Abstract read
In one paragraph

Article in Cancer medicine, 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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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

18 authors.

Shu KatoDepartment of Pharmacy, National Cancer Center Hospital East, Kashiwa, Japan.
Kaede BabaDepartment of Pharmacy, National Cancer Center Hospital East, Kashiwa, Japan.ORCID https://orcid.org/0009-0001-3035-7073
Kanako MamishinDepartment of Pharmacy, National Cancer Center Hospital East, Kashiwa, Japan.
Mao UematsuDepartment of Medical Oncology, National Cancer Center Hospital East, Kashiwa, Japan.
Mai ShimuraDepartment of Medical Oncology, National Cancer Center Hospital East, Kashiwa, Japan.
Akira HirotaDepartment of Medical Oncology, National Cancer Center Hospital East, Kashiwa, Japan.
Misao FukudaDepartment of Medical Oncology, National Cancer Center Hospital East, Kashiwa, Japan.
Nobuyuki TakahashiDepartment of Medical Oncology, National Cancer Center Hospital East, Kashiwa, Japan.ORCID https://orcid.org/0000-0002-8592-6528
Takehiro NakaoDepartment of Medical Oncology, National Cancer Center Hospital East, Kashiwa, Japan.
Hiromichi NakajimaDepartment of Medical Oncology, National Cancer Center Hospital East, Kashiwa, Japan.
Chikako FunasakaDepartment of Medical Oncology, National Cancer Center Hospital East, Kashiwa, Japan.
Chihiro KondohDepartment of Medical Oncology, National Cancer Center Hospital East, Kashiwa, Japan.
Kenichi HaranoDepartment of Medical Oncology, National Cancer Center Hospital East, Kashiwa, Japan.
Yoichi NaitoDepartment of Medical Oncology, National Cancer Center Hospital East, Kashiwa, Japan.ORCID https://orcid.org/0000-0002-8490-9064
Nobuaki MatsubaraDepartment of Medical Oncology, National Cancer Center Hospital East, Kashiwa, Japan.ORCID https://orcid.org/0000-0002-9203-4245
Ako HosonoDepartment of Medical Oncology, National Cancer Center Hospital East, Kashiwa, Japan.
Toshikatsu KawasakiDepartment of Pharmacy, National Cancer Center Hospital East, Kashiwa, Japan.ORCID https://orcid.org/0000-0002-7697-5512
Toru MukoharaDepartment of Medical Oncology, National Cancer Center Hospital East, Kashiwa, Japan.ORCID https://orcid.org/0000-0002-8573-418X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCarboplatin (CBDCA) is a mainstay of chemotherapy for ovarian cancer and its dose is determined in proportion to the estimated creatinine clearance (CCr). Serum creatinine (SCr) values necessary to estimate CCr vary by measurement method: adding 0.2 mg/dL to SCr by enzymatic methods commonly used in Japan equates to SCr calculated using the Jaffe method, which is widely adopted outside Japan. Although adjustment by adding 0.2 mg/dL to SCr by enzymatic methods may avoid the potential overdose of CBDCA, its impact on the dose intensity (DI) of chemotherapy is unclear.

methodsWe retrospectively studied patients with ovarian cancer treated with CBDCA + paclitaxel (PTX) (TC) after primary surgery. Patients were classified into Cohort A (dose-dense [dd-]TC, SCr-adjusted, n = 18), B (dd-TC, non-adjusted, n = 8), C (tri-weekly [tw-]TC, SCr-adjusted, n = 6), and D (tw-TC, non-adjusted, n = 15), and DI and DI-related measures including average relative DI (ARDI, [RDI of CBDCA + RDI of PTX]/2]) known to correlate with patients' prognoses were compared.

resultsAlthough the DI of CBDCA did not differ between Cohorts A and B, the DI of PTX and proportion of patients with ARDI ≥ 85% were higher in Cohort A than B (78 vs. 13%, p = 0.002) as a result of less frequent treatment modification. There was no difference in these measures between Cohorts C and D.

conclusionAdjustment of SCr when calculating the CBDCA dose did not compromise the DI of total CBDCA and may rather contribute to maintaining DI in patients receiving dd-TC.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsCarboplatinCreatinineOvarian NeoplasmsPaclitaxelAdultAgedAged, 80 and overFemaleHumansMiddle AgedRetrospective StudiesCarboplatinCreatininePaclitaxeladjuvant chemotherapycarboplatincreatinineovarian cancerpaclitaxel

Identifiers

PMID40145628
PMCPMC11947989

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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.