Evidence map›Paper›PMID 41709185›Full record

ArticleBMC cancer2026

Oxaliplatin induced peripheral neuropathy and associated factors among colorectal cancer patients in Tanzania.

Mohamed Salat Gonjobe, Nazima Dharsee, Emmanuel Mduma, Khamza Kibwana Maunda

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Article in BMC cancer, 2026. 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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5 · Who and what money

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4 authors.

Mohamed Salat GonjobeDepartment of Clinical Oncology, Muhimbili University of Health and Allied Sciences, P.O. Box 65001, Dar es Salaam, Tanzania. mansaa98@gmail.com.
Nazima DharseeDepartment of Clinical Oncology, Muhimbili University of Health and Allied Sciences, P.O. Box 65001, Dar es Salaam, Tanzania.
Emmanuel MdumaDepartment of Clinical Oncology, Muhimbili University of Health and Allied Sciences, P.O. Box 65001, Dar es Salaam, Tanzania.
Khamza Kibwana MaundaDepartment of Clinical Oncology, Muhimbili University of Health and Allied Sciences, P.O. Box 65001, Dar es Salaam, Tanzania.

Funding

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6 · The paper itself

Abstract

backgroundColorectal cancer (CRC) is one of the leading malignancies globally and chemotherapy forms the bulk of its management. Oxaliplatin is one of the standard drugs used for management of colorectal cancer. Oxaliplatin induced peripheral neuropathy (OIPN) is one of the most debilitating toxicities encountered which can lead to dose modification and premature treatment discontinuation with a great impact on quality of life. Therefore, we aimed to determine the prevalence, severity and factors associated with OIPN among colorectal cancer patients treated in Tanzania.

methodsThis retrospective cohort study conducted at Ocean Road Cancer Institute (ORCI) of histologically confirmed CRC patients who were on oxaliplatin-based chemotherapy regimens. Data was collected using EORT-QLQ CIPN20 questionnaire and analysis was done using SPSS version 23 and p value < 0.05 was considered statistically significant.

resultsA total of 62 patients were recruited, the prevalence of OIPN was 71% and 59.7% for acute and chronic symptoms respectively. Obese patients were 21.66 times higher at risk of suffering from chronic OIPN compared to individuals who have normal body weight (p < 0.05). Cumulative Dose ≤ 780 showed a protective effect (p < 0.005) in development of OIPN. For the severity of acute OIPN, it was found that 4.8% had grade 4 symptoms, while 8.1% had grade 3 symptoms, and 69.4% had grade 2 symptoms, and 17.7% of the patients had grade 1. In patients with chronic OIPN, 13.5% had grade 3 neuropathies, 24.3% had grade 2 and 62.2% had grade 1 neuropathy.

conclusionThe prevalence of acute and chronic OIPN among colorectal cancer patients managed at ORCI was 71.0% and 59.7% respectively, with most patients developing grade 1 and 2 neuropathy for both acute and chronic symptoms. Number of cycles, cumulative dose and BMI were the major factors associated with the neuropathy.

Indexed as

Antineoplastic AgentsAntineoplastic Combined Chemotherapy ProtocolsColorectal NeoplasmsOxaliplatinPeripheral Nervous System DiseasesAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedPrevalenceQuality of LifeRetrospective StudiesRisk FactorsAntineoplastic AgentsOxaliplatinColorectal cancerOcean Road Cancer InstituteOxaliplatinPeripheral neuropathy

Identifiers

PMID41709185
PMCPMC13020417

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