# Time to haematologist visit and non-haematological referral from primary health care during blood cancer diagnosis – findings from a large national survey in Australia

**Authors:** Mohammad Radwanur Talukder, Emily Kovacev, Bill Stavreski, Sarah DeLacey

PMC · DOI: 10.1186/s12885-026-15757-1 · BMC Cancer · 2026-02-17

## TL;DR

This study in Australia found that many blood cancer patients face long waits to see a haematologist and often get referred to other specialists during diagnosis.

## Contribution

The study provides new insights into diagnostic delays and referral patterns for blood cancers in Australia using a large national survey.

## Key findings

- 26.3% of patients had a delay of more than one month between their first PHC contact and seeing a haematologist.
- Women and regional Australians were more likely to experience extended PHC-haematologist visit intervals.
- Patients with indolent blood cancers were more likely to face delays or non-haematological referrals.

## Abstract

Blood cancers are the third most common cancer in Australia. However, little is known about their diagnostic pathway in the Australian context. This research aimed to assess the interval between first primary health care (PHC) contact and first haematologist visit, and referrals to specialists other than haematologists (non-haematological referrals) during blood cancer diagnoses.

An online national survey was conducted with patients living with blood cancers, such as leukaemia, lymphoma, multiple myeloma, myeloproliferative neoplasms (MPN) and myelodysplastic neoplasms (MDS) between October and November 2022. Univariate and adjusted logistic regression models were applied to examine sociodemographic factors (age, sex, income, residence location, country of birth, private health insurance) and type of blood cancers associated with extended PHC-haematologist visit intervals (> 1-month) and non-haematological referrals.

Of the total 1758 participants, 26.3% (95% CI 24.3, 28.4%) patients experienced an extended PHC-haematologist visit interval (> 1-month) and of 1749 participants, 24.8% (95% CI 22.8, 26.9%) patients experienced non-haematological referrals during their diagnosis stage. Women were more likely to report an extended PHC-haematologist visit interval (adjusted odds ratio aOR 1.38, 95% CI 1.10, 1.73) or non-haematological referrals (aOR 1.42, 95%CI 1.12, 1.80). Regional Australians (aOR 1.37, 95%CI 1.08, 1.73) were more likely to experience an extended PHC -haematologist visit interval, but the odds of non-haematological referrals was not significant for them. Being older (≥ 65 years) (aOR 0.59, 95% CI 0.36, 0.97) and overseas-born (aOR 0.73, 95%CI 0.54, 0.99) were associated with a lower likelihood of non-haematological referrals. Private insurance holders (aOR 1.19, 95% CI 1.05, 1.35) were also more likely to have specialist referrals other than haematologists. Patients with an indolent type of blood cancers, such as lymphomas, multiple myeloma and MDS, are more likely to experience an extended PHC-haematologist visit interval or non-haematological referrals.

A multi-pronged approach, including raising awareness of blood cancer signs and symptoms among both patients and health care professionals and improving access to GPs and specialist services, particularly in regional and rural Australia, is required to improve timely help-seeking during diagnosis. More evidence is also needed on clusters of non-specific symptoms indicative of haematological cancers underpinning guidelines and optimal care pathways to support possible use of automated software prompts and prompt diagnosis.

The online version contains supplementary material available at 10.1186/s12885-026-15757-1.

## Linked entities

- **Diseases:** blood cancer (MONDO:0002334), leukaemia (MONDO:0004355), lymphoma (MONDO:0003659), multiple myeloma (MONDO:0009693), myeloproliferative neoplasms (MONDO:0020076)

## Full-text entities

- **Diseases:** lymphadenopathy (MESH:D008206), bleeding (MESH:D006470), splenomegaly (MESH:D013163), fatigue (MESH:D005221), hairy cell leukaemia (MESH:D007943), Hodgkin (MESH:D006689), Burkitt's lymphoma (MESH:D002051), myelofibrosis (MESH:D055728), spinal cord compression (MESH:D013117), abnormal sweating (MESH:D013543), MDS (MESH:D009190), Blood Cancer (MESH:D019337), fever (MESH:D005334), disease (MESH:D004194), leucopenia (MESH:C536227), fractures (MESH:D050723), pain (MESH:D010146), Chronic leukaemia (MESH:D015451), skin problems (MESH:D012871), renal failure (MESH:D051437), polycythaemia rubra vera (MESH:D011087), shortness of breath (MESH:D004417), lump (MESH:C536531), Multiple myeloma (MESH:D009101), chronic lymphocytic leukaemia (MESH:D015461), Myeloproliferative neoplasm (MESH:D009369), acute promyelocytic leukaemia (MESH:D015473), bruising (MESH:D003288), amyloidosis (MESH:D000686), CNS lymphoma (MESH:D008223), aggressive B cell lymphoma (MESH:D016393), Leukaemia (MESH:D015458), anaemia (MESH:D000743), Hodgkin or NHL (MESH:D008228), Mantle cell lymphoma (MESH:D020522), pallor (MESH:D010167), Waldenstrom's macroglobulinaemia (MESH:D008258), follicular lymphoma (MESH:D008224), T cell lymphoblastic lymphoma (MESH:D016399), blood abnormalities (MESH:D006402), QLD (MESH:D000073605), Acute leukaemia (MESH:D054218), infection (MESH:D007239), cough (MESH:D003371), Essential thrombocythaemia (MESH:D020329)
- **Chemicals:** cholesterol (MESH:D002784)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

10 references — full list in the complete paper: https://tomesphere.com/paper/PMC12931068/full.md

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Source: https://tomesphere.com/paper/PMC12931068