1/16
Why do we use a vaccine (BCG) to treat an unrelated malignancy (bladder cancer)?

Can infections really prevent/treat cancer?

Let's find out.
2/
This story begins in 1813 when Arsène-Hippolyte Vautier reported that patients suffering from gas gangrene experienced a decrease in the size of their malignant tumors.

An explanation (or even the causative bacterium!) wasn't immediately apparent.

pubmed.ncbi.nlm.nih.gov/28202530/
3/
Decades later, Williams Coley heard about the curious case of a man with inoperable sarcoma that disappeared after erysipelas developed.

The remission was durable out to at least 7 years.

dx.doi.org/10.1097/000006…
4/
After hearing about this case, Coley wondered whether intentional injection of Streptococcus pyogenes might work too.

In 1893 he reported tumor regression in several patients with this therapy.

What was going on?

dx.doi.org/10.1097/000006…
5/
In 1929, Raymond Pearl reported another curious finding.

In an autopsy study, he found a lower frequency of cancer in those with evidence of tuberculosis.

[I'll soon post a historical note on the problems with this study.]

doi.org/10.1093/oxford…
6/
Based on the above, researchers began to study Bacillus Calmette-Guerin (BCG). Old et al found that BCG-infected mice showed increased resistance to tumors.

In one experiment, the 48-day mortality was:
😀0% in BCG infected
🙁92% in uninfected controls

pubmed.ncbi.nlm.nih.gov/14428599/
7/
The first trial of BCG in humans wasn't actually for bladder cancer. Instead, it was for acute lymphoblastic leukemia (ALL).

30 patients with ALL in remission after chemo were treated. Relapse rates were:

😐63% in BCG treated
🙁100% in controls

pubmed.ncbi.nlm.nih.gov/4182654/
8/
Although many tumor types appeared to respond to BCG, bladder cancer emerged as the perfect option for this therapy.

Why?

Injecting the attenuated bacteria in the bladder allowed for a more controlled introduction to tumor cells.

pubmed.ncbi.nlm.nih.gov/17997439/
9/
The promise of BCG therapy in bladder cancer became clear with the results of a small trial by Morales et al.

They treated 9 patients with recurrent non-muscle invasive bladder cancer with BCG and found a 12-fold reduction in recurrence.

pubmed.ncbi.nlm.nih.gov/820877/
10/
In subsequent years, BCG has also been compared head-to-head against chemotherapy and proved superior.

The probability of disease-free survival at five years:
😐45% in BCG treated
🙁18% in doxorubicin treated

pubmed.ncbi.nlm.nih.gov/1922207/
11/
Overall, meta-analyses have demonstrated the following odds ratios for tumor recurrence:

☞ 0.61 (compared with control)
☞ 0.56 (compared to mitomycin C)

pubmed.ncbi.nlm.nih.gov/16765182/
pubmed.ncbi.nlm.nih.gov/15947584/
12/
What is BCG doing to cause this anti-tumor effect? The short answer, it is:

💥Immunotherapy💥

BCG activates nearly all aspects of the immune system, including both innate and adaptive.

pubmed.ncbi.nlm.nih.gov/24492433/
13/
While we often equate the immune system with our fight against infectious diseases, it also has a key role in tumor recognition and rejection.

The emergence of checkpoint inhibitors demonstrates well the power of immunotherapy.

pubmed.ncbi.nlm.nih.gov/28783669/
14/
Another mechanism of benefit with BCG may be Trained Immunity.

This is the concept that innate immune cells (e.g., macrophages) "trained" by one infection (or vaccine) respond with a heightened response to a second, unrelated, infection.

pubmed.ncbi.nlm.nih.gov/34131332/
15/
Before closing, it's worth mentioning another way immune activation by BCG can benefit.

Reduction in non-TB infections.

For example, a recent RCT reported a decrease in new infections after BCG vaccination:
🙁42% for placebo
🙂25% for BCG

pubmed.ncbi.nlm.nih.gov/32941801/
16/16 - SUMMARY
⚡️For centuries bacterial infections have been observed to reduce tumor size
⚡️These observations led to trials of BCG for cancer, including bladder cancer
⚡️BCG acts as a form of immunotherapy, leading to immune destruction of cancer cells

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More from @tony_breu

14 Aug
As I noted in a recent tweetorial, Raymond Pearl reported a lower frequency of cancer in those with evidence of tuberculosis.

This finding led Pearl and others to treat patients with tuberculin.

Unfortunately, Pearl's original study methods suffered from bias.
More specifically, Pearl's study sample contained an overrepresentation of exposed controls (i.e., control subjects who had died from tuberculosis).

This led to an incorrect conclusion that tuberculosis is associated with decreased rates of cancer.
Pearl published a "retraction" in Science.

While arguing that "any serious student of the matter" would agree that TB and cancer are rarely found together in the same person, he admits that concluding a mechanistic connection "may have been erroneous".

pubmed.ncbi.nlm.nih.gov/17777405/
Read 5 tweets
26 Jul
1/15
Why does clostridium difficile infection (CDI) cause marked leukocytosis?

Many of you have likely seen a new WBC >20k and wondered "could this patient have CDI?"

Are you right to wonder? If so, why?
2/
To start, is there a connection?

One of the earliest studies examined patients with WBC >30k. They reported the following rates of CDI:

🔹20% of all cases (excluding those with heme malignancy)
🔹34% of patients with an infectious etiology

pubmed.ncbi.nlm.nih.gov/12032893/
3/
In another study included 60 patients with unexplained leukocytosis (WBC >15k) and found:

⚡️58% had CDI⚡️

And: leukocytosis preceded recorded symptoms of colitis in half of the patients.

pubmed.ncbi.nlm.nih.gov/14599633/
Read 15 tweets
11 May
Great list Avi!

I'll add some relevant links for a few of these.
💻K/Mg repletion often unnecessary

Here is a tweetorial on potassium repletion/replacement.

💻Wilson disease evaluation in acute liver failure often not needed

@ebtapper and @ShaniHerzig wrote a great article in the @JHospMedicine Things We Do For No Reason Series on nondirected testing for inpatients with severe liver injury.

journalofhospitalmedicine.com/jhospmed/artic…
Read 6 tweets
17 Apr
1/6
Does doxycycline protect against clostridium difficile infection (CDI)?

If so, why?

These questions came up on rounds yesterday. Here are some potential answers.
2/
One study found an adjusted hazard ratio of 0.73 for CDI with the use of doxycycline.

A separate meta-analysis supported this finding with an odds ratio of 0.62 with all tetracyclines. The forest plot is attached.

pubmed.ncbi.nlm.nih.gov/22563022/
pubmed.ncbi.nlm.nih.gov/29401273/
3/
One potential explanation is that tetracyclines have in vitro activity against C. difficile.

This was demonstrated in a study reporting that 84% of C. difficile isolates had an MIC of ≤0.25 mg/L to tetracycline.

pubmed.ncbi.nlm.nih.gov/19732094/
Read 6 tweets
2 Apr
1/13
Why doesn't hemolysis cause acute kidney injury as easily as rhabdomyolysis?

I see a lot of hemolysis and can't think of a case of AKI that resulted.

Rhabdo? I immediately worry about AKI.

If heme is the toxic molecule, shouldn't both conditions be equally nephrotoxic?
2/
🔑Heme is contained in both hemoglobin and myoglobin and is the toxic molecule in BOTH hemolysis and rhabdomyolysis.

The mechanism of heme toxicity won't be covered in this thread. Instead, we'll stick with why rhabdo causes more AKI.

pubmed.ncbi.nlm.nih.gov/31018590/
3/
Before moving on, it is important to note that hemolysis CAN cause AKI.

Historically, massive hemolysis from ABO mismatch was a major cause. Now the causes are more varied.

pubmed.ncbi.nlm.nih.gov/31668630/
Read 13 tweets
31 Mar
1/9
Great question!

From what I gather, the exact explanation for the low alkaline phosphatase in Wilson's disease remains unexplained.
2/
The first description of the association between low AP and Wilson's came in a 1986 paper by Shaver, Bhatt, and Combes.

pubmed.ncbi.nlm.nih.gov/3758940/
3/
They describe patients with acute hemolytic anemia in the setting of Wilson's disease who are noted to have low AP.

They wonder whether the acute increase in serum copper may compete with zinc for incorporation into AP.

pubmed.ncbi.nlm.nih.gov/3758940/
Read 9 tweets

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